MINÁŘ, Luboš, Ivanka KLABENEŠOVÁ, Eva JANDÁKOVÁ, Filip ZLÁMAL and Julie BIENERTOVÁ VAŠKŮ. Is human epididymis protein 4 an effective tool for the differential diagnosis of benign and malignant endometrial tumours? European Journal of Gynaecological Oncology. Montreal: IROG CANADA, 2016, vol. 37, No 5, p. 617-621. ISSN 0392-2936. Available from: https://dx.doi.org/10.12892/ejgo3090.2016.
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Basic information
Original name Is human epididymis protein 4 an effective tool for the differential diagnosis of benign and malignant endometrial tumours?
Authors MINÁŘ, Luboš (203 Czech Republic, guarantor, belonging to the institution), Ivanka KLABENEŠOVÁ (203 Czech Republic), Eva JANDÁKOVÁ (203 Czech Republic), Filip ZLÁMAL (203 Czech Republic, belonging to the institution) and Julie BIENERTOVÁ VAŠKŮ (203 Czech Republic, belonging to the institution).
Edition European Journal of Gynaecological Oncology, Montreal, IROG CANADA, 2016, 0392-2936.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30214 Obstetrics and gynaecology
Country of publisher Canada
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 0.692
RIV identification code RIV/00216224:14110/16:00091106
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.12892/ejgo3090.2016
UT WoS 000385055500004
Keywords in English Benign endometrial tumours; Endometrial cancer; Human epididymis protein 4.
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 14/11/2016 09:30.
Abstract
Purpose of investigation: This study was designed to evaluate the use of human epididymis protein 4 (HE4) as a biomarker in the differential diagnosis of malignant and benign endometrial tumours. Materials and Methods: The study, conducted between July 2009 and June 2014, included a total of 150 patients with endometrioid adenocarcinoma and a control group of 150 patients with benign endometrial lesions. The serum of all patients was analyzed with respect to HE4 and CA125 levels. The median and ranges of serum levels were determined in relation to histological results. The statistical analysis procedure employed in this study utilized logarithmic-transformed values of biomarkers and logistic regression. Results: An analysis of two groups of patients with different histologies yielded a statistically significant difference (p-value < 0.05) only in the case of HE4, in which case a cut-off value of 48.5 pmol/l resulted in an achieved sensitivity of 87.8%, a specificity of 56.6%, and a negative predictive value of 81.1%. Conclusion: In combination with clinical and ultrasound findings, HE4 could help with the differentiation of prognostically varied patient groups as well as with the decision-making process associated with the development of individual treatment plans. However, the optimal cut-off for HE4 has not been established yet and further studies are needed.
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