4.6 Review

Current evidence for second-line treatment in metastatic renal cell carcinoma after progression to immune-based combinations

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CANCER TREATMENT REVIEWS
卷 105, 期 -, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.ctrv.2022.102379

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Renal cell carcinoma; Second-line; Immune-based combinations; mRCC; Novel agents

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The recent approval of ICI-based combinations has changed the first-line standard of care for mRCC patients, but the optimal second-line treatment remains unclear. Retrospective data suggest that second-line VEGFR-TKIs may be more effective after failure of dual ICIs than after ICIs plus VEGFR-TKIs, but more prospective data is needed. Ongoing trials are evaluating novel molecules and ICI-based combinations for second-line therapy.
The recent approval of immune checkpoint inhibitor (ICI)-based combinations has redefined the first-line standard of care of metastatic renal cell carcinoma (mRCC) patients. Although the undisputed advantage of these combinations, most patients progressed, requiring subsequent therapies. The change of first-line therapy inevitably led to modification of the all mRCC treatment algorithm; to date, the most appropriate second-line options remain still unclear. The aim of our review was to provide a useful summary of the available evidence in order to overcome the doubts about treatment sequences. Retrospectively, the efficacy of second-line VEGFR-TKIs seems to be greater after failure of a dual ICIs combination rather than after ICIs plus VEGFR-TKIs, nevertheless prospective data of second-line TKIs are limited. Moreover, ICI re-challenge could be an option but, again, most data derived from retrospective series emphasizing the identification of predictive factors of response to select mRCC patients that could benefit from this strategy. Novel molecules and different ICI-based combinations are under evaluation with the aim of implementing the second-line setting. In particular, belzutifan, ciforadenant (CPI-444), and talazoparib achieved encouraging objective response rates (ORR) in phase I/II trials. Phase III trials comparing these new molecules with the standard of care are currently ongoing. The first-line regimen, and the type and duration of response emerged as crucial factors that could influence the efficacy of second-line therapy. Prognostic models that integrate clinical features and molecular biomarkers with a predictive value are warranted to guide clinicians in the decision-making process with the ultimate goal of offering to the patients the most effective therapy in a personalized, precision medicine-based, therapeutic strategy.

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