Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

FDA Approves Olaparib for First-line Maintenance Treatment of BRCA-mutated Advanced Ovarian Cancer

Patients should be selected for therapy based on an FDA-approved companion diagnostic
08 Jan 2019
Targeted Therapy;  Cytotoxic Therapy
Gynaecological Malignancies

On 19 December 2018, the US Food and Drug Administration (FDA) approved olaparib (LYNPARZA, AstraZeneca Pharmaceuticals LP) for the maintenance treatment of adult patients with deleterious or suspected deleterious germline or somatic BRCA-mutated (gBRCAm or sBRCAm) advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are in complete or partial response to first-line platinum-based chemotherapy. Patients with gBRCAm advanced epithelial ovarian, fallopian tube or primary peritoneal cancer should be selected for therapy based on an FDA-approved companion diagnostic. 

Approval was based on SOLO-1 (NCT01844986), a randomised, double-blind, placebo-controlled, multicentre trial that compared the efficacy of olaparib with placebo in patients with BRCAm advanced ovarian, fallopian tube, or primary peritoneal cancer following first-line platinum-based chemotherapy. Patients were randomised (2:1) to receive olaparib tablets 300 mg orally twice daily (n=260) or placebo (n=131). 

The primary efficacy outcome was investigator-assessed progression-free survival (PFS) evaluated according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. The trial demonstrated a statistically significant improvement in investigator-assessed PFS for olaparib compared to placebo. Estimated median PFS was not reached in the olaparib arm and was 13.8 months in the placebo arm (HR 0.30; 95% CI: 0.23-0.41; p < 0.0001). At the time of the analysis of PFS, overall survival data were not mature. 

Most common (≥10%) adverse reactions of any grade occurring in patients who received olaparib in SOLO-1 were nausea, fatigue, abdominal pain, vomiting, anaemia, diarrhoea, upper respiratory tract infection/influenza/nasopharyngitis/bronchitis, constipation, dysgeusia, decreased appetite, dizziness, neutropenia, dyspepsia, dyspnoea, urinary tract infection, leukopenia, thrombocytopenia, and stomatitis. 

FDA also approved the ­­­­BRACAnalysis CDx test (Myriad Genetic Laboratories, Inc.) to identify patients with gBRCAm advanced epithelial ovarian, fallopian tube or primary peritoneal cancer who are eligible for olaparib. The effectiveness of the ­­­­BRACAnalysis CDx test was based on the SOLO-1 trial population for whom deleterious or suspected deleterious gBRCAm status was confirmed with either prospective or retrospective testing with the ­­­­BRACAnalysis CDx test. 

The recommended olaparib dose is 300 mg (two 150 mg tablets) taken orally twice daily, with or without food, for a total daily dose of 600 mg. 

Full prescribing information for LYNPARZA is available here.

The FDA Oncology Center of Excellence Assessment Aid Pilot Project  was used for the review of this application. 

FDA granted this application priority review. 

Healthcare professionals should report all serious adverse events suspected to be associated with the use of any medicine and device to FDA’s MedWatch Reporting System.

Last update: 08 Jan 2019

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.