Development and external validation of a faecal immunochemical test-based prediction model for colorectal cancer detection in symptomatic patients

被引:47
|
作者
Cubiella, Joaquin [1 ,2 ]
Vega, Pablo [1 ]
Salve, Maria [1 ]
Diaz-Ondina, Marta [3 ]
Teresa Alves, Maria [4 ]
Quintero, Enrique [5 ,6 ]
Alvarez-Sanchez, Victoria [7 ]
Fernandez-Banares, Fernando [8 ]
Boadas, Jaume [9 ]
Campo, Rafel [10 ]
Bujanda, Luis [11 ]
Clofent, Joan [12 ]
Ferrandez, Angel [13 ]
Torrealba, Leyanira [14 ]
Pinol, Virginia [14 ]
Rodriguez-Alcalde, Daniel [15 ]
Hernandez, Vicent [2 ,16 ]
Fernandez-Seara, Javier [1 ,2 ]
机构
[1] Complexo Hosp Univ Ourense, Gastroenterol Dept, Rua Ramon Puga 52-54, Orense 32005, Spain
[2] Inst Invest Biomed IBI Ourense Pontevedra & Vigo, Rua Ramon Puga 52-54, Orense 32005, Spain
[3] Complexo Hosp Univ Ourense, Clin Anal Dept, Rua Ramon Puga 52-54, Orense 32005, Spain
[4] Univ Vigo, NECOM Grp, Campus Univ As Lagoas, Vigo 36310, Spain
[5] Univ La Laguna, Inst Univ Tecnol Biomed ITB, Gastroenterol Dept, Hosp Univ Canarias, Carretera Ofra S-N, San Cristobal Laguna 38320, Santa Cruz De T, Spain
[6] Univ La Laguna, Ctr Invest Biomed Canarias CIBICAN, Carretera Ofra S-N, San Cristobal Laguna 38320, Santa Cruz De T, Spain
[7] Complejo Hosp Pontevedra, Gastroenterol Dept, Ave Montecelo, Casas Novas 36164, Pontevedra, Spain
[8] Hosp Univ Mutua Terrassa, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Gastroenterol Dept, Placa Doctor Robert 5, Barcelona 08221, Spain
[9] Consorci Sanitari Terrassa, Gastroenterol Dept, Carr Torrebonica S-N, Barcelona 08227, Spain
[10] Corp Sanitaria & Univ Parc Tauli, Hosp Sabadell, Gastroenterol Dept, Parc Tauli 1, Barcelona 08208, Spain
[11] Univ Basque Country UPV EHU, CIBERehd, Biodonostia Inst, Donostia Hosp, Paseo Doctor Begiristain 117, San Sebastian 20080, Guipuzcoa, Spain
[12] Hosp Sagunto, Gastroenterol Dept, Ave Ramon & Cajal S-N, Valencia 46520, Spain
[13] Univ Zaragoza, CIBERehd, Serv Aparato Digestivo, Hosp Clin Univ,IIS Aragen, San Juan Bosco 15, E-50009 Zaragoza, Spain
[14] Hosp Dr Josep Trueta, Gastroenterol Dept, Ave Francia S-N, Girona 17007, Spain
[15] Hosp Univ Mostoles, Digest Dis Sect, Rio Jucar S-N, Madrid 28935, Spain
[16] Gastroenterol Dept, Vigo, Pontevedra, Spain
来源
BMC MEDICINE | 2016年 / 14卷
关键词
Colorectal cancer; Faecal immunochemical test; Colonoscopy; Diagnostic accuracy; Risk stratification; Prompt diagnosis; CONSULTATION QUESTIONNAIRE; SCORING SYSTEM; PRIMARY-CARE; RISK; HEMOGLOBIN; GUIDELINES; QUALITY; INDICATORS; DIAGNOSIS; PEOPLE;
D O I
10.1186/s12916-016-0668-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Risk prediction models for colorectal cancer (CRC) detection in symptomatic patients based on available biomarkers may improve CRC diagnosis. Our aim was to develop, compare with the NICE referral criteria and externally validate a CRC prediction model, COLONPREDICT, based on clinical and laboratory variables. Methods: This prospective cross-sectional study included consecutive patients with gastrointestinal symptoms referred for colonoscopy between March 2012 and September 2013 in a derivation cohort and between March 2014 and March 2015 in a validation cohort. In the derivation cohort, we assessed symptoms and the NICE referral criteria, and determined levels of faecal haemoglobin and calprotectin, blood haemoglobin, and serum carcinoembryonic antigen before performing an anorectal examination and a colonoscopy. A multivariate logistic regression analysis was used to develop the model with diagnostic accuracy with CRC detection as the main outcome. Results: We included 1572 patients in the derivation cohort and 1481 in the validation cohorts, with a 13.6 % and 9. 1 % CRC prevalence respectively. The final prediction model included 11 variables: age (years) (odds ratio [OR] 1.04, 95 % confidence interval [CI] 1.02-1.06), male gender (OR 2.2, 95 % CI 1.5-3.4), faecal haemoglobin >= 20 mu g/g (OR 17.0, 95 % CI 10.0-28.6), blood haemoglobin <10 g/dL (OR 4.8, 95 % CI 2.2-10.3), blood haemoglobin 10-12 g/dL (OR 1.8, 95 % CI 1.1-3.0), carcinoembryonic antigen >= 3 ng/mL (OR 4.5, 95 % CI 3.0-6.8), acetylsalicylic acid treatment (OR 0.4, 95 % CI 0.2-0.7), previous colonoscopy (OR 0.1, 95 % CI 0.06-0.2), rectal mass (OR 14.8, 95 % CI 5.3-41.0), benign anorectal lesion (OR 0.3, 95 % CI 0.2-0.4), rectal bleeding (OR 2.2, 95 % CI 1.4-3.4) and change in bowel habit (OR 1.7, 95 % CI 1.1-2.5). The area under the curve (AUC) was 0.92 (95 % CI 0.91-0.94), higher than the NICE referral criteria (AUC 0.59, 95 % CI 0.55-0.63; p < 0.001). On the basis of the thresholds with 90 % (5.6) and 99 % (3.5) sensitivity, we divided the derivation cohort into three risk groups for CRC detection: high (30.9 % of the cohort, positive predictive value [PPV] 40.7 %, 95 % CI 36.7-45.9 %), intermediate (29.5 %, PPV 4.4 %, 95 % CI 2.8-6.8 %) and low (39.5 %, PPV 0.2 %, 95 % CI 0.0-1.1 %). The discriminatory ability was equivalent in the validation cohort (AUC 0.92, 95 % CI 0.90-0.94; p = 0.7). Conclusions: COLONPREDICT is a highly accurate prediction model for CRC detection.
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页数:13
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