The BRCA1 and BRCA2 genes were discovered 25 years ago. Since then, our understanding of hereditary cancers has profoundly changed. The Basser Center was founded in 2012 to accelerate this understanding and propel progress in treatment opportunities and scientific discovery. Basser’s mission is to see a world free of the devastating effects of BRCA-related cancers.
At Basser, 25 million people affected means 25 million opportunities for a cure.
The discovery of BRCA1 and BRCA2 sparked incredible innovation in cancer research. The Basser Center at Penn Medicine’s Abramson Cancer Center turned that initial spark into a flame of promise — a focus on ensuring that future generations have better options. Basser is committed to collaborative science and compassionate clinical care. We know that approximately 25 million people are affected worldwide, but only 10% are aware of their mutation status. By raising awareness, Basser is saving lives. While our innovative research starts at Penn, it extends to best-in-class institutions around the world. This collective spirit has led to unparalleled collaboration and will push us to faster progress.
Our goal is to engage as many esteemed partners as possible in this mission. This collaborative approach is revolutionizing the field, expanding genetic testing, and spreading life-saving information to high-risk populations.
people in the general population are estimated to have a BRCA mutation
people in the Ashkenazi Jewish population have a BRCA mutation
women with ovarian cancer have a BRCA mutation
Men and women with a BRCA2 mutation have up to a 7% lifetime risk of pancreatic cancer
Men with a BRCA2 mutation have up to a 25% lifetime risk of aggressive prostate cancer
Women with a BRCA1 mutation have up to a 50% lifetime risk of ovarian cancer
Women with a BRCA1 or BRCA2 mutation have up to a 75% lifetime risk of breast cancer
The journey to understanding BRCA1 and BRCA2 began with a spark. In 2019, we recognized the 25th anniversary of the first time researchers identified the complete sequence of BRCA1 and quantified the corresponding lifetime risks of breast and ovarian cancers.
BRCA1 is cloned.
The most common BRCA1 mutation is traced back to families of Ashkenazi Jewish descent. Subsequently, two additional mutations — one in BRCA1 and one in BRCA2 — are identified as common Founder mutations in individuals of Ashkenazi Jewish descent. Mutations in BRCA1 and BRCA2 are seen in every race and ethnicity.
BRCA2 is cloned.
BRCA2 mutations are linked to male breast cancer.
BRCA2 mutations are linked to prostate cancer.
Research solidifies the role of BRCA1 in homologous recombination.
Bilateral preventive mastectomy is demonstrated to substantially reduce the incidence of breast cancer among women with mutations in BRCA1 or BRCA2.
The role of 53bp1 in regulating BRCA1 is discovered. (Penn Medicine's Roger Greenberg, MD, PhD, is currently pursuing research in this critical area.)
PARP inhibitors are shown to kill cells that do not have BRCA1 or BRCA2 protein present.
A paradigm-changing discovery by Basser Center’s Ronny Drapkin, PhD, and colleagues revealed that the majority of high-grade serous ovarian cancers arise in the fallopian tubes.
Research led by Basser Center Executive Director Susan M. Domchek, MD, showed strong evidence that removal of the ovaries improved overall survival in BRCA1 and BRCA2 mutation carriers.
Mindy and Jon Gray establish the Basser Center for BRCA.
Basser Global Prize is established and endowed by Shari and Len Potter.
FDA approved first PARP-inhibitor olaparib for BRCA-related ovarian cancer based on research led by the Basser Center. (PARP-inhibitors are a therapy that can stop cancerous cells from repairing themselves.)
Evidence shows that PARP inhibitors may be helpful in BRCA1/2-related pancreatic and prostate cancer.
Basser Center research supported the FDA approval of rucaparib for BRCA-related ovarian cancer.
FDA approved niraparib for all ovarian cancers.
Basser Center studies led to the FDA approval of olaparib and talazoparib for BRCA-related breast cancer.
Basser Center investigator Kim Reiss Binder, MD, showed that PARP Inhibitors are an effective and less toxic maintenance therapy for patients with BRCA-related pancreatic cancer.
