Showing posts with label genetic testing. Show all posts
Showing posts with label genetic testing. Show all posts

Wednesday, 11 July 2018

Hereditary vs Somatic Mutations July 2018 Chat

Tonight our topic was Hereditary vs Somatic Mutations in gynecologic cancers. Along with our regular participants we also welcomed a few new community members. We especially appreciate the attendance of Erica Bodner (@EMBOSU), a genetic counselor at MD Anderson Cancer Center for sharing her expertise on hereditary mutations and the role of genetic counselors.

You may find a complete transcript here and analytics here. The resources shared during the chat are listed at the end of this post.

Here is a sample of the responses to the questions we asked during the hour chat.

T1: What is the difference between hereditary mutations and somatic mutations?
  • hereditary mutations (aka germline) = changes or "spelling mistakes" in a gene that we inherit from a parent. The mutation is present in every cell of our body. Somatic mutations are what I think of as tumor-specific: changes that occur in the tumor or cancer
  • “When a mutation occurs within germ cells, it is called a germline mutation. Germline mutations affect every cell in an organism and are passed on to offspring. When a mutation occurs in a somatic cell, it is called a somatic mutation.”
  • There are some tricky cases where we look at a tumor for it's somatic mutations and accidentally find hereditary (germline) changes -- since those are in all of the cells, often including the tumor. It can get complicated!
T2: Which gene mutations are known to be associated with hereditary gynecologic cancers?
    • 1) a single gene is like a very long sentence...a mutation=a letter change somewhere within that sentence that causes the sentence to not make any sense to the body. There can be 100s of spots in any given gene that can have a mutation
    • (2): for gyn cancers it's often easier to think about which cancers are linked to which hereditary conditions. Ex: ~3% of endometrial cancers are due to Lynch syndrome (caused by a mutation in 1 of 5 genes: MLH1 MSH2 MSH6 PMS2 or EPCAM)
    • (3) about 10-20% of "epithelial" ovarian cancers are due to a hereditary cause...most often a mutation in BRCA1 or BRCA2, but sometimes can be due to a mutation in a Lynch syndrome gene or a "moderate penetrance" gene like RAD51D
    • Genetic mutation an alteration in DNA occurs after conception ovarian CA inherited mutation in BRCA1/BRCA2
    • Yes. BRCA associated ovarian cancers are more frequently high grade serous carcinomas whereas Lynch syndrome associated ovarian carcinomas are nonserous (most endometrioid or clear cell)
    • BRCA1 and BRCA2
      T3: What testing is needed to find hereditary mutations?
          T3 follow-up... What are the differences between clinical genetic tests and Direct To Consumer (DTC) tests?
          • T3 (1) clinical genetic tests are ordered by your genetic counselor and/or doctor for medical purposes + have high levels of quality control & regulation. DTC labs (historically) have been tests ordered by any1 from home + often used different technology+ non-med purpose
          • 2) now we're starting to see clinical-DTC Hybrids like @Color that are a little bit of both. The genetic testing area is growing & changing very fast...luckily it's our job as genetic counselors to keep track of what's out there & can help navigate you to best options
          • T3: There have been many articles recently about what DTC do and do not cover. Most would need a clinical lab test to confirm results. Genetic counseling key before to decide and after to be sure understand results
          • Evaluation of some direct-to-consumer genetic testing reveals inaccuracies and misinterpretations #gyncsm http://www.facingourrisk.org/XRAYS/inaccurate-dtc-results?utm_source=social&utm_medium=social&utm_campaign=XRAYS%202017-2018%20social%20monitoring
          • Cannot be overemphasized the importance of having ur health care team involved. Confirming DTC results in a clinical laboratory that's well versed in complex variant detection & classification is essential. This is concerning... https://www.nature.com/articles/gim201838
          T4: Do we know what somatic mutations are prevalent in gynecologic cancers?
            • I found this journal article "13 most important genes for gynaecological cancers, being BRAF, CDKN2A, CTNNB1, FBXW7, FGFR2, FGFR3, FOXL2, HRAS, KRAS, NRAS, PIK3CA, PPP2R1A and PTEN." http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0093451
            • Research on somatic mutations is early but is part of the personalized/precision medicine puzzle. BRAF, KRAS, PIK3CA and PTEN have been identified with epithelial ovarian tumors. There are also somatic BRCA mutations. 
             T5: How does knowing you have these mutations impact your healthcare decisions?
              • knowing if you have a hereditary mutation (or not) can impact cancer treatment decision making, cancer screening/prevention options, and can provide info to relatives so they can better understand their cancer risks
              • hereditary mutations can signal risk for other, separate cancers... This can be information to help guide screening and prevention (but the info might also feel like a burden, especially if you are already dealing with one cancer dx).
              • For those already diagnosed, more and more research is coming out to help select the best treatment based on which mutations are present. Genetic and tumor tests can help decide what to try when standard tx doesn't work - or even what to try first.
              • Do you chose prophylactic surgery? Vigilant testing ? #gyncsm. Tough choices
              • Women w/ OC knowing they are BRCA allows for additional treatment options on - PARP for example
              • Knowing that you are at risk for a certain cancers can be powerful information that allows you to take preventative risk reduction measures against developing those cancers
                T6: What role do genetic counselors play in helping patients understand the results of testing?
                  • My personal bias is to hope that genetic counselors have good relationships with mental health professionals to refer patients to.
                  • Personal risk is discussed. Choices are discussed. Emotional support is discussed. Information is powerful in making best decisions
                  • Genetic counseling can be especially important as multi-gene panel might be better suited given your family history (vs testing for one type of mutation).
                  • Genetic counselors can help you to navigate and piece together how your cancer history+family history impact your chance to have a hereditary mutation. We can help figure out if the testing you had was hereditary (germline) or somatic.
                  • Genetic counselors can help you weigh pro's and con's of genetic testing, and what results could mean for you and your family. Where to get tested? Does insurance cover it? We can help with that too!
                  • We can help explain your results, develop a plan for you and your family to help #endcancer. We also want to be a resource - emotional, informational, and for your family. You can find one of us at http://www.nsgc.org @GeneticCouns


