Immunoprofile of adenosquamous carcinoma in gastric cancer

Author:

Wu Cheng-Han1,Lai Cheng-Lun1,Teng Chieh-Lin Jerry1234,Fang Wen-Liang56,Huang Kuo-Hung56,Fen-Yau Li Anna57,Yu Hung-Yuan589,Chiang Nai-Jung510,Chao Yee510,Hung Yi-Ping510,Chen Ming-Huang510

Affiliation:

1. Division of Hematology/Medical Oncology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan, ROC

2. Department of Life Science, Tunghai University, Taichung, Taiwan, ROC

3. School of Medicine, Chung Shan Medical University, Taichung, Taiwan, ROC

4. College of Medicine, National Chung Hsing University, Taichung, Taiwan, ROC

5. School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan, ROC

6. Division of General Surgery, Department of Surgery, Taipei Veterans General Hospital, Taipei, Taiwan, ROC

7. Department of Pathology, Cheng Hsin General Hospital, Taipei, Taiwan, ROC

8. Division of Gastroenterology and Hepatology, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan, ROC

9. Hospitalist Ward, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan, ROC

10. Department of Oncology, Taipei Veterans General Hospital, Taipei, Taiwan, ROC

Abstract

Background: Gastric adenosquamous carcinoma (GASC) is a rare subtype of gastric cancer. Research on GASC treatment is limited, and its outcome is usually poor. We investigated the clinical features, immunoprofile of GASC, and determined the optimal treatment modality for these patients. Methods: Patients with GASC from Taipei Veterans General Hospital were retrospectively reviewed. Clinical features and treatment outcomes were evaluated. Adequate samples were examined for surrogate biomarkers for immunotherapy by IHC staining. Results: Total 14 (0.35%) GASC patients were found among 4034 gastric cancer patients. The median tumor size was 6.8 cm in 10 patients with stage III GASC, and all these patients underwent radical gastrectomy followed by adjuvant therapy. The median progression-free survival (PFS) and overall survival (OS) were 6.0 and 11.5 months, respectively. Two patients with stage IV GASC received frontline immunotherapy. Their median PFS and OS were 9.0 and 12.5 months. In immunoprofiling, 25.0% (n = 3), 75.0% (n = 9), and 33.3% (n = 4) of the samples had deficient mismatch repair (dMMR) protein, combined positive score (CPS) of ≥1, and CPS of ≥10, respectively. The univariate analysis revealed that programmed death-ligand 1 ≥5% (HR: 0.12; 95% CI: 0.01-0.97; p = 0.047) was significant associated with superior OS. One stage IV patient with CPS ≥10 and dMMR proteins received nivolumab monotherapy as frontline treatment that resulted 14-month PFS. Conclusion: Patients with GASC are more likely to yield positive results for CPS and dMMR. Biomarkers should be examined, and immunotherapy can be considered as frontline systemic treatment.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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