Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Department of Medicine Solna, Clinical Epidemiology Division, Karolinska Institutet, Stockholm, Sweden.
BMC Cancer. 2022 Aug 13;22(1):890. doi: 10.1186/s12885-022-09992-5.
While individuals with normal gastrointestinal (GI) mucosa on endoscopy have a lower risk of colorectal cancer, risks of other cancers remain unexplored.
Through Sweden's 28 pathology departments, we identified 415,092 individuals with a first GI biopsy with histologically normal mucosa during 1965-2016 and no prior cancer. These individuals were compared to 1,939,215 matched reference individuals from the general population. Follow-up began 6 months after biopsy, and incident cancer data were retrieved from the Swedish Cancer Register. Flexible parametric model was applied to estimate cumulative incidences and hazard ratios (HRs) for cancers. We also used full siblings (n = 441,534) as a secondary comparison group.
During a median follow-up of 10.9 years, 40,935 individuals with normal mucosa (incidence rate: 82.74 per 10,000 person-years) and 177,350 reference individuals (incidence rate: 75.26) developed cancer. Restricting the data to individuals where follow-up revealed no cancer in the first 6 months, we still observed an increased risk of any cancer in those with a histologically normal mucosa (average HR = 1.07; 95%CI = 1.06-1.09). Although the HR for any and specific cancers decreased shortly after biopsy, we observed a long-term excess risk of any cancer, with an HR of 1.08 (95%CI = 1.05-1.12) and a cumulative incidence difference of 0.93% (95%CI = 0.61%-1.25%) at 30 years after biopsy. An elevated risk of gastric cancer, lung cancer, and hematological malignancy (including lymphoproliferative malignancy) was also observed at 20 or 30 years since biopsy. Sibling analyses confirmed the above findings.
Individuals with a histologically normal mucosa at biopsy and where follow-up revealed no cancer in the first 6 months, may still be at increased risk of cancer, although excess risks are small.
虽然内镜下胃肠道(GI)黏膜正常的个体结直肠癌风险较低,但其他癌症的风险仍未得到探索。
通过瑞典的 28 个病理部门,我们确定了 1965 年至 2016 年间首次进行 GI 活检且组织学上黏膜正常且无既往癌症的 415092 名个体,并将这些个体与来自普通人群的 1939215 名匹配的参考个体进行比较。随访从活检后 6 个月开始,从瑞典癌症登记处获取癌症发病数据。采用灵活参数模型估计癌症的累积发生率和风险比(HR)。我们还使用全同胞(n=441534)作为次要比较组。
在中位随访 10.9 年期间,40935 名正常黏膜个体(发病率:82.74/10000 人年)和 177350 名参考个体(发病率:75.26)发生了癌症。将数据限制在最初 6 个月内没有癌症的个体中,我们仍然观察到组织学上正常黏膜个体的任何癌症风险增加(平均 HR=1.07;95%CI=1.06-1.09)。尽管活检后任何和特定癌症的 HR 短期下降,但我们观察到任何癌症的长期风险增加,HR 为 1.08(95%CI=1.05-1.12),并且在活检后 30 年时累积发病率差异为 0.93%(95%CI=0.61%-1.25%)。在活检后 20 或 30 年时,还观察到胃癌、肺癌和血液恶性肿瘤(包括淋巴增生性恶性肿瘤)的风险增加。同胞分析证实了上述发现。
在最初 6 个月内没有癌症的情况下进行活检,组织学上正常黏膜的个体可能仍然存在癌症风险增加,尽管风险增加很小。