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Synchronous metastatic gastric cancer-molecular background and clinical implications with special attention to mismatch repair deficiency
Authors:Karol Polom  Christine Böger  Elizabeth Smyth  Daniele Marrelli  Hans-Michael Behrens  Luigi Marano  Thomas Becker  Florian Lordick  Christoph Röcken  Franco Roviello
Affiliation:1. General Surgery and Surgical Oncology Department, University of Siena, Italy viale Bracci 16, 53100, Siena, Italy;2. Department of Surgical Oncology, Medical University of Gdansk, Gdansk, Poland;3. Department of Pathology, Christian-Albrechts-University, Kiel, Germany;4. Department of Gastrointestinal Oncology and Lymphoma, Royal Marsden Hospital, London and Sutton, United Kingdom;5. General, Minimally Invasive and Robotic Surgery, Department of Surgery, “San Matteo degli Infermi Hospital”–ASL Umbria 2, 06049, Spoleto, Italy;6. Department of General, Visceral, Thoracic, Transplant and Pediatric Surgery, Christian-Albrechts-University, Kiel, Germany;g. University Cancer Center Leipzig (UCCL), University Medicine Leipzig, 04103 Leipzig, Germany
Abstract:

Background

Current guidelines recommend that metastatic gastric cancer should not be treated with surgery unless this is required for symptom control. We hypothesized that patients with mismatch repair deficiency (MMRd) gastric cancer and metastatic disease detected at the timepoint of surgical resection would have superior survival compared to patients with MMRd cancers in the same setting.

Methods

Clinicopathological details and survival data were collected from prospective databases at two large European centers on patients who had undergone surgery and were diagnosed with synchronous stage IV gastric cancer (distant lymph nodes, positive peritoneal cytology, peritoneal, and distant metastases) at the timepoint of surgery. Resection specimens were tested for the presence of microsatellite instability using a standard 5 mononucleotide repeat panel.

Results

One hundred and seventy six patients with resected stage IV gastric cancer were identified. 14/176 (8.0%) had MSI-H (high) disease. There was no significant difference between the clinical and pathological characteristics of MSI and microsatellite stable (MSS) patients. No differences in the type of metastases were observed between MSI and MSS groups. Patients who were MSI-H had superior OS compared to MSS patients (median OS 15.9 vs. 8 months, p = 0.023). However, in Cox regression multivariate analysis only liver and peritoneal metastases were independent predictors of survival.

Conclusions

Surgically treated patients with MSI-H stage IV gastric cancer have a better survival than patients with MSS gastric cancer. Further analysis of the role of surgery in MSI stage IV GC is required.
Keywords:Microsatellite instability  Molecular  Stomach cancer  Prognosis  Metastasis  Microsatellite instability  MSI  Gastric cancer  GC  Microsatellite stable  MSS  Overall survival  OS  Microsatellite instability with high instability  MSI-H  European Society of Medical Oncology  ESMO  National Comprehensive Cancer Network  NCCN  Japanese Gastric Cancer Association  JGCA  Italian Gastric Cancer Research Group  GIRCG  The Cancer Genome Atlas  TCGA  World Health Organization histology  WHO histology  Deoxyribonucleic acid  DNA  Hazard ratio  HR  Mismatch repair deficiency  MMRd  Epirubicin, cisplatin, fluorouracil chemotherapy  ECF  Food and drug association  FDA  anti programmed cell death protein 1 antibody  anti-PD-1 antibody
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