A Single-Arm Phase 2 Study of Sotorasib Plus Carboplatin and Pemetrexed in Patients With Advanced Nonsquamous NSCLC With KRAS G12C Mutation (WJOG14821L, SCARLET)
- PMID: 39828218
- DOI: 10.1016/j.jtho.2025.01.006
A Single-Arm Phase 2 Study of Sotorasib Plus Carboplatin and Pemetrexed in Patients With Advanced Nonsquamous NSCLC With KRAS G12C Mutation (WJOG14821L, SCARLET)
Abstract
Introduction: The efficacy and safety of sotorasib plus platinum doublet chemotherapy in KRAS G12C-mutated nonsquamous NSCLC (nonsq NSCLC) have been previously reported with a limited follow-up period.
Methods: SCARLET is a single-arm phase 2 study involving chemotherapy-naive patients with KRAS G12C-mutated nonsq NSCLC. The participants received 960 mg daily plus four cycles of carboplatin (area under the curve = 5)/pemetrexed 500 mg/m2, followed by sotorasib/pemetrexed until disease progression. The primary end point was the overall response rate (ORR) and the secondary end points were progression-free survival (PFS), overall survival, and safety. Using plasma samples, next-generation sequencing was performed at baseline, 3 weeks, and during disease progression (the Japan Registry of Clinical Trials number 2051210086).
Results: Thirty patients were enrolled between October 2021 and July 2022 with a median follow-up of 14.8 months. ORR was 88.9% (80% confidence interval [CI]: 78.5%-94.8%, 95% CI: 70.8%-97.6%), median PFS was 6.6 months (95% CI: 5.3-16.7 mo), and median overall survival was 20.6 months (95% CI: 8.1 mo-not estimated). Among patients with programmed death-ligand 1 expression levels of 1% or higher and less than 1%, the ORRs were 82.3 and 100%, respectively, and the median PFS was 7.6 and 9.7 months, respectively. Using plasma samples, patients without KRAS G12C at baseline, without KRAS-related pathway co-alterations, or who cleared KRAS G12C at 3 weeks had better median PFS (16.7, 13.9, 8.7 mo, respectively). Tumor protein 53 mutations and EGFR and MET amplification were detected as acquired resistance.
Conclusions: In patients with KRAS G12C-mutated nonsq NSCLC, sotorasib plus carboplatin/pemetrexed reported favorable efficacy, particularly for patients with less than 1% programmed death-ligand 1, with manageable toxicity.
Keywords: KRAS G12C; Nonsquamous non–small cell lung cancer; Sotorasib.
Copyright © 2025 The Author(s). Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosure Dr. Akamatsu received honoraria from Amgen Inc., AstraZeneca K.K., Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Nippon Kayaku Co. Ltd., Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Takeda Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd.; served in an advisory role for Amgen Inc., Janssen Pharmaceutical K.K., and Sandoz; and received research funding from Amgen Inc., Chugai Pharmaceutical Co. Ltd., and Merck Sharp & Dohme K.K. Dr. Sakata received honoraria from AstraZeneca K.K., Takeda Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd. Dr. Azuma received honoraria from AstraZeneca K.K., Bristol-Myers Squibb, Chugai Pharmaceutical Co., Ltd., Merck Sharp & Dohme K.K., Ono Pharmaceutical Co., Ltd., and Takeda Pharmaceutical Co., Ltd. Dr. Yoshioka received honoraria from Amgen Inc.; AstraZeneca K.K.; Boehringer Ingelheim Japan Inc.; Bristol-Myers Squibb; Chugai Pharmaceutical Co. Ltd.; Daiichi Sankyo Co. Ltd.; Eli Lilly Japan K.K.; Kyowa