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What is it about?
This study systematically reviews and meta-analyzes the efficacy and safety of novel neoadjuvant therapies, including immune checkpoint inhibitors (ICI), molecular targeted agents (MTA), and antibody-drug conjugates, in muscle-invasive bladder cancer. Analyzing 17 trials with 1977 patients, it finds that ICI-based treatments yield higher pathologic complete response and downstaging rates than MTA, with ICI monotherapy achieving a pathologic complete response rate of 34% compared to 5% for MTA monotherapy. ICIs also demonstrate a more favorable safety profile, with fewer Grade ≥3 adverse events. The study highlights PD-L1 expression as a potential marker for ICI treatment selection and calls for randomized trials to optimize treatment algorithms and validate biomarkers. Furthermore, while ICI-chemotherapy combinations show enhanced activity, they also result in higher severe adverse event rates primarily due to chemotherapy-induced toxicities.
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Why is it important?
This research is important because it provides a comprehensive evaluation of novel neoadjuvant therapies for muscle-invasive bladder cancer, which are crucial for improving patient outcomes. The study investigates the effectiveness and safety of immune checkpoint inhibitors (ICI), molecular targeted agents (MTA), and antibody-drug conjugates, offering insights into more effective treatment options beyond traditional chemotherapy. By analyzing response rates, survival outcomes, and safety profiles, this research contributes to a better understanding of emerging therapies, guiding clinical decision-making and personalized treatment strategies for bladder cancer patients. Key Takeaways: 1. Enhanced Efficacy: Immune checkpoint inhibitors (ICI) show promising pathologic complete response and downstaging rates, surpassing traditional chemotherapy, indicating their potential as a more effective neoadjuvant treatment for muscle-invasive bladder cancer. 2. Safety Profiles: ICI-based treatments are associated with lower rates of severe adverse events compared to MTA-based treatments, highlighting their more favorable safety profile and underscoring the importance of considering adverse event rates in treatment selection. 3. Biomarker Guidance: High PD-L1 expression is linked to improved pathologic response, suggesting that PD-L1 could serve as a valuable biomarker for selecting patients who might benefit most from ICI-based therapies, paving the way for more personalized and targeted treatment approaches.
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This page is a summary of: Novel neoadjuvant therapies for muscle‐invasive bladder cancer: Systematic review and meta‐analysis, BJUI Compass, May 2025, Wiley,
DOI: 10.1002/bco2.70031.
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