# Long-term durable response to Sintilimab therapy in synchronous lung squamous cell carcinoma and gastric adenocarcinoma: a rare case report

**Authors:** Margaret Mekuriya Bassaye, Zou Jijian, Zhou Li, Shuai Han

PMC · DOI: 10.3389/fonc.2026.1679799 · Frontiers in Oncology · 2026-02-06

## TL;DR

A 64-year-old man with two rare cancers achieved long-term control using Sintilimab, an immune therapy, instead of traditional treatments.

## Contribution

Demonstrates the effectiveness of Sintilimab monotherapy in managing synchronous lung and gastric cancers.

## Key findings

- Sintilimab led to regression of lung SCC and long-term disease control.
- High PD-L1 expression in both tumors supported immune checkpoint blockade response.
- Gastric tumor progression was managed surgically after initial immune therapy.

## Abstract

Gastric cancer (GC) and lung squamous cell carcinoma (SCC) are major global causes of cancer-related morbidity and mortality, but their synchronous occurrence is exceedingly rare and poses substantial diagnostic and therapeutic challenges. This report describes a 64-year-old male with synchronous lung SCC and gastric adenocarcinoma who achieved long-term disease control with Sintilimab monotherapy. Initial imaging and biopsy confirmed poorly differentiated lung SCC (PD-L1 CPS: 2), while PET-CT and endoscopy identified a gastric lesion later confirmed as adenocarcinoma (PD-L1 CPS: 5). Despite indications for chemotherapy, the patient declined cytotoxic therapy and initially refused surgery. He was treated with Sintilimab plus Anlotinib, resulting in lung lesion regression. Progression of gastric obstruction led to gastrectomy two years later; subsequent lung recurrence was managed surgically. Both tumors showed high proliferative indices (Ki-67 ~80–90%) and PD-L1 expression, supporting responsiveness to immune checkpoint blockade. This case highlights the feasibility of immune monotherapy in managing complex synchronous malignancies, especially when standard treatments are declined.

## Linked entities

- **Proteins:** CD274 (CD274 molecule)
- **Chemicals:** Anlotinib (PubChem CID 25017411)
- **Diseases:** gastric cancer (MONDO:0001056), lung squamous cell carcinoma (MONDO:0005097), gastric adenocarcinoma (MONDO:0005036)

## Full-text entities

- **Genes:** TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, KRT20 (keratin 20) [NCBI Gene 54474] {aka CD20, CK-20, CK20, K20, KRT21}, KRT7 (keratin 7) [NCBI Gene 3855] {aka CK7, K2C7, K7, SCL}, CDX2 (caudal type homeobox 2) [NCBI Gene 1045] {aka CDX-3, CDX2/AS, CDX3}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, TP63 (tumor protein p63) [NCBI Gene 8626] {aka AIS, B(p51A), B(p51B), EEC3, KET, LMS}, KIT (KIT proto-oncogene, receptor tyrosine kinase) [NCBI Gene 3815] {aka C-Kit, CD117, MASTC, PBT, SCFR}, NAPSA (napsin A aspartic peptidase) [NCBI Gene 9476] {aka KAP, Kdap, NAP1, NAPA, NR1H2-AS1, SNAPA}
- **Diseases:** Gastric cancer (MESH:D013274), bleeding lesion (MESH:D006470), hyperemia (MESH:D006940), inability to (MESH:C564980), SCC (MESH:D002294), mass (MESH:C536030), NSCLC (MESH:D002289), disease (MESH:D004194), gastric ulcer (MESH:D013276), atrophic gastritis (MESH:D005757), melanoma (MESH:D008545), hereditary cancer syndromes (MESH:D009386), lung tumor (MESH:D008175), lung (MESH:D008171), diabetes mellitus (MESH:D003920), Cancer (MESH:D009369), adenocarcinoma (MESH:D000230), edema (MESH:D004487), gastric lesion (MESH:D013272), Lymph node metastasis (MESH:D008207), chronic hepatitis B (MESH:D019694), Li-Fraumeni syndrome (MESH:D016864), squamous lung cancer (MESH:D018307), HCC (MESH:D006528), oncologic (MESH:D000072716), necrosis (MESH:D009336), synchronous (MESH:D009378), PM (MESH:D009362), hypertension (MESH:D006973), infection (MESH:D007239), erosions (MESH:D014077), gastric obstruction (MESH:D017219), cytotoxic (MESH:D064420), ulcerated lesion (MESH:D014456)
- **Chemicals:** atezolizumab (MESH:C000594389), Sintilimab (MESH:C000632826), durvalumab (MESH:C000613593), nivolumab (MESH:D000077594), Anlotinib (MESH:C000625192), S-1 (-), H&amp;E (MESH:D006371), pembrolizumab (MESH:C582435), FDG (MESH:D019788)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12920228/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12920228/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12920228/full.md

---
Source: https://tomesphere.com/paper/PMC12920228