Clinical Trial

Hypofractionated Radiotherapy After Complete Resection for Stage II/III Thymic Epithelial Tumors

Study acronym: TET-HFRT40
Recruiting Phase 2
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Summary
This is a prospective, open-label, single-arm Phase II study designed to evaluate the safety of postoperative hypofractionated radiotherapy in patients with Stage II/III thymic epithelial tumors after complete resection. After a screening period of up to 28 days, eligible patients will receive adjuvant hypofractionated radiotherapy to a total dose of 40 Gy in 15 fractions, delivered once daily at 2.67 Gy per fraction, 5 days per week over 3 weeks. The study will primarily assess treatment-related safety and tolerability, with preliminary evaluation of efficacy, economic burden, and quality of life.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-07-08.
Trial Details
NCT Number NCT07691619
Lead Sponsor Tianjin Medical University Cancer Institute and Hospital
Conditions Thymic Epithelial Tumor
Enrollment 49 participants
Start Date 2026-07-14
Primary Completion 2027-06-30 (estimated)
Study Completion 2029-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-07-10