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免疫检查点抑制剂再治疗非小细胞肺癌的安全性和疗效:一项系统评价和荟萃分析。

Safety and efficacy of retreatment with immune checkpoint inhibitors in non-small cell lung cancer: a systematic review and meta-analysis.

作者信息

Cai Zijing, Zhan Ping, Song Yong, Liu Hongbing, Lv Tangfeng

机构信息

Department of Respiratory Medicine, Jinling Hospital, Nanjing Medical University, Nanjing, China.

Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, Nanjing, China.

出版信息

Transl Lung Cancer Res. 2022 Aug;11(8):1555-1566. doi: 10.21037/tlcr-22-140.

Abstract

BACKGROUND

Retreatment with immune checkpoint inhibitors (ICIs) might be a subsequent therapeutic option for patients with non-small cell lung cancer (NSCLC) who discontinued initial ICIs treatment because of disease progression, immune-related adverse events (irAEs) or completion of a fixed course, yet little evidence exists on the safety and efficacy of ICIs retreatment to support this strategy.

METHODS

We searched PubMed, Web of Science, Embase, Cochrane and major meeting libraries for articles about ICIs retreatment in NSCLC for systematic review and meta-analysis. The outcomes included objective response rate (ORR) and disease control rate (DCR) for efficacy and the incidence of all-grade and high-grade irAEs for safety. ICIs rechallenge implies retreatment that can be applied to patients who progressed, while ICIs resumption refers to retreatment for patients who discontinued prior treatment due to an irAE or completion of a fixed course of immunotherapy.

RESULTS

Eighteen studies were enrolled in our analysis. The pooled ORR and DCR of ICIs retreatment were respectively 20% and 54%. ICIs retreatment was associated with a decrease in ORR and DCR compared to prior ICIs treatment (ORR: OR, 0.29, 95% CI: 0.14, 0.63, P=0.002; DCR: OR, 0.53, 95% CI: 0.28-0.99, P=0.05). The pooled ORR and DCR of ICIs rechallenge were 8% and 39%. ICIs rechallenge showed a lower ORR compared with initial ICIs treatment (P<0.05). ICIs resumption presented an ORR of 34% and a DCR of 71%, showing no significant difference in ORR and DCR compared with initial ICIs treatment (P>0.05). Retreated with the same type of ICIs as before showed no difference in ORR and DCR (P>0.05), while with different ICIs was associated with a decrease in ORR and DCR in contrast to initial treatment (P<0.05). The pooled incidence of all-grade and high-grade irAEs after ICIs retreatment in patients with NSCLC were separately 41% and 13% which showed a similar incidence compared with initial ICIs treatment (P>0.05).

DISCUSSION

Retreatment with ICIs is feasible for patients with NSCLC in consideration of its encouraging efficacy and tolerable safety, especially in resumption with ICIs. When it comes to ICIs rechallenge, it is necessary to accurately identify the potential targeted beneficiary population. More large-scale prospective studies are warranted to confirm our discoveries. More attention could be paid to further exploring the efficacy and safety of retreatment concurrently with ICIs and chemotherapy.

摘要

背景

对于因疾病进展、免疫相关不良事件(irAE)或完成固定疗程而停止初始免疫检查点抑制剂(ICI)治疗的非小细胞肺癌(NSCLC)患者,ICI再治疗可能是后续的治疗选择,但关于ICI再治疗的安全性和有效性的证据很少,无法支持这一策略。

方法

我们检索了PubMed、Web of Science、Embase、Cochrane和主要会议文献库,以查找有关NSCLC患者ICI再治疗的文章,进行系统评价和荟萃分析。结果包括疗效的客观缓解率(ORR)和疾病控制率(DCR)以及安全性方面的所有级别和高级别irAE的发生率。ICI再次挑战是指可应用于病情进展患者的再治疗,而ICI恢复是指因irAE或完成固定疗程的免疫治疗而停止先前治疗的患者的再治疗。

结果

18项研究纳入我们的分析。ICI再治疗的汇总ORR和DCR分别为20%和54%。与先前的ICI治疗相比,ICI再治疗的ORR和DCR有所下降(ORR:OR,0.29,95%CI:0.14,0.63,P=0.002;DCR:OR,0.53,95%CI:0.28 - 0.99,P=0.05)。ICI再次挑战的汇总ORR和DCR分别为8%和39%。与初始ICI治疗相比,ICI再次挑战的ORR较低(P<0.05)。ICI恢复的ORR为34%,DCR为71%,与初始ICI治疗相比,ORR和DCR无显著差异(P>0.05)。与之前使用相同类型的ICI进行再治疗,ORR和DCR无差异(P>0.05),而与不同的ICI相比,与初始治疗相比ORR和DCR下降(P<0.05)。NSCLC患者ICI再治疗后所有级别和高级别irAE的汇总发生率分别为41%和13%,与初始ICI治疗相比发生率相似(P>0.05)。

讨论

考虑到其令人鼓舞的疗效和可耐受的安全性,ICI再治疗对NSCLC患者是可行的,尤其是ICI恢复治疗。对于ICI再次挑战,有必要准确识别潜在的目标受益人群。需要更多大规模的前瞻性研究来证实我们的发现。可以更多地关注进一步探索ICI与化疗同时进行再治疗的疗效和安全性。

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