Shao-Bin Chen, Hong-Rui Weng, Geng Wang, Jie-Sheng Yang, Wei-Ping Yang, Di-Tian Liu, Yu-Ping Chen, Department of Thoracic Surgery, Cancer Hospital of Shantou University Medical College, Shantou 515031, Guangdong Province, China.
World J Gastroenterol. 2013 Dec 7;19(45):8382-90. doi: 10.3748/wjg.v19.i45.8382.
To investigate the clinical characteristics, diagnosis, treatment, and prognosis of primary adenosquamous carcinoma (ASC) of the esophagus.
A total of 4015 patients with esophageal carcinoma underwent surgical resection between January 1995 and June 2012 at the Cancer Hospital of Shantou University Medical College. In 37 cases, the histological diagnosis was primary ASC. Clinical data were retrospectively analyzed from these 37 patients, who underwent transthoracic esophagectomy with lymphadenectomy. The χ(2) or Fisher's exact test was used to compare the clinicopathological features between patients with ASC and those with squamous cell carcinoma (SCC). The Kaplan-Meier and Log-Rank methods were used to estimate and compare survival rates. A Cox proportional hazard regression model was used to identify independent prognostic factors.
Primary esophageal ASC accounted for 0.92% of all primary esophageal carcinoma cases (37/4015). The clinical manifestations were identical to those of other types of esophageal cancer. All of the 24 patients who underwent preoperative endoscopic biopsy were misdiagnosed with SCC. The median survival time (MST) was 21.0 mo (95%CI: 12.6-29.4), and the 1-, 3-, and 5-year overall survival rates were 67.5%, 29.4%, and 22.9%, respectively. In multivariate analysis, only adjuvant radiotherapy (HR = 0.317, 95%CI: 0.114-0.885, P = 0.028) was found to be an independent prognostic factor. The MST for ASC patients was significantly lower than that for SCC patients [21.0 mo (95%CI: 12.6-29.4) vs 46.0 mo (95%CI: 40.8-51.2), P = 0.001]. In subgroup analyses, the MST for ASC patients was similar to that for poorly differentiated SCC patients.
Primary esophageal ASC is a rare disease that is prone to be misdiagnosed by endoscopic biopsy. The prognosis is poorer than esophageal SCC but similar to that for poorly differentiated SCC patients.
探讨食管原发性腺鳞癌(ASC)的临床特征、诊断、治疗及预后。
1995 年 1 月至 2012 年 6 月,汕头大学医学院附属肿瘤医院共对 4015 例食管癌患者进行了外科手术切除,其中 37 例的组织学诊断为原发性 ASC。对这 37 例接受经胸食管切除术和淋巴结清扫术的患者进行了回顾性临床数据分析。采用 χ(2)或 Fisher 确切概率检验比较 ASC 患者和鳞癌(SCC)患者的临床病理特征。采用 Kaplan-Meier 和 Log-Rank 方法估计和比较生存率。采用 Cox 比例风险回归模型识别独立的预后因素。
原发性食管 ASC 占所有原发性食管鳞癌的 0.92%(37/4015)。临床表现与其他类型食管癌相同。所有 24 例行术前内镜活检的患者均误诊为 SCC。中位总生存期(MST)为 21.0 个月(95%CI:12.6-29.4),1、3、5 年总生存率分别为 67.5%、29.4%和 22.9%。多因素分析显示,仅辅助放疗(HR=0.317,95%CI:0.114-0.885,P=0.028)是独立的预后因素。ASC 患者的 MST 明显低于 SCC 患者[21.0 个月(95%CI:12.6-29.4)比 46.0 个月(95%CI:40.8-51.2),P=0.001]。亚组分析显示,ASC 患者的 MST 与低分化 SCC 患者相似。
原发性食管 ASC 是一种罕见疾病,容易被内镜活检误诊。其预后较食管 SCC 差,但与低分化 SCC 患者相似。