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Three PARP inhibitors have been approved by the FDA for treating ovarian, primary peritoneal and fallopian tube cancer.
Lynparza is a PARP inhibitor approved by the
FDA to treat ovarian, fallopian tube, and primary peritoneal cancer in women who carry mutations in BRCA1 or BRCA2, and who have received three or more previous lines of chemotherapy.
Rubraca is a
PARP inhibitor that was approved by the FDA to treat women with advanced ovarian, fallopian tube, and primary peritoneal cancer who have had two or more prior treatment and who have inherited mutations in BRCA or whose tumors have BRCA mutations as detected by the FoundationFocus CDxBRCA companion diagnostic test.
Maintenance therapy is a type of treatment that is given after initial standard treatment has been completed to try to keep the cancer from returning. The goal of maintenance therapy is to extend the length of time before a new recurrence emerges or even to turn a temporary remission into a long-term cure. Two PARP inhibitors have been FDA approved for use as maintenance therapy in women with ovarian, fallopian tube and primary peritoneal cancer.
Lynparza or Zejula may be used as maintenance therapy for women with ovarian cancer who have received 2 or more lines of chemotherapy who had either a complete or partial response to the most recent line of recurrence therapy. These PARP inhibitors have been approved for maintenance therapy in women with, and women without a
BRCA mutation. However, research suggests that the agents work particularly well in women with a BRCA1 or BRCA2 mutation.
Research is now also looking at
PARP inhibitor effectiveness when combined with other agents, such as drugs that shrink blood supply and immunotherapies. You can look for research studies enrolling women with hereditary ovarian, fallopian tube, and primary peritoneal cancer by visiting FORCE's Research Study Search Tool.