Department of Gastroenterology, Kaiser Permanente San Francisco, San Francisco, California.
Department of Gastroenterology, Kaiser Permanente San Francisco, San Francisco, California; Division of Research, Kaiser Permanente Northern California, Oakland, California.
Clin Gastroenterol Hepatol. 2023 Feb;21(2):487-496.e3. doi: 10.1016/j.cgh.2022.05.006. Epub 2022 May 26.
BACKGROUND & AIMS: Recent research has demonstrated biologic plausibility for iatrogenic tumor seeding via colonoscopy as a cause of metachronous colorectal cancers (CRC). This study evaluated the association between biopsy of non-tumor sites after CRC biopsy and risk of metachronous CRC in a large community-based health care organization.
This was a retrospective case-control study of adults with an initial CRC diagnosed by colonoscopy between January 2006 and June 2018 who underwent curative resection. Cases developed a second primary (metachronous) CRC diagnosed 6 months to 4 years after the initial CRC, and were matched by age, sex, diagnosis of inflammatory bowel disease, race, and ethnicity with up to 5 controls without a second CRC diagnosis. The exposure was biopsy in the colonic segment of the metachronous CRC (or corresponding segment in controls) after tumor biopsy, ascertained with blinding to case status. Associations were evaluated using conditional logistic regression and adjusted for potential cofounders.
Among 14,119 patients diagnosed with an initial CRC during colonoscopy, 107 received a second CRC diagnosis. After exclusions for recurrent or synchronous CRC, 45 cases and 212 controls were included. There was no significant association between biopsy of non-tumor sites after initial CRC biopsy and risk of metachronous CRC in the segment of the additional biopsy site (adjusted odds ratio, 2.29; 95% confidence interval, 0.77-6.81).
Metachronous cancers are not significantly associated with biopsy of non-tumor sites after biopsy of the primary cancer. Although the sample size does not allow definite exclusion of any association, these findings do not support iatrogenic tumor seeding as a common risk factor for metachronous CRC.
最近的研究表明,结肠镜检查过程中肿瘤种植具有生物学可能性,可能是结直肠多发癌(CRC)的原因之一。本研究在一个大型社区医疗组织中评估了结直肠活检后对非肿瘤部位进行活检与 CRC 患者发生 CRC 的相关性。
这是一项回顾性病例对照研究,纳入了 2006 年 1 月至 2018 年 6 月期间通过结肠镜诊断为初始 CRC 的成年人患者,这些患者接受了根治性切除术。病例组为在初始 CRC 诊断后 6 个月至 4 年内发生第二个原发性(异时性)CRC 的患者,并按年龄、性别、炎症性肠病诊断、种族和民族与最多 5 名无第二个 CRC 诊断的对照患者进行匹配。暴露因素为在肿瘤活检后(或对照患者中相应的节段)对异时性 CRC (或对照)的结肠节段进行活检,病例状态设盲。使用条件逻辑回归评估关联,并调整潜在混杂因素。
在结肠镜检查中诊断为初始 CRC 的 14119 例患者中,有 107 例患者诊断出第二原发 CRC。排除复发或同步 CRC 后,纳入 45 例病例和 212 例对照。在初始 CRC 活检后对非肿瘤部位进行活检与额外活检部位 CRC 的发生风险之间无显著相关性(调整后的比值比,2.29;95%置信区间,0.77-6.81)。
异时性癌症与原发性癌症活检后对非肿瘤部位进行活检无显著相关性。尽管样本量不能排除任何相关性,但这些发现不支持肿瘤种植是 CRC 异时性发生的常见危险因素。