Olaparib is approved in first line maintenance for BRCA1/2-related ovarian cancer.
The journey to understanding BRCA1 and BRCA2 began with a spark. In 2019, we recognized the 25th anniversary of the first time researchers identified the complete sequence of BRCA1 and quantified the corresponding lifetime risks of breast and ovarian cancers.
BRCA1 is cloned.
The most common BRCA1 mutation is traced back to families of Ashkenazi Jewish descent. Subsequently, two additional mutations — one in BRCA1 and one in BRCA2 — are identified as common Founder mutations in individuals of Ashkenazi Jewish descent. Mutations in BRCA1 and BRCA2 are seen in every race and ethnicity.
BRCA2 is cloned.
BRCA2 mutations are linked to male breast cancer.
BRCA2 mutations are linked to prostate cancer.
Research solidifies the role of BRCA1 in homologous recombination.
Bilateral preventive mastectomy is demonstrated to substantially reduce the incidence of breast cancer among women with mutations in BRCA1 or BRCA2.
The role of 53bp1 in regulating BRCA1 is discovered. (Penn Medicine's Roger Greenberg, MD, PhD, is currently pursuing research in this critical area.)
PARP inhibitors are shown to kill cells that do not have BRCA1 or BRCA2 protein present.
A paradigm-changing discovery by Basser Center’s Ronny Drapkin, PhD, and colleagues revealed that the majority of high-grade serous ovarian cancers arise in the fallopian tubes.
Research led by Basser Center Executive Director Susan M. Domchek, MD, showed strong evidence that removal of the ovaries improved overall survival in BRCA1 and BRCA2 mutation carriers.
Mindy and Jon Gray establish the Basser Center for BRCA.
Basser Global Prize is established and endowed by Shari and Len Potter.
FDA approved first PARP-inhibitor olaparib for BRCA-related ovarian cancer based on research led by the Basser Center. (PARP-inhibitors are a therapy that can stop cancerous cells from repairing themselves.)
Evidence shows that PARP inhibitors may be helpful in BRCA1/2-related pancreatic and prostate cancer.
Basser Center research supported the FDA approval of rucaparib for BRCA-related ovarian cancer.
FDA approved niraparib for all ovarian cancers.
Basser Center studies led to the FDA approval of olaparib and talazoparib for BRCA-related breast cancer.
Basser Center investigator Kim Reiss Binder, MD, showed that PARP Inhibitors are an effective and less toxic maintenance therapy for patients with BRCA-related pancreatic cancer.
Olaparib is approved in first line maintenance for BRCA1/2-related ovarian cancer.
The Basser Center continues to extend the reach of its top researchers and clinicians by constantly innovating and collaborating to bring the best care possible to patients around the world.
Funded Research
Projects
External
Grants Awarded
Raised From Over
1,000 Donors
Pancreatic cancer is the third-leading cause of cancer deaths in the United States, and one of the most difficult cancers to treat. And while BRCA mutations are most closely associated with breast and ovarian cancers, they also lead to an increased risk for pancreatic cancer. The discovery of these relationships is already improving outcomes for affected patients. The Basser Center’s Kim Reiss Binder, MD, an Assistant Professor of Hematology-Oncology, is studying the use of PARP inhibitors for pancreatic cancer patients with a BRCA mutation.
In 2019, Dr. Reiss Binder presented preliminary results from a clinical trial that showed that switching patients with incurable pancreatic cancer to the PARP inhibitor rucaparib as maintenance therapy instead of continuing intensive chemotherapy either shrunk tumors or stopped them from growing altogether. She is now preparing to launch a national trial to use this therapy in a frontline treatment setting, in the hope that it will offer cures to more patients. These discoveries represent an opportunity to change the face of BRCA-related pancreatic cancer, and give affected patients a chance at a better and longer life.
To be able to offer a targeted therapy with much less toxicity, even if only for a subset of our patients, was an extraordinary breakthrough for our patients with metastatic pancreatic cancer. Now we will apply this same therapy to patients with curable disease, in the hope that we can save more lives.
