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含或不含抗 PD-1 的化疗方案作为一线治疗晚期尿路上皮癌的疗效和安全性。

The efficacy and safety of chemotherapy with or without anti-PD-1 for the first-line treatment of advanced urothelial carcinoma.

机构信息

Medical School of Chinese PLA, Beijing, China.

Department of Oncology, The First Medical Centre, Chinese PLA General Hospital, Beijing, China.

出版信息

Cancer Med. 2023 Dec;12(23):21129-21137. doi: 10.1002/cam4.6671. Epub 2023 Nov 21.

DOI:10.1002/cam4.6671
PMID:37990780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10726829/
Abstract

OBJECTIVE

To compare the efficacy and safety of first-line anti-PD-1 combined with chemotherapy versus chemotherapy alone in patients with advanced urothelial carcinoma (UC).

METHOD

Patients with advanced UC who received first-line treatment of chemotherapy (n = 51, gemcitabine/paclitaxel [albumin-bound] combined with platinum) or immunochemotherapy (n = 50, PD-1 inhibitors plus chemotherapy) were enrolled. The efficacy and safety were analyzed between the two groups.

RESULTS

This study included data from 101 patients, including 51 patients in the chemotherapy group and 50 patients in the immunochemotherapy group. The median progression-free survival of the immunochemotherapy group was significantly longer than that of the chemotherapy group (11.5 vs. 7.17 m, HR = 0.56, p = 0.009). The two groups' overall survival showed no significant difference (20.3 vs. 17.8 m, p = 0.204). The objective response rates and the disease control rates of the two groups were 38.0% versus 49.0% (p = 0.26) and 88.0% versus 80.4% (p = 0.29). The incidence of adverse reactions (AEs) in the immunochemotherapy group and chemotherapy group were 90.0% and 84.3% (p = 0.394), respectively, and the incidence of Grade III-IV AEs were 32.0% and 35.3% (p = 0.726), respectively.

CONCLUSION

In the first-line treatment of patients with advanced UC, anti-PD-1 therapy combined with chemotherapy might have better efficacy than chemotherapy alone, and AEs are similar between the two groups.

摘要

目的

比较一线抗 PD-1 联合化疗与单纯化疗治疗晚期尿路上皮癌(UC)患者的疗效和安全性。

方法

入组接受一线化疗(n=51,吉西他滨/紫杉醇[白蛋白结合物]联合铂类)或免疫化疗(n=50,PD-1 抑制剂联合化疗)治疗的晚期 UC 患者。分析两组患者的疗效和安全性。

结果

本研究纳入 101 例患者,化疗组 51 例,免疫化疗组 50 例。免疫化疗组的中位无进展生存期明显长于化疗组(11.5 vs. 7.17 m,HR=0.56,p=0.009)。两组的总生存期无显著差异(20.3 vs. 17.8 m,p=0.204)。两组客观缓解率和疾病控制率分别为 38.0%和 49.0%(p=0.26)和 88.0%和 80.4%(p=0.29)。免疫化疗组和化疗组不良反应(AE)发生率分别为 90.0%和 84.3%(p=0.394),3 级及以上 AE 发生率分别为 32.0%和 35.3%(p=0.726)。

结论

在晚期 UC 患者的一线治疗中,抗 PD-1 治疗联合化疗可能比单纯化疗疗效更好,且两组的 AE 相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/b5431c147d9c/CAM4-12-21129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/af2276f842a6/CAM4-12-21129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/97634ee345e6/CAM4-12-21129-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/b5431c147d9c/CAM4-12-21129-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/af2276f842a6/CAM4-12-21129-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/97634ee345e6/CAM4-12-21129-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c6df/10726829/b5431c147d9c/CAM4-12-21129-g002.jpg

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