PARP Inhibitors in the Management of Ovarian Cancer: ASCO Guideline

Author:

Tew William P.1,Lacchetti Christina2ORCID,Ellis Annie34,Maxian Kathleen5,Banerjee Susana6,Bookman Michael7ORCID,Jones Monica Brown8,Lee Jung-Min9,Lheureux Stéphanie10ORCID,Liu Joyce F.11,Moore Kathleen N.12ORCID,Muller Carolyn13,Rodriguez Patricia14ORCID,Walsh Christine15ORCID,Westin Shannon N.16ORCID,Kohn Elise C.9

Affiliation:

1. Memorial Sloan Kettering Cancer Center, New York, NY

2. American Society of Clinical Oncology, Alexandria, VA

3. SHARE Cancer Support, New York, NY

4. Ovarian Cancer Research Alliance, New York, NY

5. Ovarian Cancer Project, Williamsville, NY

6. The Royal Marsden NHS Foundation Trust and Institute of Cancer Research, London, United Kingdom

7. Kaiser Permanente, San Francisco, CA

8. DeCesaris Cancer Institute, Anne Arundel Medical Center, Annapolis, MD

9. National Cancer Institute, Bethesda, MD

10. University Health Network, Toronto, Ontario, Canada

11. Dana-Farber Cancer Institute, Boston, MA

12. Stephenson Cancer Center, Oklahoma City, OK

13. University of New Mexico, Albuquerque, NM

14. Virginia Cancer Specialists, Arlington, VA

15. Cedars-Sinai, West Hollywood, CA

16. University of Texas MD Anderson Cancer Center, Houston, TX

Abstract

PURPOSE To provide recommendations on the use of poly(ADP-ribose) polymerase inhibitors (PARPis) for management of epithelial ovarian, tubal, or primary peritoneal cancer (EOC). METHODS Randomized, controlled, and open-labeled trials published from 2011 through 2020 were identified in a literature search. Guideline recommendations were based on the review of the evidence, US Food and Drug Administration approvals, and consensus when evidence was lacking. RESULTS The systematic review identified 17 eligible trials. RECOMMENDATIONS The guideline pertains to patients who are PARPi naïve. All patients with newly diagnosed, stage III-IV EOC whose disease is in complete or partial response to first-line, platinum-based chemotherapy with high-grade serous or endometrioid EOC should be offered PARPi maintenance therapy with niraparib. For patients with germline or somatic pathogenic or likely pathogenic variants in BRCA1 (g/s BRCA1) or BRCA2 (g/s BRCA2) genes should be treated with olaparib. The addition of olaparib to bevacizumab may be offered to patients with stage III-IV EOC with g/s BRCA1/2 and/or genomic instability and a partial or complete response to chemotherapy plus bevacizumab combination. Maintenance therapy (second line or more) with single-agent PARPi may be offered for patients with EOC who have not received a PARPi and have responded to platinum-based therapy regardless of BRCA mutation status. Treatment with a PARPi should be offered to patients with recurrent EOC that has not recurred within 6 months of platinum-based therapy, who have not received a PARPi and have a g/s BRCA1/2, or whose tumor demonstrates genomic instability. PARPis are not recommended for use in combination with chemotherapy, other targeted agents, or immune-oncology agents in the recurrent setting outside the context of a clinical trial. Recommendations for managing specific adverse events are presented. Data to support reuse of PARPis in any setting are needed. Additional information is available at www.asco.org/gynecologic-cancer-guidelines .

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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