# Pathological complete response in esophageal squamous cell carcinoma complicated by malignant fistula via neoadjuvant immunotherapy, chemoradiotherapy, and nutritional support: a case report

**Authors:** Nanxi Li, Mei Lan, Wenxiu Yao, Yixiang Zhu, Qifeng Wang

PMC · DOI: 10.3389/fimmu.2026.1750544 · Frontiers in Immunology · 2026-02-11

## TL;DR

A patient with advanced esophageal cancer and a fistula achieved complete remission after a combination of immunotherapy, chemotherapy, and nutritional support.

## Contribution

Demonstrates successful pathological complete response in esophageal cancer with fistula using neoadjuvant immunotherapy and chemoradiotherapy.

## Key findings

- Patient achieved pathological complete response (pCR) after multimodal treatment.
- Pre-treatment PD-L1 positivity and CD8+ T cell infiltration correlated with treatment success.
- Nutritional support enabled completion of aggressive therapy in a complex case.

## Abstract

Esophageal cancer presents a formidable global health challenge, particularly when complicated by esophageal fistulas, which historically confer a dismal prognosis and severely limit therapeutic options. We report a challenging case of locally advanced esophageal squamous cell carcinoma (ESCC) complicated by an esophageal fistula that ultimately achieved a pathological complete response (pCR). The patient, a male in his 50s, presented with cough and dysphagia and was diagnosed with Stage IVA ESCC. Notably, an esophageal fistula was identified at the initial presentation, posing a threat to treatment. Aggressive enteral nutritional support via nasogastric tube placement and subsequent percutaneous endoscopic gastrostomy (PEG) was promptly initiated. This allowed the patient to successfully complete neoadjuvant therapy consisting of the anti-PD-1 antibody tislelizumab, paclitaxel, carboplatin, and concurrent intensity-modulated radiation therapy (IMRT). Following this multimodal regimen, the patient was reassessed as resectable following response to therapy status. Subsequent radical esophagectomy revealed no residual tumor cells in the primary lesion or dissected lymph nodes (ypT0N0M0), confirming pCR. Immunohistochemical analysis of pre-treatment biopsies demonstrated PD-L1 positivity and high infiltration of CD8+ T cells, suggesting that a robust immune-active microenvironment favored the efficacy of PD-1 blockade. This case underscores the feasibility of integrating immunotherapy with chemoradiotherapy in ESCC patients complicated by esophageal fistulas when supported by rigorous nutritional management.

## Linked entities

- **Proteins:** CD274 (CD274 molecule), CD8A (CD8 subunit alpha)
- **Chemicals:** paclitaxel (PubChem CID 36314), carboplatin (PubChem CID 426756)
- **Diseases:** esophageal squamous cell carcinoma (MONDO:0005580)

## Full-text entities

- **Genes:** CD34 (CD34 molecule) [NCBI Gene 947], SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, CDKN2A (cyclin dependent kinase inhibitor 2A) [NCBI Gene 1029] {aka ARF, CAI2, CDK4I, CDKN2, CMM2, INK4}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, DES (desmin) [NCBI Gene 1674] {aka CDCD3, CSM1, CSM2, LGMD1D, LGMD1E, LGMD2R}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, SDHB (succinate dehydrogenase complex iron sulfur subunit B) [NCBI Gene 6390] {aka CWS2, IP, MC2DN4, PGL4, PPGL4, SDH}, ANO1 (anoctamin 1) [NCBI Gene 55107] {aka DOG1, INDMS, MYMY7, ORAOV2, TAOS2, TMEM16A}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, S100A1 (S100 calcium binding protein A1) [NCBI Gene 6271] {aka S100, S100-alpha, S100A}, SPRY1 (sprouty RTK signaling antagonist 1) [NCBI Gene 10252] {aka hSPRY1}
- **Diseases:** vomiting (MESH:D014839), squamous cell carcinoma (MESH:D002294), fever (MESH:D005334), fistula (MESH:D005402), Esophageal cancer (MESH:D004938), ischemia (MESH:D007511), tuberculosis (MESH:D014376), pulmonary inflammation (MESH:D011014), ankle fracture (MESH:D064386), pCR (MESH:D005598), hepatitis (MESH:D056486), IV (MESH:D006011), nausea (MESH:D009325), lymph node metastasis (MESH:D008207), abdominal discomfort (MESH:D000007), depression (MESH:D003866), lymphadenopathies (MESH:D008206), leukopenia (MESH:D007970), pleural effusion (MESH:D010996), leiomyoma (MESH:D007889), ESCC (MESH:D000077277), esophageal fistula (MESH:D004937), spindle cell tumor (MESH:D002277), cough (MESH:D003371), weight loss (MESH:D015431), toxicities (MESH:D064420), lung invasion (MESH:D008171), diabetes (MESH:D003920), Cancer (MESH:D009369), shortness of breath (MESH:D004417), infective (MESH:D007239), coronary heart disease (MESH:D003327), pain (MESH:D010146), hypertension (MESH:D006973), sore throat (MESH:D010612), neutropenia (MESH:D009503), deaths (MESH:D003643), metastasis (MESH:D009362), dysphagia (MESH:D003680), inflammatory (MESH:D007249), atrophic gastritis (MESH:D005757), abscess (MESH:D000038)
- **Chemicals:** alcohol (MESH:D000438), DAB (MESH:C000469), tislelizumab (MESH:C000707970), toripalimab (MESH:C000656314), paclitaxel (MESH:D017239), carboplatin (MESH:D016190), sodium citrate (MESH:D000077559)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

10 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932521/full.md

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Source: https://tomesphere.com/paper/PMC12932521