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Visualizing eligibility gaps between muscle-invasive bladder cancer trials and real-world patients.

Researchers

Takaki Ichiyama, Takuma Narita, Yuya Sekine, Masanao Shinohara, Yohei Kawashima, Mizuki Kobayashi, Kazuyuki Numakura, Jotaro Mikami, Naoki Fujita, Teppei Okamoto, Hayato Yamamoto, Shintaro Narita, Satoshi Sato, Tomonori Habuchi, Chikara Ohyama, Shingo Hatakeyama

Abstract

Clinical studies in muscle-invasive bladder cancer (MIBC) often enroll younger and fitter patients than those treated in routine practice, limiting generalizability. We developed a simple eligibility gap (EG) score to quantify baseline eligibility differences between clinical studies and real-world cohorts. Eight clinical studies and eight real-world datasets were analyzed. The EG score was based on three commonly reported determinants: age, Eastern Cooperative Oncology Group performance status (ECOG PS), and cisplatin eligibility, each scaled from 0 to 33.3 points (total range: 0-99.9). Higher scores indicate younger, fitter, and more cisplatin-eligible populations. Known-groups validity was assessed by comparing EG scores across prespecified study categories expected to differ in eligibility selectivity. Sensitivity analyses using alternative fixed weighting schemes and random-weight simulations were performed to examine score robustness. Baseline characteristics differed between clinical studies and real-world cohorts. Trial populations were generally younger, had better ECOG PS, and showed higher cisplatin eligibility than real-world cohorts. EG scores followed the expected ordering across prespecified study categories, with the highest values in cisplatin-fit trials (86), intermediate values in real-world cohorts (66), and the lowest values in cisplatin-unfit/refusal trials (44), consistent with known-groups validity. Domain-specific analyses showed larger differences in age and cisplatin eligibility than in ECOG PS. Across alternative weighting scenarios, rank correlations with the equal-weight model remained high (ρ = 0.976-0.994), and the expected category-level ordering was preserved. The EG score describes eligibility differences between clinical studies and real-world MIBC populations and may aid interpretation of trial evidence across heterogeneous populations.
Source: PubMed (PMID: 42218684)View Original on PubMed
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