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INFORMATION FOR

    Smilow Shares: Breast Cancer Awareness Month: Early-Stage Breast Cancer

    October 30, 2025

    October 9, 2025

    Moderated by: Rachel Greenup, MD, MPH

    Presentations by:

    Elizabeth Berger, MD, MS, FACS

    Mariya Rozenblit, MD

    Siba Haykal, MD, PhD, FRCS, FACS

    ID
    13573

    Transcript

    • 00:00Good evening, and welcome to
    • 00:02the SmiloShares
    • 00:03early stage breast cancer session
    • 00:05entitled what patients and families
    • 00:07should know.
    • 00:08My name is doctor Rachel
    • 00:10Greenup. I'm the chief of
    • 00:11breast surgery
    • 00:13at the SMILO in the
    • 00:14department of surgery at the
    • 00:16Yale School of Medicine. And
    • 00:17tonight, we have three of
    • 00:18our esteemed colleagues, doctor Elizabeth
    • 00:20Berger,
    • 00:21doctor Siba Haykel, and doctor
    • 00:23Maria Rosenblatt.
    • 00:24And we're gonna start with
    • 00:26doctor Berger who's an assistant
    • 00:27professor of surgery in the
    • 00:29division of surgical oncology
    • 00:31who will talking be talking
    • 00:32to us about surgical updates
    • 00:34and breast cancer.
    • 00:35Doctor Berger, welcome.
    • 00:40Thank you so much for
    • 00:40that kind introduction, doctor Greenup.
    • 00:42Let me share my screen.
    • 00:49I get a thumbs up
    • 00:51so everyone can see it?
    • 00:52Great.
    • 00:53So tonight, I I'm gonna
    • 00:55spend about ten to fifteen
    • 00:56minutes talking about some of
    • 00:57the kind of updates of
    • 00:58as far as surgical care
    • 01:00in early stage breast cancer.
    • 01:02And I appreciate the time,
    • 01:03and, hopefully, we'll have time
    • 01:04for questions,
    • 01:05at the end if there
    • 01:06are some.
    • 01:07So the way we stage
    • 01:09breast cancers in just kind
    • 01:10of context as far as
    • 01:11early stage goes is is
    • 01:12multiple different ways. We think
    • 01:13about how big the tumor
    • 01:15size is, how how many
    • 01:16lymph nodes may or may
    • 01:17not be involved, and we
    • 01:19essentially come up with a
    • 01:20stage of breast cancer. And
    • 01:21doctor Rosenblatt will probably get
    • 01:22into this in more detail,
    • 01:24but the biology of tumors
    • 01:25now is so much more
    • 01:26important than stage. But we
    • 01:28still stage breast cancers based
    • 01:29upon the staging,
    • 01:31schema.
    • 01:32And what we'll be talking
    • 01:33about tonight is really this
    • 01:35category of kind of stage
    • 01:36zero, if you will, to
    • 01:37stage two breast cancer is
    • 01:38considered early stage.
    • 01:40Stage zero breast cancer, kind
    • 01:42of an enigma and doesn't
    • 01:44make that much sense, but
    • 01:45we really refer to what's
    • 01:46called ductal carcinoma in situ
    • 01:48as stage zero breast cancer.
    • 01:50Or for a lot of
    • 01:51my patients, when I say
    • 01:52a precancerous process,
    • 01:53it's in situ disease, meaning,
    • 01:55you know, the abnormal cells
    • 01:56are contained within the ducts.
    • 01:58There's no invasion that we've
    • 02:00identified.
    • 02:01And so,
    • 02:03you know, we really think
    • 02:04that this is a precancerous
    • 02:05lesion or stage
    • 02:10We still think that we
    • 02:11should take all of DCIS
    • 02:12out. We should remove it
    • 02:14surgically
    • 02:15because we thought all DCIS
    • 02:16became an invasive cancer at
    • 02:18some point.
    • 02:20Now what we know with
    • 02:21ongoing clinical trials is maybe
    • 02:23some DCIS
    • 02:24never becomes invasive cancers,
    • 02:26and we can actually safely
    • 02:28observe or survey DCIS without
    • 02:31actually having to remove it.
    • 02:33So stay tuned.
    • 02:34Hopefully, in maybe two thousand
    • 02:35and thirty, we'll hear more
    • 02:37about,
    • 02:38stage zero or precancerous lesions
    • 02:40such as DCIS
    • 02:41being able to,
    • 02:43stay in the breast, not
    • 02:44have to be removed because
    • 02:45of these ongoing clinical trials.
    • 02:48So much of breast cancer
    • 02:48care as I think everyone's
    • 02:50call knows is really based
    • 02:51upon really good clinical trial
    • 02:53data, which is really exciting
    • 02:54for all of us as
    • 02:56providers and for patients.
    • 02:58So if we're gonna talk
    • 02:59about surgery for breast cancer,
    • 03:00because surgery for breast cancer
    • 03:02is is still important,
    • 03:04we think about kind of
    • 03:05where we've we've been and
    • 03:06where we're going. So
    • 03:08doctor Halsted used to perform
    • 03:10what's called the radical mastectomy
    • 03:11where we'd remove the chest,
    • 03:13the the breast, the, pectoralis
    • 03:16major and minor muscles.
    • 03:17And now we know for
    • 03:19breast cancer care that we
    • 03:20can really preserve the breast.
    • 03:22We can often do what's
    • 03:23called lumpectomies where we do
    • 03:25breast conservation and not remove
    • 03:27the whole breast,
    • 03:28and give patients similar, you
    • 03:30know, the same outcomes from
    • 03:31their cancer care.
    • 03:37So and I recognize, but
    • 03:39the the point the point
    • 03:40of the slide is that,
    • 03:42in the nineteen seventies, we
    • 03:44started to ask these big
    • 03:45questions for surgical care for
    • 03:47breast cancer. And we realized
    • 03:49that in the nineteen seventies,
    • 03:50we didn't have to remove
    • 03:52the whole breast,
    • 03:53and we could do breast
    • 03:54conservation with radiation.
    • 03:56We then, if we pivoted
    • 03:57towards the nineteen nineties, realized
    • 03:59that we didn't have to
    • 04:00do so much axillary surgery
    • 04:02for early stage breast cancers.
    • 04:04The z eleven trial was
    • 04:06instrumental
    • 04:06in allowing our patients to
    • 04:08have less axillary surgery
    • 04:10even if they had a
    • 04:11few lymph nodes with cancer
    • 04:12in it. And now fast
    • 04:14forward to the, you know,
    • 04:16kind of present time where
    • 04:18we can do,
    • 04:19maybe even less surgery for
    • 04:20DCIS, and we just observe
    • 04:22DCIS.
    • 04:23So these are some of
    • 04:24the really, important,
    • 04:27practice changing trials for breast
    • 04:28cancer care, especially in the
    • 04:30early stage setting.
    • 04:33We even may go as
    • 04:34far as to say and,
    • 04:35again, a little bit more
    • 04:36in advanced, breast cancer settings,
    • 04:38but we even may as
    • 04:39go as to far as
    • 04:40to say, if a woman
    • 04:41gets chemotherapy before surgery and
    • 04:44there's no cancer left in
    • 04:45the breast, we may be
    • 04:46even able to avoid surgery
    • 04:48altogether.
    • 04:49This is, I think, too
    • 04:50early for prime time, not
    • 04:51not ready yet,
    • 04:53but something potentially down the
    • 04:55pipe.
    • 04:58So if we are gonna
    • 04:58do surgery for early stage
    • 05:00breast cancers,
    • 05:01what are some of the
    • 05:02updates? And I'll go through
    • 05:03these in a kind of
    • 05:04brief,
    • 05:05review
    • 05:06as far as thinking about,
    • 05:08we do have noncancerous lesions
    • 05:09that we often take out
    • 05:10for breast,
    • 05:11as breast surgeons. We do
    • 05:12a lot of now more
    • 05:13oncoplastic work, which I'll touch
    • 05:15on, briefly.
    • 05:16We have some nipple sparing
    • 05:17mastectomy updates as far as,
    • 05:19nipple as far as sensation
    • 05:21preservation
    • 05:22and, potentially, you know, different
    • 05:24options for reduction of lymphedema.
    • 05:26So a lot of women
    • 05:28will get diagnosed
    • 05:30with these things called high
    • 05:30risk lesions. They're not actually
    • 05:31breast cancers, but sometimes,
    • 05:34if they're in the breast
    • 05:35and we remove it, we
    • 05:36may find some underlying,
    • 05:38essentially, precancer or DCIS diagnoses.
