Overall, 22 of 24 patients (91.7%) in the BRCA-mutant group and 11 of 16 patients (68.8%) in the BRCA wild-type group experienced at least one olaparib-related adverse event of any grade during treatment, although this difference did not reach statistical significance (OR 5.00, 95% CI 0.78–27.08; p = 0.094).
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BRCA mutation status and olaparib-related toxicity during maintenance therapy: a real-world retrospective cohort study.
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