Department of Internal Medicine, Mayo Clinic, Phoenix, AZ.
Division of Hematology-Oncology, Mayo Clinic Cancer Center, Phoenix, AZ.
Clin Lung Cancer. 2023 Nov;24(7):591-597. doi: 10.1016/j.cllc.2023.05.005. Epub 2023 May 26.
Studies demonstrated that chemoimmunotherapy prolongs progression-free survival (PFS) and overall survival (OS) in patients with extensive-stage small-cell lung cancer (ES-SCLC) and an Eastern Cooperative Oncology Group performance status (ECOG PS) 0 or 1. However, there is little data regarding chemoimmunotherapy in patients with ES-SCLC and an ECOG PS 2 or 3. This study aims to evaluate the benefits of chemoimmunotherapy compared to chemotherapy in the first-line treatment of patients with ES-SCLC and ECOG PS 2 or 3.
This retrospective study analyzed 46 adults treated at Mayo Clinic between 2017 and 2020 with de novo ES-SCLC and an ECOG PS 2 or 3. Twenty patients received platinum-etoposide and 26 patients received platinum-etoposide and atezolizumab. Progression-free survival (PFS) and Overall survival (OS) were calculated using Kaplan-Meier methods.
PFS was longer in the chemoimmunotherapy group compared to the chemotherapy group, 4.1 months (95% confidence interval [CI]: 3.8-6.9) vs. 3.2 months (95% CI: 0.6-4.8), respectively; P = 0.0491. However, there was no statistically significant difference in the OS between the chemoimmunotherapy and chemotherapy group, 9.3 months (95% CI: : 4.9-12.8) vs. 7.6 months (95% CI: 0.6-11.9), respectively; P = .21.
Chemoimmunotherapy prolongs PFS compared to chemotherapy in patients with newly diagnosed ES-SCLC and an ECOG PS 2 or 3. No OS difference was observed among the chemoimmunotherapy and chemotherapy groups; nevertheless, this may be attributed due to the small sample size of the study.
研究表明,化疗免疫疗法可延长广泛期小细胞肺癌(ES-SCLC)和东部合作肿瘤学组表现状态(ECOG PS)为 0 或 1 的患者的无进展生存期(PFS)和总生存期(OS)。然而,对于 ECOG PS 为 2 或 3 的 ES-SCLC 患者接受化疗免疫治疗的数据很少。本研究旨在评估与化疗相比,化疗免疫疗法在 ECOG PS 为 2 或 3 的 ES-SCLC 患者一线治疗中的获益。
本回顾性研究分析了 2017 年至 2020 年间在 Mayo 诊所接受治疗的 46 例初诊为 ES-SCLC 且 ECOG PS 为 2 或 3 的成人患者。20 例患者接受铂类依托泊苷治疗,26 例患者接受铂类依托泊苷和阿替利珠单抗治疗。采用 Kaplan-Meier 法计算无进展生存期(PFS)和总生存期(OS)。
化疗免疫治疗组的 PFS 长于化疗组,分别为 4.1 个月(95%置信区间 [CI]:3.8-6.9)和 3.2 个月(95% CI:0.6-4.8);P=0.0491。然而,化疗免疫治疗组和化疗组的 OS 无统计学差异,分别为 9.3 个月(95% CI:4.9-12.8)和 7.6 个月(95% CI:0.6-11.9);P=0.21。
与化疗相比,化疗免疫疗法可延长新诊断为 ES-SCLC 且 ECOG PS 为 2 或 3 的患者的 PFS。在化疗免疫治疗组和化疗组之间未观察到 OS 差异;然而,这可能归因于研究的样本量较小。