    • 05:41So if a woman gets
    • 05:42biopsy and has what's called
    • 05:43atypical ductal hyperplasia,
    • 05:45it is something that you
    • 05:46wanna, consider seeing a breast
    • 05:48surgeon for because it may
    • 05:50be something we would talk
    • 05:51to you you about removal
    • 05:52of.
    • 05:53Someone may get diagnosed with
    • 05:54what's called LCIS or lobular
    • 05:56carcinoma in situ, and it's
    • 05:58alarming for patients and often
    • 06:00get a a phone call
    • 06:01from their primary doctor saying,
    • 06:02you know, you have an
    • 06:04carcinoma.
    • 06:05But what we know about
    • 06:06LCIS,
    • 06:07that we actually don't need
    • 06:08to take it out. It
    • 06:09doesn't become a breast cancer,
    • 06:11and it's something that we
    • 06:12can watch,
    • 06:13recognizing
    • 06:14that it's a marker of
    • 06:15risk. And then, you know,
    • 06:17further things in the breast
    • 06:18that can be diagnosed
    • 06:20are the
    • 06:21scars and papillomas.
    • 06:23All
    • 06:25some times,
    • 06:26again, considering
    • 06:29high risk lesions.
    • 06:32Some we recommend,
    • 06:34excision for, and some we
    • 06:35don't recommend excision for.
    • 06:38A lot of women ask,
    • 06:39well, how are you gonna
    • 06:40find who you're gonna be
    • 06:41able to identify to get
    • 06:42the the tumor out? And,
    • 06:43unfortunately, that little biopsy clip
    • 06:44get that gets left is
    • 06:46not big enough for us
    • 06:47as breast cancer surgeons to
    • 06:48find on our own. So
    • 06:50we need some help to
    • 06:51be able to find that
    • 06:52lesion, and it's always disappointing
    • 06:53for the patient when we
    • 06:54say we have to put
    • 06:55in another thing into the
    • 06:57breast before surgery, but it's
    • 06:59very helpful for us, to
    • 07:00be able to find accurately
    • 07:01and pinpoint exactly where we
    • 07:03need to go. So we
    • 07:04used to use wires.
    • 07:06And now,
    • 07:07because of all the sometimes
    • 07:09chaos that can happen with
    • 07:10wires, sometimes we'll use what's
    • 07:12called a tag or even
    • 07:14a smaller device that goes
    • 07:16into the breast a few
    • 07:17days before surgery,
    • 07:18and then often doesn't delay
    • 07:20surgeries.
    • 07:21A patient can get it,
    • 07:22you know, a few days
    • 07:23before on their own time,
    • 07:25and it allows
    • 07:27often
    • 07:29to you know, a little
    • 07:30bit, at different locations of
    • 07:32the breast. Wires are still
    • 07:33used. They're great technology.
    • 07:35It's a very per, kind
    • 07:36of surgeon preference and personal
    • 07:38preference for the patient as
    • 07:39well, but they're just different
    • 07:41ways to, think about localization.
    • 07:45Some women will come into
    • 07:47our our
    • 07:48clinic with, you know, these
    • 07:49very large areas of, for
    • 07:50instance, calcifications
    • 07:52or even a large breast
    • 07:53tumor,
    • 07:55where, you know, we recommend
    • 07:56surgery first.
    • 07:58And sometimes, you know, there
    • 07:59may be no other option
    • 08:01but a mastectomy.
    • 08:02But sometimes we have really
    • 08:03nice options
    • 08:04where we can do a
    • 08:04very large resection and work
    • 08:06very closely with our plastic
    • 08:07surgeons, doctor Hakal and others,
    • 08:09where we can do what's
    • 08:10called an oncoplastic reduction. And
    • 08:12so it allows us as
    • 08:13breast cancer surgeons, even an
    • 08:14early stage breast cancer, to
    • 08:16take out a large piece
    • 08:17of tissue,
    • 08:18and really reduce or, you
    • 08:20know, do what's called a
    • 08:21mastopexy lift of the breast,
    • 08:23and leave a woman with
    • 08:24an amazing, reconstructive result,
    • 08:27but still take out a
    • 08:28fair amount of breast tissue
    • 08:29and and get out the
    • 08:30cancer safely.
    • 08:32When we are taking
    • 08:35out early stage cancers, we
    • 08:37all kinda make sure that
    • 08:38we get clear margins around
    • 08:40the cancer. And I think
    • 08:41this is can be a
    • 08:42very confusing,
    • 08:43for patients to understand.
    • 08:45So when we think about
    • 08:46clear margins,
    • 08:48what essentially what we wanna
    • 08:49do is we wanna take
    • 08:50out, the cancer,
    • 08:52and then we always want
    • 08:53some healthy breast tissue
    • 08:55around that cancer.
    • 08:57And so, you know, unfortunately,
    • 08:59when we have what's called
    • 09:00a positive margin,
    • 09:01what that means is is
    • 09:02the what we hope is
    • 09:04healthy breast tissue. Again, unfortunately,
    • 09:06this is all microscopic
    • 09:07disease.
    • 09:08What we what a healthy
    • 09:09breast tissue margin we we
    • 09:11removed
    • 09:12comes back underneath the microscope
    • 09:13with some cancer on the
    • 09:14edge of that margin. And
    • 09:16that does often require us
    • 09:18to go back to the
    • 09:18operating room with the patient
    • 09:19to take, again, a little
    • 09:21bit more tissue.
    • 09:22It doesn't mean that the
    • 09:23cancer has spread all over
    • 09:24the store. It doesn't mean
    • 09:26that,
    • 09:27you know, we missed something
    • 09:29per se. Unfortunately,
    • 09:30you know, we don't have,
    • 09:32X-ray vision. If we did,
    • 09:33that would be awesome.
    • 09:35But since we don't, it's
    • 09:36just a matter of where
    • 09:37the pathologist, the doctors that
    • 09:39look at things underneath the
    • 09:40microscope, really have to examine
    • 09:41that tissue to make sure
    • 09:43that the cancer cells are
    • 09:44clean of the edge.
    • 09:47We also want cancer cells
    • 09:48clean of the edge when
    • 09:49we do DCIS,
    • 09:51surgeries as well,
    • 09:53and we always,
    • 09:54kinda shoot for this idea
    • 09:55of two millimeters from the
    • 09:56edge of the piece of
    • 09:57tissue when we take out
    • 09:58margins.
    • 10:01At Yale, the the study
    • 10:03done to look at margins
    • 10:05when we do remove breast
    • 10:06tissue around,
    • 10:08the the,
    • 10:11cancer was done,
    • 10:12by doctor Chagpar, who's no
    • 10:14longer here at Yale, but
    • 10:15she led this trial at
    • 10:16Yale. And it was a
    • 10:17really well done trial to
    • 10:20show how we can take
    • 10:21these,
    • 10:22this healthy breast tissue around
    • 10:24the cancer.
    • 10:26As far as some of
    • 10:27the mastectomy updates for early
    • 10:28stage breast cancers, so when
    • 10:30we think about mastectomies,
    • 10:33there's multiple different ways to
    • 10:34do mastectomies, multiple different types
    • 10:36of reconstruction.
    • 10:37And one of the ways
    • 10:38now is what we can
    • 10:39do is called a nipple
    • 10:40sparing mastectomy.
    • 10:42Yes, we know ducts do
    • 10:44go into the nipple, and
    • 10:45so sometimes there's fear that,
    • 10:47you know, that may increase
    • 10:48a woman's risk of developing
    • 10:49a breast cancer if they
    • 10:50have, for instance, the BRCA
    • 10:52gene and want a prophylactic
    • 10:53mastectomy.
    • 10:54Or it may you know,
    • 10:55there there may be some
    • 10:56fear about risk of recurrence,
    • 10:58if a patient has cancer
    • 10:59and has a nipple sparing
    • 11:00mastectomy.
    • 11:01And a lot of really
    • 11:02well done trials, you'll see
    • 11:03doctor Greenup on this study,
    • 11:05I should say.
    • 11:07There's been a lot of
    • 11:08work done in whether or
    • 11:09not nipple sparing mastectomies are
    • 11:11safe for our cancer patients
    • 11:12in the early stage setting
    • 11:13and in the prophylactic setting
    • 11:15for our BRCA carrier patients.
    • 11:17And what we found from
    • 11:18multiple trials now or studies,
    • 11:21I guess, I should articulate,
    • 11:22is that, it is a
    • 11:23very, very safe procedure for
    • 11:26women to have done. Not
    • 11:27everyone will qualify for a
    • 11:29nipple sparing for various reasons,
    • 11:32but,
    • 11:33you know, in the setting
    • 11:34that it's it's, a reasonable
    • 11:35operation for a patient, it's
    • 11:37safe.
