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Diagnostic and Screening Tools for Gynecologic Cancers

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  • 00:00 --> 00:03Funding for Yale Cancer Answers is
  • 00:03 --> 00:06provided by Smilow Cancer Hospital.
  • 00:06 --> 00:08Welcome to Yale Cancer Answers
  • 00:08 --> 00:10with Doctor Anees Chagpar.
  • 00:10 --> 00:11Yale Cancer Answers features
  • 00:11 --> 00:13the latest information on cancer
  • 00:13 --> 00:15care by welcoming oncologists and
  • 00:15 --> 00:17specialists who are on the forefront
  • 00:17 --> 00:19of the battle to fight cancer.
  • 00:19 --> 00:21This week it's a conversation about GYN
  • 00:21 --> 00:24cancers with Doctor Peter Dottino. Dr.
  • 00:24 --> 00:26Dottino is a professor of obstetrics,
  • 00:26 --> 00:28gynecology and reproductive sciences
  • 00:28 --> 00:30at the Yale School of Medicine,
  • 00:30 --> 00:32where Doctor Chagpar is a professor
  • 00:32 --> 00:33of surgical oncology.
  • 00:35 --> 00:37Maybe we can start off by you
  • 00:37 --> 00:39telling us a little bit more about
  • 00:39 --> 00:41yourself and what it is you do.
  • 00:42 --> 00:44I'm a board certified obstetrician,
  • 00:44 --> 00:48gynecologist is how I started and
  • 00:48 --> 00:52then I did a subspecialty training in
  • 00:52 --> 00:55gynecologic oncology almost 40 years ago.
  • 00:55 --> 00:58I'm currently board certified in both
  • 00:58 --> 01:00gynecological oncology and obstetrics
  • 01:00 --> 01:03and gynecology and my practice is pretty
  • 01:03 --> 01:06much gynecologic oncology which is women
  • 01:06 --> 01:08with cancer that affects the reproductive
  • 01:08 --> 01:11tract is what I see and treat.
  • 01:11 --> 01:14Not only do I do the surgeries
  • 01:14 --> 01:17for women with those diseases,
  • 01:17 --> 01:18but I also do the treatment
  • 01:18 --> 01:19and the treatment planning.
  • 01:19 --> 01:22I do administer chemotherapy.
  • 01:22 --> 01:26I work with radiation oncologists.
  • 01:29 --> 01:31When we talk about
  • 01:31 --> 01:32women with gynecologic cancers,
  • 01:32 --> 01:36that always seems to me to be a rather large
  • 01:36 --> 01:38bucket of of cancers.
  • 01:38 --> 01:40Can you tell us a little bit more
  • 01:40 --> 01:42about the different types of cancers,
  • 01:42 --> 01:44the frequency with which you
  • 01:44 --> 01:46see them and a little bit
  • 01:46 --> 01:47more about each of the types?
  • 01:49 --> 01:50Good question.
  • 01:50 --> 01:52So the the most common gynecologic
  • 01:52 --> 01:55cancer is uterine cancer or the other
  • 01:55 --> 01:58name it goes by is endometrial cancer.
  • 01:58 --> 02:02And there's roughly about 65,000
  • 02:02 --> 02:06cases in the US a year of women
  • 02:06 --> 02:09that get uterine cancer.
  • 02:09 --> 02:12Uterine cancer is the one
  • 02:12 --> 02:14gynecologic malignancy that is
  • 02:14 --> 02:17increasing in incidence every year
  • 02:17 --> 02:20and that is thought to be due to
  • 02:20 --> 02:24the increasing rates of obesity in our
  • 02:24 --> 02:27society because obesity is directly
  • 02:27 --> 02:30related to women getting endometrial
  • 02:30 --> 02:33cancer, but if you look at the the most common
  • 02:33 --> 02:36overall cancers that affect women today,
  • 02:36 --> 02:38it's number one breast,
  • 02:38 --> 02:41#2 lung and #3 colon.
  • 02:41 --> 02:42But what's going to happen in the
  • 02:42 --> 02:44next two to five years is that
  • 02:44 --> 02:46Colon will fall out of the third
  • 02:46 --> 02:48spot because of all the colonoscopy
  • 02:48 --> 02:50screening that's taking place.
  • 02:50 --> 02:52And uterine cancer will be the
  • 02:52 --> 02:54third most common cancer that
  • 02:54 --> 02:57affects women overall after breast
  • 02:57 --> 03:00and lung cancer following
  • 03:00 --> 03:03Endometrial cancer, ovarian cancer,
  • 03:03 --> 03:06which there's about 22,000 new cases,
  • 03:06 --> 03:10here in the US.
  • 03:10 --> 03:11And unfortunately,
  • 03:11 --> 03:14without a screening test to
  • 03:14 --> 03:17diagnose this disease early,
  • 03:17 --> 03:1985% of the ladies who actually present
  • 03:19 --> 03:22or walk into my office and need
  • 03:22 --> 03:24some specialist who treats ovarian
  • 03:24 --> 03:27cancer will be in very advanced
  • 03:27 --> 03:30stages, stage three and stage 4.
  • 03:30 --> 03:32Following endometrial cancer,
  • 03:32 --> 03:36we will have cervical cancer roughly about
  • 03:36 --> 03:4014,000 cases to 12,000 cases a year.