                    If you are a patient or caregiver you may continue this discussion on the Smart Patients Platform ( https://www.smartpatients.com/gyncsm ). 

                    We hope you will join us for the next #gyncsm chat: Wednesday, August 8, 2018 on "What is OK during treatment?" where we'll touch on things like vitamins, supplements, exercise, etc.
                    Have a good month.

                    Dee
                    #gyncsm Co-moderator


                    RESOURCES
                    Germline vs Somatic mutations
                    https://biologywise.com/germline-mutation-vs-somatic-mutation

                    National Society of Genetic Counselors
                    https://www.nsgc.org/

                    FORCE
                    http://www.facingourrisk.org/understanding-brca-and-hboc/getting-tested.php
                    http://www.facingourrisk.org/XRAYS/inaccurate-dtc-results?utm_source=social&utm_medium=social&utm_campaign=XRAYS%202017-2018%20social%20monitoring

                    SGO
                    https://www.sgo.org/newsroom/position-statements-2/genetic-testing-for-gynecologic-cancer/

                    Salon - What Genetic Testing Didn't Tell Me About My Cancer
                    https://www.salon.com/2018/06/24/what-genetic-testing-didnt-tell-me-about-my-cancer/

                    CURE Magazine - Cancer Redefined Personalized Medicine
                    https://www.curetoday.com/community/rick-boulay/2018/07/cancer-redefined-personalized-medicine

                    NATURE - False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care
                    https://www.nature.com/articles/gim201838

                    New York Times - The Online Gene Test Finds a Dangerous Mutation...
                    https://www.nytimes.com/2018/07/02/health/gene-testing-disease-nyt.html?nytmobile=0

                    @NIH Fact Sheet
                    https://www.genome.gov/pages/health/patientspublicinfo/genetictestingfactsheet.pdf

                    Designing a High-Throughput Somatic Mutation Profiling Panel Specifically for Gynaecological Cancers
                    http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0093451

                    Friday, 6 July 2018

                    July 11, 2018 Hereditary vs Somatic Mutations


                    The topic of the #gyncsm community's second ever chat was Genetics and Personalized Medicine. Since that day in October 2013 we have learned much more about the mutations associated with gynecologic cancer. This month we will be discussing Hereditary vs Somatic Mutations.

                    If you want to know...
                    • The differences between hereditary and somatic mutations
                    • The gene mutations associated with hereditary gynecologic cancers
                    • What testing is needed to find hereditary mutations
                    • What somatic mutations are prevalent in gynecologic cancers
                    • How knowing you have these mutations can impact your healthcare decisions
                    • What role genetics counselors play in understanding test results
                    ...then be sure to join us on Wednesday July 11, 2018 at 9pm ET. 

