Zhu N, Huang Y Q, Song Y M, Zhang S Z, Zheng S, Yuan Y
Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China Department of Medical Oncology, Key Labaratory of Cancer Prevention and Intervention, Ministry of Education, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.
Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, Ministry of Education, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310009, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2022 Jul 25;25(7):612-620. doi: 10.3760/cma.j.cn441530-20211127-00478.
To investigate the effects of high risk factors questionnaire (HRFQ), Asia-Pacific colorectal screening (APCS) score and their combinations with fecal immunochemical test (FIT) in screening advanced colorectal neoplasia, in order to provide an evidence for further optimization of cancer screening program. A retrospective cohort study method was used to summarize and analyze the results of colorectal tumor screening in Jiashan County, Zhejiang Province from March 2017 to July 2018. Those with severe diseases that were not suitable for colonoscopy and those with mental and behavioral abnormalities who can not cooperate with the screening were excluded. Those who met any one or more of the followings in the HRFQ questionnaire were classified as high-risk people of HRFQ: (1) first-degree relatives with a history of colorectal cancer; (2) subjects with a history of cancer or any other malignant tumor; (3) subjects with a history of intestinal polyps; (4) those with two or more of the followings: chronic constipation (constipation lasted for more than 2 months per year in the past two years), chronic diarrhea (diarrhea lasted for more than 3 months in the past two years, and the duration of each episode was more than one week), mucus and bloody stools, history of adverse life events (occurring within the past 20 years and causing greater trauma or distress to the subject after the event), history of chronic appendicitis or appendectomy, history of chronic biliary disease or cholecystectomy. In this study, those who were assessed as high risk by HRFQ were recorded as "HRFQ (+)", and those who were not at high risk were recorded as "HRFQ (-)". The APCS questionnaire provided risk scores based on 4 risk factors including age, gender, family history and smoking: (1) age: 2 points for 50-69 years old, 3 points for 70 years old and above; (2) gender: 1 point for male, 0 point for women; (3) family history: 2 points for first-degree relatives suffering from colorectal cancer; (4) smoking: 1 point for current or past smoking, 0 point for non-smokers. The population was divided into low-risk (0-1 point), intermediate-risk (2-3 points), and high-risk (4-7 points). Those who were assessed as high risk by APCS were recorded as "APCS (+)", and those with intermediate and low risk were recorded as "APCS (-)". The hemoglobin threshold for a positive FIT was set to 100 μg/L. Those who were assessed as high risk by APCS with positive FIT were recorded as "APCS+FIT (+)". Those who were assessed as high risk by APCS with negative FIT, those who were assessed by APCS as low-middle risk with positive FIT, and those who were assessed by APCS as low-middle with negative FIT were all recorded as "APCS+FIT(-)". Observation indicators in this study were as follows: (1) the screening compliance rate of the cohort and the detection of advanced colorectal tumors; (2) positive predictive value, negative predictive value, sensitivity and specificity of HRFQ and APCS and their combination with FIT for screening advanced colorectal tumors; (3) comparison of the detection rate between HRFQ and APCS questionnaire for different colorectal lesions. Using SPSS 21.0 software, the receiver operating characteristic (ROC) curve was drawn to evaluate the clinical value of HRFQ and APCS combined with FIT in screening advanced colorectal tumors. From 2017 to 2018 in Jiashan County, a total of 53 268 target subjects were screened, and 42 093 people actually completed the questionnaire, with a compliance rate of 79.02%. A total of 8145 cases underwent colonoscopy. A total of 3607 cases among HRFQ positive population (5320 cases) underwent colonoscopy, and the colonoscopy compliance rate was 67. 80%; 8 cases were diagnosed with colorectal cancer and 88 cases were advanced colorectal adenoma. A total of 2977 cases among APCS positive population (11 942 cases) underwent colonoscopy, and the colonoscopy compliance rate was 24.93%; 17 cases were diagnosed with colorectal cancer and 148 cases were advanced colorectal adenoma. The positive rate of HRFQ screening was lower than that of APCS [12.6% (5320/42 093) vs. 28.4% (11 942/42 093), χ=3195. 547, <0.001]. In the FIT positive population (6223 cases), a total of 4894 cases underwent colonoscopy, and the colonoscopy compliance rate was 78.64%; 34 cases were diagnosed with colorectal cancer and 224 cases were advanced adenoma. The positive predictive values of HRFQ and APCS and their combination with FIT for screening advanced colorectal tumors were 2.67%, 5.54%, 5.44%, and 8.56%; negative predictive values were 94.89%, 96.85%, 96.11% and 96.99%; sensitivity was 29.27%, 50.30%, 12.20 % and 39.02%; specificity was 55.09%, 64.03%, 91.11% and 82.51%, respectively. The ROC curves constructed by HRFQ, APCS, FIT, HRFQ+FIT and APCS+FIT indicated that APCS+FIT presented the highest efficacy in screening advanced colorectal tumors (AUC: 0.608, 95%CI: 0.574-0.642). The comparison of the detection rates of different colorectal lesions between HRFQ and APCS questionnaires showed that there were no significant differences in detection rate of inflammatory polyps and hyperplastic polyps between the two questionnaires (both >0.05). However, as compared to HRFQ questionnaire, APCS questionnaire had higher detection rates in non-advanced adenomas [26.10% (777/2977) vs. 19.43% (701/3607), χ=51.228, <0.001], advanced adenoma [4.97% (148/2977) vs. 2.44% (88/3607), χ=30.249, <0.001] and colorectal cancer [0.57% (17 /2977) vs. 0.22% (8/3607), χ=5.259, =0.022]. APCS has a higher detection rate of advanced colorectal tumors than HRFQ. APCS combined with FIT can further improve the effectiveness of advanced colorectal tumor screening.