  • 03:40 --> 03:42And then we have the rarer types
  • 03:42 --> 03:45which would be vaginal cancer
  • 03:45 --> 03:47and vulvar cancer which affects
  • 03:47 --> 03:50the skin on the outside.
  • 03:50 --> 03:53And then that makes up the the range
  • 03:53 --> 03:56of what we see as gynecologic oncologist.
  • 03:57 --> 04:00You know it's so interesting that
  • 04:00 --> 04:02you say that endometrial cancer
  • 04:02 --> 04:04will likely take the third spot
  • 04:04 --> 04:07instead of colon cancer in large
  • 04:07 --> 04:10part due to the fact that we have
  • 04:10 --> 04:12good screening for colon cancers.
  • 04:12 --> 04:15Are there good screening techniques for
  • 04:15 --> 04:18for the GYN cancers that you mentioned?
  • 04:19 --> 04:24Well, if you look historically the
  • 04:24 --> 04:26screening test that was devised
  • 04:26 --> 04:29I think in the late 1930s,
  • 04:29 --> 04:32the Pap test was one of the
  • 04:32 --> 04:33first screening tests
  • 04:33 --> 04:36in all of cancer and that was
  • 04:36 --> 04:38designed to screen for cervical
  • 04:38 --> 04:41cancer because back in that time
  • 04:41 --> 04:43range cervical cancer was the most
  • 04:43 --> 04:45common cancer that affected women.
  • 04:45 --> 04:48And over the years the Pap test
  • 04:48 --> 04:51has been refined and now not only does
  • 04:51 --> 04:54it pick up cervical cancer but most
  • 04:54 --> 04:56importantly it picks up the precancerous
  • 04:56 --> 04:59lesions that affect the cervix.
  • 04:59 --> 05:02And so what that means is that when somebody
  • 05:02 --> 05:04has a precancerous lesion,
  • 05:04 --> 05:07we can eradicate those in an office setting,
  • 05:07 --> 05:09either with cryotherapy,
  • 05:09 --> 05:11which is freezing it,
  • 05:11 --> 05:14we can use laser to vaporize it,
  • 05:14 --> 05:17or we can just simply excise the lesion.
  • 05:17 --> 05:20And that's why in this country the
  • 05:20 --> 05:22incidence of cervical cancer went
  • 05:22 --> 05:25from the most common cancer to the
  • 05:25 --> 05:2713th most least likely of cancers
  • 05:27 --> 05:30for women because the Pap
  • 05:30 --> 05:32test for women in general access
  • 05:32 --> 05:33health care has made a huge impact.
  • 05:39 --> 05:42If you look at the rest of the
  • 05:42 --> 05:44world and developing
  • 05:44 --> 05:46countries who don't for economic
  • 05:46 --> 05:49reasons have access to PAP testing,
  • 05:49 --> 05:50cervical cancer is either the
  • 05:50 --> 05:52number one or #2 killer of women.
  • 05:52 --> 05:55But worldwide because there is an absence
  • 05:55 --> 05:57of a screening modality and it's
  • 05:58 --> 05:59an absolute tragedy that
  • 05:59 --> 06:01we have a screening modality,
  • 06:01 --> 06:03but yet it
  • 06:03 --> 06:05remains one of the number one and
  • 06:05 --> 06:07#2 killers of women worldwide.
  • 06:07 --> 06:09I mean I guess the other thing that's
  • 06:09 --> 06:11unfortunate for cervical cancer
  • 06:11 --> 06:13is that we also have a vaccine?
  • 06:13 --> 06:16That's correct and that's beginning
  • 06:16 --> 06:18to make an impact
  • 06:18 --> 06:20because I think the vaccines
  • 06:20 --> 06:22now are maybe 10 to 12 years old.
  • 06:22 --> 06:24And so in addition to the
  • 06:24 --> 06:26Pap test with the vaccine,
  • 06:26 --> 06:30this should be and will be
  • 06:30 --> 06:32hopefully an eradicable disease.
  • 06:32 --> 06:36There's still a lot of
  • 06:36 --> 06:38stumbling blocks in the developing
  • 06:38 --> 06:40world to the uptake of the vaccine,
  • 06:40 --> 06:42but in the developing nations there has
  • 06:42 --> 06:45been huge uptake in the
  • 06:45 --> 06:47vaccine and this will make between
  • 06:47 --> 06:49the Pap test and the vaccine
  • 06:49 --> 06:52will make an enormous impact on
  • 06:52 --> 06:54eradication of cervical cancer.
  • 06:54 --> 06:57I'll give you an example that
  • 06:57 --> 07:00roughly maybe 15-18 years ago I used
  • 07:00 --> 07:02to do about 70 radical operations
  • 07:02 --> 07:06for cervical cancer a year.
  • 07:06 --> 07:08Currently now I will do maybe one or
  • 07:08 --> 07:11two a year, that's how good the
  • 07:11 --> 07:14Pap test has been in identifying
  • 07:14 --> 07:16these precancerous lesions that are
  • 07:16 --> 07:19just so easily treatable.
  • 07:25 --> 07:27In my practice people that have
  • 07:27 --> 07:28cervical cancer usually they've
  • 07:28 --> 07:30either migrated here from countries
  • 07:30 --> 07:33that did not have PAP screening
  • 07:33 --> 07:35unfortunately or some people have
  • 07:35 --> 07:36fallen through the healthcare
  • 07:36 --> 07:39cracks in our system and they just
  • 07:39 --> 07:42either don't have money or they don't
  • 07:42 --> 07:45have access to PAP testing,
  • 07:45 --> 07:48which is also a tragedy.
