Breast Cancer 2010 David B. Pearlstone, MD MBA FACS Co-Director, Breast Division John Theurer Cancer Center Chief, Division of Breast Surgery Hackensack.

Slides:



Advertisements
Similar presentations
How will you approach the 35 year old, with a 2 x 2 x 2cm, firm, mobile, well circumscribed non tender mass on the right breast?
Advertisements

Breast Cancer Early Detection is Your Best Protection
Which of the following increases a women’s risk for Breast Cancer? A.Starting her menses at age 14 or older B.Breastfeeding C.Extremely dense breast tissue.
†Source: U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2011 Incidence and Mortality Web-based Report. Atlanta (GA): Department.
Breast and Prostate Cancer Prevention
Breast MR Imaging Workshop th September 2014 High-Risk Screening Evidence-based Clinical Indications for Breast MRI Dr. Muhamad Zabidi Ahmad, AMDI.
Breast Density A patient guide.
10 November 2011 Genetic counseling for breast cancer risk Aichu Huang, MS. CGC. Department of Medical Genetics National Taiwan University Hospital.
1 GINA for Health Professionals The Genetic Information Nondiscrimination Act May 2010 Developed Under a Grant from The Pew Charitable Trusts Copyright.
Hereditary Factors in Breast Cancer
Hereditary breast and ovarian cancer Who should be screened and How? Symposium on Cancer Waterloo Inn October 31, 2007 Mala Bahl, MD, MSc.
Hereditary Breast & Ovarian Cancer Syndrome HBOC Tammy McKamie RN MSN OCN Cancer Genetics Educator Clinical Oncology Patient Navigator.
Breast Cancer Risk and Risk Assessment Models
YOLANDA LAWSON M.D., F.A.C.O.G MADEWELL OBGYN ASSOCIATE ATTENDING BAYLOR UNIVERSITY MEDICAL CENTER Women's Health Screening Guidelines.
Type Of Cancer:Location: CarcinomaEpithelial Cells SarcomaConnective Tissue LeukemiaCirculatory / Lymphatic.
Copyright © 2005 Pearson Education, Inc., publishing as Benjamin Cummings PowerPoint ® Lecture prepared by Jan Campbell T H E B A S I C S SIXTH EDITION.
April 6, o What is cancer? o Cancer statistics o Cancer prevention and early detection o Cancer disparities o Cancer survivorship o Cancer research.
The Harvard Health Caucus Genetic Privacy: Legal & Ethical Frameworks Allan T. Bombard, MD, FACOG, FACS, FACMG Medical Director, Aetna Women’s Health Program.
Otis W. Brawley, M.D. Chief Medical and Scientific Officer Executive Vice President American Cancer Society Professor of Hematology, Medical Oncology,
Breast Cancer 101 Barbara Lee Bass, MD, FACS Professor of Surgery
The Facts about Breast Cancer
Breast Imaging Made Brief and Simple
Breast cancer screening Recommendations for breast cancer screening چه شواهدی برای خطر وجود دارد؟ برای غربالگری چه باید کرد؟
Breast Cancer By George Rezk.
Screening Tests for Brest & Cervical Cancer
Breast Cancer This slide goes first.
The Cancer Pedigree BRCA What?. Outline Introduction: Understanding the weight of genetics in Ovarian Breast Cancer BRCA 1 and BRCA 2 Genes – Function.
Genetics and Ovarian Cancer June 16, 2015 Ovarian Cancer Alliance of Oregon and SW Washington Becky Clark, MS, CGC Genetic Counselor.
Breast Health/Breast Cancer Awareness Program Workplace Session Copyright © 2008 by Susan G. Komen for the Cure. All rights reserved.
The Mammary Glands Pages Mammary Glands © 2015 Pearson Education, Inc.  Modifies sweat glands  Present in both sexes; functional only in females.
Breast Cancer. This Presentation provided by The American Cancer Society The University of Georgia Cooperative Extension Service The Department of Human.
Breast cancer screening Mammography is the most widely used screening modality, with solid evidence of benefit for women aged 40 to 74 years Clinical breast.