                    The CDC has a wealth of information on genes and genetics at https://www.genome.gov/education/ or check out this Fact Sheet from the NIH  https://www.genome.gov/pages/health/patientspublicinfo/genetictestingfactsheet.pdf

                    We look forward to having you join us on the 11th. 

                    Dee

                    Wednesday, 9 March 2016

                    March Chat Genetic Counselors and Gynecologic Cancer Risk

                    "Genetics is an integral part of cancer prevention. Know your genetics. Get to know a GC."
                    -Mary Freivogel 

                    For this month's chat, we were joined by the National Society of Genetic Counselors (@GeneticCouns) Past President Joy Larsen Haidle (@JoyLarsenHaidle) and NSGC President-elect Mary Freivogel (@MaryFreivogel) to discuss Genetic Counselors and Understanding Gynecologic Cancer Risk. We had 45 participants and achieved over 1.7 million impressions.  Additional analytics may be found here. 

                    A small sample of the responses to each of our topic questions appear below. You may read the full transcript here.  (Please scroll down for a list of valuable resource shared during the chat. )

                    T1: What is genetic counseling and why it is recommended prior to genetic testing?
                    • @GeneticCouns help estimate #cancer risk, discuss test options & explain how test results might be used in your medical care 
                    • We (Genetic Counselors) help to make sure genetic testing is the right choice for you and your family! 
                    • Not everyone would benefit from a genetic test. Talk to a #geneticcounselor to learn if testing is useful for you.
                    • Genetic counselors help people understand & adapt to med,psych & familial implications of genetic contributions to disease… 
                    T2a: Who should consider genetic testing? How does it help those already diagnosed w/ a GYN cancer? Does it impact treatment plans?
                    • T2A @SGO_org recommends genetic testing: https://t.co/Q3rMU66Qey
                    • Cancer diagnosis before age 50 or strong family history of cancer often warrants genetic testing.
                    T2b: Have you had genetic testing? What influenced your decision? If yes, did you have a genetic counselor?
                    • T2 #Gyncsm: Family history of #ColonCancer, brother tested positive for #Lynchsyndrome. Having a child influenced decision, and yes! 
                    • T2 My gyn onc spoke to me about genetic testing. I then talked to a genetic counselor re: my "pedigree" and she recommended the test
                    • T2 yes had genetic testing. Breast & ovarian cancer in family. #brca mutation 3 generations 
                    T3: Which genetic mutations are known to increase risk for gyn cancers? Do these mutations also impact risks for other cancers?
                    • T3 At least 24 genes are associated with ovarian cancer risk. Several have uterine cancer risk.
                    • T3 A genetic counselor can help determine the best test based on your personal and family history. #gyncsm @GeneticCouns 
                    • Many more than BRCA1/2! Lynch syndrome is colon, uterine, ovarian, stomach cancer, etc... Talk to a GC if you are concerned! #gyncsm 
                    • T3 Many mutations associated with Gyn Cancers: BRCA 1/2, Lynch Syndrome, Cowdens' Syndrome. Li Fraumeni . Often other cancers too.
                    • T3: Many people, even PJS patients, don't know that Peutz-Jeghers Syndrome adds risk for gyn or breast cancer
                    T4a: How can people access genetic counseling? What prep work is needed? Are referrals required?
                    T4b: Does insurance cover genetic counseling? Are there protections against discrimination based on genetic test results?
                    • Most but not all insurance covers both the genetics consultation and the testing 
                    • GC for BRCA1/2 testing is often covered as preventive service as per the Affordable Care Act. Check your policy for details. 
                    • Talk to your GC/MD about testing options--if cost is a barrier, there may be financial assistance available to help! 
                    • Risk of genetic discrimination is very low. Often far outweighed by info gained from genetic testing. Talk to a GC!
                    •  Life insurance is a HUGE problem , not protected under #GINA. Seek coverage PRIOR to genetic counseling/testing. 
                    T5a: Let's talk about the term "risk". If mutations are found that increase my cancer risk, what does that really mean for me?
                    • Everyone has a chance of developing cancer. Having a mutation raises the chance above the general population.
                    • #Cancer risk is not the same with all genes. Some genes confer low, medium or high risk.
                    • An average woman has a 1.5% chance of developing ovarian cancer. BRCA1 mutation raises chance to 45%. Lynch 4-24%. 
                    • Some women will consider surgery to decrease their cancer #risk. Speak to a @GeneticCouns to discuss your cancer
                    T6: Where can those with a genetic mutation find the latest info and get help weighing options for preventative action or treatment?
                    • @GeneticCouns has resources. Talk to a genetic counselor to help gather current info tailored to you. https://t.co/6DC5QzpmDQ
                    • We recommend people see only CGC Certified Genetic Counselor
                    • Where can you find the latest info and get help w options for prevention or treatment? A genetics counselor!
                    T7: How and when to share test results with family can be tough. What are some tips?