  • 07:48 --> 07:50What about for endometrial cancer,
  • 07:50 --> 07:52do we have any kind of screening for that?
  • 07:53 --> 07:57No, there is no screening test that
  • 07:57 --> 08:00will detect endometrial cancer today.
  • 08:00 --> 08:02And there's work being
  • 08:02 --> 08:06done on that and one of
  • 08:06 --> 08:08the sort of pushbacks from the
  • 08:08 --> 08:10general community is that endometrial
  • 08:10 --> 08:13cancer, because women start having
  • 08:13 --> 08:16abnormal bleeding very early in
  • 08:16 --> 08:19the course of the disease,
  • 08:19 --> 08:21which leads most of them to
  • 08:21 --> 08:23see physicians very early,
  • 08:23 --> 08:26so probably about 3/4 of the disease that
  • 08:26 --> 08:30we see today is because
  • 08:30 --> 08:32they have bleeding, they come in,
  • 08:32 --> 08:35they have a a biopsy of the uterus
  • 08:35 --> 08:37that cancer is usually detected
  • 08:37 --> 08:39in very early stage one.
  • 08:39 --> 08:42And the cure rates in stage one
  • 08:42 --> 08:44are relatively high exceeding
  • 08:44 --> 08:49over 85 to the low 90% cure rates.
  • 08:49 --> 08:50That's fantastic.
  • 08:50 --> 08:53The caveat I would put to that,
  • 08:53 --> 08:55much like cervical cancer where there is
  • 09:00 --> 09:02a well defined precancerous lesion,
  • 09:02 --> 09:05we also know that there are well
  • 09:05 --> 09:07defined precancerous lesions of
  • 09:07 --> 09:10the uterus called hyperplasia.
  • 09:10 --> 09:13And the time it takes to go from a
  • 09:13 --> 09:15mild hyperplasia to uterine cancer
  • 09:15 --> 09:19is roughly about 8 to 9 years.
  • 09:19 --> 09:21So it's slow growing.
  • 09:21 --> 09:23And what that tells you is
  • 09:23 --> 09:25that if you could pick up these
  • 09:25 --> 09:26precancerous lesions,
  • 09:26 --> 09:29those could be treated without
  • 09:29 --> 09:31surgery in most cases,
  • 09:31 --> 09:32usually with hormonal treatments,
  • 09:32 --> 09:36those can be reversed and spare ladies
  • 09:36 --> 09:39the exposure to hysterectomy,
  • 09:39 --> 09:41potential surgical complications
  • 09:41 --> 09:44and also a loss of time from
  • 09:44 --> 09:46work from family and so forth.
  • 09:46 --> 09:48So there's
  • 09:48 --> 09:50a lot of work being directed towards,
  • 09:51 --> 09:54how can we detect these precancerous
  • 09:54 --> 09:57stages or the earliest cancer stages.
  • 09:57 --> 09:57Because again,
  • 09:57 --> 09:59if you can avoid a hysterectomy,
  • 09:59 --> 10:02that would just be a homerun.
  • 10:04 --> 10:06So tell us more about the
  • 10:06 --> 10:07screening that's being developed.
  • 10:07 --> 10:09Screening has kind of passed
  • 10:09 --> 10:11through a number of different stages.
  • 10:11 --> 10:13And one of the first things that
  • 10:13 --> 10:15had come on that probably about
  • 10:15 --> 10:1810-12 years ago was the use of what
  • 10:18 --> 10:21we call a transvaginal ultrasound,
  • 10:21 --> 10:23where an ultrasound probe is
  • 10:23 --> 10:24inserted into the vagina,
  • 10:24 --> 10:27goes directly against the cervix
  • 10:27 --> 10:30and it allows you to measure very
  • 10:30 --> 10:32accurately in millimeters the
  • 10:32 --> 10:34thickness of the lining of the uterus.
  • 10:34 --> 10:37And we know for certain
  • 10:37 --> 10:38ranges of patients
  • 10:38 --> 10:40how thick we would expect it to be,
  • 10:40 --> 10:43what would be considered normal and
  • 10:43 --> 10:45what would be considered abnormal
  • 10:45 --> 10:47and it was hoped that the
  • 10:47 --> 10:49use of this would lead to
  • 10:49 --> 10:50identifying precursor cases.
  • 10:50 --> 10:55But what we didn't find out what that
  • 10:55 --> 10:58those studies that were done was that
  • 10:58 --> 11:01ultrasound is not inexpensive #1 and #2
  • 11:01 --> 11:03we didn't know what interval do you use?
  • 11:03 --> 11:05Like with your mammogram you do
  • 11:05 --> 11:08it every year, do you do it every two years?
  • 11:08 --> 11:10And the same thing with the Pap
  • 11:10 --> 11:11test, we've now refined
  • 11:11 --> 11:13it so some women can get a PAP
  • 11:13 --> 11:14every year.
  • 11:14 --> 11:18Some may use it every two to three years.
  • 11:18 --> 11:20One of the tasks that
  • 11:22 --> 11:24I with my colleagues have been
  • 11:24 --> 11:26working on is a procedure
  • 11:26 --> 11:27called the uterine lavage.