Early Detection Is Your Best Protection. Breast Cancer Statistics for Women A woman has a one in eight chance of developing breast cancer in her lifetime.
Ovarian Cancer National Alliance Ovarian Cancer: What All Women Need to Know.
GENETIC TESTING: WHAT DOES IT REALLY TELL YOU? Lori L. Ballinger, MS, CGC Licensed Genetic Counselor University of New Mexico Cancer Center.
Cancer Risk Assessment Judith A Westman MD Clinical Director Division of Human Genetics.
Breast Cancer Inheritance
Atoosa Adibi MD. Department of Radiology Isfahan University Of Medical Sciences.
Breast Cancer Methods for Early Detection. Breast Cancer What It Is Methods of Early Detection Risk Factors.
1 MAMMOGRAPHY RADIOGRAPHIC IMAGING OF THE BREAST Part 2 -Statistics A mammogram can find breast cancer when it is very small -- 2 to 3 years before you.
Breast Cancer. What is this Disease? Second leading cause of cancer death in women Malignant (cancerous) tumor –Develops from cells in the breast that.
Ovarian Cancer Risk Reduction Taking oral contraceptives for 5 years can reduce your risk of ovarian cancer by up to 50% Hankinson SE, Colditz GA, Hunter.
Breast Cancer Breast Cancer DR/FATMA AL-THOUBAITY ASSOCIATE PROFESSOR SURGICAL CONSULTANT.
National Breast Cancer Awareness Month sources: National Cancer Institute ( and American Cancer Society ( Employee Wellness.
Shiva Sharma SHO to Professor Redmond.  Introduction  Increased risk groups  Consideration of genetic testing  Management of patients with mutation.
March 10, 2014 NURS 330 Human Reproductive Health.
Breast Cancer and Ethical Issues Regarding Insurance Coverage! By Jenn Butt Heidi Keefe Melissa Snyder Rachel Malinowski.
Genetics: For this Generation and the Next
BREAST CANCER: Half a million women later… Amy Miglani M.D September 3, 2004.
COMMON LIFESTYLE DISEASES: CANCER EMS 355 By: Dr. Bushra Bilal.
Breast Cancer. Breast cancer is a disease in which malignant cells form in the tissues of the breast – “National Breast Cancer Foundation” The American.
Javad Jamshidi Fasa University of Medical Sciences, December 2015 Cancer Genetics Session 4 Medical Genetics.
Cancer 101: A Cancer Education and Training Program for [Target Population] Date Location Presented by: Presenter 1 Presenter 2.
By: Kaylee Copas. What is cancer? Cancer is the uncontrolled growth of abnormal cells in the body. Cancerous cells are also called malignant cells.
Breast Cancer.  Breast Cancer is a form of cancer that affects both genders; although it is more common in women.  It is caused by a malignant tumor.
By: Anthony, Sophia, Jessica, Terrance, and Sierra.
Genetic Counseling Yahwardiah Siregar Sry Suryani W Mutiara Indah Sari.
Genomic Medicine Rebecca Tay Oncology Registrar. What is Genomic Medicine? personalised, precision or stratified medicine.
Breast Cancer in Young Women by Kim Wooden 1. Facts While the majority of women who develop breast cancer are postmenopausal, younger women are more likely.
The Elliott Breast Center * Baton Rouge, LA *
Brent Hannah. Breast Cancer  Uncontrolled cell growth in the breast as a result of mutation or abnormal change in the regulation of cell growth  Second.
BREAST SELF- AWARENESS FOR OUR COMMUNITY Updated 3/2015.
Hereditary Cancer Predisposition: Updates in Genetic Testing
Breast cancer screening recommendations
Cancer screening PROF .MAZIN AL-HAWAZ.
Breast Imaging Ravi Adhikary, MD.
Genetic Counseling & Testing for Cancer Risk
Breast Cancer.
Genetic Cancer Screening Medicare Insurance Clients
Specific Tumor Suppressor Genes
Presentation transcript:

Breast Cancer 2010 David B. Pearlstone, MD MBA FACS Co-Director, Breast Division John Theurer Cancer Center Chief, Division of Breast Surgery Hackensack University Medical Center

Outline – Epidemiology – Screening – Work up Genomics or ‘personalized medicine’ – diagnosis and treatment – breast & ovarian cancer

Breast Cancer 101 Statistics Most commonly diagnosed cancer among women; 27% of all cancers diagnosed in women are breast cancers. Second most common cause of cancer deaths among women, after lung cancer; 15% of all women who die of cancer, die of breast cancer.

Incidence of Cancers Among Women Jemal et al, Cancer Statistics, 2009 CA Cancer J Clin 2009;59:225

Cancer Deaths Among Women Jemal et al, Cancer Statistics, 2009 CA Cancer J Clin 2009;59:225

Cancer Cases and Cancer Deaths “Find more, Die less” Jemal et al, Cancer Statistics, 2009 CA Cancer J Clin 2009;59:225

Breast Cancer 101 Biology any cell can produce malignancy – glandular/ductal cells – high turnover – Adenocarcinomas ductal adenocarcinoma, ‘garden variety breast cancer’

ACS Screening Recommendations Women should know how their breasts normally feel and report any breast change promptly to their health care providers. Breast self-exam (BSE) is an option for women starting in their 20s. Yearly mammograms are recommended starting at age 40 and continuing for as long as a woman is in good health. Women at high risk (greater than 20% lifetime risk) should get an MRI and a mammogram every year. Women at moderately increased risk (15% to 20% lifetime risk) should talk with their doctors about the benefits and limitations of adding MRI screening to their yearly mammogram. Yearly MRI screening is not recommended for women whose lifetime risk of breast cancer is less than 15%. Clinical breast exam (CBE) should be part of a periodic health exam, about every 3 years for women in their 20s and 30s and every year for women 40 and over. Cancer_Detection_Guidelines_36.asp?sitearea=PED

Breast Self Exam Women should know how their breasts normally feel and report any breast change promptly to their health care providers. Breast self-exam (BSE) is an option for women starting in their 20s. Monthly – Cycle – Shower

Breast Self Exam Don’t be intimidated You know yourself better than you think you do

Breast Imaging Mammography Ultrasound MRI Microwave imaging Thermography Electroimpedence

Breast Imaging Mammography 40 mammogram Yearly mammograms are recommended starting at age 40 and continuing for as long as a woman is in good health. Exceptions personal history strong family history Role of ultrasound in early screening Evolving field

Breast Imaging MRI Women at high risk (greater than 20% lifetime risk) should get an MRI and a mammogram every year. Women at moderately increased risk (15% to 20% lifetime risk) should talk with their doctors about the benefits and limitations of adding MRI screening to their yearly mammogram. Yearly MRI screening is not recommended for women whose lifetime risk of breast cancer is less than 15%.

Annual Exam Clinical breast exam (CBE) should be part of a periodic health exam, about every 3 years for women in their 20s and 30s and every year for women 40 and over.

Annual Exam History symptoms (mass, pain, discharge, skin changes), gyn history, family history, endocrine therapy history PERSONAL HISTORY OF BREAST CANCER Physical visual v. palpable, skin changes, nipple, axilla/supraclavicular Imaging

Annual Exam Genetics consultation/discussion Analysis of risk Risk reduction

The Dread “Finding” “I think you should see a breast specialist.” Work up Biopsy FNA core needle excisional palpable wire localized ~80% negative rate

Genomics Diagnosis BRCA1 & BRCA2 other genotypes treatment options – observation – medical – surgical FAMILY HISTORY – Most breast cancers are sporadic – Few are familial – Even fewer are ‘genetic’ – IF YOU DON’T HAVE THE MUTATION, YOU ARE NOT OFF THE HOOK

Genomics Breast Cancer Risk with BRCA Mutation 12 % of women in the general population will develop breast cancer sometime during their lives 60% of women who have inherited a harmful mutation in BRCA1 or BRCA2 will develop breast cancer sometime during their lives. In other words, a woman who has inherited a harmful mutation in BRCA1 or BRCA2 is about five times more likely to develop breast cancer than a woman who does not have such a mutation.

Genomics BRCA1 &BRCA2 Tumor suppressor genes Not just breast cancer BRCA1: cervical, uterine, pancreas, colon cancer male breast cancer, testicular, prostate BRCA2: pancreas, stomach, gall bladder, melanoma

Genomics BRCA1 &BRCA2 The BRCA1 gene is located on the long (q) arm of chromosome 17 at band 21, from base pair 38,449,840 to base pair 38,530,994 The BRCA2 gene is located on the long (q) arm of chromosome 13 at position 12.3 (13q12.3), from base pair 31,787,616 to base pair 31,871,804

Genomics BRCA1

Genomics BRCA1 & BRCA2 Certain variations of the BRCA1 gene lead to an increased risk for breast cancer. Researchers have identified hundreds of mutations in the BRCA1 gene, many of which are associated with an increased risk of cancer. Women who have an abnormal BRCA1 or BRCA2 gene have up to an 85% risk of developing breast cancer by age 70; increased risk of developing ovarian cancer is about 55% for women with BRCA1 mutations and about 25% for women with BRCA2 mutations