The PARP Inhibitor study investigates whether patients can safely discontinue intravenous chemotherapy and, instead, keep their cancer in check with a pill.
Basser Center Executive Director Susan M. Domchek, MD, led a multicenter study evaluating the combination of the drugs olaparib and durvalumab in patients with germline (inherited) BRCA-related breast and ovarian cancer with advanced disease. The study results found that this combination shows promise. This research will be published in The Lancet Oncology 2020.
“Patients with responses showed durable benefit,” Dr. Domchek says of the breast cancer cohort, “and progression-free survival and overall survival compared well with standard-of-care therapy for these populations.” While additional analysis is needed to determine which types of patients would benefit most from these combination therapies, it offers the hope of new viable and less toxic treatment options for patients.
An additional study of individuals with advanced BRCA1/2 cancer of many types treated with avelumab (an immune therapy) and talazoparib (a PARP inhibitor) has just closed to accrual and final results are being eagerly awaited.
The hope is that by combining these two therapies we are able to prolong a patient’s response, helping them fight their disease longer.
The REACH study (A Randomized Study of an eHealth Delivery Alternative for Cancer Genetic Testing for Hereditary Predisposition in Metastatic Breast and Ovarian Cancer Patients) evaluates the effectiveness of an eHealth delivery alternative to traditional genetic counseling in 400 patients with advanced breast and ovarian cancer.
“This alternative delivery model for genetic testing has the potential to provide equal or improved patient outcomes while reducing patient and genetic provider time, and increasing genetic testing in patients who can benefit.”
Dr. Drapkin has created an animal model of ovarian cancer that replicates the origins of the disease, which he has hypothesized begin in the fallopian tubes. The model allows him to explore the genomic complexity of humans and to study tumor-host interactions.
“The models allow us to safely observe how the immune system reacts to ovarian cancer tumors and study whether the genetic make-up of the tumor influences those interactions.”
The goal of Dr. Greenberg’s research is to identify and target mechanisms of resistance to PARP inhibitors (PARPi) and Platinum-based chemotherapies in BRCA1 and BRCA2 mutant cancers.
“We are working to unravel the mysteries of how DNA damage influences the immune system's response to cancer cells, and how PARP inhibitors themselves create immune responses. These kinds of insights can absolutely contribute to more personalized care.”
Dr. Vonderheide, Director of the Abramson Cancer Center, is working to test a novel vaccine that prevents BRCA1/2-related cancer when administered to healthy individuals who carry BRCA1/2 mutations, while also analyzing the immunobiology of mutant BRCA1/2-associated tumors in humans.
“Having completed the first-in-human clinical trial of our novel vaccine, we designed and wrote the protocol for a clinical trial to test this vaccine in healthy BRCA1/2 carriers. We have FDA approval for the protocol and are thrilled that the trial will open later this year, once issues of COVID-19 make it safe for us to do so.”
Dr. Nathanson’s team is expanding on their prior finding that a subset of BRCA1/2-related cancers do not display loss of heterozygosity (the loss of the second “bad” copy). They are also evaluating the immune response in BRCA1/2-related breast and ovarian cancers.
“The goal of this work is to probe more deeply into immune system function in BRCA mutation carriers and in those with related cancers. These studies have the potential not only to shed more light on BRCA cancers, but on the function of the immune system in general.”
Katherine L. Nathanson, MD, graduated from Penn’s Perelman School of Medicine in 1993, and has had an illustrious career ever since. She is one of the world’s foremost experts in cancer genetics and genomics. Now, in addition to her roles as Deputy Director of Penn Medicine’s Abramson Cancer Center and Director of Genetics at the Basser Center, Dr. Nathanson is the inaugural chair of the Pearl Basser Professorship in BRCA-Related Research. The professorship was established and endowed by Shari and Len Potter in honor of Shari and Mindy Gray’s mother, Pearl Basser, who died in 2017.