  • 11:27 --> 11:29And what that means is when a
  • 11:29 --> 11:31woman comes in for her Pap test,
  • 11:31 --> 11:34which literally takes 15 seconds to do,
  • 11:34 --> 11:36after we do the Pap test,
  • 11:36 --> 11:39then we take about a teaspoon of saline
  • 11:39 --> 11:43and we put it
  • 11:43 --> 11:45inside the uterus and then we rinse
  • 11:45 --> 11:47out the inside of the uterus and we
  • 11:47 --> 11:49take that fluid and we take it to our
  • 11:49 --> 11:52laboratory and we look for specific
  • 11:52 --> 11:55different protein markers that are
  • 11:55 --> 11:57indicative of these precancerous
  • 11:57 --> 12:00and early cancer states.
  • 12:00 --> 12:04And so far today we've done this
  • 12:04 --> 12:06uterine lavage technique on over
  • 12:06 --> 12:10750 women and we found this to
  • 12:10 --> 12:13be as a screening test greater
  • 12:13 --> 12:16than 90% sensitive and specific.
  • 12:16 --> 12:20So we are currently expanding that
  • 12:20 --> 12:23to increase our numbers and that's
  • 12:23 --> 12:26something that again it's easy to do,
  • 12:26 --> 12:30it's very inexpensive like a Pap test,
  • 12:30 --> 12:32and it can pick up these
  • 12:32 --> 12:33kind of precancerous conditions.
  • 12:35 --> 12:36That's amazing.
  • 12:36 --> 12:38It sounds like that could really have
  • 12:38 --> 12:41a huge impact for uterine cancer.
  • 12:41 --> 12:43When do you think that might become
  • 12:44 --> 12:46something that we can see
  • 12:46 --> 12:48in regular clinical practice?
  • 12:51 --> 12:52The way these are going now,
  • 12:52 --> 12:56it possibly could be
  • 12:56 --> 12:5918 to 24 months you know depending
  • 12:59 --> 13:01upon you know a lot of external
  • 13:01 --> 13:03factors and how soon it takes to
  • 13:03 --> 13:05recruit this many patients
  • 13:05 --> 13:07or to get your application to the
  • 13:07 --> 13:09FDA for approval and so forth.
  • 13:09 --> 13:12But it's very, very encouraging.
  • 13:12 --> 13:14Fantastic. Well, we're going to take
  • 13:14 --> 13:16a short break for a medical minute.
  • 13:16 --> 13:18Please stay tuned to learn more
  • 13:18 --> 13:20about the care of GYN cancers with
  • 13:20 --> 13:22my guest doctor Peter Dottino.
  • 13:22 --> 13:24Funding for Yale Cancer Answers
  • 13:24 --> 13:26comes from Smilow Cancer Hospital,
  • 13:26 --> 13:28where their one-of-a-kind
  • 13:28 --> 13:29Sexuality, intimacy,
  • 13:29 --> 13:31and menopause program combines medical
  • 13:31 --> 13:33and psychological interventions
  • 13:33 --> 13:35for women who experience sexual
  • 13:35 --> 13:37dysfunction after cancer.
  • 13:37 --> 13:40Smilowcancerhospital.org.
  • 13:40 --> 13:43Over 230,000 Americans will be
  • 13:43 --> 13:45diagnosed with lung cancer this year,
  • 13:45 --> 13:47and in Connecticut alone there
  • 13:47 --> 13:50will be over 2700 new cases.
  • 13:50 --> 13:52More than 85% of lung cancer
  • 13:52 --> 13:54diagnosis are related to smoking,
  • 13:54 --> 13:57and quitting even after decades of use,
  • 13:57 --> 13:59can significantly reduce your risk
  • 13:59 --> 14:01of developing lung cancer each day.
  • 14:01 --> 14:04Patients with lung cancer are surviving
  • 14:04 --> 14:06thanks to increased access to advanced
  • 14:06 --> 14:08therapies and specialized care.
  • 14:08 --> 14:10New treatment options and surgical
  • 14:10 --> 14:11techniques are giving lung cancer
  • 14:11 --> 14:13survivors more hope than they
  • 14:13 --> 14:14have ever had before.
  • 14:14 --> 14:17Clinical trials are currently underway
  • 14:17 --> 14:19at federally designated Comprehensive
  • 14:19 --> 14:21cancer centers such as the battle
  • 14:21 --> 14:23two trial at Yale Cancer Center and
  • 14:23 --> 14:25Smilow Cancer Hospital to learn if a
  • 14:25 --> 14:28drug or combination of drugs based
  • 14:28 --> 14:30on personal biomarkers can help to
  • 14:30 --> 14:33control non small cell lung cancer.
  • 14:33 --> 14:35More information is available
  • 14:35 --> 14:36at yalecancercenter.org.
  • 14:36 --> 14:38You're listening to Connecticut public radio.
  • 14:40 --> 14:42Welcome back to Yale Cancer Answers.
  • 14:42 --> 14:43This is doctor Anees Chagpar
  • 14:43 --> 14:45and I'm joined tonight by my guest,
  • 14:45 --> 14:47doctor Peter Dottino.
  • 14:47 --> 14:49We're talking about the care of
  • 14:49 --> 14:51patients with Gyn cancers and
  • 14:51 --> 14:53diagnostic and screening tools.
