Literature DB >> 32332003

An elevated CA 19-9 is associated with invasive cancer and worse survival in IPMN.

D Ciprani1, V Morales-Oyarvide1, M Qadan1, T Hank1, M Weniger1, J M Harrison1, C Rodrigues1, N K Horick2, M Mino-Kenudson3, C R Ferrone1, A L Warshaw1, K D Lillemoe1, C Fernández-Del Castillo4.   

Abstract

BACKGROUND: Current guidelines for IPMN include an elevated serum carbohydrate antigen (CA) 19-9 among the worrisome features. However, the correlation of CA 19-9 with histological malignant features and survival is unclear. Serum CEA is also currently used for preoperative management of IPMN, although its measurement is not evidence-based. Accordingly, we aimed to assess the role of these tumor markers as predictors of malignancy in IPMN.
METHODS: IPMN resected between 1998 and 2018 at Massachusetts General Hospital were analyzed. Clinical, pathological and survival data were collected and compared to preoperative levels of CA 19-9 and CEA. Receiver operating characteristic (ROC) and Cox regression analyses were performed considering cut-offs of 37 U/ml (CA 19-9) and 5 μg/l (CEA).
RESULTS: Analysis of 594 patients showed that preoperative CA 19-9 levels > 37 U/ml (n = 128) were associated with an increased likelihood of invasive carcinoma when compared to normal levels (45.3% vs. 18.0%, P < 0.001), while there was no difference with respect to high-grade dysplasia (32.9% vs 31.9%, P = 0.88). The proportion of concurrent pancreatic cancer was higher in patients with CA 19-9 > 37 U/ml (17.2% vs 4.9%, P < 0.001). An elevated CA 19-9 was also associated with worse overall and disease-free survival (HR = 1.943, P = 0.007 and HR = 2.484, P < 0.001 respectively). CEA levels did not correlate with malignancy.
CONCLUSION: In patients with IPMN, serum CA19-9 > 37 U/ml is associated with invasive IPMN and concurrent pancreatic cancer as well as worse survival, but not with high-grade dysplasia. Serum CEA appears to have minimal utility in the management of these patients.
Copyright © 2020 IAP and EPC. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CA 19-9; CEA; Intraductal papillary mucinous neoplasm; Malignancy; Survival

Mesh:

Substances:

Year:  2020        PMID: 32332003     DOI: 10.1016/j.pan.2020.04.002

Source DB:  PubMed          Journal:  Pancreatology        ISSN: 1424-3903            Impact factor:   3.996


  11 in total

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Authors:  Joseph R Habib; Benedict Kinny-Köster; Neda Amini; Sami Shoucair; John L Cameron; Elizabeth D Thompson; Elliot K Fishman; Ralph H Hruban; Ammar A Javed; Jin He; Christopher L Wolfgang
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Review 3.  UEG position paper on pancreatic cancer. Bringing pancreatic cancer to the 21st century: Prevent, detect, and treat the disease earlier and better.

Authors:  Patrick Michl; Matthias Löhr; John P Neoptolemos; Gabriele Capurso; Vinciane Rebours; Nuria Malats; Mathilde Ollivier; Luigi Ricciardiello
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4.  Extracellular Vesicle Analysis Allows for Identification of Invasive IPMN.

Authors:  Katherine S Yang; Debora Ciprani; Aileen O'Shea; Andrew S Liss; Robert Yang; Sarah Fletcher-Mercaldo; Mari Mino-Kenudson; Carlos Fernández-Del Castillo; Ralph Weissleder
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Review 5.  Intraductal Pancreatic Mucinous Neoplasms: A Tumor-Biology Based Approach for Risk Stratification.

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Review 6.  Humoral Predictors of Malignancy in IPMN: A Review of the Literature.

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8.  The molecular, immune features, and risk score construction of intraductal papillary mucinous neoplasm patients.

Authors:  Xing Huang; Yipeng Feng; Dawei Ma; Hanlin Ding; Gaochao Dong; Yan Chen; Xiaochen Huang; Jingyuan Zhang; Xinyu Xu; Chen Chen
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9.  Nomogram to predict malignancy in branch duct type intraductal papillary mucinous neoplasms.

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Review 10.  Pathology of intraductal papillary mucinous neoplasms.

Authors:  Naziheh Assarzadegan; Elizabeth Thompson; Kevan Salimian; Matthias M Gaida; Lodewijk A A Brosens; Laura Wood; Syed Z Ali; Ralph H Hruban
Journal:  Langenbecks Arch Surg       Date:  2021-05-28       Impact factor: 2.895

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