Guven Deniz Can, Sahin Taha Koray, Kilickap Saadettin
Medical Oncology Clinic, Health Sciences University, Elazig City Hospital, 23280 Elazig, Turkey.
Internal Medicine Clinic, Sultanhanı Hospital, 68000 Aksaray, Turkey.
Cancers (Basel). 2023 Dec 28;16(1):156. doi: 10.3390/cancers16010156.
After the success of immunotherapy in the treatment of advanced non-small cell lung cancer (NSCLC), the benefit of neoadjuvant chemoimmunotherapy was compared with chemotherapy for localized NSCLC in several trials. However, the available studies had variable study designs, and study cohorts had limited follow-up times. Therefore, we conducted a systematic review and meta-analysis to evaluate the benefit of adding immunotherapy to neoadjuvant chemotherapy in patients with localized NSCLC.
We conducted a systematic review using Pubmed, Web of Science, and Scopus databases for studies published until 5 December 2023. This protocol was registered in the PROSPERO database (Registration Number: CRD42023466337). We performed the meta-analyses with the generic inverse-variance method with a fixed effects model.
Overall, 7 studies encompassing 2993 patients were included in the analyses. The use of neoadjuvant chemoimmunotherapy was associated with a 41% reduction in the risk of progression or death compared to neoadjuvant chemotherapy (HR: 0.59, 95% CI: 0.52-0.66, < 0.0001) and a lower risk of death (HR: 0.67, 95% CI: 0.55-0.82, < 0.0001). The neoadjuvant chemoimmunotherapy improved pCR rates compared to chemotherapy (21.8% vs. 3.8%, OR: 7.04, 95% CI: 5.23-9.47, < 0.0001), while high-grade adverse events were higher with neoadjuvant chemoimmunotherapy (OR: 1.18, 95% CI: 1.02-1.36, = 0.0300).
The available evidence demonstrates a statistically significant and clinically meaningful event-free survival benefit and possibly an overall survival benefit with neoadjuvant chemoimmunotherapy with a slight increase in high-grade toxicities.
免疫疗法在晚期非小细胞肺癌(NSCLC)治疗中取得成功后,多项试验比较了新辅助化疗免疫疗法与单纯化疗对局限性NSCLC的疗效。然而,现有研究的设计各不相同,且研究队列的随访时间有限。因此,我们进行了一项系统评价和荟萃分析,以评估在局限性NSCLC患者的新辅助化疗中添加免疫疗法的益处。
我们使用PubMed、科学网和Scopus数据库对截至2023年12月5日发表的研究进行了系统评价。该方案已在PROSPERO数据库中注册(注册号:CRD42023466337)。我们采用固定效应模型的通用逆方差法进行荟萃分析。
总体而言,分析纳入了7项研究,共2993例患者。与新辅助化疗相比,新辅助化疗免疫疗法使疾病进展或死亡风险降低了41%(HR:0.59,95%CI:0.52 - 0.66,P < 0.0001),死亡风险更低(HR:0.67,95%CI:0.55 - 0.82,P < 0.0001)。与化疗相比,新辅助化疗免疫疗法提高了病理完全缓解(pCR)率(21.8%对3.8%,OR:7.04,95%CI:5.23 - 9.47,P < 0.0001),而新辅助化疗免疫疗法的高级别不良事件发生率更高(OR:1.18,95%CI:1.02 - 1.36,P = 0.0300)。
现有证据表明,新辅助化疗免疫疗法在无事件生存方面具有统计学显著且临床有意义的益处,可能对总生存也有益处,不过高级别毒性略有增加。