  • 14:53 --> 14:55And right before the break,
  • 14:55 --> 14:58Doctor Dottino was telling us about how
  • 14:58 --> 15:00Pap smears have really revolutionized
  • 15:00 --> 15:03the care for cervical cancer and some
  • 15:03 --> 15:06of his recent work looking at lavage,
  • 15:06 --> 15:07which can be done at the same
  • 15:07 --> 15:10time as a pap smear that can
  • 15:10 --> 15:12screen for endometrial cancer,
  • 15:12 --> 15:16which is set to become the third
  • 15:16 --> 15:18most common cancer in women.
  • 15:18 --> 15:20So doctor Dottino,
  • 15:20 --> 15:22the other cancer that women often
  • 15:22 --> 15:25talk about and think about in terms
  • 15:25 --> 15:27of GYN cancers is ovarian cancer.
  • 15:27 --> 15:31Can you tell us a little bit more about
  • 15:31 --> 15:35ovarian cancer in terms of its prognosis and
  • 15:35 --> 15:38kind of how it presents?
  • 15:38 --> 15:40It's often called the silent cancer.
  • 15:40 --> 15:40Is that right?
  • 15:41 --> 15:43You know, it is called that,
  • 15:43 --> 15:47but it turns out that it's actually
  • 15:47 --> 15:50not a silent cancer and by that I
  • 15:50 --> 15:53mean the following, it turns out that
  • 15:53 --> 15:55extensive studies that have been done
  • 15:55 --> 15:58show that all women will have symptoms
  • 15:58 --> 16:01for at least three to four months and
  • 16:01 --> 16:04those symptoms they usually report to
  • 16:04 --> 16:08their doctor or they feel that those
  • 16:08 --> 16:09symptoms are with
  • 16:09 --> 16:10menopause or with aging.
  • 16:10 --> 16:11These would be symptoms of,
  • 16:11 --> 16:14say, what we call early satiety,
  • 16:14 --> 16:16so that when you eat something you have
  • 16:16 --> 16:18a couple of bites but you feel full.
  • 16:18 --> 16:20Sometimes it could be urinary frequency,
  • 16:20 --> 16:22where you think maybe I'm getting
  • 16:22 --> 16:22a little older,
  • 16:22 --> 16:24I could have a urinary infection.
  • 16:24 --> 16:26Sometimes it could be symptoms
  • 16:26 --> 16:27of where it's a little difficult
  • 16:27 --> 16:30to buckle your pants and
  • 16:30 --> 16:32your pants feel very tight.
  • 16:32 --> 16:35And it could be lower back
  • 16:35 --> 16:37pain or pain with intercourse,
  • 16:37 --> 16:38sexual intercourse.
  • 16:38 --> 16:42And those symptoms could go sometimes
  • 16:42 --> 16:44with either urinary infection,
  • 16:44 --> 16:47GI inflammation or many other things
  • 16:47 --> 16:48and most often either patients
  • 16:48 --> 16:50don't think that they possibly
  • 16:50 --> 16:52could be developing ovary
  • 16:52 --> 16:55cancer and a lot of times even
  • 16:55 --> 16:56their primary care physicians,
  • 16:56 --> 16:59whether that be a primary care OBGYN
  • 16:59 --> 17:02or a Primary Health care provider
  • 17:02 --> 17:04don't think that these could
  • 17:04 --> 17:06be related to ovary cancer.
  • 17:06 --> 17:11And because of the delay,
  • 17:11 --> 17:1485% of the ladies who actually finally
  • 17:14 --> 17:17make it in to see myself or anybody else
  • 17:17 --> 17:19who's a gynecologic oncologist will
  • 17:19 --> 17:22either be in stage three or stage four.
  • 17:22 --> 17:25And at that stage actually the medical
  • 17:25 --> 17:27student can establish the diagnosis
  • 17:27 --> 17:30because the stomach area and
  • 17:30 --> 17:32the abdominal area is swollen with
  • 17:32 --> 17:34fluid and patients are unable to
  • 17:34 --> 17:37eat, their legs could be swollen.
  • 17:37 --> 17:39So at that point it's very
  • 17:39 --> 17:42easy to make a diagnosis and that
  • 17:42 --> 17:45course then usually follows some kind
  • 17:45 --> 17:47of an ultra radical surgery procedure
  • 17:47 --> 17:50to remove all of the disease and
  • 17:50 --> 17:53then either six or eight months of
  • 17:53 --> 17:57chemotherapy and then what we call
  • 17:57 --> 17:59maintenance or consolidation
  • 17:59 --> 18:02therapy to keep the disease away.
  • 18:02 --> 18:05And so even in the best of circumstances,
  • 18:05 --> 18:08most people with advanced disease
  • 18:08 --> 18:10unfortunately will relapse even
  • 18:10 --> 18:12after having ultra radical surgery.
  • 18:12 --> 18:16Six or eight months of chemotherapy.
  • 18:16 --> 18:18So it's a difficult disease,
  • 18:18 --> 18:20but what we do know that about 8%
  • 18:20 --> 18:22of ovarian cancer is picked up by
  • 18:22 --> 18:25mistake where somebody may have a
  • 18:25 --> 18:26gallbladder operation and they look
  • 18:26 --> 18:29at the ovary and they see there's
  • 18:29 --> 18:31something abnormal or they may go
  • 18:31 --> 18:33for an MRI for back pain that they
  • 18:33 --> 18:36may see a growth on the ovary.
