Zhao Yang, Xu Xiaoqing, Sun Yuhan, Yu Xinyang, Qi Yuanfu, Dai Xin
First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Department of Medical Oncology, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Front Oncol. 2024 Sep 16;14:1468784. doi: 10.3389/fonc.2024.1468784. eCollection 2024.
In recent years, some clinical studies of first-line treatment for advanced-stage urothelial carcinoma (aUC) have reached the main endpoint, showing inconsistent clinical efficacy. We hope to explore the efficacy and safety of first-line treatment for aUC.
The relevant literature from January 2000 to February 2024 was searched, and the R language (version 4.3.1) was used to perform a network meta-analysis based on the JAGS package and GEMTC package under the Bayesian framework. The main indicators included OS, PFS, ORR and adverse events of grade 3 or higher. This study has been registered in PROSPERO (CRD42024525372).
A total of 8 RCTs involving 5539 patients and 12 treatments were included. Pembrolizumab plus Enfortumab Vedotin (PEM+EV) was significantly better than other groups in OS, PFS and ORR. In terms of OS, PEM+EV was significantly better than nivolumab plus platinum-based chemotherapy (NIVO+platinumCT) (HR=0.60; 95% CI: 0.45-0.81), PEM+platinumCT (HR=0.55; 95%CI: 0.42-0.72), atezolizumab (ATE) + platinumCT (HR=0.57; 95%CI: 0.43-0.75) and platinumCT (HR=0.47; 95%CI: 0.38-0.58). In terms of PFS, PEM+EV was also significantly better than NIVO+platinumCT (HR=0.62; 95%CI: 0.48-0.82), PEM+platinumCT (HR=0.58; 95%CI: 0.45-0.74), ATE+platinumCT (HR=0.55; 95%CI: 0.43-0.69) and platinumCT (HR=0.45; 95%CI: 0.38-0.54). In terms of ORR, PEM+EV had a significant be nefit compared with other treatment measures, which was 2.63 times that of platinumCT (OR=2.63; 95%CI: 2.00-3.45). The adverse events of grade 3 or higher in immunotherapy (ATE, PEM, durvalumab) was significantly lower than other treatment measures.
PEM+EV can significantly prolong OS and PFS compared with other treatments, and has a higher ORR. The adverse events of grade 3 or higher of ATE was the lowest.
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024525372, identifier CRD42024525372.
近年来,一些晚期尿路上皮癌(aUC)一线治疗的临床研究达到了主要终点,临床疗效存在不一致性。我们希望探讨aUC一线治疗的疗效和安全性。
检索2000年1月至2024年2月的相关文献,使用R语言(版本4.3.1)在贝叶斯框架下基于JAGS包和GEMTC包进行网络荟萃分析。主要指标包括总生存期(OS)、无进展生存期(PFS)、客观缓解率(ORR)以及3级或更高等级的不良事件。本研究已在国际前瞻性系统评价注册库(PROSPERO)注册(注册号:CRD42024525372)。
共纳入8项随机对照试验(RCT),涉及5539例患者和12种治疗方法。帕博利珠单抗联合恩杂鲁胺(PEM+EV)在OS、PFS和ORR方面显著优于其他组。在OS方面,PEM+EV显著优于纳武利尤单抗联合铂类化疗(NIVO+铂类CT)(风险比[HR]=0.60;95%置信区间[CI]:0.45-0.81)、PEM+铂类CT(HR=0.55;95%CI:0.42-0.72)、阿替利珠单抗(ATE)+铂类CT(HR=0.57;95%CI:0.43-0.75)和铂类CT(HR=0.47;95%CI:0.38-0.58)。在PFS方面,PEM+EV也显著优于NIVO+铂类CT(HR=0.62;95%CI:0.48-0.82)、PEM+铂类CT(HR=0.58;95%CI:0.45-0.74)、ATE+铂类CT(HR=0.55;95%CI:0.43-0.69)和铂类CT(HR=0.45;95%CI:0.38-0.54)。在ORR方面,PEM+EV与其他治疗措施相比有显著优势,是铂类CT的2.63倍(优势比[OR]=2.63;95%CI:2.00-3.45)。免疫治疗(ATE、PEM、度伐利尤单抗)3级或更高等级的不良事件显著低于其他治疗措施。
与其他治疗方法相比,PEM+EV可显著延长OS和PFS,且ORR更高。ATE的3级或更高等级不良事件最低。
https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024525372,标识符CRD42024525372