    • 11:39Contralateral prophylactic mastectomy. So this
    • 11:42is a whole another discussion
    • 11:43about when a woman has
    • 11:44an affected breast with breast
    • 11:46cancer.
    • 11:47What about removing the other
    • 11:49breast? You know, there's a
    • 11:50lot of discussion about whether
    • 11:51breast cancer spreads from one
    • 11:53breast to the other, and
    • 11:54that's actually not the case.
    • 11:55We know that breast cancers
    • 11:56don't spread from the right
    • 11:58breast, for instance, to the
    • 11:59left breast, but we do
    • 12:00know that a woman's at
    • 12:01a higher risk of developing
    • 12:03a contralateral cancer if they
    • 12:04have a breast cancer in
    • 12:05one of their breast.
    • 12:07What we do know is
    • 12:08that
    • 12:09removing the contralateral breast does
    • 12:11decrease that woman's risk of
    • 12:13getting a breast cancer, but
    • 12:14doesn't improve their survival from
    • 12:16their actual cancer in their
    • 12:17in their breast.
    • 12:19It's something to consider. It's
    • 12:20definitely a conversation to have
    • 12:22with your surgeon.
    • 12:24And, you know, some women
    • 12:25elect to do it for
    • 12:25a very personal reason, and
    • 12:27some women don't. It's just
    • 12:28something to always kind of
    • 12:30think about.
    • 12:32As far as nipple sin
    • 12:34neurotization
    • 12:35now, so,
    • 12:36there is some
    • 12:38data to suggest that we
    • 12:40may be able to reneurotize
    • 12:42or essentially give sensation to
    • 12:44the mastectomy skin when we
    • 12:46remove the breast. Oftentimes, we
    • 12:48remove the breast, the skin
    • 12:49is innervated or gets its
    • 12:50sensation from the breast, And
    • 12:52so the skin loses sensation.
    • 12:54It becomes numb.
    • 12:55And now, you know, there
    • 12:57is some,
    • 12:58ability
    • 12:59to find these nerves along
    • 13:01the the outside part of
    • 13:03the breast,
    • 13:04connect,
    • 13:05what's called an allograph. So
    • 13:06it's a cadaver nerve,
    • 13:08and then so that also
    • 13:10into nerves underneath the nipple
    • 13:12to try to preserve some
    • 13:13sensation.
    • 13:15There's
    • 13:16some data to suggest that
    • 13:18it works and then some
    • 13:19data to suggest that it's
    • 13:20it's not perfect,
    • 13:22and that it doesn't always
    • 13:23work. And so, you know,
    • 13:25I think this is, you
    • 13:26know, kinda two weeks continued.
    • 13:29You know, I think often
    • 13:30it's worth a try, and
    • 13:32then, you know, sometimes,
    • 13:34you know, we'll just have
    • 13:35to see what the data
    • 13:36shows as far as long
    • 13:37term outcomes,
    • 13:38because it may not, hold
    • 13:40true to for every woman.
    • 13:44There's been a lot of
    • 13:46changes in the way we
    • 13:48think about removing lymph nodes
    • 13:49underneath the armpit for early
    • 13:50stage breast cancers, which is
    • 13:52really exciting for patients.
    • 13:54We used to have to
    • 13:55remove all the lymph nodes
    • 13:56underneath the armpit all the
    • 13:57time, and it caused a
    • 13:58lot of morbidity for our
    • 14:00patients. And now what we
    • 14:01know, we can really only
    • 14:02have to remove a few
    • 14:03lymph nodes off in called
    • 14:05a sentinel lymph node biopsy
    • 14:06and leave the the rest
    • 14:08of the lymph nodes to
    • 14:09avoid that really, you know,
    • 14:10unfortunate risk of what's called
    • 14:12lymphedema, the swelling of the
    • 14:13arm.
    • 14:14As I spoke, earlier on,
    • 14:16the z eleven trial was
    • 14:17the trial in the early
    • 14:18two thousands that showed us
    • 14:20that if a woman has
    • 14:21only one or two positive
    • 14:23lymph nodes at the time
    • 14:24of surgery, we don't have
    • 14:26to necessarily remove all the
    • 14:27lymph nodes.
    • 14:29Now we even know
    • 14:31that with women who have
    • 14:32early stage slow growing cancers,
    • 14:35the hormone receptor positive breast
    • 14:36cancers,
    • 14:37we actually don't even have
    • 14:38to remove lymph nodes at
    • 14:40all. So we don't even
    • 14:41have to do that sentinel
    • 14:42lymph node biopsy.
    • 14:44If a woman has small
    • 14:45cancers, hormone receptor positive,
    • 14:48two trials were done, kind
    • 14:50of right near each other,
    • 14:51one in Europe and one
    • 14:53in the UK,
    • 14:54that showed us that there
    • 14:55was no difference in outcomes
    • 14:56whether we actually remove lymph
    • 14:58nodes at all.
    • 15:00This was just a a
    • 15:01little bit more detail on
    • 15:02the sound trial that allowed
    • 15:04us again to show if
    • 15:05a woman has a normal
    • 15:06axillary ultrasound before surgery, we
    • 15:09do breast conservation.
    • 15:11We don't have to remove
    • 15:12lymph nodes. And this was
    • 15:13the INSEMA trial in Europe,
    • 15:15again, showing essentially the same
    • 15:17results. As you can see,
    • 15:18the surgical complications
    • 15:20are real when we have
    • 15:22to remove lymph nodes, and
    • 15:24they did a really nice
    • 15:24job demonstrating that when we
    • 15:26omit removing lymph nodes, women
    • 15:28have a lot less, surgical
    • 15:30complications.
    • 15:32We give neoadjuvant chemotherapy, meaning
    • 15:34chemotherapy before surgery and sometimes
    • 15:37still early stage breast cancers
    • 15:38if they're more aggressive, like
    • 15:39the triple negative setting and
    • 15:41the HER2 positive setting.
    • 15:42And now what we know
    • 15:43is
    • 15:44that if we remove lymph
    • 15:46nodes after chemotherapy
    • 15:49and there's no cancer left
    • 15:50in any of them, we
    • 15:52don't have to take out
    • 15:52all that lymph nodes underneath
    • 15:54the armpit.
    • 15:55However, stay tuned because even
    • 15:58now, when we have a
    • 15:59few lymph nodes that still
    • 16:00have cancer in it after
    • 16:01chemotherapy,
    • 16:02we may not need to
    • 16:03take out all the rest
    • 16:04of them, and we may
    • 16:05be able to, offer the
    • 16:07patient radiation alone. So these
    • 16:09results are hopefully coming in
    • 16:10the next four to five
    • 16:11to ten years,
    • 16:13but I think this will
    • 16:13be practice changing patients
    • 16:15as
    • 16:16well.
    • 16:19And doctor Hickall may get
    • 16:20into this in a little
    • 16:21bit more detail later, but
    • 16:22we now know that if
    • 16:23we do have to remove
    • 16:24all the lymph nodes, even
    • 16:25still for an early stage
    • 16:26breast cancer, it can happen.
    • 16:28We can do techniques now
    • 16:29to hopefully avoid, the horrible
    • 16:31complication of lymphedema,
    • 16:33where we can connect a
    • 16:35vein and a lymphatic, a
    • 16:37little channel in the armpit.
    • 16:38And, again, I ideally, allow
    • 16:40our patients to suffer less
    • 16:42from potential complications of lymphedema.
    • 16:45There are ongoing clinical trials
    • 16:47in this country looking at
    • 16:48this very idea to hopefully
    • 16:50have to show that there
    • 16:52are good outcomes with it,
    • 16:54but stay tuned as well.
    • 16:56And I think that's all
    • 16:57I have. Thank you so
    • 16:58much for the time, and
    • 16:59I'd love to take questions
    • 17:00at the end.
    • 17:01Thank you so much, doctor
    • 17:03Berger. And we're gonna move
    • 17:04on to our two additional
    • 17:05speakers. We'll take questions at
    • 17:07the end, and I'll be
    • 17:08responding in real time in
    • 17:09the chat.
    • 17:11This is really meant to
    • 17:12highlight our multidisciplinary
    • 17:13team approach.
    • 17:14Next up is doctor Siva
    • 17:16Haykal, associate professor of plastic
    • 17:18surgery and section chief of
    • 17:20oncoplastic
    • 17:21reconstruction.
    • 17:22Tonight, she'll be talking about
    • 17:24breast reconstruction
    • 17:25and early stage breast cancer.
    • 17:26Thank you, doctor Haykel.
    • 17:28Thank you so much, doctor
    • 17:29Greenup, and thank you, doctor
    • 17:31Berger, for an amazing talk.
    • 17:33I'll be sharing my screen.
    • 17:42Please let me know if
    • 17:43you can see it.