  • 18:36 --> 18:38And what we do know that if ovary
  • 18:38 --> 18:40cancer is picked up in stage one,
  • 18:40 --> 18:43the cure rates are over 90% long term
  • 18:43 --> 18:46survivors that's greater than 10 years.
  • 18:46 --> 18:48So what we've been struggling with in
  • 18:48 --> 18:50the field is to develop a screening
  • 18:50 --> 18:53tool that would allow us to pick it
  • 18:53 --> 18:55up in early stage because an early
  • 18:55 --> 18:59stage cure is possible.
  • 18:59 --> 19:01Cure is remotely possibly even in advanced disease
  • 19:01 --> 19:02unfortunately
  • 19:02 --> 19:03even today.
  • 19:04 --> 19:07And so what has been your progress
  • 19:07 --> 19:09in terms of developing screening
  • 19:09 --> 19:11tools for ovarian cancer?
  • 19:11 --> 19:13Can you tell us more about
  • 19:13 --> 19:14whether there are any bright
  • 19:14 --> 19:15lights on the horizon there?
  • 19:16 --> 19:19Sure. We've got
  • 19:19 --> 19:22a blood test that was
  • 19:22 --> 19:24developed and it's called a CA 125
  • 19:24 --> 19:27and that was a blood test that
  • 19:27 --> 19:29again is about 25 years old now,
  • 19:29 --> 19:32but it was one of the first markers that
  • 19:32 --> 19:34was found to be in the blood for ovary
  • 19:34 --> 19:36cancer and we thought that
  • 19:36 --> 19:38that would be a home run.
  • 19:38 --> 19:40But what unfortunately we found out as
  • 19:40 --> 19:43the test went into widespread use is that
  • 19:43 --> 19:45there were many other things besides
  • 19:45 --> 19:48cancer that would make the test elevated,
  • 19:48 --> 19:51such as uterine fibroids,
  • 19:51 --> 19:52endometriosis.
  • 19:52 --> 19:54These are benign conditions
  • 19:54 --> 19:55that could affect women.
  • 19:55 --> 19:57Any kind of inflammation in
  • 19:57 --> 20:00the body or the pelvic area
  • 20:00 --> 20:02like diverticular disease could
  • 20:02 --> 20:05elevate this so that it had
  • 20:05 --> 20:07no value, it turns out,
  • 20:07 --> 20:09as a screening test for
  • 20:09 --> 20:13ovarian cancer at all,
  • 20:13 --> 20:15unfortunately.
  • 20:15 --> 20:18The other thing that again,
  • 20:18 --> 20:21as we discussed in the first
  • 20:21 --> 20:23segment you're using the uterine lavage,
  • 20:23 --> 20:26what we found is 2 things have happened
  • 20:26 --> 20:31one through multiscale Genomics we are able to
  • 20:31 --> 20:33demonstrate, not myself,
  • 20:33 --> 20:35but in the archaeological
  • 20:35 --> 20:36community, that
  • 20:36 --> 20:39the majority of ovary cancer actually
  • 20:39 --> 20:42does not originate in the ovary,
  • 20:42 --> 20:44but it originates in the
  • 20:44 --> 20:46end of the fallopian tube.
  • 20:46 --> 20:49The thought of the fallopian
  • 20:49 --> 20:52tube that sits over the ovary
  • 20:52 --> 20:55and collects an egg and so
  • 20:55 --> 20:57that portion of the fallopian tube
  • 20:57 --> 20:59it develops a precancerous lesion,
  • 21:02 --> 21:04which has been estimated by
  • 21:04 --> 21:06mathematical modeling to take about
  • 21:06 --> 21:096 years until it turns into cancer.
  • 21:09 --> 21:09Now,
  • 21:09 --> 21:12when we were doing our uterine lavage
  • 21:12 --> 21:14for screening for uterine cancer,
  • 21:14 --> 21:15we noticed by chance that we were
  • 21:15 --> 21:17actually picking up cells
  • 21:17 --> 21:19from the fallopian tube that would
  • 21:19 --> 21:21fall into the uterus and that
  • 21:21 --> 21:23would give us a clue and
  • 21:23 --> 21:25we have now done this test and
  • 21:25 --> 21:29been able to detect early ovarian
  • 21:29 --> 21:31cancer utilizing this test.
  • 21:31 --> 21:35So we think that it will be a
  • 21:35 --> 21:37combined test that uterine lavage
  • 21:37 --> 21:40that will allow us to detect early and
  • 21:40 --> 21:42endometrial and early ovarian cancer.
  • 21:42 --> 21:44So we're very excited about it.
  • 21:44 --> 21:47It's kind of what we call the Holy
  • 21:47 --> 21:49Grail in this field because early detection,
  • 21:49 --> 21:51it becomes a game changer,
  • 21:51 --> 21:52absolute game changer.
  • 21:54 --> 21:56And it certainly sounds exciting.
  • 21:56 --> 21:59The one question that I would have
  • 21:59 --> 22:02is it sounds like the test for
  • 22:02 --> 22:04ovarian cancer is really dependent
  • 22:04 --> 22:07upon those cells dropping into the
  • 22:07 --> 22:10the uterus from the fallopian tube.
