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度伐利尤单抗联合或不联合替西木单抗治疗头颈部复发或转移性鳞状细胞癌患者的系统评价和荟萃分析。

Durvalumab with or without tremelimumab for patients with recurrent or metastatic squamous cell carcinoma of the head and neck: a systematic review and meta-analysis.

机构信息

Department of Otolaryngology-Head and Neck Surgery, BenQ Medical Center, The Affiliated BenQ Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

The Nanjing Medical Key Laboratory of Laryngopharynx and Head and Neck Neoplasm, BenQ Medical Center, The Affiliated BenQ Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.

出版信息

Front Immunol. 2024 Jan 17;14:1302840. doi: 10.3389/fimmu.2023.1302840. eCollection 2023.

Abstract

OBJECTIVE

Head and neck squamous cell carcinoma (HNSCC) ranks as the sixth most prevalent cancer worldwide, significantly impacting patients' quality of life. Immune checkpoint inhibitors (ICI) have been employed in the treatment of recurrent/metastatic (R/M)-HNSCC patients. This meta-analysis aims to assess the efficacy and safety of durvalumab monotherapy compared to the combination of durvalumab and tremelimumab in R/M-HNSCC patients.

METHODS

Relevant studies were systematically searched in PubMed, Embase, and Cochrane Library databases. All articles comparing durvalumab monotherapy with the combination with durvalumab and tremelimumab in R/M-HNSCC treatment were included. Additionally, the references of identified studies were screened if necessary.

RESULT

A total of 1298 patients from three studies comparing durvalumab with durvalumab and tremelimumab in treating R/M-HNSCC were include in this meta-analysis. Our findings revealed no significant difference in objective response rate (ORR) [odds ratio (OR): 1.15, 95% confidence interval (CI): 0.85 to 1.56, P = 0.36] and disease control rate (DCR) (OR=1.08, 95%CI: 0.86 to 1.37, P = 0.51). Similar outcomes were observed in overall survival (OS), progression-free survival (PFS), and duration of response (DoR). Regarding safety, there was no significant difference in the incidence of treatment-related adverse events (trAEs) between the two groups (OR=1.26, 95%CI: 0.81 to 1.94, P = 0.30). However, patients treated with the combination therapy exhibited a higher incidence of grade 3-4 trAEs (OR=1.93, 95%CI: 1.36 to 2.73, P = 0.0002) and a greater likelihood of discontinuing treatment due to trAEs (OR=2.07, 95%CI: 1.12 to 3.85, P = 0.02). There was no significant difference in the occurrence of severe trAEs leading to death (OR=1.36, 95%CI: 0.47 to 3.96, P = 0.57).

CONCLUSION

This meta-analysis suggests that R/M-HNSCC patients receiving the combination of durvalumab and tremelimumab may achieve comparable outcomes in terms of ORR, DCR, OS, PFS, and DoR, without significant differences. However, the combination therapy is associated with a higher incidence of grade 3-4 trAEs and an increased likelihood of treatment discontinuation due to trAEs. These findings highlight the need for cautious consideration of the combination of durvalumab and tremelimumab in R/M-HNSCC patients, which should be further evaluated in high-quality studies.

摘要

目的

头颈部鳞状细胞癌(HNSCC)是全球第六大常见癌症,显著影响患者的生活质量。免疫检查点抑制剂(ICI)已被用于治疗复发性/转移性(R/M)-HNSCC 患者。本荟萃分析旨在评估度伐利尤单抗单药与度伐利尤单抗联合 Tremelimumab 治疗 R/M-HNSCC 患者的疗效和安全性。

方法

系统检索 PubMed、Embase 和 Cochrane Library 数据库中比较度伐利尤单抗单药与度伐利尤单抗联合 Tremelimumab 治疗 R/M-HNSCC 的相关研究。纳入所有比较度伐利尤单抗单药与度伐利尤单抗联合 Tremelimumab 治疗 R/M-HNSCC 的研究。必要时,还对确定的研究的参考文献进行筛选。

结果

本荟萃分析共纳入了 3 项研究的 1298 例 R/M-HNSCC 患者,这些研究比较了度伐利尤单抗与度伐利尤单抗联合 Tremelimumab 治疗 R/M-HNSCC。我们的研究结果显示,客观缓解率(ORR)[比值比(OR):1.15,95%置信区间(CI):0.85 至 1.56,P = 0.36]和疾病控制率(DCR)(OR=1.08,95%CI:0.86 至 1.37,P = 0.51)无显著差异。总生存期(OS)、无进展生存期(PFS)和缓解持续时间(DoR)也观察到相似的结果。关于安全性,两组治疗相关不良事件(TRAE)的发生率无显著差异(OR=1.26,95%CI:0.81 至 1.94,P = 0.30)。然而,联合治疗组的患者出现 3-4 级 TRAE 的发生率更高(OR=1.93,95%CI:1.36 至 2.73,P = 0.0002),因 TRAE 而停药的可能性更高(OR=2.07,95%CI:1.12 至 3.85,P = 0.02)。严重 TRAE 导致死亡的发生率无显著差异(OR=1.36,95%CI:0.47 至 3.96,P = 0.57)。

结论

本荟萃分析表明,接受度伐利尤单抗联合 Tremelimumab 治疗的 R/M-HNSCC 患者在 ORR、DCR、OS、PFS 和 DoR 方面可能具有相似的疗效,无显著差异。然而,联合治疗与 3-4 级 TRAE 的发生率更高和因 TRAE 而停药的可能性增加有关。这些发现强调了在 R/M-HNSCC 患者中应谨慎考虑度伐利尤单抗联合 Tremelimumab,这需要在高质量的研究中进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68d0/10827947/cfe40b027a56/fimmu-14-1302840-g001.jpg

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