Department of Surgery, UCLA David Geffen School of Medicine, Los Angeles, California, USA.
Department of Pathology, UCLA David Geffen School of Medicine, Los Angeles, California, USA.
J Surg Oncol. 2021 Feb;123(2):389-398. doi: 10.1002/jso.26279. Epub 2020 Nov 4.
This study investigated the influence of the transcription factor SMAD4 on overall patient survival following surgical resection of pancreatic ductal adenocarcinoma (PDAC).
The SMAD4 status of 125 surgically resected PDAC specimens at a large academic center from 2014 to 2017 was routinely determined prospectively and correlated with clinicopathologic characteristics and overall survival.
SMAD4 loss was identified in 62% of patients and was not associated with overall survival (OS). On multivariate Cox proportional hazards survival analysis, histologic grade was the best predictor of survival in the SMAD4(-) population (adjusted hazard ratio = 4.8, p < .0001). In the SMAD4(+) population, histologic grade was not associated with survival on multivariate analysis. In the SMAD4(-) population, median OS for well/moderately differentiated patients and poorly differentiated patients was 39.6 and 8.6 months, respectively.
In this large cohort of resected PDAC, routine SMAD4 assessment identified a subpopulation of patients with SMAD4(-) and histologically poorly differentiated tumors that had significantly poor prognosis with median OS of 8.6 months. Characterization of the role of SMAD4 within the context of poorly differentiated tumors may help settle the controversy regarding SMAD4 in PDAC and lead to identification of personalized therapeutic strategies for subgroups of PDAC.
本研究旨在探讨转录因子 SMAD4 对接受胰腺导管腺癌(PDAC)手术切除患者总生存的影响。
本研究前瞻性地常规检测了 2014 年至 2017 年在一家大型学术中心接受手术切除的 125 例 PDAC 标本的 SMAD4 状态,并将其与临床病理特征和总生存相关联。
62%的患者存在 SMAD4 缺失,但与总生存(OS)无关。在多变量 Cox 比例风险生存分析中,组织学分级是 SMAD4(-)人群中生存的最佳预测因素(调整后的危险比=4.8,p<0.0001)。在 SMAD4(+)人群中,组织学分级在多变量分析中与生存无关。在 SMAD4(-)人群中,分化良好/中度和分化差患者的中位 OS 分别为 39.6 个月和 8.6 个月。
在本研究的大型 PDAC 切除队列中,常规的 SMAD4 评估确定了一组 SMAD4(-)和组织学上分化差的患者,其预后明显较差,中位 OS 为 8.6 个月。在分化差的肿瘤中明确 SMAD4 的作用,可能有助于解决 PDAC 中 SMAD4 的争议,并确定 PDAC 亚组的个体化治疗策略。