                    If you would like to continue this discussion, feel free to join us on Smart Patients at https://www.smartpatients.com/gyncsm.

                    Be sure to mark your calendar for our next chat on Wednesday, April 10  at 9pm ET as we discuss Re-envisioning Ovarian Cancer Survivorship. Our guests will be Dr. Don S. Dizon (@drdonsdizon) and Dr. Teresa Hagan ( @TLHagan). We hope to see you then.

                    Dee
                    #gyncsm co-moderator

                    RESOURCES:
                    Find a Genetic Counselor near you at https://t.co/JHZReh6ReE

                    @GeneticCouns blog will help you prepare for a genetic counseling visit. https://t.co/murxf0ekQH


                    @BeBrightPink Collect Family History  https://t.co/S8JvCebcpE

                    SGO position statements on genetic testing https://www.sgo.org/newsroom/position-statements-2/genetic-testing-for-gynecologic-cancer/

                    Surgeon General's Family Health History Initiative https://t.co/0ynYRl339L

                    Genetic Discrimination information https://t.co/xJhGNF7VnZ 

                    GENETIC TESTING, PRIVACY AND DISCRIMINATION https://t.co/x2Z1aTACg1

                    https://t.co/o8hs49pDGn genetic discrimination laws and protections

                    OCS:Development of the Risk of Ovarian Cancer Algorithm and RoOCA Screening Trials http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572791/

                    Hereditary cancer risk resources: @FacingOurRisk @BeBrightPink @Sharsheret @Hc_chat @BRCAinfo @BRCAresponder 

                    Communicating genetic test results: https://t.co/waFU48JsXi

                    After receiving +test results https://t.co/ROLi0rlFbc via Cancer Communication Research University of South Florida 

                    Oct 9,2013 Genetics and Personalized Medicine Chat https://t.co/T0ZjaCI4Bg

                    Genetic Testing and Ovarian Cancer  #gyncsm Community: https://t.co/uMVhorzjFa 

                    Genetic Counseling - Understanding Genetics - NCBI Bookshelf  https://t.co/Zi3UwQpRoE

                    Genetic Counseling Infographic  https://t.co/SZKjfF1caj 

                    Friday, 4 March 2016

                    March 9, 2016 Genetic Counselors and Understanding Gyn Cancer Risk

                    We are thrilled to be welcoming the leadership of the National Society of Genetic Counselors (@GeneticCouns) as our guests during the March 9, 2016 chat beginning at 9pmET (8CT/6PT). In July 2015 we shared on this blog a post titled, "Genetic Testing and Ovarian Cancer", which first appeared on the NSGC website. This month we will be expanding on that post and will be chatting about the role of genetic counselors in all gynecologic cancers as well as gynecologic cancer risks.

                    The topics questions are:
                    T1: What is genetic counseling and why it is recommended prior to genetic testing?

                    T2a: Who should consider genetic testing? How does it help those already diagnosed with a GYN cancer? Does it impact treatment plans?
                    T2b: Have you had genetic testing? What influenced your decision? If yes, did you have a genetic counselor?

                    T3: Which genetic mutations are known to increase risk for gynecologic cancers? Do these gene mutations impact risks for other cancers?

                    T4a: How can people access genetic counseling? What prep work is needed? Are referrals required? 
                    T4b: Does insurance cover genetic counseling? Are there protections against discrimination based on genetic test results?

                    T5a: Let's talk about the term "risk". If mutations are found that increase my cancer risk, what does that really mean for me? 
                    T5b: For those who have had genetic counseling and/or testing, how did the results impact your health care?

                    T6: Where can those with a genetic mutation find the latest info and get help weighing options for preventative action or treatment? 

                    T7: How and when to share test results with family can be tough. What are some tips?

