Hage M, Siersema P D, van Dekken H, Steyerberg E W, Dees J, Kuipers E J
Depts of Gastroenterology and Hepatology, Pathology and Public Health, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.
Scand J Gastroenterol. 2004 Dec;39(12):1175-9. doi: 10.1080/00365520410003524.
Data on cancer risk in patients with long-segment Barrett's oesophagus (BO) from older studies are often difficult to interpret, since the definition of BO has evolved from an endoscopical to a histological diagnosis. In this work the diagnoses in the Rotterdam BO cohort on current standards was redefined to obtain more accurate data on cancer risk in patients who had not undergone standard endoscopic surveillance. In addition, it was determined which patient factors present at index endoscopy were associated with neoplastic progression in BO.
The Rotterdam BO cohort comprises all patients with > or =3 cm BO, diagnosed at endoscopy between 1973 and 1984. In the present study, only patients with intestinal metaplasia were included (n = 105). Follow-up data were obtained by questionnaires and/or interviews with patients or treating physicians. A Kaplan-Meier analysis was used to estimate 20-year risks.
The mean length of the BO was 7.1 cm (range: 3-15 cm). Cancer in BO developed in 6/105 (6%) patients, and high-grade dysplasia (HGD) in 5/105 (5%) patients during 1329 patient-years of follow-up, which equals one cancer case per 221 patient-years and one HGD case per 266 patient-years. After a mean follow-up of 12.7 years, 72 (69%) patients had died; only 4 of them died of oesophageal cancer or its treatment. A longer length of BO was associated with an increased risk of progression to HGD or cancer (P < 0.02). Six of 24 patients who ever had low-grade dysplasia progressed to HGD or cancer 2-16 years after a diagnosis of BO.
The annual risk of developing HGD or adenocarcinoma in patients with long-segment BO is 0.83%. Death due to adenocarcinoma is, however, uncommon, even in a cohort of patients with long-segment BO.
早期研究中关于长节段巴雷特食管(BO)患者癌症风险的数据常难以解读,因为BO的定义已从内镜诊断发展为组织学诊断。在本研究中,按照当前标准重新定义了鹿特丹BO队列中的诊断,以获取未接受标准内镜监测患者更准确的癌症风险数据。此外,还确定了初次内镜检查时存在的哪些患者因素与BO的肿瘤进展相关。
鹿特丹BO队列包括1973年至1984年间内镜诊断为≥3 cm BO的所有患者。在本研究中,仅纳入了肠化生患者(n = 105)。通过问卷调查和/或对患者或治疗医生的访谈获取随访数据。采用Kaplan-Meier分析来估计20年风险。
BO的平均长度为7.1 cm(范围:3 - 15 cm)。在1329患者年的随访期间,105例患者中有6例(6%)发生了BO癌,5例(5%)发生了高级别异型增生(HGD),即每221患者年发生1例癌症病例,每266患者年发生1例HGD病例。平均随访12.7年后,72例(69%)患者死亡;其中只有4例死于食管癌或其治疗。BO长度较长与进展为HGD或癌症的风险增加相关(P < 0.02)。24例曾有低级别异型增生的患者中有6例在BO诊断后2至16年进展为HGD或癌症。
长节段BO患者发生HGD或腺癌的年风险为0.83%。然而,即使在长节段BO患者队列中,腺癌导致的死亡也不常见。