Clinical Trial

RT for Adenocarcinoma/Adenosquamous Carcinoma

Active, Not Recruiting Phase 1/2
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Summary
This study aims to establish a prospective cohort of locally advanced cervical adenocarcinoma to provide a better way to monitor its efficacy and provide precise treatment. The key problems to be solved are as follows: 1. Establish an observational prospective cohort of locally advanced ADC and randomly divide patients with residual cervical tumors in the primary site after CCRT into the local treatment group (salvage surgery or supplementary radiotherapy) or the systemic treatment group. 2. Collect cervical biopsy tissues before and after CCRT in patients with residual cervical tumors, explore the genomic characteristics, and predict whether they can benefit from targeted/immunotherapy in the future.
Trial Details
NCT Number NCT07153952
Lead Sponsor Peking Union Medical College Hospital
Collaborators: The First Affiliated Hospital of Xiamen University, Heilongjiang Provicial Hospital, Liaoning Cancer Hospital & Institute, Women's Hospital School Of Medicine Zhejiang University, Luohe Central Hospital
Conditions Cervical Adenocarcinoma, Cervical Adenosquamous Carcinoma, Radiotherapy
Enrollment 60 participants
Start Date 2025-01-01
Primary Completion 2027-01-01 (estimated)
Study Completion 2028-01-01 (estimated)
Updated on ClinicalTrials.gov 2025-09-04