    • 17:48Great. Thank you.
    • 17:50Okay. Great. So we're gonna
    • 17:51talk about breast reconstruction,
    • 17:53and,
    • 17:55I'm open to questions at
    • 17:56the end. Hopefully, I can
    • 17:57answer some of the questions
    • 17:58by going through,
    • 18:00some of the slides and
    • 18:01some of the techniques where,
    • 18:03breast,
    • 18:04breast cancer surgeons are working
    • 18:06in collaboration with reconstructive
    • 18:09surgeons,
    • 18:10in order to achieve a
    • 18:11great outcome.
    • 18:13So let's talk about breast
    • 18:14reconstruction. So it can either
    • 18:16be immediate, which is at
    • 18:18the time of mastectomy,
    • 18:19and we'll talk about lumpectomy
    • 18:21as well, or it can
    • 18:22be delayed, which is any
    • 18:23day after the mastectomy.
    • 18:26How do we determine the
    • 18:28best options,
    • 18:29and, how do we make
    • 18:30a decision? So it has
    • 18:32to do with patient preference,
    • 18:34the need for postoperative treatments
    • 18:36such as chemotherapy or radiation,
    • 18:39whether we have donor sites,
    • 18:40and I'll talk about what
    • 18:41that means,
    • 18:43other medical issues, and recovery
    • 18:45time.
    • 18:46So I'll first talk about
    • 18:47oncoplastic
    • 18:48reconstruction.
    • 18:49So doctor Berger mentioned it
    • 18:51a little bit, but oncoplastic
    • 18:53reconstruction
    • 18:54basically involves,
    • 18:57rearranging breast tissue after a
    • 18:59lumpectomy for breast cancer
    • 19:01to achieve a better aesthetic
    • 19:03result. So when a portion
    • 19:04of the breast is removed,
    • 19:06it can cause some dimples,
    • 19:08some divots in the breast,
    • 19:10and it can cause some
    • 19:11asymmetry between the two breasts.
    • 19:13So this is a great
    • 19:15option for people who have
    • 19:17large or very, what we
    • 19:18call, tootic or saggy breasts.
    • 19:21So a breast reduction is
    • 19:22typically done on the other
    • 19:24side as well,
    • 19:26and or and or a
    • 19:28breast lift.
    • 19:31Now let's talk about implant
    • 19:32based reconstruction.
    • 19:34So there are some techniques
    • 19:35that involve putting in an
    • 19:37implant right away. So that's
    • 19:39when we put an implant
    • 19:41at the time of a
    • 19:42mastectomy.
    • 19:43It eliminates the need for
    • 19:45what we call a tissue
    • 19:46expander.
    • 19:48It's a breast reconstruction
    • 19:49that can be completed in
    • 19:51one step,
    • 19:52and people who are good
    • 19:53candidates for this are really
    • 19:55based on the breast size,
    • 19:57the cancer size,
    • 19:59and the type of mastectomy
    • 20:01required.
    • 20:02And frequently, it's done when,
    • 20:05we try to keep the
    • 20:06nipple areola.
    • 20:07However, this is not the
    • 20:09gold standard.
    • 20:10It can lead to high
    • 20:12revision rates.
    • 20:14The gold standard for implant
    • 20:16based reconstruction
    • 20:17is what we call a
    • 20:18two stage procedure.
    • 20:20So in the first stage,
    • 20:22we put either a tissue
    • 20:23expander
    • 20:24above or underneath the muscle
    • 20:26and most commonly now above
    • 20:28the muscle.
    • 20:29This looks sort of like
    • 20:30a balloon. It has,
    • 20:32a magnetic port in it,
    • 20:34and it's covered by the
    • 20:35skin.
    • 20:37And this requires
    • 20:39filling of that,
    • 20:40balloon
    • 20:42in clinic every one to
    • 20:43two weeks, and we fill
    • 20:45it to the size that
    • 20:46we're happy with or you're
    • 20:47happy with.
    • 20:48And it involves the second
    • 20:50stage. So that means going
    • 20:52back to the operating room,
    • 20:54removing the expander, and putting
    • 20:56in an implant.
    • 20:57Because this is kinda what
    • 20:59it looks like. Sometimes it's
    • 21:00covered with a special type
    • 21:02of mesh.
    • 21:03And,
    • 21:04in clinic, we use a
    • 21:06mag we use a magnetic
    • 21:08finder. We find the magnetic
    • 21:10port, and we put a
    • 21:11needle through the skin
    • 21:13into the tissue expander, and
    • 21:15we fill up that space.
    • 21:16So, typically, we start filling
    • 21:19about two to three weeks
    • 21:20after surgery.
    • 21:21The expansion process can take
    • 21:23up to
    • 21:36treatment as required.
    • 21:39What are the advantages of
    • 21:40implant based reconstruction?
    • 21:42It's a quicker procedure.
    • 21:44It's a shorter recovery time.
    • 21:47You get to choose the
    • 21:48size of your reconstruction.
    • 21:50We're only operating on one
    • 21:52side.
    • 21:53The disadvantage is it can
    • 21:54be more than one surgery.
    • 21:56We can sometimes see and
    • 21:58palpate the implant.
    • 22:00If it's placed under the
    • 22:01muscle, the muscle can cause
    • 22:03animation.
    • 22:04There's always a risk of
    • 22:06infection.
    • 22:07There's a risk of what
    • 22:08we call capsular contracture, which
    • 22:10is the body forming
    • 22:12a capsule around the implant,
    • 22:14which
    • 22:15commonly happens. However, sometimes it
    • 22:18can become
    • 22:19hard and painful
    • 22:21and can distort the implant.
    • 22:23Implants can also rupture.
    • 22:25Any radiation can lead to
    • 22:27a higher failure rate, and
    • 22:29there's a few things associated
    • 22:31with implants that are less
    • 22:33common and actually very rare,
    • 22:35but we frequently
    • 22:36talk about and you should
    • 22:37discuss with your reconstructive surgeon,
    • 22:40which are anaplastic large cell
    • 22:41lymphoma and breast implant illness,
    • 22:44which are related to safety,
    • 22:46related to some types of
    • 22:47implants,
    • 22:48which are not always used,
    • 22:51in all practices.
    • 22:53Doctor Berger alluded to, sensation
    • 22:55preservation.
    • 22:58So this is frequently
    • 23:00done when we can preserve
    • 23:02the nipple
    • 23:03and the areola,
    • 23:04which can which is done
    • 23:06in, some patients. Again, the
    • 23:08tumor has to be far
    • 23:09away enough from the nipple
    • 23:11areola so that we can
    • 23:12keep it.
    • 23:13And then the breast have
    • 23:14to has to already has
    • 23:15a nice shape,
    • 23:17to it so that we
    • 23:18can preserve the nipple areola.
    • 23:20So when that's done, we
    • 23:21can do we can preserve
    • 23:23sensation in two ways.
    • 23:25One of them by connecting
    • 23:27a nerve
    • 23:28that comes off the shelf
    • 23:30that has been processed,
    • 23:32or we can take a
    • 23:33nerve
    • 23:34from the side of the
    • 23:35breast that's not involved in
    • 23:36the cancer
    • 23:38and transfer it over to
    • 23:39try to bring back sensation.
    • 23:42Now the sensation is not
    • 23:43like normal sensation.
    • 23:45It's not erogenous
    • 23:46sensation,
    • 23:48but, we think with some
    • 23:49studies that we can bring
    • 23:51back sensation,
    • 23:53better than not having this
    • 23:54done at all.
    • 23:56The other type of re
    • 23:58re breast reconstruction is called
    • 23:59autologous tissue reconstruction.
    • 24:02Can you guys still hear
    • 24:03me?
    • 24:05Okay. Great. Sorry. I think
    • 24:06you lost the signal.
    • 24:08And that means using your
    • 24:10own tissue. So that can
    • 24:12come from different areas.
    • 24:14So there it can come
    • 24:15from the abdomen, the belly.
    • 24:17That's called a deep flap.
    • 24:18It can come from the
    • 24:19thighs. That can is called
    • 24:21the tug flap or the
    • 24:22pad flap. It can come
    • 24:24from the buttocks, the eye
    • 24:26gap, or the s cap,
    • 24:27or it can come from
    • 24:28the back.
    • 24:29So that's using,
    • 24:30the patient's own tissues to
    • 24:32create a breast mound. It
    • 24:34avoids all the complications
    • 24:36related to implants,
    • 24:37and it's a pretty nice
    • 24:38donor site. So let's talk
    • 24:40about the options.
    • 24:41The most common one is
    • 24:43called the deep flap. That
    • 24:45stands for deep inferior epigastric
    • 24:47perforator flap. That just means
    • 24:49the vessels that we actually
    • 24:51use.
