Selpercatinib, a novel, highly selective and potent, inhibitor of RET, demonstrated clinically meaningful antitumor activity with manageable toxicity in heavily pretreated and treatment-naive RET fusion-positivenon-small-cell lung cancer patients in a Phase I/II clinical trial. LIBRETTO-431 (NCT04194944) is a randomized, global, multicenter, open-label, Phase III trial, evaluating selpercatinib versus carboplatin or cisplatin and pemetrexed chemotherapy with or without pembrolizumab in treatment-naive patients with locally advanced/metastatic RET fusion-positive nonsquamous non-small-cell lung cancer. The primary end point is progression-free survivalby independent review. Key secondary end points include overall survival, response rate, duration of responseand progression-free survival. Clinical trial registration: NCT04194944 (ClinicalTrials.gov).

Phase III study of selpercatinib vs chemotherapy +/- pembrolizumab in untreated RET positive non-small-cell lung cancer

Novello, Silvia;
2021-01-01

Abstract

Selpercatinib, a novel, highly selective and potent, inhibitor of RET, demonstrated clinically meaningful antitumor activity with manageable toxicity in heavily pretreated and treatment-naive RET fusion-positivenon-small-cell lung cancer patients in a Phase I/II clinical trial. LIBRETTO-431 (NCT04194944) is a randomized, global, multicenter, open-label, Phase III trial, evaluating selpercatinib versus carboplatin or cisplatin and pemetrexed chemotherapy with or without pembrolizumab in treatment-naive patients with locally advanced/metastatic RET fusion-positive nonsquamous non-small-cell lung cancer. The primary end point is progression-free survivalby independent review. Key secondary end points include overall survival, response rate, duration of responseand progression-free survival. Clinical trial registration: NCT04194944 (ClinicalTrials.gov).
2021
17
7
763
773
Phase III trial; RET fusion-positive; RET kinase inhibitor; RET rearrangement; non-small-cell lung cancer; selpercatinib; targeted therapy
Solomon, Benjamin J; Zhou, Cai Cun; Drilon, Alexander; Park, Keunchil; Wolf, Jürgen; Elamin, Yasir; Davis, Hannah M; Soldatenkova, Victoria; Sashegyi,...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1762572
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