Sinonasal NUT carcinoma: A consecutive case series and systematic review

Author:

Ramesh Uma12ORCID,Contrera Kevin J.1ORCID,Shakibai Nasim1,Su Shirley Y.1ORCID,Brahimaj Bledi3,Roberts Dianna1,Williams Michelle D.4,Ferrarotto Renata5ORCID,Phan Jack6,Gunn Gary Brandon6,Raza Shaan3,DeMonte Franco3,Hanna Ehab Y.1

Affiliation:

1. Department of Head and Neck Surgery The University of Texas M. D. Anderson Cancer Center Houston Texas USA

2. School of Medicine Baylor College of Medicine Houston Texas USA

3. Department of Neurosurgery The University of Texas M. D. Anderson Cancer Center Houston Texas USA

4. Department of Pathology The University of Texas M. D. Anderson Cancer Center Houston Texas USA

5. Department of Thoracic‐Head & Neck Medical Oncology The University of Texas M. D. Anderson Cancer Center Houston Texas USA

6. Department of Radiation Oncology The University of Texas M. D. Anderson Cancer Center Houston Texas USA

Abstract

AbstractBackgroundSinonasal NUT carcinoma is an extremely rare, lethal malignancy with limited literature.MethodsA case series was conduction of all patients with sinonasal NUT carcinoma at a single institution between 2010 and 2022. Survival and associated were evaluated. A systematic review of the literature was performed.ResultsIn 12 patients, followed for a median of 1.5 years, the median overall survival (OS) and disease‐specific survival (DSS) were both 14.6 months. Patients with maxillary sinus tumors were 91% more likely to survive (hazard ratio [HR]: 0.094, 95% confidence interval [CI]: 0.011–0.78, p = 0.011). Patients with higher‐stage disease stage had worse OS (stage IVb‐c vs. III‐IVa, p = 0.05). All three patients who were alive with no evidence of disease received induction chemotherapy.ConclusionFor patients with sinonasal NUT carcinoma, the median survival was 15 months but better with lower‐stage and maxillary tumors. Induction chemotherapy may be beneficial.

Publisher

Wiley

Subject

Otorhinolaryngology

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