Metastatic Organotropism Differential Treatment Response in Urothelial Carcinoma: A Systematic Review and Network Meta-analysis of Randomized Controlled Trials

医学 转移性尿路上皮癌 肿瘤科 内科学 危险系数 转移瘤切除术 杜瓦卢马布 转移 阿替唑单抗 荟萃分析 临床终点 随机对照试验 置信区间 癌症 彭布罗利珠单抗 免疫疗法 膀胱癌 尿路上皮癌
作者
Mehdi Kardoust Parizi,Akihiro Matsukawa,Kensuke Bekku,Jakob Klemm,Arman Alimohammadi,Ekaterina Laukhtina,Pierre I. Karakiewicz,Sever Chiujdea,Mohammad Abufaraj,Johanna Krauter,Shahrokh F. Shariat
出处
期刊:European Urology Oncology [Elsevier]
标识
DOI:10.1016/j.euo.2023.11.001
摘要

The optimal therapeutic agent with respect to metastatic sites is unclear in advanced urothelial carcinoma (UC).To investigate the metastatic organotropism differential treatment response in patients with advanced or metastatic UC.A systematic search and network meta-analysis (NMA) was performed according to the Preferred Reporting Items for Systematic Reviews and Meta-analyses statement. The primary endpoints of interest were the objective response rate, overall survival (OS), and progression-free survival with respect to different metastatic sites.Twenty-six trials comprising 9082 patients met our eligibility criteria, and a formal NMA was conducted. Durvalumab plus tremelimumab as first-line systemic therapy was significantly associated with better OS than chemotherapy in visceral metastasis (hazard ratio [HR] 0.81, 95% confidence interval [CI] 0.67-0.98). Pembrolizumab as second-line systemic therapy was significantly associated with better OS than chemotherapy in patients with visceral metastasis (HR 0.75, 95% CI 0.60-0.95). Atezolizumab as second-line systemic therapy was significantly associated with better OS than chemotherapy in patients with liver metastasis (in the population of >5% of tumor-infiltrating immune cells) and lymph node metastasis (HR 0.51, 95% CI 0.28-0.96, and HR 0.59, 95% CI 0.37-0.96, respectively).Administration of immune-oncology treatments with respect to metastatic sites in patients with advanced or metastatic UC might have a positive impact on survival outcomes in both the first- and the second-line setting. Nevertheless, further investigations focusing on metastatic organotropism differential response with reliable oncological outcomes are needed to identify the optimal management strategy for these patients.Although the supporting evidence for oncological benefits of therapeutic systemic agents with respect to metastatic sites is not yet strong enough to provide a recommendation in advanced or metastatic urothelial carcinoma, clinicians may take into account tumor organotropism only in discussion with the patient fully informed on the optimal treatment decision to be taken.
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