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◇ medRxiv2026-08-11· oncology

Phase I Trial Representation and Geographical Distribution in Mesothelioma and Thymic Epithelial Tumors

S. Mishra, M. Qorbani, K. Canaslan, R. Maniar, A. H. Emami, F. M. Nia, G. Janbabi, Z. Rezaei, F. Ardeshir-Larijani

原始摘要(英文原文)· Original abstract
Background and Purpose: Rare thoracic tumors face persistent exclusion from clinical trials. To address this, we characterized the representation, geographical distribution, mechanisms of action, and clinical outcomes of Phase I trials in thymic epithelial tumors (TETs) and mesothelioma. Materials and Methods: Phase I solid-tumor trials from Jan 1995 to Jan 2026 were identified on ClinicalTrials.gov and processed using Python to extract trial status. A Python pipeline identified TET and mesothelioma trials and divided them into resulted and non-resulted trials. Resulted trials underwent manual review, and publication status was verified through PubMed, Google Scholar, and LARVOL CLIN. Results: Of 6,610 Phase I trials screened, 3.1% (n=203) included rare thoracic tumors. Among these, 11.3% (n=23) reported results, 34.8% (8/23) advanced beyond Phase I, and 21.7% (n=5) were published in high-impact journals (IF > 10). Targeted therapies dominated classifications (65.2%), followed by immunotherapies (34.8%) and antibody-drug conjugates (ADCs; 8.7%). Reported efficacy outcomes showed wide ranges: objective response rate (ORR, 0-44%), progression-free survival (PFS, 1.3-8.3 months), and overall survival (OS, 3.0-19.3 months). Fatigue was the most frequent toxicity, observed in 58% of targeted therapy trials and 100% of immunotherapy and ADC cohorts. No novel agents achieved subsequent disease-specific FDA approval. Geographically, among 96 trial locations, 49.0% were concentrated in Europe and 21.9% in the United States. Conclusions: Current Phase I trials exhibit a striking scarcity of research for mesothelioma and TETs, concentrated predominantly in high-income regions. Bridging this gap requires prioritizing rare thoracic tumors and building clinical infrastructure in underrepresented countries to enhance trial access and diversity. Keywords: Thymic epithelial tumors, Mesothelioma, Phase I clinical trials, ClinicalTrials.gov, Rare thoracic malignancies.
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