                    If you would like to read more about genetic counselors and genetic testing check out these sites:

                    We look forward to you joining us!

                    Dee
                    Co-moderator

                    Tuesday, 29 September 2015

                    Hereditary Breast and Ovarian Cancer Week



                    [posted updated 9/2016, 9/2017, 9/2018]

                    The #gyncsm community has chatted about gynecologic cancer risks, the genetics of cancer (Genetics and Personalized Medicine), Genetic Counselors and Understanding Gyn Cancer Risk and Hereditary vs Somatic Mutations. HBOC week gives us another opportunity to share resources and information on hereditary ovarian and breast cancers.

                    About 15% of the ovarian cancers diagnosed are due to germline (inherited and passed on to offspring) mutations in the BRCA1 and BRCA2 genes. Having these mutations increases the risk of ovarian cancer by 15-50%. “Nearly one-third of women with hereditary ovarian carcinoma have no close relatives with cancer, and 35% of women with hereditary ovarian carcinoma are older than 60 years at diagnosis”(NCI). 

                    The Society of Gynecologic Oncology released a Clinical Practice statement in 2014 stating that all women diagnosed with ovarian, tubal and primary peritoneal cancer regardless of age or family history should receive counseling and be offered a genetic test. (https://www.sgo.org/clinical-practice/guidelines/genetic-testing-for-ovarian-cancer/)

                    F.O.R.C.E. (Facing Our Risk of Cancer Empowered) has played a crucial role in raising awareness, providing information and supporting research into hereditary breast and ovarian cancers. "The goal of HBOC Week and Previvor Day is to raise awareness about hereditary cancer. HBOC Week marks the transition between National Ovarian Cancer Awareness Month and National Breast Cancer Awareness Month and recognizes anyone affected by hereditary breast or ovarian cancer, including women and men with BRCA mutations, people with a family history of cancer, breast and ovarian cancer survivors, and previvors, individuals who carry a strong predisposition to cancer but have not developed the disease."

                    We hope you find these resources helpful. 


                    Hereditary Cancer Resources:

                    Bright Pink
                    www.bebrightpink.org
                    F.O.R.C.E. (Facing Our Risk of Cancer Empowered)
                    http://www.facingourrisk.org/
                    Sharsheret
                    http://www.sharsheret.org/
                    BRCA Mutation
                    http://www.cancer.gov/cancertopics/factsheet/Risk/BRCA
                    Lynch syndrome
                    http://www.cancer.net/cancer-types/lynch-syndrome
                    Cowden syndrome
                    http://www.cancer.net/cancer-types/cowden-syndrome
                    Li-Fraumeni syndrome
                    https://www.lfsassociation.org/what-is-lfs/
                    Peutz-Jeghers syndrome
                    https://www.cancer.net/cancer-types/peutz-jeghers-syndrome



                    Genetics: 
                    National Society of Genetics Counselors http://nsgc.org/
                    Find a Counselor Tool: http://nsgc.org/p/cm/ld/fid=164


                    Dee
                    #gyncsm Co-Founder 

                    Thursday, 23 July 2015

                    Genetic Testing and Ovarian Cancer

                    Genetic Testing and Ovarian Cancer originally appeared as a blog post on the National Society of Genetics Counselors (NSGC) website on Mar 23, 2015. It was written by Leigha Ann Senter-Jamieson, MS, LGC. Thank you  NSGC and Liegha Senter-Jamieson for allowing us to share this important information with the #gyncsm community.  



                    DNA Double Helix
                    As a genetic counselor specializing in ovarian cancer, I was heartened to learn about a recently approved chemotherapy treatment for women with a type of inherited ovarian cancer. In December, the US. Food and Drug Administration granted accelerated approval of Lynparza (also known as olaparib) for women whose ovarian cancer is caused by an inherited mutation in the BRCA1 or BRCA2 gene. Currently, this treatment is only for women whose cancer has failed to respond to three other types of chemotherapy.

                    Precision Medicine
                    This is an exciting example of how our understanding of the role of genetics in cancer is advancing the field of precision medicine, and bringing hope to women with ovarian cancer or anyone with a cancer that’s resistant to many of our standard treatments.

                    If you or a close relative has ovarian cancer, you may want to learn more about this treatment option, and consider genetic testing and genetic counseling. Genetic counseling both before and after the test is key.

