# Toripalimab-based chemoimmunotherapy for unresectable sinonasal NUT carcinoma of the maxillary sinus: a case report

**Authors:** Dan Yu, Ling Lin, Jian Tan, Xinglong Wang, Yonghui Xie, Zhiyong Huang, Bei Guo

PMC · DOI: 10.3389/fimmu.2026.1763340 · Frontiers in Immunology · 2026-02-24

## TL;DR

A 31-year-old man with an aggressive maxillary sinus cancer showed partial response to toripalimab-based chemoimmunotherapy, suggesting this treatment could help manage similar rare cancers.

## Contribution

First reported case of toripalimab-based chemoimmunotherapy showing partial response in unresectable maxillary sinus NUT carcinoma.

## Key findings

- The patient showed early radiologic improvement after three cycles of toripalimab, docetaxel, and cisplatin.
- Partial tumor regression was observed after six cycles of treatment, with stable residual disease at follow-up.
- PD-L1 expression in tumor and immune cells may support the use of PD-1 blockade in this cancer type.

## Abstract

Nuclear protein in testis (NUT) carcinoma is an extremely rare and highly aggressive epithelial malignancy driven by NUTM1 rearrangements. Sinonasal involvement is uncommon and often presents with non-specific clinical and radiologic features, leading to delayed diagnosis. Optimal management remains undefined, and outcomes are poor when complete resection is not feasible.

A 31-year-old man developed progressive numbness and swelling of the left cheek after tooth extraction. Imaging revealed a soft-tissue mass involving the left maxillary sinus with adjacent maxillofacial soft-tissue extension. Endoscopic biopsy demonstrated a poorly differentiated carcinoma with diffuse punctate nuclear NUT expression, high proliferative index (Ki-67 ~50%), and PD-L1 expression in both tumor cells and immune cells. ^18F-FDG PET-CT showed no regional or distant metastases. Given unresectability, the patient received toripalimab (240 mg) combined with docetaxel and cisplatin every 3 weeks. MRI after three cycles showed early radiologic improvement, and further tumor regression was observed after six cycles, consistent with a partial response. The patient subsequently continued on toripalimab-based maintenance therapy with ongoing stable residual disease at the latest follow-up (approximately 5 months after therapy initiation and 6 months from diagnosis).

To our knowledge, this is the first reported case of toripalimab-based chemoimmunotherapy demonstrating an early partial response and short-term disease control in unresectable maxillary sinus NUT carcinoma. It supports the potential role of PD-1 blockade integrated with platinum–taxane chemotherapy as a component of multimodal management for sinonasal NUT carcinomas.

## Linked entities

- **Genes:** NUTM1 (NUT midline carcinoma family member 1) [NCBI Gene 256646]
- **Proteins:** NUTM1 (NUT midline carcinoma family member 1), CD274 (CD274 molecule), Mki67 (antigen identified by monoclonal antibody Ki 67)
- **Chemicals:** docetaxel (PubChem CID 148124), cisplatin (PubChem CID 5460033), 18F-FDG (PubChem CID 68614)
- **Diseases:** NUT carcinoma (MONDO:0005563), maxillary sinus cancer (MONDO:0001748)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, NUTM1 (NUT midline carcinoma family member 1) [NCBI Gene 256646] {aka C15orf55, FAM22H, NUT}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}
- **Diseases:** metastases (MESH:D009362), NUT carcinoma of the maxillary sinus (MESH:D008444), Sinonasal involvement (MESH:C535701), numbness (MESH:D006987), Nuclear protein in testis (NUT) carcinoma (MESH:D013736), NUT carcinoma (MESH:D009369), swelling (MESH:D004487), epithelial malignancy (MESH:D002277)
- **Chemicals:** taxane (MESH:C080625), docetaxel (MESH:D000077143), cisplatin (MESH:D002945), -FDG (MESH:D019788), platinum (MESH:D010984), Toripalimab (MESH:C000656314)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12971447/full.md

## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12971447/full.md

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Source: https://tomesphere.com/paper/PMC12971447