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Selpercatinib and the Crossover Conundrum: Potential Impact of Postprogression Therapies on Overall Survival.

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Journal of clinical oncology : official journal of the American Society of Clinical Oncology 📖 저널 OA 33% 2022: 4/6 OA 2024: 4/10 OA 2025: 30/61 OA 2026: 34/143 OA 2022~2026 2026 p. JCO2502375 Cancer Immunotherapy and Biomarkers
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PubMed DOI OpenAlex 마지막 보강 2026-04-29
OpenAlex 토픽 · Cancer Immunotherapy and Biomarkers Lung Cancer Treatments and Mutations Lung Cancer Diagnosis and Treatment

Duke ES, Bradford D, Sinha AK, Li X, Mishra-Kalyani PS, de Claro RA, Larkins E, Drezner N

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Overall survival (OS) should be evaluated in all randomized cancer trials, even when not the primary end point, as it is clinically meaningful and measures both safety and efficacy.

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APA Elizabeth S. Duke, Diana Bradford, et al. (2026). Selpercatinib and the Crossover Conundrum: Potential Impact of Postprogression Therapies on Overall Survival.. Journal of clinical oncology : official journal of the American Society of Clinical Oncology, JCO2502375. https://doi.org/10.1200/JCO-25-02375
MLA Elizabeth S. Duke, et al.. "Selpercatinib and the Crossover Conundrum: Potential Impact of Postprogression Therapies on Overall Survival.." Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2026, pp. JCO2502375.
PMID 41996652 ↗

Abstract

Overall survival (OS) should be evaluated in all randomized cancer trials, even when not the primary end point, as it is clinically meaningful and measures both safety and efficacy. Crossover from the control to experimental arms in randomized trials may be incorporated to allow access to promising investigational treatments after progression on a control arm. The results of Study LIBRETTO-431, an ex-US multiregional, open-label, randomized, active-controlled trial of selpercatinib versus platinum-based and pemetrexed chemotherapy with or without pembrolizumab in patients with treatment-naïve advanced fusion-positive non-small cell lung cancer, highlight the challenges of interpreting OS in trials with high crossover rates and variable postprogression therapies. Trial results demonstrated a large improvement in progression-free survival with an acceptable safety profile, but were accompanied by an immature OS analysis with a hazard ratio of 1.26, favoring the chemoimmunotherapy arm. Regardless of the position of OS in the end point hierarchy, it is critical that OS analyses include prespecified plans for data collection and analytical methods to account for the potential impact of postprogression therapies on the interpretation of study results.

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