Advocacy

FORCE advocates for families facing hereditary breast and ovarian cancer in areas such as access to care, research funding, insurance, and privacy.

Advocacy > Issues > FDA Approval of Lynparza: A Win for the HBOC Community

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Newsflash

6/1/2018
FORCE staff are attending the American Society of Clinical Oncology (ASCO) annual meeting in Chicago.

5/9/18
We joined 80 patient advocacy, medical, and industry orgs in urging Congress to enact legislation to modernize FDA oversight of clinical laboratory diagnostics. Read letter...

5/8/2018
FORCE, along with over 100 other organizations, is advocating for continued funding of DoD research programs. Read our letters to Senate and House leaders.

4/17/18
FORCE and over 100 patient and professional health orgs reached out to Congressional leaders to oppose expansion of short-term health insurance plans. Read letter...

4/12/18
FDA finalizes guidances to accelerate development of reliable, beneficial next generation sequencing-based tests. Read press release...

4/9/2018
FORCE joined other organizations in urging Utah to clarify and protect coverage of breast reconstruction after cancer for its Medicaid recipients. Read more...

FDA Approval of Lynparza: A Win for the HBOC Community

Treatments & Therapies

Overview

FORCE was one of a handful of advocacy organizations to testify in favor of accelerated approval of olaparib at the FDA hearing of the Oncology Drug Advisory Committee (ODAC) in June 2014. ODAC voted against approval at the conclusion of that meeting and early word from the FDA was that more research was needed before it would approve this therapy. The BRCA cancer community is grateful that the FDA reconsidered and approved this treatment.

PARP inhibitors are “targeted therapy” drugs that target tumors based on their unique biology. Developing these “smart” drugs requires a greater understanding of how cancer cells differ from other cells, and identifying cellular vulnerabilities. Targeted therapy uses specific treatments to attack the weaknesses of certain cancers based on their cellular genetic traits. PARP inhibitors block an enzyme used by cells to repair damage to their DNA. In people with BRCA mutations, PARP inhibitors may work by keeping cancer cells from repairing themselves once they’ve been damaged by chemotherapy, while sparing healthy cells.

Despite early positive findings, PARP inhibitor research almost came to a halt several years ago due in part to the challenge of studying drugs that may only benefit small subsets of a larger cancer patient population. Fortunately, thanks to champions within the scientific, advocacy and biotech communities, this important research continued. FDA approval of Lynparza is the culmination of these ongoing efforts, and hopefully only the beginning for this promising class of drugs. See our blog about this decision and read our article on this milestone.

PARP inhibitors are being studied as treatment for a variety of BRCA and BRCA-like cancers. FORCE continues for support these efforts via encouraging genetic testing of those diagnosed with cancer and supporting clinical trial enrollment.  

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