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Clinical Trial Summary

This study seeks to determine the safety and efficacy of shortening the primary and nodal adjuvant radiation therapy course from 2 Gy x 25 fractions to 3.6 Gy x 10 fractions in merkel cell carcinoma patients who may or may not be receiving immunotherapy.


Clinical Trial Description

- To estimate the 2-year local control rate for adjuvant hypofractionated RT to the primary tumor bed. - To estimate the 2-year nodal control rate for adjuvant hypofractionated RT to the primary draining nodal basin. Secondary Objectives - To determine MCC disease outcomes including:time to non-nodal locoregional recurrence, time to nodal recurrence, time to distant mestasis, disease-free-survival and disease-specific survival for patients receiving hypofractionated adjuvant RT. - To assess acute and late RT associated toxicity within or neighboring the radiated field. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05100095
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Devarati Mitra
Phone (713) 563-1339
Email dmitra@mdanderson.org
Status Recruiting
Phase Phase 2
Start date December 14, 2021
Completion date September 1, 2028

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