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Clinical Trial Summary

To determine the histopathological response rate to neo-adjuvant nivolumab and nivolumab plus ipilimumab at time of standard of care(surgery ± radiotherapy).in patients with cutaneous squamous cell carcinoma.


Clinical Trial Description

This is an investigator-initiated randomized non-comparative phase II trial consisting of 40 patients with resectable stage III-IVa CSCC randomized 1:1 to ARM A: 2 courses of nivolumab 3 mg/kg in week 0 and 2, or ARM B: 2 courses of nivolumab 3 mg/kg in week 0 and 2 plus 1 course of ipilimumab 1mg/kg in week 0. Both treatment arms are neo-adjuvant and applied prior to standard of care (consisting of surgery at week 4 with or without adjuvant radiotherapy). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04620200
Study type Interventional
Source The Netherlands Cancer Institute
Contact Thomas Boere, MD
Phone + 31 0205129111
Email th.boere@nki.nl
Status Recruiting
Phase Phase 2
Start date August 11, 2020
Completion date November 1, 2024

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