                    What Genetic Testing Can Tell You
                    Genetic testing for ovarian cancer can provide information beyond whether a specific type of chemotherapy might be effective. It can tell you whether your particular type of cancer is hereditary and whether your close relatives, men included, may be at increased risk for developing ovarian cancer or other cancers, and whether they should consider being tested. Data suggest that up to 15 percent of women with ovarian cancer have a BRCA1 or BRCA2 mutation. These genes are associated with a 50 percent to 80 percent lifetime risk of breast cancer and a 20 to 40 percent lifetime risk of ovarian cancer in women, as well as an increased risk for breast cancer in men. These cancer risks are much higher than the risks faced by the general population. Because of this, women with the BRCA gene mutations are advised to begin cancer screenings at an earlier age and have them more often. Some women also consider having surgery to remove their ovaries or their breasts, which significantly lowers their risk of developing cancer. Since men may also inherit a BRCA1 or BRCA2 mutation, genetic testing is important for male relatives to consider as well since their screening would be adjusted if they were found to have the mutation.
                    Genetic counseling both before and after [genetic testing] is key.

                    While BRCA1 and BRCA2 mutations are the most common causes of hereditary ovarian cancer, there are less common genetic causes of the disease. In fact, many women with ovarian cancer now choose to have more extensive genetic testing utilizing what is often referred to as multi-gene panel testing. These tests analyze many genes at once and often include the BRCA genes. Multi-gene panels usually include other well-known genes that are less commonly associated with ovarian cancer risk. For some of the genes included in these tests, there are no published guidelines regarding cancer screening so it’s up to your cancer genetics care team to design a screening plan based on the available data.

                    The Role of Genetic Counseling
                    The information provided by genetic testing can be extremely useful, but it can also be overwhelming. A genetic counselor can help you decide which genetic test is right for you, guide you through the test results and what they mean for you and your family, and help you consider your options for screening, prevention or treatment.  
                    If you’d like to speak with a genetic counselor, you can locate one in your area using NSGC’s “Find a Genetic Counselor” tool.


                    Leigha Senter-Jamieson, MS, LGC is a member of the National Society of Genetic Counselors 2015 Board of Directors and is associate professor in the Division of Human Genetics in the Department of Internal Medicine at The Ohio State University



                    Dee
                    Co-moderator #gyncsm

                    Friday, 8 May 2015

                    May Chat : Advances in Personalized Medicine for GYN Cancer

                    Our October 2013 chat topic was "Genetics and Personalized Medicine". Many new developments and initiatives have occurred since then. During our May 13, 2015 (9pm EST) chat we will provide an update on advances made in personalized medicine and how they impact the care of patients with gynecologic cancers.

                    In addition to our regular Health Care Moderators, Dr. Scott Richard (@sdr2md) Director of the Division of Gynecologic Oncology at Hahnemann University Hospital and Kelly Mellott and Dr. Juan Avila from Helomics™ Corporation (former known as Precision Therapeutics; they will be tweeting as @HelomicsCancer) will join us for this important discussion. Helomics™ Corporation is a healthcare company that develops innovative diagnostics for the oncology field. PLEASE NOTE: Helomics' participation in this chat is NOT an endorsement of the company's products or services by the #gyncsm community or our health care moderators.

                    The discussion questions are:

                    T1A: What are some misconceptions you've heard about personalized medicine?
                    T1B: What personalized medicine options are currently available to gyn cancer patients? What is tested - tumor tissue, blood?
                    T2: How does genetic testing impact treatment decisions? What genetic tests are recommended for gyn cancers?
                    T3: How can I discuss personalized medicine options with my cancer care team? What if my doctor doesn't believe in these options?
                    T4A: How do you think the President’s Precision Medicine Initiative will affect patients/ research?
                    T4B: What are the challenges to bringing the benefit of personalized medicine to gyn cancer patients? How will patient care change?

                    To prepare for our discussion you may read  President Obama's Precision Medicine Initiative Fact Sheet . Additional articles/resources may be found on the CDC's Public Health Genomics page and on the NCI's Precision Medicine and Targeted Therapy page.

                    We look forward to having you join our discussion or come and "lurk and learn".

                    Dee
                    #gyncsm co-founder and co-moderator

                    Supplements / Vitamins Are they helpful? May 8, 2019 Chat

                    We were pleased to have Stacy Kennedy MPH,RD (@stacykennedyrd) join us for this informative chat on vitamins and supplements.  You may find ...