    • 24:52So this is a cross
    • 24:53section of the belly where
    • 24:54we have skin and fat
    • 24:56and the muscle.
    • 24:58There's little vessels that are
    • 24:59less than one millimeter in
    • 25:01size that really penetrate through
    • 25:03that muscle
    • 25:04and give blood supply to
    • 25:06the skin and the fat.
    • 25:07So we get a CT
    • 25:08scan of the belly first,
    • 25:10and during the surgery,
    • 25:12we find those little vessels.
    • 25:14We follow them all the
    • 25:15way down to the groin
    • 25:16where they come from, where
    • 25:17they become slightly larger, so
    • 25:19about two to three millimeters.
    • 25:21We disconnect them from that
    • 25:23area,
    • 25:24and we reconnect them in
    • 25:25vessels underneath a small piece
    • 25:27of rib.
    • 25:29This is called microsurgery.
    • 25:31We use loops and a
    • 25:32microscope to do this, and
    • 25:33it can be a long
    • 25:34procedure.
    • 25:36You end up with a
    • 25:37scar from hip to hip
    • 25:38and a scar around the
    • 25:39belly button like a tummy
    • 25:41tuck.
    • 25:42Half of the belly is
    • 25:44used for one side, half
    • 25:45is used for the other
    • 25:47side, and we create a
    • 25:48breast out of it.
    • 25:50We can also bring in
    • 25:51a little nerve to try
    • 25:53to bring back sensation
    • 25:55and try to,
    • 25:57you know, to create the
    • 25:58sensation
    • 25:59similar to what I talked
    • 26:00about earlier.
    • 26:02I'm sorry. I have a
    • 26:03little child in the background.
    • 26:05And we also have,
    • 26:07however,
    • 26:08it's, again, not like normal
    • 26:10sensation,
    • 26:12but we do know that
    • 26:13with time, even without using
    • 26:15a nerve graft, we can
    • 26:16bring back since the, the
    • 26:19nerves actually grow from the
    • 26:20side,
    • 26:21of the body to try
    • 26:23to bring back sensation into
    • 26:25the flap.
    • 26:26One side takes about six
    • 26:28hours.
    • 26:29Two sides takes about ten
    • 26:30hours.
    • 26:31This admit patients have to
    • 26:33admit be admitted for about
    • 26:35two to three days. The
    • 26:36first twenty four hours are
    • 26:38the most important because we
    • 26:39watch to make sure that
    • 26:41everything is working okay.
    • 26:43The advantages are that most
    • 26:45of the reconstruction is done
    • 26:46at the time of surgery.
    • 26:48We're using your own tissues.
    • 26:50It's lifelong. It's the best
    • 26:52substitute for a natural looking
    • 26:53breast.
    • 26:54The benefits is a tummy
    • 26:56tuck.
    • 26:57However, it's a longer procedure.
    • 26:59It's a longer recovery time.
    • 27:01It's a separate donor site.
    • 27:04It may require revision surgeries.
    • 27:06There's a possibility of it
    • 27:08not working, which is which
    • 27:09doesn't happen very often.
    • 27:11We can only use the
    • 27:12belly once, and there's obviously
    • 27:14more scars because we're operating
    • 27:16in another area.
    • 27:18Other areas that we can
    • 27:19take it from is the
    • 27:20buttocks,
    • 27:21the thighs
    • 27:23as well.
    • 27:24Now let's talk about using
    • 27:26implants with your own tissue.
    • 27:28So that is a procedure
    • 27:30where we can take,
    • 27:31in cases, for example, of
    • 27:33radiation,
    • 27:34where we can take skin
    • 27:36and fat and sometimes the
    • 27:38muscle
    • 27:39and swing it over to
    • 27:40the breast
    • 27:41along with a tissue expander
    • 27:43of an or an implant,
    • 27:45to recreate a breast.
    • 27:48Now I also wanna talk
    • 27:49about what we call aesthetic
    • 27:51flat closure.
    • 27:52So plastic surgeon can be
    • 27:54involved in after mastectomies
    • 27:56in patients who do not
    • 27:57want reconstruction,
    • 27:59but do not want redundant
    • 28:01skin in that area. So
    • 28:02we can do different techniques
    • 28:04to try to make sure
    • 28:05that we have scars,
    • 28:08that look aesthetic
    • 28:10and to make sure that
    • 28:11there are no irregularities
    • 28:13in the chest.
    • 28:15Now the advantages of implant
    • 28:17and autologous based reconstruction, which
    • 28:18I mentioned earlier, is that
    • 28:20it can be used in
    • 28:21patients who had radiation,
    • 28:23in patients who are too
    • 28:25thin or have had a
    • 28:26tummy tuck. The disadvantages
    • 28:28is the disadvantages of an
    • 28:29implant
    • 28:30or using tissue from other
    • 28:32part of the body.
    • 28:34If we have to remove
    • 28:35the nipple areola, then we
    • 28:36can reconstruct the nipple areola,
    • 28:39and that's usually done by
    • 28:40either bunching up some tissue,
    • 28:42kinda like origami, to make
    • 28:43a nipple or an elevation
    • 28:45out of it.
    • 28:46And other techniques that we
    • 28:47use are,
    • 28:49tattooing.
    • 28:50One of our APRNs will
    • 28:52do that, and we have,
    • 28:54they're involved in,
    • 28:56clinical and operative care for
    • 28:58breast, breast cancer patients.
    • 29:00They're certified in tattoo art.
    • 29:03Doctor Berger alluded to,
    • 29:06a technique that we use
    • 29:07for prevention.
    • 29:09So one technique is called
    • 29:11immediate lymphatic reconstruction,
    • 29:13Most importantly, to prevent,
    • 29:16to prevent lymphedema,
    • 29:17it's the way that we
    • 29:18actually remove the lymph nodes
    • 29:20by making sure that we
    • 29:22try to preserve the lymphatic
    • 29:23vessels at the same time.
    • 29:25But if all of the
    • 29:27lymph nodes are removed and
    • 29:28have to be removed,
    • 29:30then what we can do
    • 29:31is we can try to
    • 29:32find those little lymph nodes
    • 29:34again by using a microscope.
    • 29:36Those are very, very small
    • 29:38in size. They're less than
    • 29:39one millimeter in size.
    • 29:41And we find a vein
    • 29:42of equal size, and we
    • 29:44reroute them. We perform a
    • 29:46bypass.
    • 29:47The suture that we use
    • 29:48to bring those together is
    • 29:49actually finer than a hair,
    • 29:51so you can imagine that
    • 29:52that's very small.
    • 29:54And we our goal is
    • 29:56to hopefully prevent lymphedema.
    • 29:59This adds about an hour
    • 30:00to an hour and a
    • 30:01half to the case, and
    • 30:02we think by looking at
    • 30:04studies that it has the
    • 30:06ability to reduce the chances
    • 30:07of lymphedema by about fifty
    • 30:09percent.
    • 30:10It doesn't necessarily mean that
    • 30:12absolutely
    • 30:13would not have lymphedema,
    • 30:15but it definitely
    • 30:16is,
    • 30:17is worth, worth trying.
    • 30:20Thank you very much for
    • 30:21listening, and,
    • 30:22I welcome any questions that
    • 30:24may come at the end
    • 30:25of this talk.
    • 30:28Thank you very much, doctor
    • 30:30Haykel.
    • 30:31And, we'll move on to
    • 30:32doctor Maria Rosenblatt.
    • 30:34Doctor Rosenblatt is an assistant
    • 30:36professor of medicine in the
    • 30:37division of medical oncology,
    • 30:40and she'll be talking with
    • 30:41us this evening about updates
    • 30:42in systemic therapy.
    • 30:44Welcome, doctor Rosenblitt.
    • 30:46Thank you so much.
    • 30:49Okay. So I'm gonna be
    • 30:50talking about systemic therapy for
    • 30:52breast cancer.
    • 30:55And as we've heard so
    • 30:56far,
    • 30:57really, the treatment of breast
    • 30:59cancer is a multidisciplinary
    • 31:00approach,
    • 31:01and this involves the breast
    • 31:03surgeon, the radiation oncologist, and
    • 31:05the medical oncologist.
    • 31:07And each part of the
    • 31:09team has a slightly different
    • 31:11goal. So the goal of
    • 31:12the breast surgeon
    • 31:13is to remove the known
    • 31:14cancer,
    • 31:15to obtain negative margins as
    • 31:17we heard about, to evaluate
    • 31:18the lymph nodes,
    • 31:20and
    • 31:21to remove involved lymph nodes.