Kirin; Merck, Merck Sharp & Dohme K.K.; Nippon Kayaku Co. Ltd.; Nipro Pharma; Novartis Pharma K.K.; Ono Pharmaceutical Co. Ltd.; Otsuka Pharmaceutical; Pfizer Inc.; and Taiho Pharmaceutical Co. Ltd. Dr. Uemura received honoraria from Amgen Inc., AstraZeneca K.K., Boehringer Ingelheim Japan Inc., Chugai Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Novartis Pharma K.K., Ono Pharmaceutical Co., Ltd., and Taiho Pharmaceutical Co., Ltd. Dr. Tsuchiya-Kawano received honoraria from AstraZeneca K.K.; Bristol-Myers Squibb; Chugai Pharmaceutical Co. Ltd.; Kyowa Kirin, Merck Sharp & Dohme K.K.; Ono Pharmaceutical Co. Ltd.; Takeda Pharmaceutical Co. Ltd.; and Taiho Pharmaceutical Co. Ltd. Dr. Sato received honoraria from AstraZeneca K.K.; Boehringer Ingelheim Japan Inc.; Bristol-Myers Squibb; Chugai Pharmaceutical Co. Ltd.; Daiichi Sankyo Co. Ltd.; Eli Lilly Japan K.K.; Kyowa Kirin, Merck Sharp & Dohme K.K.; Nippon Kayaku Co. Ltd.; Novartis Pharma K.K.; Ono Pharmaceutical Co. Ltd.; Pfizer Inc.; Takeda Pharmaceutical Co. Ltd.; and Taiho Pharmaceutical Co. Ltd. Dr. Sakamoto received honoraria from AstraZeneca K.K.; Chugai Pharmaceutical Co., Ltd.; Daiichi Sankyo Co., Ltd.; Eli Lilly, Japan K.K.; and Hisamitsu Pharmaceutical Co. Inc.; Kyowa Kirin, Illumina, Janssen Pharma K.K.; Merck, Merck Sharp & Dohme K.K.; Novartis Pharma K.K.; Ono Pharmaceutical Co. Ltd.; Pfizer Inc.; Takeda Pharmaceutical Co. Ltd.; and Taiho Pharmaceutical Co. Ltd. Dr. Ninomiya received honoraria from AstraZeneca K.K.; Boehringer Ingelheim Japan Inc.; Bristol-Myers Squibb; Chugai Pharmaceutical Co. Ltd.; Daiichi Sankyo Co. Ltd.; Elekta K.K.; Eli Lilly Japan K.K.; Janssen Pharma K.K.; Kyowa Kirin, Merck Sharp & Dohme K.K.; Nippon Kayaku Co. Ltd.; Ono Pharmaceutical Co. Ltd.; Pfizer Inc.; Takeda Pharmaceutical Co. Ltd.; and Taiho Pharmaceutical Co. Ltd. Dr. Toyozawa received honoraria from AstraZeneca K.K., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Nippon Kayaku Co. Ltd., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Takeda Pharmaceutical Co. Ltd., Taiho Pharmaceutical Co. Ltd., and Thermo Fisher Scientific, and received institutional research funding from AbbVie, Amgen Inc., AnHeart Therapeutics, Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Novartis Pharma K.K., Pfizer Inc., and Takeda Pharmaceutical Co. Ltd. Dr. Shukuya received honoraria from AstraZeneca K.K., Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Nippon Kayaku Co. Ltd., Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Takeda Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd., and received institutional research funding from AstraZeneca KK, Boehringer Ingelheim Japan Inc., Chugai Pharmaceutical Co. Ltd., Merck Sharp & Dohme K.K., and Novartis Pharma K.K. Prof. Kozuki received honoraria from Amgen Inc., AstraZeneca K.K., Bayer, Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eisai, Eli Lilly Japan K.K., Kyowa Kirin, Merck, Merck Sharp & Dohme K.K., Nippon Kayaku Co. Ltd., Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Sawai, Takeda Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd.; received consulting fees from AbbVie, AstraZeneca K.K., Bayer, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Ono Pharmaceutical Co. Ltd., and Pfizer Inc.; and received institutional research funding from AbbVie, Amgen Inc., AstraZeneca K.K., Bayer, Boehringer Ingelheim Japan