VISSER, Nicole C. M., Louis J. M. VAN DER PUTTEN, Alex VAN EGERSCHOT, Koen K. VAN DE VIJVER, Maria SANTACANA, Peter BRONSERT, Marc HIRSCHFELD, Eva COLAS, Antonio GIL-MORENO, Angel GARCIA, Gemma MANCEBO, Francesc ALAMEDA, Camilla KRAKSTAD, Ingvild L. TANGEN, Jutta HUVILA, Stefanie SCHRAUWEN, Martin KOSKAS, Francine WALKER, Vít WEINBERGER, Luboš MINÁŘ, Jitka HAUSNEROVÁ, Marc P. L. M. SNIJDERS, Saskia VAN DEN BERG-VAN ERP, Xavier MATIAS-GUIU, Jone TROVIK, Frederic AMANT, Leon F. A. G. MASSUGER, Johan BULTEN and Johanna M. A. PIJNENBORG. Addition of IMP3 to L1CAM for discrimination between low- and high-grade endometrial carcinomas: a European Network for Individualised Treatment of Endometrial Cancer collaboration study. Human pathology. Philadelphia, PA: W.B. Saunders Company, 2019, vol. 89, JUL 2019, p. 90-98. ISSN 0046-8177. Available from: https://dx.doi.org/10.1016/j.humpath.2019.04.014.
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Basic information
Original name Addition of IMP3 to L1CAM for discrimination between low- and high-grade endometrial carcinomas: a European Network for Individualised Treatment of Endometrial Cancer collaboration study
Authors VISSER, Nicole C. M. (528 Netherlands, guarantor), Louis J. M. VAN DER PUTTEN (528 Netherlands), Alex VAN EGERSCHOT (528 Netherlands), Koen K. VAN DE VIJVER (56 Belgium), Maria SANTACANA (724 Spain), Peter BRONSERT (276 Germany), Marc HIRSCHFELD (276 Germany), Eva COLAS (724 Spain), Antonio GIL-MORENO (724 Spain), Angel GARCIA (724 Spain), Gemma MANCEBO (724 Spain), Francesc ALAMEDA (724 Spain), Camilla KRAKSTAD (578 Norway), Ingvild L. TANGEN (578 Norway), Jutta HUVILA (246 Finland), Stefanie SCHRAUWEN (56 Belgium), Martin KOSKAS (250 France), Francine WALKER (250 France), Vít WEINBERGER (203 Czech Republic, belonging to the institution), Luboš MINÁŘ (203 Czech Republic, belonging to the institution), Jitka HAUSNEROVÁ (203 Czech Republic, belonging to the institution), Marc P. L. M. SNIJDERS (528 Netherlands), Saskia VAN DEN BERG-VAN ERP (528 Netherlands), Xavier MATIAS-GUIU (724 Spain), Jone TROVIK (578 Norway), Frederic AMANT (56 Belgium), Leon F. A. G. MASSUGER (528 Netherlands), Johan BULTEN (528 Netherlands) and Johanna M. A. PIJNENBORG (528 Netherlands).
Edition Human pathology, Philadelphia, PA, W.B. Saunders Company, 2019, 0046-8177.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30109 Pathology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 2.735
RIV identification code RIV/00216224:14110/19:00112954
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1016/j.humpath.2019.04.014
UT WoS 000477688900011
Keywords in English Endometrial carcinoma; Diagnostic biomarker; Prognostic biomarker; IMP3; L1CAM
Tags 14110230, 14110411, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Tereza Miškechová, učo 341652. Changed: 17/2/2020 08:55.
Abstract
Discrimination between low- and high-grade endometrial carcinomas (ECs) is clinically relevant but can be challenging for pathologists, with moderate interobserver agreement. Insulin-like growth factor-II mRNA-binding protein 3 (IMP3) is an oncofoetal protein that is associated with nonendometrioid endometrial carcinomas but has been limited studied in endometrioid carcinomas. The aim of this study is to investigate the diagnostic and prognostic value of IMP3 in the discrimination between low- and high-grade ECs and its added value to L1CAM. IMP3 and L1CAM expression was assessed in tumors from 378 patients treated for EC at 1 of 9 participating European Network for Individualised Treatment of Endometrial Cancer centers. IMP3 was expressed in 24.6% of the tumors. In general, IMP3 was more homogeneously expressed than L1CAM. IMP3 expression was significantly associated with advanced stage, nonendometrioid histology, grade 3 tumors, deep myometrial invasion, lymphovascular space invasion, distant recurrences, overall mortality, and disease-related mortality. Simultaneous absence of IMP3 and Ll CAM expression showed the highest accuracy for identifying low-grade carcinomas (area under the curve 0.766), whereas simultaneous expression of IMP3 and L1CAM was strongly associated with high-grade carcinomas (odds ratio 19.7; 95% confidence interval 9.2-42.2). Even within endometrioid carcinomas, this combination remained superior to IMP3 and L1CAM alone (odds ratio 8.6; 95% confidence interval 3.4-21.9). In conclusion, IMP3 has good diagnostic value and together with L1CAM represents the optimal combination of diagnostic markers for discrimination between low- and high-grade ECs compared to IMP3 and L1CAM alone. Because of the homogenous expression of IMP3, this marker might be valuable in preoperative biopsies when compared to the more patchy L1CAM expression. (C) 2019 Elsevier Inc. All rights reserved.
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