“We are thrilled to be able to honor my mother, Pearl, and help the Basser Center provide better options and hope to individuals and families with BRCA mutations,” says Shari Potter, pictured here with her husband Len and Dr. Nathanson. “Pearl would be proud knowing that someone of Dr. Nathanson’s exceptional caliber holds a professorship in her name.”
The Basser Center’s research arm includes multiple grants to researchers pursuing various BRCA1 and BRCA2 investigations. In 2019, 14 individual research projects received funding both at Penn Medicine, as well as at institutions in Boston, Washington, D.C., Philadelphia, and Israel.
Dan Powell, PhD, and his team launched a phase I clinical trial to study CAR T cell therapy that targets a protein expressed in 90% of all ovarian cancers. The results of this trial are encouraging and offer the promise of new clinical strategies for both BRCA-related ovarian cancer and ovarian cancer at large.
Ben Black, PhD, is exploring the mechanistic underpinnings of how mutations in the PARP-1 enzyme generate resistance to PARP inhibitors (PARPi), as has been observed in the clinic during the treatment of breast and ovarian cancer. He has published his initial observations made with Basser funding in the prestigious journal Science.
Working in collaboration with Roger Greenberg, MD, PhD, Junwei Shi, PhD, is using CRISPR-based genetic screening approaches to study the PARP enzyme and better understand its efficacy in BRCA-related breast and ovarian cancers.
Sarah Kim, MD, Ashley Haggerty, MD, MSCE, and Ronny Drapkin, MD, PhD, lead the Women Choosing Surgical Prevention (WISP) trial, which seeks to investigate whether removal of fallopian tubes alone can safely improve sexual function and menopausal symptoms compared to standard risk-reducing removal of both the ovaries and fallopian tubes.
Fiona Simpkins, MD, and Eric Brown, PhD, are exploring preliminary findings that distinct combinations of PARPi, ATRi, and WEE1i differ in treatment effectiveness depending on BRCA status in high-grade serous ovarian cancers.
Using the robust resources of the Penn Medicine Biobank, Kara Maxwell, PhD, is studying the contribution of BRCA1/2 mutations to localized high-grade prostate cancer.
Mehran Makvandi, PharmD, and Austin Pantel, MD, are developing a shared resource for clinical studies of PET (positron emission tomography) imaging of PARP-1 (Poly [ADP-ribose] polymerase 1) to direct targeted cancer therapy.
The 2019 YLC Young Investigator Award went to Kim Reiss Binder, MD, for her work studying the development and testing of new treatments for pancreatic cancer and other GI malignancies.
The 2019 Pearl and Philip Basser Innovation Research Award went to Mehran Makvandi, PharmD, RPh, BCNP, whose research continues to advance the understanding of BRCA with a particular contribution toward the influence of PARP-1 and associated therapy opportunities.
Susan M. Domchek, MD, and Katherine L. Nathanson, MD, are working in partnership with the global Consortium of Investigators of Modifiers of BRCA (CIMBA) to better understand the other factors that influence the development of BRCA-related cancers in order to provide individuals with a BRCA1/2 mutation more precise, personalized guidance on cancer prevention.
Dan Powell, PhD, and his team launched a phase I clinical trial to study CAR T cell therapy that targets a protein expressed in 90% of all ovarian cancers. The results of this trial are encouraging and offer the promise of new clinical strategies for both BRCA-related ovarian cancer and ovarian cancer at large.
Ben Black, PhD, is exploring the mechanistic underpinnings of how mutations in the PARP-1 enzyme generate resistance to PARP inhibitors (PARPi), as has been observed in the clinic during the treatment of breast and ovarian cancer. He has published his initial observations made with Basser funding in the prestigious journal Science.
Working in collaboration with Roger Greenberg, MD, PhD, Junwei Shi, PhD, is using CRISPR-based genetic screening approaches to study the PARP enzyme and better understand its efficacy in BRCA-related breast and ovarian cancers.
Sarah Kim, MD, Ashley Haggerty, MD, MSCE, and Ronny Drapkin, MD, PhD, lead the Women Choosing Surgical Prevention (WISP) trial, which seeks to investigate whether removal of fallopian tubes alone can safely improve sexual function and menopausal symptoms compared to standard risk-reducing removal of both the ovaries and fallopian tubes.
