4.6 Article

Adherence to PARP inhibitor therapy among women with ovarian cancer

期刊

GYNECOLOGIC ONCOLOGY
卷 163, 期 2, 页码 262-268

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ygyno.2021.08.025

关键词

Oral anticancer agents; Adherence; PARP inhibitors; Ovarian cancer

资金

  1. Merck
  2. NIH BIRCWH [K12HD043446]

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This study evaluated medical adherence for ovarian cancer patients receiving PARP inhibitor therapy and found that a quarter of patients may be sub-optimally adherent. Factors such as age, comorbidities, insurance plan, and year of PARP inhibitor initiation were not significantly associated with non-adherence. Further research should focus on identifying at-risk patients and interventions to improve adherence.
Objective: The objective of this study was to evaluate medical adherence for patients with ovarian cancer who initiated treatment with a PARP inhibitor therapy, and to identify factors associated with nonadherence. Methods: We used the MarketScan Database to identify ovarian cancer patients who initiated PARP inhibitor therapy between January 1, 2008 and December 31, 2017. The primary outcome was adherence defined ask 80% proportion of days covered (PDC). A secondary outcome included adherence assessed using the medication pos-session ratio (MPR). Multivariable logistic regression analysis was performed to assess relation between PDC and explanatory variables. Sensitivity analysis was performed to evaluate impact of dose-adjustments and toxicity-related delays on adherence. Results: Among 170,976 patients diagnosed with ovarian cancer, 151 patients met inclusion criteria. The me-dian time from diagnosis to initiating therapy was 33 months. Overall, 40 (26.5%) were non-adherent based on a PDC less than 80%. Non-adherent patients were more likely to receive niraparib and have a longer duration of therapy (p < 0.05). We found no significant impact of age, comorbidities, insurance plan, or year of PARP inhibitor initiation on non-adherence. In a sensitivity analysis to assess different definition of adherence, non-adherence ranged from 11.3% to 41.1%. When accounting for possible dose-adjustments, 21.2% of patients were non-adherent. Conclusion: This population based study of ovarian cancer patients found that a quarter of patients may be sub-optimally adherent to PARP inhibitor therapy. Future research should focus on identification of patients at risk for nonadherence and interventions to lower nonadherence among these patients. (c) 2021 Published by Elsevier Inc.

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