Department of Medical Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, China.
Department of Medical Oncology, Shanghe County People's Hospital, Jinan, Shandong, China.
Signal Transduct Target Ther. 2024 Sep 16;9(1):241. doi: 10.1038/s41392-024-01957-3.
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.
对于复发广泛期小细胞肺癌(ES-SCLC)患者,治疗选择仍然有限。本研究旨在评估安罗替尼联合信迪利单抗加化疗作为二线或更后线治疗 ES-SCLC 患者的疗效和安全性。这是一项在山东省肿瘤医院进行的 II 期临床试验(ChiCTR2100049390)。纳入的患者为 ES-SCLC,且至少接受过一次系统治疗。试验设计包括联合治疗(信迪利单抗、安罗替尼和白蛋白紫杉醇),共 6 个 21 天周期,随后进行维持信迪利单抗治疗。主要终点为客观缓解率(ORR)。进行循环肿瘤 DNA 测序进行探索性分析。2021 年 7 月至 2023 年 4 月,共纳入 25 例符合条件的患者。确认的 ORR 为 60%(95%CI:38.7-78.9%),疾病控制率为 76%(95%CI:54.9-90.6%)。中位无进展生存期(mPFS)为 6.0 个月(95%CI:5.4-9.7),6 个月 PFS 率为 49.2%。中位总生存期(mOS)为 13.4 个月(95%CI:11.8-NR),12 个月生存率为 62.2%。任何级别的治疗相关不良事件(TRAEs)发生在 80%的患者中,最常见的是疲劳(40%)和恶心(32%)。TRAEs 为 3 级或更高的占 12%。ctDNA 分析表明,治疗期间血液肿瘤突变负担较低与更长的 PFS 和 OS 相关,并且 KMT2D 突变可能与治疗耐药相关。这种联合治疗作为二线或更后线治疗 ES-SCLC 显示出有前景的疗效和可管理的安全性,基因组学见解为治疗反应提供了潜在的生物标志物。