Genomics Who is most likely to have a BRCA mutation? Three specific mutations, two in the BRCA1 gene and one in the BRCA2 gene, are the most common mutations found in these genes in the Ashkenazi Jewish population. In one study, 2.3 percent of participants (120 out of 5,318) carried one of these three mutations This frequency is about five times higher than that found in the general population. Norwegian, Dutch, and Icelandic peoples, also have higher frequencies of specific BRCA1 and BRCA2 mutations. Frequencies of specific BRCA1 and BRCA2 mutations may vary among individual racial and ethnic groups in the United States, including African Americans, Hispanics, Asian Americans, and non-Hispanic whites.

Genomics Who Should Get BRCA Tested? – For women who are not of Ashkenazi Jewish descent: two first-degree relatives (mother, daughter, or sister) diagnosed with breast cancer, one of whom was diagnosed at age 50 or younger; three or more first-degree or second-degree (grandmother or aunt) relatives diagnosed with breast cancer regardless of their age at diagnosis; a combination of first- and second-degree relatives diagnosed with breast cancer and ovarian cancer (one cancer type per person); a first-degree relative with cancer diagnosed in both breasts (bilateral breast cancer); a combination of two or more first- or second-degree relatives diagnosed with ovarian cancer regardless of age at diagnosis; a first- or second-degree relative diagnosed with both breast and ovarian cancer regardless of age at diagnosis; and breast cancer diagnosed in a male relative.

Genomics Who Should Get BRCA Tested? – For women of Ashkenazi Jewish descent: any first-degree relative diagnosed with breast or ovarian cancer; and two second-degree relatives on the same side of the family diagnosed with breast or ovarian cancer. DO YOU REALLY WANT TO BE TESTED?

Genomics Genetic Discrimination GINA – Enacted 2008 – protect U.S. citizens against discrimination based on their genetic information in relation to health insurance and employment. – The parts of the law relating to health insurers will take effect between May 2009 and May 2010 – The parts relating to employers will take effect by November – does not cover life insurance, disability insurance, and long-term care insurance. – does not cover members of the military.

Genomics Genetic Discrimination Some of the protections under GINA with regard to health insurance include the following: – Premiums or contributions to a group health plan cannot be increased based on the genetic information of an individual(s) enrolled in the plan. – Insurers cannot require an individual or family member to undergo a genetic test before enrollment in a group health plan. – Insurers cannot request, require, or purchase genetic information about an individual before the person’s enrollment in a group health plan – Health insurers cannot use genetic information as the only basis upon which to claim a pre-existing condition is present and, therefore, to deny coverage.

Genomics Genetic Discrimination Some of the protections under GINA with regard to employment include the following: – Employers cannot refuse to hire and cannot fire individuals based on their genetic information. – Employers cannot discriminate against employees because of their genetic information. – Employers cannot request, require, or purchase genetic information about an employee except under specific circumstances. – Employers cannot disclose an employee's genetic information except under specific circumstances.

Genomics BRCA & Ovarian Cancer 1.4 % of women in the general population will be diagnosed with ovarian cancer 15 to 40 % of women who have a BRCA1 or BRCA2 mutation will be diagnosed with ovarian cancer.

Genomics Other Genetic Mutations Mutations in several other genes, including TP53, PTEN, STK11/LKB1, CDH1, CHEK2, ATM, MLH1, and MSH2, have been associated with hereditary breast and/or ovarian tumors. The majority of hereditary breast cancers can be accounted for by inherited mutations in BRCA1 and BRCA2. Overall, it has been estimated that inherited BRCA1 and BRCA2 mutations account for 5 to 10 percent of breast cancers and 10 to 15 percent of ovarian cancers among white women in the United States

Genomics Myriad Genetics BRCA1 and BRCA2 are patented in the United States by Myriad Genetics This US patent has been challenged by the American Civil Liberties Union

Breast Cancer & You Monthly breast self exam Annual practitioner exam Annual mammogram Know your family history BE PROACTIVE

Breast Cancer 2010 David B. Pearlstone, MD MBA FACS Co-Director, Breast Division John Theurer Cancer Center Chief, Division of Breast Surgery Hackensack University Medical Center