Fiona Simpkins, MD, and Eric Brown, PhD, are exploring preliminary findings that distinct combinations of PARPi, ATRi, and WEE1i differ in treatment effectiveness depending on BRCA status in high-grade serous ovarian cancers.
Using the robust resources of the Penn Medicine Biobank, Kara Maxwell, PhD, is studying the contribution of BRCA1/2 mutations to localized high-grade prostate cancer.
Mehran Makvandi, PharmD, and Austin Pantel, MD, are developing a shared resource for clinical studies of PET (positron emission tomography) imaging of PARP-1 (Poly [ADP-ribose] polymerase 1) to direct targeted cancer therapy.
The 2019 YLC Young Investigator Award went to Kim Reiss Binder, MD, for her work studying the development and testing of new treatments for pancreatic cancer and other GI malignancies.
The 2019 Pearl and Philip Basser Innovation Research Award went to Mehran Makvandi, PharmD, RPh, BCNP, whose research continues to advance the understanding of BRCA with a particular contribution toward the influence of PARP-1 and associated therapy opportunities.
Susan M. Domchek, MD, and Katherine L. Nathanson, MD, are working in partnership with the global Consortium of Investigators of Modifiers of BRCA (CIMBA) to better understand the other factors that influence the development of BRCA-related cancers in order to provide individuals with a BRCA1/2 mutation more precise, personalized guidance on cancer prevention.
Securing funding for high-risk, high-reward research is both today’s biggest opportunity and biggest challenge in the fight against BRCA-related cancer. Such support gives Basser the flexibility to explore novel research ideas and bring new treatments from bench to bedside as quickly as possible. We are grateful to Jay Lieberman and The Derfner Foundation, Christine and Jordan Kaplan, and the Paul Klingenstein Family Foundation for their unrestricted support of our work.
Principal Investigator Ralph Scully, PhD, of Beth Israel Deaconess Medical Center/Harvard Medical School is expanding on a previous study on the use of the Escherichia coli Tus/Ter replication fork barrier and FANCM on the repair of stalled replication forks in mammalian cells.
Alejandra Hurtado de Mendoza Casaus, PhD, of Georgetown University in Washington, D.C., is exploring how to increase awareness and use of genetic counseling and testing services among Latina women at risk of hereditary breast and ovarian cancer.
Principal Investigator Kavitha Sarma, PhD, of The Wistar Institute is studying novel approaches for diagnostic and therapeutic applications in BRCA1/2 deficient cancers.
Principal Investigator Eitan Friedman, MD, PhD, of Sheba Medical Center in Israel is focusing on Jewish women who carry a BRCA1 mutation.
Principal Investigator Ralph Scully, PhD, of Beth Israel Deaconess Medical Center/Harvard Medical School is expanding on a previous study on the use of the Escherichia coli Tus/Ter replication fork barrier and FANCM on the repair of stalled replication forks in mammalian cells.
Alejandra Hurtado de Mendoza Casaus, PhD, of Georgetown University in Washington, D.C., is exploring how to increase awareness and use of genetic counseling and testing services among Latina women at risk of hereditary breast and ovarian cancer.
Principal Investigator Kavitha Sarma, PhD, of The Wistar Institute is studying novel approaches for diagnostic and therapeutic applications in BRCA1/2 deficient cancers.
Principal Investigator Eitan Friedman, MD, PhD, of Sheba Medical Center in Israel is focusing on Jewish women who carry a BRCA1 mutation.
Each year, the Basser Global Prize recognizes a pioneering scientist who has advanced BRCA1/2-related research. In 2019, Douglas Easton, PhD, and Antonis Antoniou, PhD, Professors in the Department of Public Health and Primary Care at the University of Cambridge, and members of the Cancer Research UK Cambridge Centre, became the recipients of the seventh annual Basser Global Prize.
