Department of Oncology, Oxford Cancer and Haematology Centre, Oxford, UK.
Br J Surg. 2012 Feb;99(2):239-45. doi: 10.1002/bjs.7758.
Positron emission tomography combined with computed tomography (PET-CT) is increasingly being used in the staging of oesophageal cancer. Some recent reports suggest it may be used to predict survival. None of these studies, however, reported on the prognostic value of PET-CT performed before neoadjuvant chemotherapy and surgery. The aim of this study was to determine whether pretreatment PET-CT could predict survival.
Consecutive patients with oesophageal adenocarcinoma who underwent PET-CT before neoadjuvant chemotherapy and resection were included. Maximum standardized uptake value (SUV(max)), fluorodeoxyglucose (FDG)-avid tumour length and the presence of FDG-avid local lymph nodes were determined for all patients. Kaplan-Meier survival analysis was performed and multivariable analysis used to identify independent prognostic factors.
A total of 121 patients were included (mean age 63 years, 97 men) of whom 103 underwent surgical resection. On an intention-to-treat basis, overall survival was significantly worse in patients with FDG-avid local lymph nodes (P < 0·001). SUV(max) and FDG-avid tumour length did not predict survival (P = 0·276 and P = 0·713 respectively). The presence of FDG-avid local lymph nodes was an independent predictor of poor overall survival (hazard ratio (HR) 4·75, 95 per cent confidence interval 2·14 to 10·54; P < 0·001) and disease-free survival (HR 2·97, 1·40 to 6·30; P = 0·004).
The presence of FDG-avid lymph nodes, but not SUV(max) or FDG-avid tumour length, was an independent adverse prognostic factor.
正电子发射断层扫描结合计算机断层扫描(PET-CT)越来越多地用于食管癌的分期。一些最新报告表明,它可能用于预测生存。然而,这些研究均未报告新辅助化疗和手术前 PET-CT 的预后价值。本研究旨在确定术前 PET-CT 是否可预测生存。
纳入了连续接受新辅助化疗和切除术的食管腺癌患者。对所有患者确定最大标准化摄取值(SUV(max))、氟脱氧葡萄糖(FDG)阳性肿瘤长度和 FDG 阳性局部淋巴结的存在。进行 Kaplan-Meier 生存分析和多变量分析以确定独立的预后因素。
共纳入 121 例患者(平均年龄 63 岁,97 例男性),其中 103 例行手术切除。在意向治疗的基础上,有 FDG 阳性局部淋巴结的患者总体生存率显著降低(P<0·001)。SUV(max)和 FDG 阳性肿瘤长度不能预测生存(P=0·276 和 P=0·713)。FDG 阳性局部淋巴结的存在是总体生存率差的独立预测因子(危险比(HR)4·75,95%置信区间 2·14 至 10·54;P<0·001)和无病生存率(HR 2·97,1·40 至 6·30;P=0·004)。
FDG 阳性淋巴结的存在,而不是 SUV(max)或 FDG 阳性肿瘤长度,是独立的不良预后因素。