FDA Approval Summary: Olaparib Monotherapy in Patients with Deleterious Germline BRCA-Mutated Advanced Ovarian Cancer Treated with Three or More Lines of Chemotherapy

On December 19, 2014, the FDA approved olaparib capsules (Lynparza; AstraZeneca) for the treatment of patients with deleterious or suspected deleterious germline BRCA-mutated (gBRCAm) advanced ovarian cancer who have been treated with three or more prior lines of chemotherapy. The BRACAnalysis CDx (...

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Veröffentlicht in:Clinical cancer research 2015-10, Vol.21 (19), p.4257-4261
Hauptverfasser: Kim, Geoffrey, Ison, Gwynn, McKee, Amy E, Zhang, Hui, Tang, Shenghui, Gwise, Thomas, Sridhara, Rajeshwari, Lee, Eunice, Tzou, Abraham, Philip, Reena, Chiu, Haw-Jyh, Ricks, Tiffany K, Palmby, Todd, Russell, Anne Marie, Ladouceur, Gaetan, Pfuma, Elimika, Li, Hongshan, Zhao, Liang, Liu, Qi, Venugopal, Rajesh, Ibrahim, Amna, Pazdur, Richard
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Sprache:eng
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Zusammenfassung:On December 19, 2014, the FDA approved olaparib capsules (Lynparza; AstraZeneca) for the treatment of patients with deleterious or suspected deleterious germline BRCA-mutated (gBRCAm) advanced ovarian cancer who have been treated with three or more prior lines of chemotherapy. The BRACAnalysis CDx (Myriad Genetic Laboratories, Inc.) was approved concurrently. An international multicenter, single-arm trial enrolled 137 patients with measurable gBRCAm-associated ovarian cancer treated with three or more prior lines of chemotherapy. Patients received olaparib at a dose of 400 mg by mouth twice daily until disease progression or unacceptable toxicity. The objective response rate (ORR) was 34% with median response duration of 7.9 months in this cohort. The most common adverse reactions (≥20%) in patients treated with olaparib were anemia, nausea, fatigue (including asthenia), vomiting, diarrhea, dysgeusia, dyspepsia, headache, decreased appetite, nasopharyngitis/pharyngitis/upper respiratory infection, cough, arthralgia/musculoskeletal pain, myalgia, back pain, dermatitis/rash, and abdominal pain/discomfort. Myelodysplatic syndrome and/or acute myeloid leukemia occurred in 2% of the patients enrolled on this trial.
ISSN:1078-0432
1557-3265
DOI:10.1158/1078-0432.CCR-15-0887