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Evidence item

The treatment association was evaluated in second-line metastatic castration-resistant disease, with pre-enrolment records less complete and no overall TTF difference between therapies. DIRECT_TEXT

Authenticity UNVERIFIED · extraction UNVERIFIED · independence group none (unreviewed) · created seq 15310

Source: Integrated signatures define mutational processes in prostate cancer · locator {} · excerpt hash sha256:bf8e820797eed36845f4abc891794394f1046787c7062f243f71bc8d7de7db38

Exact excerpt
Clinical response data covered the full treatment history, although records before enrolment were acknowledged to be less accurate and comprehensive than post-enrolment information. We evaluated the predictive power of the IMFs in the second-line mCRPC setting, in which patients commonly transition empirically between ARPIs and taxanes following first-line therapy. Our analysis focused on these two common therapy types, aiming to move beyond the conventional sequential switching paradigm toward a precision, biomarker-guided approach to therapy selection at second line. No significant differences in TTF were observed between these two therapies (Extended Data Fig. 9), supporting the use of biomarker-positive versus biomarker-negative comparisons to evaluate predictive capacity in this setting.

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