Proposed Nomogram Predicting the Individual Risk of Malignancy in the Patients With Branch Duct Type Intraductal Papillary Mucinous Neoplasms of the Pancreas

This study evaluated individual risks of malignancy and proposed a nomogram for predicting malignancy of branch duct type intraductal papillary mucinous neoplasms (BD-IPMNs) using the large database for IPMN. Although consensus guidelines list several malignancy predicting factors in patients with B...

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Veröffentlicht in:Annals of surgery 2017-12, Vol.266 (6), p.1062-1068
Hauptverfasser: Jang, Jin-Young, Park, Taesung, Lee, Selyeong, Kim, Yongkang, Lee, Seung Yeoun, Kim, Sun-Whe, Kim, Song-Cheol, Song, Ki-Byung, Yamamoto, Masakazu, Hatori, Takashi, Hirono, Seiko, Satoi, Sohei, Fujii, Tsutomu, Hirano, Satoshi, Hashimoto, Yasushi, Shimizu, Yashuhiro, Choi, Dong Wook, Choi, Seong Ho, Heo, Jin Seok, Motoi, Fuyuhiko, Matsumoto, Ippei, Lee, Woo Jung, Kang, Chang Moo, Han, Ho-Seong, Yoon, Yoo-Seok, Sho, Masayuki, Nagano, Hiroaki, Honda, Goro, Kim, Sang Geol, Yu, Hee Chul, Chung, Jun Chul, Nagakawa, Yuichi, Seo, Hyung Il, Yamaue, Hiroki
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Sprache:eng
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Zusammenfassung:This study evaluated individual risks of malignancy and proposed a nomogram for predicting malignancy of branch duct type intraductal papillary mucinous neoplasms (BD-IPMNs) using the large database for IPMN. Although consensus guidelines list several malignancy predicting factors in patients with BD-IPMN, those variables have different predictability and individual quantitative prediction of malignancy risk is limited. Clinicopathological factors predictive of malignancy were retrospectively analyzed in 2525 patients with biopsy proven BD-IPMN at 22 tertiary hospitals in Korea and Japan. The patients with main duct dilatation >10 mm and inaccurate information were excluded. The study cohort consisted of 2258 patients. Malignant IPMNs were defined as those with high grade dysplasia and associated invasive carcinoma. Of 2258 patients, 986 (43.7%) had low, 443 (19.6%) had intermediate, 398 (17.6%) had high grade dysplasia, and 431 (19.1%) had invasive carcinoma. To construct and validate the nomogram, patients were randomly allocated into training and validation sets, with fixed ratios of benign and malignant lesions. Multiple logistic regression analysis resulted in five variables (cyst size, duct dilatation, mural nodule, serum CA19-9, and CEA) being selected to construct the nomogram. In the validation set, this nomogram showed excellent discrimination power through a 1000 times bootstrapped calibration test. A nomogram predicting malignancy in patients with BD-IPMN was constructed using a logistic regression model. This nomogram may be useful in identifying patients at risk of malignancy and for selecting optimal treatment methods. The nomogram is freely available at http://statgen.snu.ac.kr/software/nomogramIPMN.
ISSN:0003-4932
1528-1140
DOI:10.1097/SLA.0000000000001985