    • 31:23The radiation oncologist
    • 31:25then tries to mop up
    • 31:26any microscopic
    • 31:28disease in the breast,
    • 31:29and the regional lymph nodes,
    • 31:31and this is usually done
    • 31:33after surgery, so after a
    • 31:35lumpectomy.
    • 31:36And sometimes in special circumstances,
    • 31:38it might be recommended after
    • 31:39a mastectomy.
    • 31:40And the goal of that
    • 31:41treatment is to reduce local
    • 31:43recurrence, so the risk of
    • 31:45the breast cancer coming back
    • 31:46in the same breast.
    • 31:48As the medical oncologist, my
    • 31:50goal is to really mop
    • 31:51up any microscopic disease that
    • 31:53might be anywhere else in
    • 31:54the body. And my goal
    • 31:56is to decrease the risk
    • 31:58of what we call distant
    • 31:59recurrence, so the risk that
    • 32:00this cancer
    • 32:01might come back in other
    • 32:02parts of the body.
    • 32:04And we call that, the
    • 32:06risk of developing metastatic recurrence.
    • 32:13Okay. So how do we
    • 32:14decide,
    • 32:15what kind of medical treatment
    • 32:17to offer? And this is
    • 32:18a really complex decision that
    • 32:20we put a lot of
    • 32:20thought into. And we heard
    • 32:22a little bit from Doctor.
    • 32:23Berger about stage. So we
    • 32:25think about what size is
    • 32:26the tumor, how many lymph
    • 32:28nodes are involved,
    • 32:30are we worried about any
    • 32:31distant metastatic sites? And then
    • 32:34we think about the patient
    • 32:35in front of us. What
    • 32:36is their age? What are
    • 32:37their other medical problems?
    • 32:39What is their life expectancy?
    • 32:41What are their values?
    • 32:43And then we also think
    • 32:45about
    • 32:46additional characteristics.
    • 32:48So just as doctor Berger
    • 32:49mentioned, it's not just about
    • 32:50tumor size and lymph nodes,
    • 32:52it's also about the molecular
    • 32:53makeup of that tumor. So
    • 32:55we know that,
    • 32:57whether it's a hormone positive
    • 32:58or HER2 positive or triple
    • 33:00negative breast cancer,
    • 33:02The type of breast cancer
    • 33:03has a very different prognosis.
    • 33:06We also think about grade,
    • 33:07meaning how aggressive does this
    • 33:09cancer look under the microscope,
    • 33:11and we sometimes do special
    • 33:13types of gene expression testing
    • 33:15to try to help us
    • 33:16figure out what is the
    • 33:17risk of this cancer coming
    • 33:18back.
    • 33:20So in terms of the
    • 33:21timing of the therapy, we
    • 33:23think about it, in two
    • 33:25large buckets, meaning adjuvant or
    • 33:27neoadjuvant
    • 33:28approach.
    • 33:29When we talk about an
    • 33:30adjuvant approach, that's when we
    • 33:32have a discussion with the
    • 33:33surgeon,
    • 33:34and we come up with
    • 33:35a plan that we recommend
    • 33:37surgery first.
    • 33:38After surgery,
    • 33:40we think about whether
    • 33:42the person would benefit from
    • 33:43the addition of chemotherapy,
    • 33:46if they have a HER2
    • 33:47positive breast cancer, whether they
    • 33:49need HER2 targeted therapy,
    • 33:51and then if radiation is
    • 33:53needed. And then if it's
    • 33:54a hormone positive breast cancer,
    • 33:56we would add on something
    • 33:57called endocrine therapy at the
    • 33:59end.
    • 34:00Sometimes we prefer a neoadjuvant
    • 34:02approach, and this is often
    • 34:04when chemotherapy
    • 34:06is recommended before surgery.
    • 34:08And this is often done
    • 34:09in larger tumors
    • 34:11where there might be a
    • 34:12lot of lymph nodes that
    • 34:13we're hoping to shrink before
    • 34:15surgery,
    • 34:16or if it's a more
    • 34:17aggressive cancer like a triple
    • 34:19negative breast cancer or HER2
    • 34:21positive breast cancer.
    • 34:22And sometimes,
    • 34:24we recommend
    • 34:26systemic treatment first because how
    • 34:28the tumor responds to the
    • 34:29treatment can actually be very
    • 34:31important information for us as
    • 34:32medical oncologists.
    • 34:35And when the patient gets
    • 34:37to surgery,
    • 34:38we are looking for something
    • 34:39called a complete pathologic
    • 34:41response. So if we did
    • 34:42systemic therapy first
    • 34:44and the whole tumor,
    • 34:47was killed off by the
    • 34:48therapy and it looks just
    • 34:49like scar tissue under the
    • 34:50microscope,
    • 34:51prognostically, that's very important and
    • 34:53predicts a very low risk
    • 34:54of recurrence.
    • 34:56The radiation,
    • 34:57question is up to the
    • 34:59radiation oncologist
    • 35:00and really depends on,
    • 35:02what type of surgery,
    • 35:04was recommended.
    • 35:05And then once again, if
    • 35:06it's hormone positive, we would
    • 35:08end,
    • 35:08we would add on endocrine
    • 35:10therapy at the end.
    • 35:12So this is an example
    • 35:13of an oncotype, but this
    • 35:15is a test that we
    • 35:16commonly send for hormone positive
    • 35:18breast cancers.
    • 35:19And what this does is
    • 35:20it takes a small piece
    • 35:21of tissue from the original
    • 35:23breast tumor
    • 35:24and sends it off to
    • 35:25a special lab to look
    • 35:26at a certain number of
    • 35:27genes in the tumor itself
    • 35:29that help to predict how
    • 35:31aggressive that cancer is and
    • 35:33what is the risk of
    • 35:33the cancer coming back. And
    • 35:35so what the report gives
    • 35:37you is a number.
    • 35:38And in general, anything above
    • 35:40twenty five suggests that there's
    • 35:42a benefit to chemotherapy,
    • 35:44and it also gives you
    • 35:45this number called distant recurrence
    • 35:47risk at nine years. And
    • 35:49so what that number tells
    • 35:50you is over the next
    • 35:52nine years,
    • 35:53what is the risk of
    • 35:54this cancer coming back in
    • 35:56other parts of the body,
    • 35:57so coming back as a
    • 35:58metastatic breast cancer.
    • 36:00And,
    • 36:01if you take endocrine therapy,
    • 36:04it gives you the the
    • 36:05risk with the endocrine therapy.
    • 36:08In general, we know that
    • 36:09endocrine therapy reduces risk by
    • 36:11about fifty percent. So if
    • 36:13you don't take endocrine therapy,
    • 36:15you can double that number.
    • 36:17And then it also gives
    • 36:18you the number for absolute
    • 36:19chemotherapy
    • 36:20benefit.
    • 36:21And so often if it's
    • 36:22a high oncotype,
    • 36:24that absolute benefit is usually
    • 36:25greater than fifteen percent, and
    • 36:27that's when we'll be recommending
    • 36:29chemotherapy.
    • 36:32Here at Yale, we have
    • 36:33developed several different pathways,
    • 36:36to help standardize,
    • 36:38the decision for when to
    • 36:39send Oncotype.
    • 36:41And so wherever you go
    • 36:43as a patient across the
    • 36:44Yale network,
    • 36:45the different physicians will be
    • 36:47following the same algorithm.
    • 36:49And this can be really
    • 36:50helpful because for some tumors
    • 36:51that are very small, that
    • 36:53have very low risk features,
    • 36:54we often don't even have
    • 36:56to send an oncotype.
    • 36:57And then for some tumors
    • 36:59that are very large and
    • 37:00are very high risk and
    • 37:01we know that that person
    • 37:02needs chemotherapy,
    • 37:04we often don't have to
    • 37:05send oncotype either. And then
    • 37:07sometimes there are these gray
    • 37:08areas, and that's when these
    • 37:09pathways can be really helpful.
    • 37:11And if you're a physician
    • 37:12and you're on the call,
    • 37:14and you're
    • 37:16looking for some guidance for
    • 37:17when to send an oncotype,
    • 37:19you can click the pathways
    • 37:20tab in epic.
    • 37:22And so this has been
    • 37:23developed for both premenopausal
    • 37:25and postmenopausal
    • 37:26women with hormone positive breast
    • 37:27cancer.
    • 37:28And then in the adjuvant
    • 37:30setting,
    • 37:31where,
    • 37:32somebody has already completed surgery,
    • 37:35chemotherapy if they needed it,
    • 37:37and radiation,
    • 37:38We also think about ways
    • 37:39that we can optimize what
    • 37:41we call endocrine therapy. So
    • 37:42we want to block estrogen
    • 37:44in hormone positive breast cancer.
