Dulai Gareth S, Shekelle Paul G, Jensen Dennis M, Spiegel Brennan M R, Chen Jaime, Oh David, Kahn Katherine L
Greater Los Angeles Veterans Administration Healthcare System, Department of Medicine, Division of Gastroenterology, UCLA School of Medicine, Los Angeles, CA 90073, USA.
Am J Gastroenterol. 2005 Apr;100(4):775-83. doi: 10.1111/j.1572-0241.2005.41300.x.
No published data are available on the risk of further neoplastic progression in Barrett's patients stratified by baseline dysplasia status. Our aims were to estimate and compare the risk of progression to high-grade dysplasia or cancer in groups of Barrett's patients stratified by baseline dysplasia status.
Consecutive Barrett's cases from 1988-2002 were identified via pathology databases in a regional VA health-care system and medical record data were abstracted. The risk of progression to high-grade dysplasia or cancer was measured and compared in cases with versus without low-grade dysplasia within 1 yr of index endoscopy using survival analysis.
A total of 575 Barrett's cases had 2,775 patient-years of follow-up. There were 13 incident cases of high-grade dysplasia and two of cancer. The crude rate of high-grade dysplasia or cancer was 1 of 78 patient-years for those with baseline dysplasia versus 1 of 278 patient-years for those without (p= 0.001). One case of high-grade dysplasia in each group underwent successful therapy. One incident cancer case underwent successful resection and the other was unresectable. Two cases with high-grade dysplasia later developed cancer, one died postoperatively, the other was unresectable. When these two cases were included (total of four cancers), the crude rate of cancer was 1 of 274 patient-years for those with baseline dysplasia versus 1 of 1,114 patient-years for those without.
In a large cohort study of Barrett's, incident malignancy was uncommon. The rate of progression to high-grade dysplasia or cancer was significantly higher in those with baseline low-grade dysplasia. These data may warrant reevaluation of current Barrett's surveillance strategies.
目前尚无按基线发育异常状态分层的巴雷特食管患者发生进一步肿瘤进展风险的公开数据。我们的目的是估计并比较按基线发育异常状态分层的巴雷特食管患者组进展为高级别发育异常或癌症的风险。
通过一个地区退伍军人医疗保健系统的病理数据库识别出1988年至2002年的连续巴雷特食管病例,并提取病历数据。使用生存分析方法测量并比较初次内镜检查后1年内有和没有低级别发育异常的病例进展为高级别发育异常或癌症的风险。
总共575例巴雷特食管病例有2775人年的随访时间。有13例高级别发育异常新发病例和2例癌症病例。基线有发育异常者高级别发育异常或癌症的粗发病率为每78人年1例,而基线无发育异常者为每278人年1例(p = 0.001)。每组各有1例高级别发育异常病例接受了成功治疗。1例癌症新发病例接受了成功切除,另一例无法切除。2例高级别发育异常病例后来发展为癌症,1例术后死亡,另一例无法切除。当纳入这2例病例(共4例癌症)时,基线有发育异常者癌症的粗发病率为每274人年1例,而基线无发育异常者为每1114人年1例。
在一项关于巴雷特食管的大型队列研究中,恶性肿瘤新发病例并不常见。基线有低级别发育异常者进展为高级别发育异常或癌症的发生率显著更高。这些数据可能需要对当前巴雷特食管的监测策略进行重新评估。