期刊
GASTRIC CANCER
卷 25, 期 3, 页码 640-651出版社
SPRINGER
DOI: 10.1007/s10120-022-01280-2
关键词
Epstein-Barr virus (EBV); Stomach neoplasms; Histopathological response; Microsatellite instability (MSI); Mucinous differentiation
资金
- Cancer Center Amsterdam
- Netherlands Organization for Health Research and Development (ZonMW) [848101003]
This study found that EBV positivity and high microsatellite instability (MSI) were positive prognostic factors in resectable gastric cancer. However, the benefits of perioperative treatment for MSI-high tumors remain uncertain. Interestingly, MSI-high tumors with substantial histopathological response were predominantly of the mucinous phenotype. These findings suggest that mucinous phenotype could be an important parameter in future clinical trials for MSI-high patients.
Background Epstein-Barr virus positivity (EBV+) and microsatellite instability (MSI-high) are positive prognostic factors for survival in resectable gastric cancer (GC). However, benefit of perioperative treatment in patients with MSI-high tumors remains topic of discussion. Here, we present the clinicopathological outcomes of patients with EBV+, MSI-high, and EBV-/MSS GCs who received either surgery only or perioperative treatment. Methods EBV and MSI status were determined on tumor samples collected from 447 patients treated with surgery only in the D1/D2 trial, and from 451 patients treated perioperatively in the CRITICS trial. Results were correlated to histopathological response, morphological tumor characteristics, and survival. Results In the D1/D2 trial, 5-year cancer-related survival was 65.2% in 47 patients with EBV+, 56.7% in 47 patients with MSI-high, and 47.6% in 353 patients with EBV-/MSS tumors. In the CRITICS trial, 5-year cancer-related survival was 69.8% in 25 patients with EBV+, 51.7% in 27 patients with MSI-high, and 38.6% in 402 patients with EBV-/MSS tumors. Interestingly, all three MSI-high tumors with moderate to complete histopathological response (3/27, 11.1%) had substantial mucinous differentiation. No EBV+ tumors had a mucinous phenotype. 115/402 (28.6%) of EBV-/MSS tumors had moderate to complete histopathological response, of which 23/115 (20.0%) had a mucinous phenotype. Conclusions In resectable GC, MSI-high had favorable outcome compared to EBV-/MSS, both in patients treated with surgery only, and in those treated with perioperative chemo(radio)therapy. Substantial histopathological response was restricted to mucinous MSI-high tumors. The mucinous phenotype might be a relevant parameter in future clinical trials for MSI-high patients.
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