    • 37:47And in addition to our
    • 37:48estrogen blocking pills, we now
    • 37:50have something called CDK four
    • 37:52six inhibitors, and these are
    • 37:54pills
    • 37:54that actually inhibit the cell
    • 37:56cycle. So if there's any
    • 37:57microscopic
    • 37:58cancer cells left over anywhere,
    • 38:00it actually inhibits their growth
    • 38:02and helps to kill them
    • 38:03off, and we often give
    • 38:04these in combination with estrogen
    • 38:06blockers.
    • 38:08And so this is often,
    • 38:10saved for patients who have
    • 38:12a high risk of recurrence,
    • 38:14and so we've developed pathways
    • 38:15here at Yale to help
    • 38:16with that decision making as
    • 38:18well.
    • 38:19And oftentimes, it depends on
    • 38:21the tumor size. So larger
    • 38:22tumors,
    • 38:24higher oncotypes,
    • 38:26more lymph node involvement at
    • 38:28the time of diagnosis.
    • 38:31The other thing that we
    • 38:32often think about as medical
    • 38:34oncologist is whether somebody is
    • 38:36eligible for clinical trials.
    • 38:38And clinical trials are really
    • 38:39important because it's a really
    • 38:41great way to
    • 38:43try to,
    • 38:44optimize therapy for someone that
    • 38:46we're seeing
    • 38:47and either get a drug
    • 38:49early,
    • 38:50before it's on the market,
    • 38:52or hopefully get, just a
    • 38:54better approach to treatment.
    • 38:56So one of the big
    • 38:57questions currently in the field
    • 38:58is, can we think about
    • 39:00ways to
    • 39:02chemotherapy
    • 39:03in young women with hormone
    • 39:05positive breast cancer?
    • 39:06And the reason why this
    • 39:07comes up is because,
    • 39:09after doing this for many
    • 39:11decades in breast cancer, we're
    • 39:12not sure if it's really
    • 39:14the chemotherapy
    • 39:15drugs themselves
    • 39:16that are showing benefit in
    • 39:18this patient population
    • 39:19or whether it's the chemotherapy
    • 39:21putting these women into early
    • 39:23menopause
    • 39:23and whether it's actually the
    • 39:25menopausal status,
    • 39:26that is causing the benefit
    • 39:28that we see.
    • 39:29So there's currently a clinical
    • 39:31trial being run by the
    • 39:32NRG called BR009,
    • 39:35and this is looking for
    • 39:36young women who have
    • 39:38oncotype below twenty five, which
    • 39:40we generally think of as
    • 39:42low risk,
    • 39:43but they may have a
    • 39:44positive lymph node and randomizing
    • 39:47them to chemotherapy,
    • 39:49which is the standard of
    • 39:50care
    • 39:51versus
    • 39:52not doing chemotherapy, but really
    • 39:54optimizing
    • 39:55their estrogen blocking and putting
    • 39:57them into early menopause.
    • 39:59And so this is an
    • 40:00important trial and something to
    • 40:02think about,
    • 40:03especially if if you are
    • 40:04a young woman being diagnosed
    • 40:06or you know somebody who's
    • 40:07being diagnosed,
    • 40:08because we're really starting to
    • 40:10think that maybe it's not
    • 40:12so much the chemotherapy,
    • 40:13but the actual menopause status,
    • 40:15that may be benefiting
    • 40:18these young women.
    • 40:20And then we also know
    • 40:21that there's probably a subgroup
    • 40:23of hormone positive breast cancers
    • 40:25that are really high risk,
    • 40:27high risk for coming back.
    • 40:29And so how can we
    • 40:30escalate and optimize treatment for
    • 40:32those patients?
    • 40:33And so there's a trial
    • 40:34being run by Swag here
    • 40:36at Yale called, two two
    • 40:38zero six that is looking
    • 40:39at something called mamaprint, which
    • 40:41is very similar to Oncotype,
    • 40:43but is a different assay
    • 40:44looking at a different set
    • 40:45of genes.
    • 40:46And for patients who score
    • 40:48in the in that really
    • 40:49high risk category called high
    • 40:51risk two or MP two,
    • 40:53they're being randomized to adding
    • 40:56immunotherapy
    • 40:57to chemotherapy.
    • 40:58In general,
    • 40:59we don't think of hormone
    • 41:01positive breast cancer,
    • 41:03as a cancer that's very
    • 41:04responsive to immunotherapy,
    • 41:06But we think that there
    • 41:07might be a subgroup of
    • 41:08these very aggressive, fast growing
    • 41:11hormone positive breast cancers that
    • 41:12may benefit, and that's what
    • 41:14that trial is looking at.
    • 41:17We also wanna think about
    • 41:18how can we tailor chemotherapy
    • 41:20for triple negative breast cancer.
    • 41:23And so there is a
    • 41:24trial also out of SWOG
    • 41:26that is looking at,
    • 41:28patients with early stage triple
    • 41:31negative breast cancer
    • 41:32and randomizing
    • 41:33to
    • 41:35standard of care,
    • 41:36chemotherapy,
    • 41:38versus standard of care chemotherapy,
    • 41:40but without the AC.
    • 41:42And the AC drugs,
    • 41:44often referred to as the
    • 41:46red devil on the Internet,
    • 41:48are the ones that have
    • 41:49the most toxicity
    • 41:50in terms of the chemotherapies
    • 41:52that we use
    • 41:53and also have a small
    • 41:55but significant risk of potentially
    • 41:57heart failure in the future.
    • 41:59So we would like to
    • 42:00avoid them as much as
    • 42:01we can, And so we're
    • 42:02hopeful that because triple negative
    • 42:05tends to be more responsive
    • 42:06to immunotherapy,
    • 42:08we're hoping that this trial
    • 42:09will show that we can
    • 42:10avoid anthracyclines
    • 42:12or AC in the future.
    • 42:16And so the other thing
    • 42:17that I think about, for
    • 42:18hormone positive breast cancers in
    • 42:20particular is how can we
    • 42:22tailor our treatments
    • 42:23to decrease the risk of
    • 42:24late recurrence. So in general,
    • 42:26most breast
    • 42:27cancers, if they come back,
    • 42:29they often come back in
    • 42:30the first five years,
    • 42:32but hormone positive breast cancers
    • 42:34can come back late. So
    • 42:35even as far as ten
    • 42:37years out sometimes.
    • 42:39And we don't really have
    • 42:40a good way to detect
    • 42:41them
    • 42:42besides continuing to screen with
    • 42:44our breast imaging with mammograms
    • 42:46and ultrasounds.
    • 42:47So this is, a trial
    • 42:49called KEATS, that is now
    • 42:50open at Yale and will
    • 42:52be open across several different
    • 42:54sites through the TBCRC.
    • 42:56And this is looking at
    • 42:57using a novel test called
    • 42:59circulating tumor DNA,
    • 43:02to see whether we can
    • 43:03detect
    • 43:04cancer coming back at just
    • 43:06the microscopic
    • 43:07level.
    • 43:07And so for patients who
    • 43:09are more than five years
    • 43:10out from diagnosis with hormone
    • 43:12positive breast cancer, who have
    • 43:13completed all of their prior
    • 43:15treatments,
    • 43:17on this trial, they can
    • 43:18get the ctDNA test, which
    • 43:20is a blood test every
    • 43:21three months.
    • 43:23And if they end up
    • 43:24coming back positive on this
    • 43:26test
    • 43:27and they don't have cancer
    • 43:28yet on their scans,
    • 43:30we're gonna be treating them
    • 43:31with elocestrant,
    • 43:32which is a pill.
    • 43:33And it's one of these
    • 43:35newer
    • 43:36estrogen receptor degraders.
    • 43:38So not just a blocker,
    • 43:39but actually degrading the estrogen
    • 43:41receptor.
    • 43:42And we're hopeful that by,
    • 43:45intervening
    • 43:45at the microscopic
    • 43:47state, we can prevent these
    • 43:49cells from growing back into
    • 43:50a tumor and growing back
    • 43:52into a breast cancer recurrence.
    • 43:55So thank you very much,
    • 43:56and I hope that if
    • 43:58you're a patient or a
    • 43:59family member or a treating
    • 44:01physician that you think about
    • 44:02clinical trials or at least
    • 44:04discuss clinical trials with your
    • 44:06oncologist. Thank you.
    • 44:08Thank you very much, doctor
    • 44:10Rosenblatt.
    • 44:12So we've answered many questions
    • 44:14in the chat. This has
    • 44:15been a fast and furious
    • 44:16overview on updates in early
    • 44:18stage breast cancer. We learned,
    • 44:20surgical therapy from doctor Berger,
    • 44:23options for reconstruction from doctor
    • 44:25Hakal as well as updates
    • 44:27and systemic therapy
    • 44:28from doctor Rosenblit.
