Department of Medical Oncology, Antalya City Hospital, Antalya, Turkey.
Department of Medical Oncology, Ankara Bilkent City Hospital, Ankara, Turkey.
Expert Opin Pharmacother. 2024 Aug;25(11):1555-1563. doi: 10.1080/14656566.2024.2391007. Epub 2024 Aug 11.
We aimed to evaluate the efficacy and safety of granulocyte-colony stimulating factor (G-CSF) prophylaxis during chemoimmunotherapy with carboplatin plus etoposide and atezolizumab in extensive-stage small cell lung cancer (ES-SCLC).
This retrospective, multicenter study enrolled ES-SCLC patients receiving carboplatin plus etoposide and atezolizumab, categorized into G-CSF and non-G-CSF groups. Demographic and disease-related data were collected. Response rates, progression-free survival (PFS), overall survival (OS), and toxicity were analyzed.
Of 119 patients (median age: 63 years), the overall response rate (ORR) and disease control rate (DCR) were 72.3% and 81.5%, respectively. In the G-CSF group, the ORR was 76.4% compared to 60.0% in the non-G-CSF group ( = 0.33), and the DCR was 85.4% versus 70.0%, respectively ( = 0.46). Median PFS was 8.3 months (95% CI, 6.8-9.8) in the G-CSF group and 6.8 months (95% CI, 6.2-7.5) in the non-G-CSF group ( = 0.24). Median OS was 13.8 months (95% CI, 9.6-18.1) for the G-CSF group and 10.6 months (95% CI, 7.9-13.3) for the non-G-CSF group ( = 0.47). Grade 3 ≥ adverse events were similar between groups (49.4% vs. 33.3%, respectively, = 0.12).
G-CSF prophylaxis can be safely used in ES-SCLC patients undergoing carboplatin plus etoposide and atezolizumab regimen without significantly altering efficacy or increasing toxicity.
我们旨在评估在广泛期小细胞肺癌(ES-SCLC)患者中使用卡铂+依托泊苷和阿替利珠单抗化疗免疫治疗时,使用粒细胞集落刺激因子(G-CSF)预防的疗效和安全性。
这项回顾性、多中心研究纳入了接受卡铂+依托泊苷和阿替利珠单抗治疗的 ES-SCLC 患者,将其分为 G-CSF 组和非 G-CSF 组。收集人口统计学和疾病相关数据。分析了反应率、无进展生存期(PFS)、总生存期(OS)和毒性。
在 119 名患者(中位年龄:63 岁)中,总缓解率(ORR)和疾病控制率(DCR)分别为 72.3%和 81.5%。在 G-CSF 组中,ORR 为 76.4%,而非 G-CSF 组为 60.0%( = 0.33),DCR 分别为 85.4%和 70.0%( = 0.46)。G-CSF 组的中位 PFS 为 8.3 个月(95%CI,6.8-9.8),而非 G-CSF 组为 6.8 个月(95%CI,6.2-7.5)( = 0.24)。G-CSF 组的中位 OS 为 13.8 个月(95%CI,9.6-18.1),而非 G-CSF 组为 10.6 个月(95%CI,7.9-13.3)( = 0.47)。两组的 3 级及以上不良事件发生率相似(分别为 49.4%和 33.3%, = 0.12)。
在接受卡铂+依托泊苷和阿替利珠单抗方案治疗的 ES-SCLC 患者中,使用 G-CSF 预防不会显著改变疗效或增加毒性,是安全的。