  • 22:10 --> 22:14Do all cells do that or would you miss some?
  • 22:15 --> 22:17Well, that's what
  • 22:17 --> 22:20we're trying to work out now,
  • 22:20 --> 22:23but we do know that there is peristalsis
  • 22:23 --> 22:26in the muscular length of
  • 22:26 --> 22:29the tube because the tube
  • 22:29 --> 22:31has what they call it the end of the tube,
  • 22:31 --> 22:33is these fimbria, which are tiny,
  • 22:33 --> 22:36like fingers that sit on top of the ovary.
  • 22:36 --> 22:38So that when a woman ovulates and
  • 22:38 --> 22:41an egg burst out of the ovary,
  • 22:41 --> 22:44the fimbria pick up the egg and put it into
  • 22:44 --> 22:47the fallopian tube and then the muscles,
  • 22:47 --> 22:49the peristaltic motion of the tube
  • 22:49 --> 22:52brings the egg down into the uterus
  • 22:52 --> 22:54so that it can be fertilized.
  • 22:55 --> 22:57What we theorize that those same
  • 22:57 --> 22:59precancerous cells are just moved
  • 22:59 --> 23:02along and dropped into the tube
  • 23:02 --> 23:04will that be everybody
  • 23:04 --> 23:06that we will have to workout
  • 23:06 --> 23:08as we go along with our test?
  • 23:10 --> 23:12So it's something to be seen,
  • 23:12 --> 23:14but that is a distinct
  • 23:14 --> 23:15possibility that
  • 23:15 --> 23:17we're definitely picking up these
  • 23:17 --> 23:18precancerous cells.
  • 23:18 --> 23:19There's no question about that.
  • 23:19 --> 23:22And I mean one would
  • 23:22 --> 23:25surmise that picking up some of them,
  • 23:25 --> 23:27even if you don't pick up all of
  • 23:27 --> 23:30them would still be a real boon for
  • 23:30 --> 23:32a cancer where there really isn't
  • 23:32 --> 23:35any other screening test available.
  • 23:36 --> 23:37No question about that.
  • 23:37 --> 23:39So one of the other ways we're
  • 23:39 --> 23:41approaching this is the same techniques
  • 23:41 --> 23:43that we use to analyze the uterine
  • 23:43 --> 23:46lavage fluid where we take the test,
  • 23:46 --> 23:48the lavage for a woman.
  • 23:48 --> 23:50Right now, we also take a blood sample.
  • 23:50 --> 23:51And interestingly,
  • 23:51 --> 23:53what we find is the same signal
  • 23:53 --> 23:55that we're picking up in the
  • 23:55 --> 23:58lavage we can pick up in the blood.
  • 23:58 --> 24:00So it may be that the test is
  • 24:00 --> 24:03done in combination where we do
  • 24:03 --> 24:05a lavage plus a blood sample.
  • 24:05 --> 24:07So that way we might cover for
  • 24:07 --> 24:10those patients where the cells
  • 24:10 --> 24:12actually don't fall into the uterus.
  • 24:13 --> 24:18And so now we have a good
  • 24:18 --> 24:21screening test for cervical cancer.
  • 24:21 --> 24:24We potentially have one for uterine
  • 24:24 --> 24:26cancer and maybe even ovarian cancer.
  • 24:26 --> 24:28The other two cancers that you
  • 24:28 --> 24:31mentioned at the top of the show
  • 24:31 --> 24:33were vulvar and vaginal cancers.
  • 24:33 --> 24:35Anything on the horizon
  • 24:35 --> 24:37for screening in those two cancers?
  • 24:38 --> 24:40For vulvar cancer which is really
  • 24:40 --> 24:43a skin cancer and it's on the
  • 24:43 --> 24:44external part,
  • 24:44 --> 24:48and so the most important thing for that is
  • 24:48 --> 24:49going to be education.
  • 24:49 --> 24:51And it's education of not only
  • 24:51 --> 24:54patients but primary care providers.
  • 24:54 --> 24:56Because when a woman complains the
  • 24:56 --> 24:58typical complaints for vulvar
  • 24:58 --> 25:02cancer are itching, dryness,
  • 25:02 --> 25:05cracking skin and
  • 25:05 --> 25:07those are often ignored where
  • 25:07 --> 25:09somebody will say go to the
  • 25:09 --> 25:11drugstore and put on some cortisone
  • 25:11 --> 25:13cream and that will make it better.
  • 25:13 --> 25:15But the key thing is that if
  • 25:15 --> 25:16somebody has these symptoms and
  • 25:16 --> 25:18their lasting greater than a month,
  • 25:18 --> 25:20you should see a specialist and
  • 25:20 --> 25:23we will then look at their skin
  • 25:23 --> 25:25with a microscope or the colposcope.
  • 25:25 --> 25:27And more often than not we will
  • 25:27 --> 25:30always take a small skin biopsy to
  • 25:30 --> 25:32make sure that there is no malignancy
  • 25:32 --> 25:35because if all cancer is caught early,
  • 25:35 --> 25:38it becomes also curable.
