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Clinical Trial Summary

This is a single arm phase II study that will evaluate the combination of pembrolizumab, docetaxel, and cisplatin or carboplatin (PDC) as single treatment modality in patients with stage II-IVb (T2-4, any N, M0) squamous cell carcinoma of the nasal cavity/paranasal sinuses (PNS SCC).


Clinical Trial Description

Primary Objective -Increase overall response rate (ORR), following pembrolizumab combined with induction chemotherapy prior to radiation, from historical 60% with induction chemotherapy alone to 80%. Secondary Objective - Improve the following efficacy endpoints relative to historical results with chemotherapy alone: progression free survival (PFS), overall survival (OS), organ [orbital, maxillary, cranial] preservation rate (OPR), and locoregional failure (LRF). - To determine safety and tolerability of pembrolizumab combined with induction chemotherapy and chemoradiation in patients with PNS SCC. - Correlate immune phenotype in tumors and blood, including T cell infiltration and PD-L1 status, with treatment outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05027633
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Renata Ferrarotto
Phone (713) 745-6774
Email rferrarotto@mdanderson.org
Status Recruiting
Phase Phase 2
Start date November 2, 2021
Completion date March 30, 2026

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