Sintilimab combined with anlotinib and chemotherapy as second-line or later therapy in extensive-stage small cell lung cancer: a phase II clinical trial

IF 40.8 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Signal Transduction and Targeted Therapy Pub Date : 2024-09-16 DOI:10.1038/s41392-024-01957-3
Xiao Han, Jun Guo, Lingyu Li, Yong Huang, Xue Meng, Linlin Wang, Hui Zhu, Xiangjiao Meng, Qian Shao, Xing Li, Yan Zhang, Jin Wang, Yanhua Chen, Yingjie Zhang, Yiru Chen, Changbin Zhu, Zhehai Wang
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Abstract

Treatment options for patients with relapsed extensive-stage small cell lung cancer (ES-SCLC) remain scarce. This study aims to evaluate the efficacy and safety of combining anlotinib and sintilimab plus chemotherapy as a second line or later therapy for ES-SCLC patients. This is a phase II clinical trial (ChiCTR2100049390) conducting at Shandong Cancer Hospital. Patients with ES-SCLC and received at least one prior systemic treatment were enrolled. The trial design involved a combination therapy (sintilimab, anlotinib, and nab-paclitaxel) administered over six 21-day cycles, followed by maintenance sintilimab therapy. The primary endpoint was objective response rate (ORR). Circulating tumor DNA sequencing was employed for exploratory analysis. From July 2021 to April 2023, 25 eligible patients were enrolled. The confirmed ORR was 60% (95% CI: 38.7–78.9%) and the DCR was 76% (95% CI: 54.9–90.6%). The mPFS was 6.0 months (95% CI: 5.4–9.7), and the 6-month PFS rate was 49.2%. The mOS was 13.4 months (95% CI: 11.8-NR), with a 12-month survival rate of 62.2%. Treatment-related adverse events (TRAEs) of any grade occurred in 80% of patients, with the most common being fatigue (40%) and nausea (32%). TRAEs of Grade 3 or higher were reported in 12% of patients. ctDNA analysis indicated that low on-treatment blood tumor mutation burden was associated with longer PFS and OS and a potential role of KMT2D mutation in treatment resistance. This combination therapy shows promising efficacy and a manageable safety profile as a second-line or later treatment for ES-SCLC, with genomic insights providing potential biomarkers for treatment response.

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辛替利单抗联合安罗替尼和化疗作为广泛期小细胞肺癌的二线或后期治疗:II 期临床试验
复发的广泛期小细胞肺癌(ES-SCLC)患者的治疗方案仍然很少。本研究旨在评估安罗替尼和辛替利单抗联合化疗作为ES-SCLC患者二线或后期治疗的有效性和安全性。这是山东省肿瘤医院开展的一项II期临床试验(ChiCTR2100049390)。ES-SCLC患者既往至少接受过一次系统治疗。试验设计包括6个21天周期的联合治疗(辛替利单抗、安罗替尼和纳伯-紫杉醇),随后是辛替利单抗的维持治疗。主要终点是客观反应率(ORR)。循环肿瘤DNA测序用于探索性分析。从2021年7月到2023年4月,共有25名符合条件的患者入组。确诊ORR为60%(95% CI:38.7-78.9%),DCR为76%(95% CI:54.9-90.6%)。mPFS为6.0个月(95% CI:5.4-9.7),6个月PFS率为49.2%。mOS为13.4个月(95% CI:11.8-NR),12个月生存率为62.2%。80%的患者发生了任何级别的治疗相关不良事件(TRAEs),最常见的是疲劳(40%)和恶心(32%)。ctDNA分析表明,低治疗时血液肿瘤突变负荷与较长的PFS和OS有关,KMT2D突变在耐药中可能起作用。这种联合疗法作为ES-SCLC的二线或后期治疗,显示出良好的疗效和可控的安全性,其基因组学见解为治疗反应提供了潜在的生物标志物。
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来源期刊
Signal Transduction and Targeted Therapy
Signal Transduction and Targeted Therapy Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
44.50
自引率
1.50%
发文量
384
审稿时长
5 weeks
期刊介绍: Signal Transduction and Targeted Therapy is an open access journal that focuses on timely publication of cutting-edge discoveries and advancements in basic science and clinical research related to signal transduction and targeted therapy. Scope: The journal covers research on major human diseases, including, but not limited to: Cancer,Cardiovascular diseases,Autoimmune diseases,Nervous system diseases.
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