Department of Surgery, Division of General Surgery, David Geffen School of Medicine at University of California, Los Angeles.
Department of Medicine, David Geffen School of Medicine at University of California, Los Angeles.
JAMA Surg. 2014 Feb;149(2):145-53. doi: 10.1001/jamasurg.2013.2690.
Treatment of patients with locally advanced/borderline resectable (LA/BR) pancreatic ductal adenocarcinoma (PDAC) is not standardized.
To (1) perform a detailed survival analysis of our institution's experience with patients with LA/BR PDAC who were downstaged and underwent surgical resection and (2) identify prognostic biomarkers that may help to guide a decision for the use of adjuvant therapy in this patient subgroup.
DESIGN, SETTING, AND PARTICIPANTS: Retrospective observational study of 49 consecutive patients from a single institution during 1992-2011 with American Joint Committee on Cancer stage III LA/BR PDAC who were initially unresectable, as determined by staging computed tomography and/or surgical exploration, and who were treated and then surgically resected.
Clinicopathologic variables and prognostic biomarkers SMAD4, S100A2, and microRNA-21 were correlated with survival by univariate and multivariate Cox proportional hazard modeling.
All 49 patients were deemed initially unresectable owing to vascular involvement. After completing preoperative chemotherapy for a median of 7.1 months (range, 5.4-9.6 months), most (75.5%) underwent a pylorus-preserving Whipple operation; 3 patients (6.1%) had a vascular resection. Strikingly, 37 of 49 patients were lymph-node (LN) negative (75.5%) and 42 (85.7%) had negative margins; 45.8% of evaluable patients achieved a complete histopathologic (HP) response. The median overall survival (OS) was 40.1 months (range, 22.7-65.9 months). A univariate analysis of HP prognostic biomarkers revealed that perineural invasion (hazard ratio, 5.5; P=.007) and HP treatment response (hazard ratio, 9.0; P=.009) were most significant. Lymph-node involvement, as a marker of systemic disease, was also significant on univariate analysis (P=.05). Patients with no LN involvement had longer OS (44.4 vs 23.2 months, P=.04) than LN-positive patients. The candidate prognostic biomarkers, SMAD4 protein loss (P=.01) in tumor cells and microRNA-21 expression in the stroma (P=.05), also correlated with OS. On multivariate Cox proportional hazard modeling of HP and prognostic biomarkers, only SMAD4 protein loss was significant (hazard ratio, 9.3; P=.004).
Our approach to patients with LA/BR PDAC, which includes prolonged preoperative chemotherapy, is associated with a high incidence of LN-negative disease and excellent OS. After surgical resection, HP treatment response, perineural invasion, and SMAD4 status should help determine who should receive adjuvant therapy in this select subset of patients.
局部晚期/边界可切除(LA/BR)胰腺导管腺癌(PDAC)患者的治疗尚未标准化。
(1)对本机构接受降期手术切除的 LA/BR PDAC 患者的生存情况进行详细分析,(2)确定可能有助于指导该患者亚组使用辅助治疗的预后生物标志物。
设计、地点和参与者:对 1992 年至 2011 年期间在单一机构接受治疗的 49 例连续患者进行回顾性观察性研究,这些患者为美国癌症联合委员会(AJCC)III 期 LA/BR PDAC,初始时因分期 CT 和/或手术探查结果认为不可切除。
采用单因素和多因素 Cox 比例风险模型对临床病理变量和预后生物标志物 SMAD4、S100A2 和 microRNA-21 与生存进行相关性分析。
49 例患者均因血管受累而被认为初始时不可切除。在接受中位时间为 7.1 个月(范围为 5.4-9.6 个月)的术前化疗后,大多数患者(75.5%)接受了保留幽门的胰十二指肠切除术;3 例患者(6.1%)进行了血管切除术。显著的是,49 例患者中有 37 例(75.5%)为淋巴结(LN)阴性,42 例(85.7%)为切缘阴性;45.8%的可评估患者获得了完全组织病理学(HP)反应。中位总生存期(OS)为 40.1 个月(范围为 22.7-65.9 个月)。HP 预后生物标志物的单因素分析显示,神经周围侵犯(风险比,5.5;P=.007)和 HP 治疗反应(风险比,9.0;P=.009)是最重要的影响因素。作为全身疾病标志物的 LN 受累在单因素分析中也有意义(P=.05)。无 LN 受累的患者 OS 更长(44.4 个月比 23.2 个月,P=.04)。候选预后生物标志物,肿瘤细胞中 SMAD4 蛋白缺失(P=.01)和基质中 microRNA-21 表达(P=.05),也与 OS 相关。在 HP 和预后生物标志物的多因素 Cox 比例风险模型中,只有 SMAD4 蛋白缺失具有统计学意义(风险比,9.3;P=.004)。
我们对 LA/BR PDAC 患者采用的方法包括延长术前化疗,与 LN 阴性疾病的高发生率和良好的 OS 相关。在接受手术切除后,HP 治疗反应、神经周围侵犯和 SMAD4 状态应有助于确定在该特定患者亚组中谁应接受辅助治疗。