進行性尿路上皮がんの治療効果を時間軸で再評価~RMSTによる再解析で、従来法では見えにくかった治療差を明確化~

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2026-03-03 東京科学大学

東京科学大学大学院医歯学総合研究科の研究チームは、進行性尿路上皮がんの一次治療を対象とした7つの臨床試験(5,321例、10比較)を解析し、従来のハザード比に基づく評価では治療効果を十分に捉えられない可能性を示した。解析の結果、全生存期間の10解析中5件、無増悪生存期間の5解析中3件で比例ハザード仮定が成立していないことが判明した。そこで比例ハザード仮定に依存しない指標である制限付き平均生存期間(RMST)とネットワークメタ解析を用いて再評価したところ、免疫チェックポイント阻害薬単剤は治療初期に化学療法より不利となる傾向が確認された。一方、エンホルツマブベドチンとペムブロリズマブの併用療法は36か月時点で5.7か月の生存延長を示し、最も高い治療効果を示した。本研究は、時間軸に基づく新たながん治療評価の重要性を示し、個別化治療戦略の構築に貢献すると期待される。

進行性尿路上皮がんの治療効果を時間軸で再評価~RMSTによる再解析で、従来法では見えにくかった治療差を明確化~
図1. 化学療法と比較した各治療法のRMST差

<関連情報>

制限平均生存期間を用いた進行尿路上皮癌の治療の再評価:系統的レビューとネットワークメタアナリシス Re-evaluating Treatments for Advanced Urothelial Carcinoma Using Restricted Mean Survival Time: A Systematic Review and Network Meta-analysis

Shugo Yajima, Wei Chen, Kohei Hirose, Akihiro Hirakawa, Kenji Tanabe, Motohiro Fujiwara, Hiroshi Fukushima, Hajime Tanaka, Hitoshi Masuda, Yasuhisa Fujii, Soichiro Yoshida
European Urology Open Science  Available online: 6 February 2026
DOI:https://doi.org/10.1016/j.euros.2026.01.013

Abstract

Background and objective

The proportional hazards (PH) assumption may not hold for immune checkpoint inhibitor (ICI) trials because of delayed treatment effects. We assessed PH validity in trials of first-line treatment in advanced urothelial carcinoma (UC) and compared treatments using restricted mean survival time (RMST).

Methods

We conducted a systematic review and network meta-analysis (NMA) of phase 2/3 randomized controlled trials published between 2015 and 2025 evaluating ICIs or antibody-drug conjugates. Seven trials involving 5321 patients with ten treatment comparisons were analyzed. Individual patient data were reconstructed from Kaplan-Meier curves. The PH assumption was tested using Schoenfeld residuals (p < 0.05 indicating violation). RMST-based NMA was performed at 6-mo intervals up to 36 mo.

Key findings and limitations

The PH assumption was violated in 50% of overall survival (OS) comparisons and 60% of progression-free survival comparisons. ICI monotherapy regimens demonstrated a significant early detriment at 12 mo in comparison to chemotherapy (PD-1 inhibitors: −0.8 mo, p = 0.007; PD-L1 inhibitors: −0.9 mo, p < 0.001) that was completely masked by nonsignificant hazard ratios. Enfortumab vedotin + pembrolizumab was associated with a superior RMST benefit of 5.7 mo (95% confidence interval 3.3–8.1) at the 36-mo time point. Study limitations include the sparse network structure and heterogeneous patient eligibility criteria across trials.

Conclusions and clinical implications

Half of modern UC trials violate PH assumptions, with time-dependent treatment effects that can be obscured by traditional analyses. RMST analysis quantifies the magnitude and clinical impact of early ICI monotherapy detriment that is not captured by nonsignificant hazard ratios. Enfortumab vedotin plus pembrolizumab demonstrated the largest RMST benefit in this analysis, although this finding is based on a single pivotal trial and requires validation in additional studies and real-world settings. These findings support the value of RMST analysis as a complementary approach for evaluating time-dependent treatment effects in immunotherapy trials.

Patient summary

We analyzed clinical trials of treatments for advanced bladder cancer and found that traditional statistical methods may miss important treatment patterns. Our analysis shows that immunotherapy alone may perform worse than chemotherapy initially, but the treatment effect improves over time. The combination of enfortumab vedotin and pembrolizumab provides the best outcomes for patients at all time points.

医療・健康
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