Abushanab Aws Khalid, Mustafa Mus'ab Theeb, Mousa Mahmoud Taysir, Albanawi Renad Fawwaz, Alkhalaileh Razan Mohammad, Alqudah Ghaith Nahar, Abu Zaina Razan Feras, Abu Sitta Zaina Ammar, Almasri Issa Mohammad, Abuquteish Dua
Faculty of Medicine, The Hashemite University, Zarqa, Jordan.
Department of Microbiology, Pathology and Forensic Medicine, Faculty of Medicine, The Hashemite University, Zarqa, Jordan.
Expert Rev Anticancer Ther. 2025 Feb;25(2):167-179. doi: 10.1080/14737140.2025.2460537. Epub 2025 Feb 3.
Immune checkpoint inhibitors (ICIs) are currently the primary approach for managing NSCLC. However, numerous combination therapies are currently under investigation. Our goal is to investigate the overall efficacy and safety of ICIs and taxane-based chemotherapy.
We conducted a systematic review and meta-analysis, searching web databases for relevant literature. We limited our eligibility to phase II/III randomized clinical trials involving advanced/metastatic NSCLC patients.
We performed a meta-analysis encompassing nineteen studies derived from sixteen RCTs. For patients with sq-NSCLC PD-L1 ≥ 50%, using ICIs plus taxane significantly improve PFS and OS with HR of 0.58 (95% CI, 0.45-0.74, < 0.0001) and 0.41 (95% CI, 0.33-0.50, < 0.00001), respectively. For patients with non-sq NSCLC PD-L1 1-49%, the analysis revealed significant improvement of OS and PFS with HR of 0.64 (95% CI, 0.47-0.88, = 0.005) and 0.62 (95% CI, 0.47-0.81, = 0.0004), respectively. For TRAEs of all grades, ICIs plus taxane resulted with no significant difference compared to control group with risk ratio (RR) 1.00 (95% CI 0.99-1.02).
The analysis revealed significant improvement in efficacy of ICIs with taxane in advanced/metastatic NSCLC patients compared with ICI/taxane monotherapy. PROSPERO (CRD42023447532).
免疫检查点抑制剂(ICIs)是目前治疗非小细胞肺癌(NSCLC)的主要方法。然而,目前有许多联合疗法正在研究中。我们的目标是研究ICIs与紫杉烷类化疗的总体疗效和安全性。
我们进行了一项系统评价和荟萃分析,在网络数据库中搜索相关文献。我们将纳入标准限定为涉及晚期/转移性NSCLC患者的II/III期随机临床试验。
我们进行了一项荟萃分析,纳入了来自16项随机对照试验(RCT)的19项研究。对于鳞状NSCLC(sq-NSCLC)患者且PD-L1≥50%,使用ICIs联合紫杉烷可显著改善无进展生存期(PFS)和总生存期(OS),风险比(HR)分别为0.58(95%置信区间[CI],0.45-0.74,P<0.0001)和0.41(95%CI,0.33-0.50,P<0.00001)。对于非鳞状NSCLC患者且PD-L1为1%-49%,分析显示OS和PFS有显著改善,HR分别为0.64(95%CI,0.47-0.88,P=0.005)和0.62(95%CI,0.47-0.81,P=0.0004)。对于所有级别的治疗相关不良事件(TRAEs),ICIs联合紫杉烷与对照组相比无显著差异,风险比(RR)为1.00(95%CI 0.99-1.02)。
分析显示,与ICIs/紫杉烷单药治疗相比,ICIs联合紫杉烷在晚期/转移性NSCLC患者中的疗效有显著改善。国际前瞻性系统评价注册库(PROSPERO)(CRD42023447532)。