Bertaglia Valentina, Petrelli Fausto, Dottorini Lorenzo, Carnio Simona, Morelli Anna Maria, Nepote Alessandro, Maccioni Antonio, Scartozzi Mario, Solinas Cinzia, Novello Silvia
Department of Oncology, University of Turin, San Luigi Gonzaga Hospital, Orbassano, Torino, Italy.
Oncology Unit, ASST Bergamo Ovest, Treviglio, Bergamo, Italy.
Semin Oncol. 2025 Feb;52(1):14-18. doi: 10.1053/j.seminoncol.2024.11.001. Epub 2024 Dec 31.
Small-cell lung cancer (SCLC) accounts for 10%-15% of all lung cancers. At diagnosis, nearly two thirds of patients with SCLC have extensive stage (ES), with a median overall survival (OS) less than 12 months. The combination of protein-death-1/protein-death-ligand-1 (PD-1/PD-L1) immune checkpoint inhibitors (ICIs) with first-line platinum plus etoposide chemotherapy has changed the therapeutic landscape for ES-SCLC. Older adults represent most of the cancers diagnosed and deaths by age group, with an expected increase over the next decade. In the real-world setting, about 30%-40% of patients with a diagnosis of SCLC are reported to be over 70-years-old at the time of diagnosis. However, this subgroup of patients is underrepresented in clinical trials. Based on this evidence, we performed this systematic review to define the activity of ICIs plus chemotherapy in older patients with previously untreated ES-SCLC.
This systematic review was carried out in accordance with the statement in the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA). A systematic search on multiple electronic databases was conducted from inception to the end of April to identify randomized trials that prospectively evaluated chemotherapy ± PD-1/PD-L1 ICIs. When more than one report of the same study was available, the most recent data (with longer follow-up and/or higher number of patients) was considered. The primary endpoint of the study was efficacy, in terms of overall survival, progression-free survival, and disease control rate.
We selected six randomized clinical trials that enrolled 3396 patients in the meta-analysis. In the experimental arm, 670 patients were 65 years of age and older compared to 504 in the control arm. In the subgroup of patients ≥65 years, adding ICIs to chemotherapy led to a significant benefit in OS [hazard ratio (HR) 0.80, 95% confidence interval (CI) 0.72-0.90). There was moderate but not-significant heterogenity among the trials (I = 47%, P = 0.07).
This systematic review found that the combination of chemotherapy plus ICIs improved OS among older patients with ES-SCLC. Biomarker and comprehensive geriatric assessment are needed to improve the identification and selection of patients with cancer that are uniformly defined as older.
小细胞肺癌(SCLC)占所有肺癌的10%-15%。在确诊时,近三分之二的SCLC患者处于广泛期(ES),中位总生存期(OS)不足12个月。蛋白死亡-1/蛋白死亡配体-1(PD-1/PD-L1)免疫检查点抑制剂(ICI)与一线铂类加依托泊苷化疗联合应用改变了ES-SCLC的治疗格局。按年龄组划分,老年人占确诊癌症和死亡病例的大多数,预计在未来十年会有所增加。在现实环境中,据报道约30%-40%的SCLC确诊患者在确诊时年龄超过70岁。然而,这一亚组患者在临床试验中的代表性不足。基于这一证据,我们进行了这项系统评价,以确定ICI联合化疗在先前未治疗的ES-SCLC老年患者中的疗效。
本系统评价按照系统评价和Meta分析的首选报告项目(PRISMA)指南中的声明进行。从数据库建立至4月底,在多个电子数据库中进行系统检索,以识别前瞻性评估化疗±PD-1/PD-L1 ICI的随机试验。当同一研究有多个报告时,考虑最新数据(随访时间更长和/或患者数量更多)。研究的主要终点是疗效,以总生存期、无进展生存期和疾病控制率衡量。
我们选择了六项随机临床试验,纳入荟萃分析的患者有3396例。试验组有670例患者年龄在65岁及以上,对照组有504例。在≥65岁的患者亚组中,化疗加用ICI可显著改善总生存期[风险比(HR)0.80,95%置信区间(CI)0.72-0.90]。试验之间存在中度但不显著的异质性(I² = 47%,P = 0.07)。
本系统评价发现,化疗加ICI可改善ES-SCLC老年患者的总生存期。需要生物标志物和综合老年评估来改善对统一界定为老年的癌症患者的识别和选择。