4.7 Article

PARP Inhibitors in the Management of Ovarian Cancer: ASCO Guideline

Journal

JOURNAL OF CLINICAL ONCOLOGY
Volume 38, Issue 30, Pages 3468-+

Publisher

AMER SOC CLINICAL ONCOLOGY
DOI: 10.1200/JCO.20.01924

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Funding

  1. Janssen-Cilag (Inst)
  2. GlaxoSmithKline (Inst)
  3. Eli Lilly (Inst)
  4. AstraZeneca (Inst)
  5. AstraZeneca
  6. Roche
  7. Merck (Inst)
  8. Boston Biomedical (Inst)
  9. Acetylon (Inst)
  10. Bristol Myers Squibb
  11. Agenus
  12. CytomX Therapeutics
  13. Tesaro (Inst)
  14. Clovis Oncology
  15. Vigeo Therapeutics (Inst)
  16. Arch Oncology (Inst)
  17. PTC Therapeutics
  18. Genentech (Inst)
  19. Lilly Foundation (Inst)
  20. Advaxis
  21. Verastem
  22. Novartis Pharmaceuticals UK
  23. Agenus (Inst)
  24. Takeda
  25. Stem CentRx (Inst)
  26. Immunogen
  27. Bayer
  28. Novogen
  29. Stemcentrx
  30. Celgene
  31. Tesaro
  32. Kite Pharma
  33. GOG Foundation (Inst)
  34. Atara Biotherapeutics (Inst)

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PURPOSETo provide recommendations on the use of poly(ADP-ribose) polymerase inhibitors (PARPis) for management of epithelial ovarian, tubal, or primary peritoneal cancer (EOC).METHODSRandomized, 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.RESULTSThe systematic review identified 17 eligible trials.RECOMMENDATIONSThe guideline pertains to patients who are PARPi naive. 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/sBRCA1) or BRCA2 (g/sBRCA2) genes should be treated with olaparib. The addition of olaparib to bevacizumab may be offered to patients with stage III-IV EOC with g/sBRCA1/2 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/sBRCA1/2, 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.

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