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Lymphocyte-Rich Gastric Cancer: Associations with Epstein-Barr Virus, Microsatellite Instability, Histology, and Survival

机译:淋巴细胞丰富的胃癌:与爱泼斯坦-巴尔病毒,微卫星不稳定性,组织学和生存的关联。

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Lymphocyte-rich gastric carcinomas may have a better prognosis than cancers without a pronounced host inflammatory response. Two subsets of gastric cancer—Epstein-Barr virus-positive and microsatellite instability high—have been associated with a lymphocyte-rich phenotype. We assessed relationships between tumor-infiltrating lymphocytes, Epstein-Barr virus status, microsatellite instability status, and cancer-specific survival in 110 resected gastric cancers. Seven patients had Epstein-Barr virus-positive cancer, including 4 (3.7%) of 107 consecutive patients. Tumors from 17 patients (16%) were designated microsatellite instability high on the basis of negative immunohistochemical staining for MLH1; all tumors had intact expression of MSH2 and MSH6. Epstein-Barr virus-positive cancers had increased tumor-infiltrating lymphocytes compared with Epstein-Barr virus-negative cancers (median 450/10 HPF versus 21/10 HPF, P versus 20/HPF, P < .001). Microsatellite instability–high cancers affected older patients and were more likely to be intestinal in the Lauren classification and expanding in the Ming classification. By univariate analysis, decreased risk of death from gastric cancer was significantly associated with low tumor stage, expanding growth pattern, increasing tumor-infiltrating lymphocyte count, and microsatellite instability–high status. High tumor-infiltrating lymphocyte count and microsatellite instability–high status retained statistical significance as favorable prognostic factors after adjustment for tumor stage in multivariate analysis. Tumor-infiltrating lymphocyte count retained statistical significance as a favorable prognostic factor after adjustment for microsatellite instability–high status; but microsatellite instability–high status did not remain a significant independent prognosticator after adjustment for tumor-infiltrating lymphocyte count. The association between microsatellite instability–high cancers and high tumor-infiltrating lymphocyte counts may account for the association of microsatellite instability–high gastric cancers with improved survival.
机译:与没有明显宿主炎症反应的癌症相比,富含淋巴细胞的胃癌的预后可能更好。胃癌的两个子集-Epstein-Barr病毒阳性和高微卫星不稳定性-与富含淋巴细胞的表型有关。我们评估了110例切除的胃癌中肿瘤浸润淋巴细胞,爱泼斯坦-巴尔病毒状态,微卫星不稳定性状态和特定于癌症的生存率之间的关系。 7例患者患有爱泼斯坦-巴尔病毒阳性,包括107例连续患者中的4例(3.7%)。根据MLH1免疫组化染色阴性,将17位患者(16%)的肿瘤定为高微卫星不稳定性。所有肿瘤均完整表达了MSH2和MSH6。与爱泼斯坦-巴尔病毒阴性的癌症相比,爱泼斯坦-巴尔病毒阳性的癌症的肿瘤浸润淋巴细胞增加(中位数450/10 HPF对21/10 HPF,P对20 / HPF,P <.001)。微卫星不稳定-高癌会影响老年患者,在Lauren分级中更可能是肠道,而在Ming分级中则扩大。通过单因素分析,胃癌死亡风险的降低与肿瘤的低分期,扩大的生长方式,增加的肿瘤浸润淋巴细胞计数以及微卫星不稳定(高状态)密切相关。在多因素分析中调整肿瘤分期后,高肿瘤浸润淋巴细胞计数和微卫星不稳定性-高状态保留了统计学意义,作为有利的预后因素。调整微卫星不稳定性(高状态)后,肿瘤浸润淋巴细胞计数仍具有统计学意义,可作为有利的预后因素。但是在调整了肿瘤浸润淋巴细胞计数后,微卫星不稳定性(高状态)仍不是重要的独立预后指标。微卫星不稳定性(高癌症)与高肿瘤浸润淋巴细胞计数之间的关联可能解释了微卫星不稳定性(高胃癌)与生存改善之间的关联。

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