  • 25:38 --> 25:40And so most
  • 25:40 --> 25:41cases we see are advanced,
  • 25:42 --> 25:44the advanced cases are where women
  • 25:44 --> 25:47have lived for years on these salves,
  • 25:47 --> 25:51creams and so forth that they just keep
  • 25:51 --> 25:52getting and nobody's thought,
  • 25:52 --> 25:54well wait a minute, you know
  • 25:54 --> 25:57there's got to be a reason for this
  • 25:57 --> 25:59and the emphasis really is to
  • 25:59 --> 26:01to take a biopsy and primary care
  • 26:01 --> 26:03doctors are more than capable of
  • 26:03 --> 26:05taking the biopsy because it's just
  • 26:05 --> 26:07looking at the skin and the lesions.
  • 26:09 --> 26:11Very easy to identify.
  • 26:11 --> 26:13Vaginal cancers now are also
  • 26:13 --> 26:15going to be picked up with
  • 26:16 --> 26:19A Pap test also because the Pap
  • 26:19 --> 26:21test can pick up the same kinds
  • 26:21 --> 26:23of precancerous cells that we
  • 26:23 --> 26:25see in cervical cancer can also
  • 26:25 --> 26:27occur in vaginal cancers.
  • 26:27 --> 26:29So the PAP tests can be very
  • 26:29 --> 26:31effective in that way also.
  • 26:31 --> 26:32So you know,
  • 26:32 --> 26:34it's really a matter
  • 26:34 --> 26:36of getting people to
  • 26:36 --> 26:37understand their bodies and always
  • 26:37 --> 26:39to ask that question or you know
  • 26:39 --> 26:41I tell my patients for
  • 26:41 --> 26:42specifically for ovarian cancer
  • 26:42 --> 26:45if they have this constellation
  • 26:45 --> 26:47of symptoms of early satiety,
  • 26:47 --> 26:49a little bit of abdominal swelling
  • 26:49 --> 26:50or discomfort or whatever,
  • 26:50 --> 26:52and if pain or discomfort
  • 26:52 --> 26:54lasts more than four weeks,
  • 26:54 --> 26:56go to your doctor and you say,
  • 26:56 --> 27:00prove to me that I don't have ovary cancer.
  • 27:00 --> 27:03Rather than just continue to live
  • 27:03 --> 27:05with the the symptoms get multiple
  • 27:05 --> 27:08urine cultures and the like and
  • 27:08 --> 27:09two months later,
  • 27:09 --> 27:10you'll find out that those symptoms
  • 27:10 --> 27:12were really of a developing cancer,
  • 27:12 --> 27:13which is unfortunate.
  • 27:14 --> 27:16Yeah, I think that you know
  • 27:16 --> 27:18very often those symptoms,
  • 27:18 --> 27:22right feeling of bloatedness.
  • 27:22 --> 27:24You know, a little bit of urinary frequency,
  • 27:24 --> 27:27a little bit of abdominal pain.
  • 27:27 --> 27:30There can be so many other things
  • 27:30 --> 27:32and many patients think that the
  • 27:32 --> 27:34last thing on their mind is that
  • 27:34 --> 27:37this could be an ovarian cancer,
  • 27:37 --> 27:38particularly if they don't
  • 27:38 --> 27:40have a family history,
  • 27:40 --> 27:44they don't have a genetic mutation.
  • 27:44 --> 27:46And so they tend to put that at
  • 27:46 --> 27:48the bottom of the list.
  • 27:49 --> 27:50Right. And we need to move it up.
  • 27:50 --> 27:52Because if we think about it right,
  • 27:52 --> 27:53the genetic mutations,
  • 27:53 --> 27:56particularly the BRCA genes,
  • 27:56 --> 27:59those are going to account for roughly about
  • 27:59 --> 28:0215 to 18% of people who get ovarian cancer.
  • 28:02 --> 28:04So that means 85% of these are
  • 28:04 --> 28:06going to people going to be in
  • 28:06 --> 28:07people without a family history,
  • 28:07 --> 28:09without a genetic mutation
  • 28:09 --> 28:12that we hardly can identify.
  • 28:12 --> 28:15And so it behooves us,
  • 28:15 --> 28:17again, it's like when we
  • 28:17 --> 28:19all taught our medical students.
  • 28:19 --> 28:22If somebody has pelvic pain, you know,
  • 28:22 --> 28:24give me a differential diagnosis.
  • 28:24 --> 28:26And not three things,
  • 28:26 --> 28:27give me 15 things,
  • 28:27 --> 28:28because if you don't think
  • 28:28 --> 28:30about it as a possibility,
  • 28:30 --> 28:31you'll never find it.
  • 28:31 --> 28:33Doctor Peter Dottino is a
  • 28:33 --> 28:35professor of obstetrics, gynecology,
  • 28:35 --> 28:36and reproductive sciences at
  • 28:36 --> 28:39the Yale School of Medicine.
  • 28:39 --> 28:41If you have questions,
  • 28:41 --> 28:43the address is canceranswers@yale.edu,
  • 28:43 --> 28:45and past editions of the program
  • 28:45 --> 28:48are available in audio and written
  • 28:48 --> 28:49form at yalecancercenter.org.
  • 28:49 --> 28:51We hope you'll join us next week to
  • 28:51 --> 28:53learn more about the fight against
  • 28:53 --> 28:55cancer here on Connecticut Public Radio.
  • 28:55 --> 28:57Funding for Yale Cancer Answers is
  • 28:57 --> 29:00provided by Smilow Cancer Hospital.