Inc., Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eisai, Eli Lilly Japan K.K., Gilead Sciences, IQVIA Services Japan, Kyowa Kirin, Labcorp Development Japan, Merck, Merck Sharp & Dohme K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Sanofi, and Taiho Pharmaceutical Co. Ltd. Dr. Daga received honoraria from AstraZeneca K.K. Dr. Kato received honoraria from Amgen Inc., AstraZeneca K.K., BeiGene, Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., GlaxoSmithKline, Janssen, Merck, Merck Sharp & Dohme K.K., Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Takeda Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd.; received institutional research funding from AbbVie, Amgen Inc., Arrivent, AstraZeneca K.K., Bayer, BeiGene, Blue Print, Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., Gilead Sciences, GlaxoSmithKline, Haihe, Janssen, Merck, Merck Sharp & Dohme K.K., Novartis Pharma K.K., Pfizer Inc., Regeneron, and Takeda Pharmaceutical Co. Ltd.; and participated on the Data Safety Monitoring or Advisory Boards of AstraZeneca K.K., BeiGene, Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Janssen, Merck, Merck Sharp & Dohme, Novartis Pharma K.K., and Pfizer Inc. Eli Lilly, a Japanese K.K. Dr. Takahashi received honoraria from Amgen Inc., AstraZeneca K.K., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., and Takeda Pharmaceutical Co. Ltd. and institutional research funding from Amgen Inc., AnHeart Therapeutics, AstraZeneca K.K., Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan K.K., Janssen, Merck, Merck Sharp & Dohme K.K., and Pfizer Inc. Dr. Koh received honoraria from Amgen Inc., Chugai Pharmaceutical Co. Ltd., Guardant Health Japan Corp., Novartis Pharma K.K., Takeda Pharmaceutical Co. Ltd., CytoGen, and Tosoh Corp. and received institutional research funding from Boehringer Ingelheim Japan, AstraZeneca K.K., Chugai Pharmaceutical Co. Ltd., Takeda Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Takeda Pharmaceutical Co. Ltd., Tosoh Corp., and ZEON Corp. Prof. Morita received honoraria from AstraZeneca K.K.; Bristol-Myers Squibb; Chugai Pharmaceutical Co., Ltd.; Eli Lilly, Japan K.K.; Merck Sharp & Dohme K.K.; and Ono Pharmaceutical Co., Ltd. Prof. Yamamoto received honoraria from AbbVie G.K., Accuray Japan K.K., Amgen Inc., AstraZeneca K.K., Boehringer Ingelheim Japan Inc., Chugai Pharmaceutical Co. Ltd., Daiichi Sankyo Co. Ltd., Eli Lilly Japan K.K., Guardant Health Japan Corp., Janssen Pharmaceutical K.K., Kyorin, Merck Sharp & Dohme K.K., Merck, Miyarisan pharmaceutical, Novartis Pharma K.K., Ono Pharmaceutical Co. Ltd., Pfizer Inc., Takeda Pharmaceutical Co. Ltd., Taiho Pharmaceutical Co. Ltd., Terumo, and Tsumura & Co.; received consulting fees from Amgen Inc., AstraZeneca K.K., Chugai Pharmaceutical Co. Ltd., Eli Lilly Japan K.K., Merck Sharp & Dohme K.K., Novartis Pharma K.K., and Ono Pharmaceutical Co. Ltd.; and received institutional research funding from A2 Healthcare Co., AbbVie G.K., Amgen Inc., Asahi Kasei, AstraZeneca K.K., Boehringer Ingelheim Japan Inc., Bristol-Myers Squibb, Chugai Pharmaceutical Co. Ltd., EPS Co, IQVIA Japan Inc., Janssen Pharmaceutical K.K., Mebix, Novartis Pharma K.K., Merck Sharp & Dohme K.K., Ono Pharmaceutical Co. Ltd., and Taiho Pharmaceutical Co. Ltd. The remaining authors declare no conflict of interest.
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