一线免疫检查点抑制剂+化疗在台湾广泛期小细胞肺癌患者中的应用

IF 2.4
Ying-Ting Liao, Ruei-Lin Sun, Hsu-Ching Huang, Chia-I Shen, Yen-Han Tseng, Yung-Hung Luo, Yuh-Min Chen, Chi-Lu Chiang
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引用次数: 0

摘要

背景:免疫检查点抑制剂(ICIs)与铂和依托泊苷(EP)联合用于广泛期小细胞肺癌(ES-SCLC)的一线(1L)治疗中,已经证明了生存益处。我们研究了台湾ES-SCLC患者接受1L ICI + EP治疗的真实结局、不良事件(ae)和预后因素。方法:我们分析ES-SCLC患者接受ICI + EP或单独EP作为1L治疗的临床特征、客观缓解率、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和治疗相关ae。结果:ICI + EP治疗33例,单独EP治疗199例。1L ICI + EP组的OS比1L EP组长(中位数:13.9个月vs 8.5个月,p = 0.003)。基线肝转移与较短的1L PFS相关,而接受巩固性胸部放疗(cTRT)与较长的1L PFS相关。基线肝转移、严重血液学ae(分级≥3)和中性粒细胞与淋巴细胞比值(NLR)≥4与较短的生存期相关。结论:在1L化疗中加入ICIs可提高ES-SCLC的生存率,但需要密切监测ae。cTRT增强局部肿瘤控制,改善PFS。肝转移与较短的PFS和OS相关。在接受免疫化疗的ES-SCLC患者中,严重的血液学ae和NLR升高预示着不良的OS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
First-line immune checkpoint inhibitors plus chemotherapy in Taiwanese patients with extensive-stage small-cell lung cancer.

Background: Immune checkpoint inhibitors (ICIs) have demonstrated survival benefits when combined with platinum and etoposide (EP) in first-line (1L) treatment for extensive-stage small-cell lung cancer (ES-SCLC). We investigated the real-world outcomes, adverse events (AEs), and prognostic factors of Taiwanese patients with ES-SCLC receiving 1L ICI + EP.

Methods: We analyzed the clinical characteristics, objective response rates, disease control rates (DCR), progression-free survival (PFS), overall survival (OS), and treatment-related AEs of patients with ES-SCLC who received ICI + EP or EP alone as 1L treatment.

Results: A total of 33 patients received ICI + EP, and 199 received EP alone. The 1L ICI + EP group had longer OS than did the 1L EP group (median: 13.9 months vs 8.5 months; p = 0.003). Baseline liver metastasis was associated with shorter 1L PFS, whereas undergoing consolidative thoracic radiotherapy (cTRT) was associated with longer 1L PFS. Baseline liver metastasis, severe hematological AEs (grade ≥ 3), and a neutrophil-to-lymphocyte ratio (NLR) of ≥4 were associated with shorter OS.

Conclusion: Adding ICIs to 1L chemotherapy provides survival benefits in ES-SCLC, while close monitoring for AEs is required. cTRT enhances local tumor control and improves PFS. Liver metastasis is associated with shorter PFS and OS. Severe hematological AEs and an elevated NLR predict poor OS in patients with ES-SCLC undergoing immunochemotherapy.

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