为探讨高危因素问卷(HRFQ)、亚太结直肠癌筛查(APCS)评分及其与粪便免疫化学试验(FIT)联合应用于筛查进展期结直肠肿瘤的效果,为进一步优化癌症筛查方案提供依据。采用回顾性队列研究方法,总结分析2017年3月至2018年7月浙江省嘉善县结直肠肿瘤筛查结果。排除患有严重疾病不适合结肠镜检查者以及存在精神和行为异常无法配合筛查者。在HRFQ问卷中,符合以下任何一项或多项者被列为HRFQ高危人群:(1)有结直肠癌家族史的一级亲属;(2)有癌症或其他恶性肿瘤病史的受试者;(3)有肠息肉病史的受试者;(4)有以下两项或更多项者:慢性便秘(过去两年中每年便秘持续超过2个月)、慢性腹泻(过去两年中腹泻持续超过3个月,且每次发作持续时间超过1周)、黏液血便、不良生活事件史(发生在过去20年内,事件发生后对受试者造成较大创伤或困扰)、慢性阑尾炎或阑尾切除术史、慢性胆道疾病或胆囊切除术史。本研究中,被HRFQ评估为高危者记录为“HRFQ(+)”,非高危者记录为“HRFQ(-)”。APCS问卷根据年龄、性别、家族史和吸烟4个风险因素提供风险评分:(1)年龄:50 - 69岁为2分,70岁及以上为3分;(2)性别:男性为1分,女性为0分;(3)家族史:有患结直肠癌的一级亲属为2分;(4)吸烟:目前或既往吸烟者为1分,非吸烟者为0分。人群分为低风险(0 - 1分)、中风险(2 - 3分)和高风险(4 - 7分)。被APCS评估为高危者记录为“APCS(+)”,中低风险者记录为“APCS(-)”。FIT阳性的血红蛋白阈值设定为100μg/L。被APCS评估为高危且FIT阳性者记录为“APCS+FIT(+)”。被APCS评估为高危但FIT阴性者、被APCS评估为中低风险但FIT阳性者以及被APCS评估为中低风险且FIT阴性者均记录为“APCS+FIT(-)”。本研究的观察指标如下:(1)队列的筛查依从率及进展期结直肠肿瘤的检出情况;(2)HRFQ和APCS及其与FIT联合应用筛查进展期结直肠肿瘤的阳性预测值、阴性预测值、敏感性和特异性;(3)HRFQ和APCS问卷对不同结直肠病变的检出率比较。使用SPSS 21.0软件绘制受试者工作特征(ROC)曲线,评估HRFQ和APCS联合FIT在筛查进展期结直肠肿瘤中的临床价值。2017 - 2018年嘉善县共筛查53268名目标受试者,实际完成问卷42093人,依从率为79.02%。共8145例接受结肠镜检查。HRFQ阳性人群(5320例)中3607例接受结肠镜检查,结肠镜检查依从率为67.80%;8例诊断为结直肠癌,88例为进展期结直肠腺瘤。APCS阳性人群(11942例)中2977例接受结肠镜检查,结肠镜检查依从率为24.93%;17例诊断为结直肠癌,148例为进展期结直肠腺瘤。HRFQ筛查阳性率低于APCS [12.6%(5320/42093)对28.4%(11942/42093),χ = 3195.547,P < 0.001]。在FIT阳性人群(6223例)中,共4894例接受结肠镜检查,结肠镜检查依从率为78.64%;34例诊断为结直肠癌,224例为进展期腺瘤。HRFQ、APCS及其与FIT联合应用筛查进展期结直肠肿瘤的阳性预测值分别为2.67%、5.54%、5.44%和8.56%;阴性预测值分别为94.89%、96.85%、96.11%和96.99%;敏感性分别为29.27%、50.30%、12.20%和39.02%;特异性分别为55.09%、64.03%、91.11%和82.51%。HRFQ、APCS、FIT、HRFQ+FIT和APCS+FIT构建的ROC曲线表明,APCS+FIT在筛查进展期结直肠肿瘤中效能最高(AUC:0.608,95%CI:0.574 - 0.642)。HRFQ和APCS问卷对不同结直肠病变检出率的比较显示,两者在炎性息肉和增生性息肉检出率上无显著差异(均P > 0.05)。然而,与HRFQ问卷相比,APCS问卷在非进展期腺瘤[26.10%(777/2977)对19.43%(701/3607),χ = 51.228,P < 0.001]、进展期腺瘤[4.97%(148/2977)对2.44%(88/3607),χ = 30.249,P < 0.001]和结直肠癌[0.57%(17/2977)对0.22%(8/3607),χ = 5.259,P = 0.022]的检出率上更高。APCS对进展期结直肠肿瘤的检出率高于HRFQ。APCS联合FIT可进一步提高进展期结直肠肿瘤筛查的有效性。