For the First Time, a Drug is Indicated Specifically for BRCA-Mutated Breast Cancer
Posted on January 14, 2018
Source:
Medscape
The US Food and Drug Administration (FDA) has extended the approval of olaparib (Lynparza, AstraZeneca) to include the treatment of metastatic breast cancer in patients who carry the specific inherited BRCA mutation.
These patients can be identified by using the FDA-approved genetic test, BRAC Analysis CDx (Myriad Genetic Laboratories).
About 10% to 15% of patients with any type of breast cancer have a BRCA mutation, the agency notes.
Olaparib acts as an inhibitor of the enzyme poly-(ADP-ribose) polymerase (PARP), which is involved in the repair of damaged DNA, it explains.
By blocking this enzyme, DNA inside the cancerous cells with damaged BRCA genes may be less likely to be repaired, leading to cell death and possibly a slowdown or stoppage of tumor growth.
Olaparib is already approved for use in germline BRCA-mutated ovarian cancer. The initial approval, granted in 2014, was for use in BRCA-mutated advanced ovarian cancer in patients who have received three or more treatments of chemotherapy. Earlier this year, the FDA granted approval for maintenance use in patients with recurrent epithelial ovarian, fallopian tube cancer, or primary peritoneal cancer whose tumors have completely or partially responded to chemotherapy.
In addition to olaparib, another PARP inhibitor has been approved for use in BRCA ovarian cancer ― rucaparib (Rubraca, Clovis Oncology). A third PARP inhibitor, niraparib (Zejula, Tesaro), is approved for use in ovarian cancer irrespective of whether or not the patients carries a BRCA mutation.
Olapraib becomes the first PARP inhibitor to be approved for use in breast cancer.
"This class of drugs has been used to treat advanced BRCA-mutated ovarian cancer and has now shown efficacy in treating certain types of BRCA-mutated breast cancer," commented Richard Pazdur, MD, director of the FDA's Oncology Center of Excellence and acting director of the Office of Hematology and Oncology Products in the FDA's Center for Drug Evaluation and Research.
"This approval demonstrates the current paradigm of developing drugs that target the underlying genetic causes of a cancer, often across cancer types," he added.
Clinical Trial Data
The agency notes that the safety and efficacy of olaparib in the treatment of breast cancer were determined on the basis of findings from the OlympyiAD trial, a randomized clinical trial of 302 patients with HER2-negative metastatic breast cancer with a germline BRCA mutation.