i3S-Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal.
Ipatimup-Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Int J Cancer. 2022 Mar 1;150(5):868-880. doi: 10.1002/ijc.33872. Epub 2021 Dec 9.
Surgical resection with lymphadenectomy and perioperative chemotherapy is the universal mainstay for curative treatment of gastric cancer (GC) patients with locoregional disease. However, GC survival remains asymmetric in West- and East-world regions. We hypothesize that this asymmetry derives from differential clinical management. Therefore, we collected chemo-naïve GC patients from Portugal and South Korea to explore specific immunophenotypic profiles related to disease aggressiveness and clinicopathological factors potentially explaining associated overall survival (OS) differences. Clinicopathological and survival data were collected from chemo-naïve surgical cohorts from Portugal (West-Europe cohort [WE-C]; n = 170) and South Korea (East-Asia cohort [EA-C]; n = 367) and correlated with immunohistochemical expression profiles of E-cadherin and CD44v6 obtained from consecutive tissue microarrays sections. Survival analysis revealed a subset of 12.4% of WE-C patients, whose tumors concomitantly express E-cadherin_abnormal and CD44v6_very high, displaying extremely poor OS, even at TNM stages I and II. These WE-C stage-I and -II patients tumors were particularly aggressive compared to all others, invading deeper into the gastric wall (P = .032) and more often permeating the vasculature (P = .018) and nerves (P = .009). A similar immunophenotypic profile was found in 11.9% of EA-C patients, but unrelated to survival. Tumours, from stage-I and -II EA-C patients, that display both biomarkers, also permeated more lymphatic vessels (P = .003), promoting lymph node (LN) metastasis (P = .019), being diagnosed on average 8 years earlier and submitted to more extensive LN dissection than WE-C. Concomitant E-cadherin_abnormal/CD44v6_very-high expression predicts aggressiveness and poor survival of stage-I and -II GC submitted to conservative lymphadenectomy.
手术切除加淋巴结清扫和围手术期化疗是局部区域疾病胃癌(GC)患者根治性治疗的普遍基础。然而,GC 的生存率在西方国家和东亚地区仍然存在差异。我们假设这种差异源于不同的临床管理。因此,我们从葡萄牙和韩国收集了未经化疗的 GC 患者,以探讨与疾病侵袭性相关的特定免疫表型特征,以及可能解释相关总生存(OS)差异的临床病理因素。从葡萄牙(西欧队列[WE-C];n=170)和韩国(东亚队列[EA-C];n=367)未经化疗的手术队列中收集临床病理和生存数据,并与连续组织微阵列切片中获得的 E-钙粘蛋白和 CD44v6 的免疫组织化学表达谱相关联。生存分析显示,WE-C 患者中有 12.4%的患者肿瘤同时表达 E-钙粘蛋白异常和 CD44v6 非常高,其 OS 极差,即使在 TNM 分期 I 和 II 期也是如此。与所有其他患者相比,这些 WE-C 分期 I 和 II 期患者的肿瘤具有更强的侵袭性,更深地侵犯胃壁(P=.032),更常侵犯脉管系统(P=.018)和神经(P=.009)。在 11.9%的 EA-C 患者中也发现了类似的免疫表型谱,但与生存无关。来自 EA-C 分期 I 和 II 期的肿瘤,如果同时显示这两种生物标志物,也更易穿透淋巴管(P=.003),促进淋巴结(LN)转移(P=.019),平均诊断时间早 8 年,接受的 LN 清扫范围也比 WE-C 更广泛。同时表达 E-钙粘蛋白异常/CD44v6 非常高预测接受保守淋巴结清扫的分期 I 和 II 期 GC 的侵袭性和不良生存。