Tomotherapy for sinonasal teratocarcinosarcoma with SMARCA4 deletion and CTNNB1 mutation: A case report and literature review

Sinonasal teratocarcinosarcoma (SNTCS) is a rare and aggressive malignant tumor that is difficult to diagnose and lacks a standard therapeutic strategies. Here, we report a case of SNTCS harboring a <i>SMARCA4</i> deletion and a <i>CTNNB1</i> mutation. Following incomplete surgical resection, the patient received synchronous postoperative chemotherapy with tomotherapy (TOMO) radiation and achieved a complete response lasting for > 47 months with tolerated side effects. This case suggests that <i>SMARCA4</i> deletion and <i>CTNNB1</i> mutation may be key molecular events in the development of SNTCS, potentially providing valuable clues for its diagnosis. Moreover, to the best of our knowledge, this is the first case demonstrating that TOMO technology can be a beneficial option for SNTCS radiotherapy.

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Publication Details

Journal
Precision Radiation Oncology
Published
2025-12-01
DOI
https://doi.org/10.1002/pro6.70038
Primary Topic
Chromatin Remodeling and Cancer
Type
article
Field-Weighted Citation Impact
0.00

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article

Tomotherapy for sinonasal teratocarcinosarcoma with SMARCA4 deletion and CTNNB1 mutation: A case report and literature review

Fanglei Duan, Peng Xu, Yue Zhao, Jianping Zhou et al.
Precision Radiation Oncology
Chromatin Remodeling and Cancer
article

Tomotherapy for sinonasal teratocarcinosarcoma with SMARCA4 deletion and CTNNB1 mutation: A case report and literature review

Fanglei Duan, Peng Xu, Yue Zhao, Jianping Zhou, Siyu Xie, Yang Liu, Lei Yang, Shun Lu, Chenghui Ren
article en

Abstract

Sinonasal teratocarcinosarcoma (SNTCS) is a rare and aggressive malignant tumor that is difficult to diagnose and lacks a standard therapeutic strategies. Here, we report a case of SNTCS harboring a <i>SMARCA4</i> deletion and a <i>CTNNB1</i> mutation. Following incomplete surgical resection, the patient received synchronous postoperative chemotherapy with tomotherapy (TOMO) radiation and achieved a complete response lasting for > 47 months with tolerated side effects. This case suggests that <i>SMARCA4</i> deletion and <i>CTNNB1</i> mutation may be key molecular events in the development of SNTCS, potentially providing valuable clues for its diagnosis. Moreover, to the best of our knowledge, this is the first case demonstrating that TOMO technology can be a beneficial option for SNTCS radiotherapy.

Precision Radiation OncologyVol. 9(4)
Chengdu Medical College (CN), Sichuan Cancer Hospital (CN)
Department of Science and Technology of Sichuan Province, Chengdu Science and Technology Program
Openalex Percentile: Top 63%
Chromatin Remodeling and Cancer
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