Introduction: We investigated the clinicopathological features and prognoses of the new molecularly defined entities in latest edition of the World Health Organization (WHO) classification of sinonasal carcinoma (SNC).
Methods: Integrated data were combined into an individual patient data (IPD) meta-analysis.
Results: We included 61 studies with 278 SNCs including 25 IDH2-mutant, 41 NUT carcinoma, 187 SWI/SNF loss, and 25 triple negative SNCs (without IDH2 mutation, NUTM1 rearrangement, and SWI/SNF inactivation) for analyses. Compared to other molecular groups, NUT carcinoma was associated with a younger age at presentation and an inferior disease-specific survival. Among SNCs with SWI/SNF inactivation, SMARCB1-deficient tumors presented later in life and were associated with a higher rate of radiotherapy administration. SMARCA4-deficiency was mostly found in teratocarcinosarcoma while SMARCB1-deficient tumors were associated with undifferentiated carcinoma and non-keratinizing squamous cell carcinoma.
Conclusion: Our study facilitates our current understanding of this developing molecular-defined spectrum of tumors and their prognoses.
Keywords: IDH2; SMARCA4; SMARCB1; nut; sinonasal carcinoma; sinonasal undifferentiated carcinoma.
Copyright © 2023 Vuong, Le, Le, Le, El-Rassi, McKinney and Dunn.