LIBRETTO-432, a phase III study of adjuvant selpercatinib or placebo in stage IB-IIIA RET fusion-positive non-small-cell lung cancer

Author:

Tsuboi Masahiro1ORCID,Goldman Jonathan W2,Wu Yi-Long3ORCID,Johnson Melissa L4,Paz-Ares Luis5,Yang James Chih-Hsin6,Besse Benjamin7,Su Weiji8,Chao Bo H9,Drilon Alexander10

Affiliation:

1. National Cancer Center Hospital East, Kashiwa, Japan

2. David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA 90095, USA

3. Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital & Guangdong Academy of Medical Sciences, Guangzhou, China

4. Sarah Cannon Research Institute, Nashville, TN 37203, USA

5. Department of Medical Oncology, Hospital Universitario 12 de Octubre, H120-CNIO Lung Cancer Unit, Universidad Complutense & Ciberonc, Madrid, Spain

6. Department of Oncology, National Taiwan University Hospital & Graduate Institute of Oncology, National Taiwan University, Taipei, Taiwan

7. Gustave Roussy, Villejuif France & Paris Saclay University, France

8. Eli Lilly & Company, Indianapolis, IN 46225, USA

9. Eli Lilly & Company, New York, NY 10016, USA

10. Department of Medicine, Memorial Sloan-Kettering Cancer Center & Weill Cornell Medical College, New York, NY 10065, USA

Abstract

Selpercatinib, a first-in-class, highly selective and potent central nervous system-active RET kinase inhibitor demonstrated clinically meaningful activity with manageable toxicity in pretreated and treatment-naive advanced/metastatic RET fusion-positive non-small-cell lung cancer (NSCLC). LIBRETTO-432 is a global, randomized, double-blind, phase III trial evaluating selpercatinib versus placebo in stage IB-IIIA, RET fusion-positive NSCLC, previously treated with definitive surgery or radiation; participants must have undergone available anti-cancer therapy (including chemotherapy or durvalumab) or not be suitable for it, per investigator's discretion. The primary end point is investigator-assessed event-free survival (EFS) in the primary analysis population (stage II-IIIA RET fusion-positive NSCLC). Key secondary end points include EFS in the overall population, overall survival, and time to distant disease recurrence in the central nervous system.

Funder

Eli Lilly and Company

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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