Past Recipients of the Global Prize include:2018: Maria Jasin, PhD
2017: Ashok Venkitaraman, MBBS, PhD
2016: Steven Narod, MD, FRCPC, PhD (hon), FRSC
2015: David Livingston, MD
2014: Mary-Claire King, PhD
2013: Alan Ashworth, PhD, FRS
We are deeply honored to be selected for this award by the Basser Center. Basser is known and respected around the world for its efforts to make a difference for patients with inherited BRCA1/2 mutations.
The Basser Global Prize will be critical in supporting our research on the prevention and early detection of cancer in BRCA1 and BRCA2 mutation carriers.
Numerous, ongoing studies are helping to improve access to genetic counseling and testing, and increase awareness of BRCA mutation risk.
The BRCA Founder Outreach (BFOR) Study, a collaboration between Basser and four other institutions around the country, developed a new model to make genetic testing more accessible. This pilot study used an online platform to offer free genetic testing to over 4,000 people of Ashkenazi Jewish ancestry with the goal of ultimately developing a larger international study.
Our team of six genetic counselors offers top-tier genetic counseling and testing services both on-site at the Basser Center and through telemedicine. Thanks to philanthropic support from Tamsen and Michael Brown, a research coordinator is now on staff to help facilitate a research project evaluating methods of sharing genetic test results with family members.
We are evaluating an alternative delivery model for genetic testing to all patients with pancreatic cancer and men with metastatic prostate cancer. By integrating genetic testing into the standard of care, we can meet the increasing demands of the genetics community and provide results needed for time-sensitive medical management decisions.
This fully staffed unit enables investigators to open clinical trials on BRCA and related mutations that affect a variety of cancer types, significantly enhancing and streamlining our clinical trials. Initially funded by private philanthropy, this model is being adopted by other disease areas across the Abramson Cancer Center.
An attorney, author, wife, and mother of three with a family history of cancer, Shannon is also an advocate for patients through her work with Basser’s Young Leadership Council (YLC).
Shannon Pulaski is 36 years old and a BRCA mutation carrier, which means she has up to a 75% chance of developing breast cancer and up to a 50% chance of developing ovarian cancer in her lifetime. Shannon’s mother and aunt were both diagnosed with ovarian cancer in their 50s, making her risk all the more real.
“The most challenging part about having a BRCA mutation for me is — hands down — worrying about my children,” Shannon says. “Even with all the steps I can take to be proactive, there still is so much uncertainty and concern that the mutation will be passed on.”
Shannon is an active member of the YLC and is focused on supporting and accelerating BRCA-related research.
“I was particularly drawn to the YLC because of its focus on funding research that is meaningful to the BRCA community,” she says. Shannon is also dedicated to increasing awareness of BRCA, noting, “Having knowledge allows you to have options. Having options allows you to take control of your health, be proactive, and feel empowered.”
I desperately hope that there are better options in the future so our children do not have to be faced with the difficult decisions and challenges a BRCA mutation bring.
Let’s stop the march of these insidious mutations from one generation to the next and make this the last generation of BRCA cancers in all of our families.
At the Basser Center, we are taking a comprehensive approach to a complex problem, tackling the challenge of BRCA from all sides. The last 25 years have seen remarkable progress in the field of hereditary cancer from prevention to detection, to better understanding to better treatments. Because of this immense amount of progress, we are incredibly hopeful about the next 25 years.
The Basser Center’s holistic line of attack on BRCA mutations is a multipronged and multifaceted effort ranging from prevention and screening to raising awareness and counseling.
A preventative vaccine clinical trial to test immune response and safety in healthy individuals who have a BRCA mutation has been approved by the FDA. The trial is slated to open in 2020.
The Basser Center is evaluating new models of providing genetic counseling to patients. Expanding on the Penn Telegenetics Program, Basser is using a variety of digital health platforms and EMR-based approaches to improve identification of individuals at risk.