    • 44:31I think the last thing
    • 44:32we'd love to share with
    • 44:33our attendees is that we
    • 44:35do make decisions as a
    • 44:36multi disciplinary cancer team. So
    • 44:38patients that
    • 44:39come to any site across
    • 44:41the Yale Smilow network
    • 44:43will meet with a medical
    • 44:45oncologist,
    • 44:46surgeon, radiation oncologist, and plastic
    • 44:48surgeon,
    • 44:49and we work as a
    • 44:50cohesive united team in patients
    • 44:52care.
    • 44:53I think there's one last
    • 44:55question in the chat, doctor
    • 44:56Rosenblatt, about a lobular
    • 44:59carcinoma with an oncotype
    • 45:01of thirty four
    • 45:02and,
    • 45:03some concern about how estrogen
    • 45:05gene expression,
    • 45:08being borderline positive
    • 45:10and how that
    • 45:12information
    • 45:13influences your recommendations for systemic
    • 45:16therapy.
    • 45:22That's a great question. So
    • 45:24Oncotype
    • 45:25was really designed to
    • 45:27answer the question of, is
    • 45:29there benefit to chemotherapy
    • 45:31or not?
    • 45:32And it really wasn't designed
    • 45:34to
    • 45:36kind of investigate
    • 45:38how hormone
    • 45:39positive a breast cancer is.
    • 45:41So we still do rely
    • 45:42on
    • 45:43looking at the tumor under
    • 45:45the microscope, and that would
    • 45:46be a discussion with your
    • 45:49team, including the pathologist
    • 45:51in terms of how,
    • 45:53how much estrogen positivity you're
    • 45:55seeing in that case.
    • 45:57In general,
    • 45:58even for borderline
    • 46:00positive
    • 46:01cases,
    • 46:02it looks like in this
    • 46:03case, it was
    • 46:05ninety percent is what I'm
    • 46:06understanding
    • 46:07from
    • 46:08the report.
    • 46:10We would go ahead and
    • 46:11treat that as an estrogen,
    • 46:14hormone positive breast cancer.
    • 46:16There are borderline cases where
    • 46:18the estrogen positivity is very
    • 46:20low, and that becomes just
    • 46:21a very complex discussion with
    • 46:23your medical oncologist.
    • 46:24And in that case, they
    • 46:26might
    • 46:27tailor the chemotherapy
    • 46:28and offer you a slightly
    • 46:29different chemotherapy
    • 46:31if it's borderline.
    • 46:33Thank you very much. There's
    • 46:35another question about
    • 46:38what we recommend for young
    • 46:39women who are
    • 46:42thinking about future pregnancy
    • 46:44and have an estrogen positive
    • 46:46tumor. Unfortunately,
    • 46:48the positive trial, which was
    • 46:50run out of Dana Farber
    • 46:51but included multiple institutions
    • 46:53across the country and the
    • 46:55world,
    • 46:56did look at young women.
    • 46:57They were forty two or
    • 46:59younger who
    • 47:00were treated for hormone receptor
    • 47:02positive breast cancer and received
    • 47:04between eighteen and thirty months
    • 47:06of anti estrogen therapy or
    • 47:08hormone,
    • 47:10endocrine therapy to target their
    • 47:12breast cancer. They went on
    • 47:13to take a break for
    • 47:14pregnancy and
    • 47:16potential breastfeeding, and their pregnancy
    • 47:18success was very good
    • 47:21as well as the risk
    • 47:22of a recurrence
    • 47:23was similar to the women
    • 47:25who did not go ahead
    • 47:26with pregnancy. So the data
    • 47:27we currently have
    • 47:29is showing great promise
    • 47:32that it's safe for select
    • 47:33women with hormone receptor positive
    • 47:36breast cancers to take a
    • 47:38break for pregnancy and,
    • 47:40future,
    • 47:41breastfeeding.
    • 47:42And this is certainly something
    • 47:44you should discuss with your
    • 47:46oncology team. It's important that
    • 47:48you're at a right stage
    • 47:49of your cancer treatment and
    • 47:51that we can monitor you
    • 47:52as well as possible during
    • 47:54and after pregnancy.
    • 47:57There's another question about,
    • 48:00a recent article on spike
    • 48:02proteins
    • 48:03and the aggressive new cancers.
    • 48:05Doctor Rosenblatt, I'd I'd defer
    • 48:07to you if you're able
    • 48:08to answer this question.
    • 48:11I don't see this question
    • 48:12about the spike proteins.
    • 48:15It says, any comment on
    • 48:17the recent article on spike
    • 48:18protein and aggressive new cancers?
    • 48:22I'm not exactly sure what
    • 48:24this article is referring to.
    • 48:26There is a lot of
    • 48:27research out there trying to
    • 48:29figure out,
    • 48:30better ways of predicting aggressiveness
    • 48:33and recurrence, so that's probably
    • 48:34what that's referring to.
    • 48:37It's nothing that has reached,
    • 48:38you know, standard of care
    • 48:40yet. It hasn't entered mainstream
    • 48:42practice.
    • 48:43But, yeah, I I look
    • 48:44forward to reading more about
    • 48:45it.
    • 48:46Okay.
    • 48:47And then there's another question
    • 48:49about tracking recurrences
    • 48:51and HER2 positive versus
    • 48:53hormone receptor
    • 48:54positive HER2 negative cancers.
    • 48:57I'll dive in very quickly
    • 48:58as a surgeon. I think
    • 49:00locally, we're examining your skin.
    • 49:02We're looking at any changes.
    • 49:04There can be there was
    • 49:06another comment and question in
    • 49:08the chat. There can be
    • 49:09ongoing changes in the breast
    • 49:10tissue
    • 49:11after surgery, reconstruction, and radiation
    • 49:14for even a couple years,
    • 49:15but most cancer patients should
    • 49:17be under surveillance with their
    • 49:18oncology team.
    • 49:20We decide to survey people
    • 49:22for a distant recurrence in
    • 49:24the setting of of symptoms
    • 49:26or abnormal labs, and doctor
    • 49:27Rosenblitz really an expert in
    • 49:29ctDNA.
    • 49:30So I'll, turn that over
    • 49:32to her.
    • 49:34Yeah. So the main surveillance
    • 49:36mechanism, like we mentioned, is
    • 49:38physical exam and then breast
    • 49:40imaging.
    • 49:42In breast cancer, we have
    • 49:43not seen any benefit
    • 49:44from PET scans or CAT
    • 49:46scans, and so we don't
    • 49:47do them because
    • 49:49the risk of the radiation
    • 49:50from the scans actually outweighs
    • 49:52any any benefit in terms
    • 49:54of finding a recurrence.
    • 49:56And we don't have good
    • 49:57blood tests either. There are
    • 49:59blood tests out there called
    • 50:00tumor markers and we use
    • 50:01them for metastatic breast cancer
    • 50:03all the time, But for
    • 50:04early stage breast cancer, they've
    • 50:06been shown to have what's
    • 50:08called low sensitivity and low
    • 50:09specificity. So they can be
    • 50:11negative and there can still
    • 50:12be a cancer and they
    • 50:13can be positive and there
    • 50:14could be no cancer. So
    • 50:16they're not very helpful to
    • 50:17us. And that's why we're
    • 50:18trying to develop this new
    • 50:19blood test called circulating tumor
    • 50:21DNA.
    • 50:22Right now, we're looking at
    • 50:23it just in the research
    • 50:25setting because we don't know
    • 50:27yet how helpful this test
    • 50:28is, and we don't have
    • 50:30a treatment option. We need
    • 50:31to investigate what treatment we
    • 50:33can give if that test
    • 50:34is positive.
    • 50:35So there are trials going
    • 50:36on for that for both
    • 50:37hormone positive and HER2 positive
    • 50:39and triple negative breast cancer.
    • 50:41So if you're really interested,
    • 50:43please look out for those
    • 50:44trials.
    • 50:45They're in very early stages,
    • 50:47but we'll probably see more
    • 50:48of those clinical trials in
    • 50:50the next couple of years.
    • 50:54Alright. Well, thank you to
    • 50:55my esteemed colleagues,
    • 50:57for joining us tonight and
    • 50:58sharing your knowledge, and thank
    • 51:00you to all the attendees
    • 51:01for joining us for this
    • 51:02Milo shares. We,
    • 51:04encourage you to attend our
    • 51:06future sessions in the month
    • 51:07of October, which as many
    • 51:09of you know is breast
    • 51:10cancer awareness month. And please
    • 51:12reach out,
    • 51:14to any member of our
    • 51:15program if you or family
    • 51:17or friends need to be
    • 51:18seen.
    • 51:19We wish you all well,
    • 51:21and
    • 51:21thank you again for joining.