Sample Danielle C, Samadder N Jewel, Pappas Lisa M, Boucher Kenneth M, Samowitz Wade S, Berry Therese, Westover Michelle, Nathan Deepika, Kanth Priyanka, Byrne Kathryn R, Burt Randall W, Neklason Deborah W
Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope, Salt Lake City, UT, 84112-5550, USA.
University of Utah School of Medicine, 175 North Medical Drive East, Salt Lake City, UT, 84132, USA.
BMC Gastroenterol. 2018 Jul 16;18(1):115. doi: 10.1186/s12876-018-0841-8.
Patients with familial adenomatous polyposis (FAP) frequently undergo colectomy to reduce the 70 to 90% lifetime risk of colorectal cancer. After risk-reducing colectomy, duodenal cancer and complications from duodenal surgeries are the main cause of morbidity. Our objective was to prospectively describe the duodenal and gastric polyp phenotype in a cohort of 150 FAP patients undergoing pre-screening for a chemoprevention trial and analyze variables that may affect recommendations for surveillance.
Individuals with a diagnosis of FAP underwent prospective esophagogastroduodenoscopy using a uniform system of mapping of size and number of duodenal polyps for a 10 cm segment. Gastric polyps were recorded as the total number.
The distribution of the count and sum diameter of duodenal polyps were statistically different in two genotype groups, those with APC mutations associated with classic FAP had a greater count (median 17) and sum diameter of polyps (median 32 mm) than those with APC mutations associated with attenuated FAP (median count 4 and median sum diameter of 7 mm) (p < 0.0001). The number of gastric polyps did not differ based on genotype (p = 0.67) but advancing age correlated with severity of gastric polyposis (p = 0.019). Spigelman (modified) staging of II or greater was found in 88% of classic FAP patients and 48% attenuated FAP patients. Examples of severe and mild upper GI phenotype are observed in patients with identical APC mutations, showing that the APC mutation location is not absolutely predictive of an upper GI phenotype.
Most FAP patients have duodenal and gastric polyps which become more prevalent and advanced with age. Standard upper endoscopic surveillance is recommended based on personal history independent of APC mutation location.
NCT 01187901 registered August 24, 2010, prospective to enrollment.
家族性腺瘤性息肉病(FAP)患者常接受结肠切除术以降低70%至90%的终生患结直肠癌风险。在进行降低风险的结肠切除术后,十二指肠癌和十二指肠手术并发症是发病的主要原因。我们的目标是前瞻性地描述150名接受化学预防试验预筛查的FAP患者队列中的十二指肠和胃息肉表型,并分析可能影响监测建议的变量。
诊断为FAP的个体接受前瞻性食管胃十二指肠镜检查,使用统一系统对十二指肠息肉的大小和数量进行10厘米节段的映射。胃息肉记录为总数。
在两个基因型组中,十二指肠息肉的数量和总直径分布存在统计学差异,与经典FAP相关的APC突变患者的息肉数量(中位数17)和总直径(中位数32毫米)比与轻度FAP相关的APC突变患者(中位数数量4和中位数总直径7毫米)更多(p<0.0001)。胃息肉的数量在不同基因型之间没有差异(p=0.67),但年龄增长与胃息肉病的严重程度相关(p=0.019)。88%的经典FAP患者和48%的轻度FAP患者的斯皮格尔曼(改良)分期为II期或更高。在具有相同APC突变的患者中观察到严重和轻度上消化道表型的例子,表明APC突变位置并非绝对可预测上消化道表型。
大多数FAP患者有十二指肠和胃息肉,其随着年龄增长而更普遍和严重。建议根据个人病史进行标准的上消化道内镜监测,而不依赖于APC突变位置。
NCT 01187901于2010年8月24日注册,前瞻性入组。