Payal Shah, MD, and Vivek Narayan, MD, MS, are working on the efficacy of PARP inhibitors in patients with BRCA-related breast and prostate cancers, respectively. Dr. Shah is examining olaparib in combination with other drugs, specifically fulvestrant and palbociclib. Dr. Narayan is examining the optimal sequencing of hormonal therapy, chemotherapy and PARP inhibitors in prostate cancer.
An emerging priority is to offer education on genetic testing to primary care physicians, many of whom are uncertain of when to recommend testing, and for which patients. Basser is creating platforms to provide physicians and other healthcare providers with the most up-to-date information about risk management, screening, prevention, and treatment for patients with a BRCA mutation.
Basser is replacing fear with hope, and I couldn’t be prouder and more honored to be a part of it.
LATINX & BRCA is a comprehensive initiative to raise awareness, provide education and resources in Spanish, and build a support system for the Latinx community affected by BRCA mutations and related cancers. This new program was founded in partnership with women’s health advocate Alejandra Campoverdi.
I was able to substantially lower my chance of having to battle cancer because I was aware of my BRCA mutation. More Black families should be empowered with the same information.
Black women are substantially less likely to undergo genetic counseling and testing for BRCA mutations compared to white women, even though research suggests that the rate of BRCA mutations may be higher among Black women than it is for white. To help address these disparities, we have partnered with Erika Stallings, the co-chair of the YLC on the Black & BRCA initiative, to provide educational resources, assistance in finding a genetic counselor, and to offer a network of support for the African-American community.
The Parents Leadership Community (PLC) seeks to address the unique challenges faced by families with a BRCA mutation. The group, led by co-chairs Shari Potter, Susan Getz, and Raquel Haas, will be a supportive forum for parents while also providing resources to stay informed on the last advances in BRCA research.
The Young Leadership Council’s (YLC) more than 100 members from around the world stay informed about the latest research advances and raise support individually and through events to propel research, patient care, and educational initiatives.
Basser is replacing fear with hope, and I couldn’t be prouder and more honored to be a part of it.
LATINX & BRCA is a comprehensive initiative to raise awareness, provide education and resources in Spanish, and build a support system for the Latinx community affected by BRCA mutations and related cancers. This new program was founded in partnership with women’s health advocate Alejandra Campoverdi.
I was able to substantially lower my chance of having to battle cancer because I was aware of my BRCA mutation. More Black families should be empowered with the same information.
Black women are substantially less likely to undergo genetic counseling and testing for BRCA mutations compared to white women, even though research suggests that the rate of BRCA mutations may be higher among Black women than it is for white. To help address these disparities, we have partnered with Erika Stallings, the co-chair of the YLC on the Black & BRCA initiative, to provide educational resources, assistance in finding a genetic counselor, and to offer a network of support for the African-American community.
The Parents Leadership Community (PLC) seeks to address the unique challenges faced by families with a BRCA mutation. The group, led by co-chairs Shari Potter, Susan Getz, and Raquel Haas, will be a supportive forum for parents while also providing resources to stay informed on the last advances in BRCA research.
The Young Leadership Council’s (YLC) more than 100 members from around the world stay informed about the latest research advances and raise support individually and through events to propel research, patient care, and educational initiatives.
The mission of the Basser Center is simple: Create a central hub to tackle all things BRCA related, focus intensely on this multi-generational challenge, assemble a world class team, and provide the resources they need to make a difference.
The Basser Leadership Council advocates, informs, and engages on behalf of the Basser Center. The Council enhances and supports the Center’s mission and provides hope to patients and families by securing the resources needed to accelerate BRCA-related research, care, and education.
The Young Leadership Council’s (YLC) more than 100 members from around the world stay informed about the latest research advances and raise support individually and through events to propel research, patient care, and educational initiatives. Learn more at Basser.org/YLC.
Your support at any level benefits individuals and families affected by a BRCA mutation, pioneering research at Basser and around the globe, and enhances lifesaving outreach and educational programs.
*Gifts listed below are from January 1, 2019, through December 31, 2019, and reflect cumulative giving during that time period.
The Basser Center for BRCA has received many generous and thoughtful gifts in honor, memory, and celebration of the following individuals.