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YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer

OBJECTIVE: To evaluate the use of YKL-40 in the discrimination between benign and malignant adnexal mass and to determine its prognostic value in assessing residual tumor after primary cytoreduction and platinum sensitivity in serous epithelial ovarian carcinoma (EOC). MATERIALS AND METHODS: During...

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Autores principales: Kahramanoğlu, İlker, Tokgözoğlu, Nedim, Turan, Hasan, Şal, Veysel, Şimşek, Gönül, Gelişgen, Remise, Beşe, Tugan, Demirkıran, Fuat, Arvas, Macit, Uzun, Hafize
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127478/
https://www.ncbi.nlm.nih.gov/pubmed/30202628
http://dx.doi.org/10.4274/tjod.28459
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author Kahramanoğlu, İlker
Tokgözoğlu, Nedim
Turan, Hasan
Şal, Veysel
Şimşek, Gönül
Gelişgen, Remise
Beşe, Tugan
Demirkıran, Fuat
Arvas, Macit
Uzun, Hafize
author_facet Kahramanoğlu, İlker
Tokgözoğlu, Nedim
Turan, Hasan
Şal, Veysel
Şimşek, Gönül
Gelişgen, Remise
Beşe, Tugan
Demirkıran, Fuat
Arvas, Macit
Uzun, Hafize
author_sort Kahramanoğlu, İlker
collection PubMed
description OBJECTIVE: To evaluate the use of YKL-40 in the discrimination between benign and malignant adnexal mass and to determine its prognostic value in assessing residual tumor after primary cytoreduction and platinum sensitivity in serous epithelial ovarian carcinoma (EOC). MATERIALS AND METHODS: During the three years from January 2015 to December 2017, a nonconsecutive series of 100 patient (60 malignant, 40 benign) who underwent surgery for an adnexal mass were enrolled in the study. Preoperatively, serum samples were collected for YKL-40 level analysis. RESULTS: YKL-40 [receiver operator characteristics (ROC)-area under curve (AUC)=0.83] was a significantly better predictor of EOC than cancer antigen-125 (ROC-AUC=0.75). Using a cut-off for YKL-40 of 47.7 ng/mL had a sensitivity of 80% and a specificity of 70%. Higher serum YKL-40 levels were associated with advanced stage, higher grade, residual tumor after primary cytoreduction and recurrence. Platinum-sensitive patients had significantly elevated levels of YKL-40 compared with platinum-resistant or refractory patients. CONCLUSION: The results obtained from our study support the use of serum YKL-40 for the discrimination between malignant and benign ovarian tumors. YKL-40 levels in patients with serous EOC may also predict disease residual disease after primary cytoreduction and recurrence. Further studies are needed to understand the relationship between YKL-40 and platinum sensitivity.
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spelling pubmed-61274782018-09-10 YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer Kahramanoğlu, İlker Tokgözoğlu, Nedim Turan, Hasan Şal, Veysel Şimşek, Gönül Gelişgen, Remise Beşe, Tugan Demirkıran, Fuat Arvas, Macit Uzun, Hafize Turk J Obstet Gynecol Clinical Investigation OBJECTIVE: To evaluate the use of YKL-40 in the discrimination between benign and malignant adnexal mass and to determine its prognostic value in assessing residual tumor after primary cytoreduction and platinum sensitivity in serous epithelial ovarian carcinoma (EOC). MATERIALS AND METHODS: During the three years from January 2015 to December 2017, a nonconsecutive series of 100 patient (60 malignant, 40 benign) who underwent surgery for an adnexal mass were enrolled in the study. Preoperatively, serum samples were collected for YKL-40 level analysis. RESULTS: YKL-40 [receiver operator characteristics (ROC)-area under curve (AUC)=0.83] was a significantly better predictor of EOC than cancer antigen-125 (ROC-AUC=0.75). Using a cut-off for YKL-40 of 47.7 ng/mL had a sensitivity of 80% and a specificity of 70%. Higher serum YKL-40 levels were associated with advanced stage, higher grade, residual tumor after primary cytoreduction and recurrence. Platinum-sensitive patients had significantly elevated levels of YKL-40 compared with platinum-resistant or refractory patients. CONCLUSION: The results obtained from our study support the use of serum YKL-40 for the discrimination between malignant and benign ovarian tumors. YKL-40 levels in patients with serous EOC may also predict disease residual disease after primary cytoreduction and recurrence. Further studies are needed to understand the relationship between YKL-40 and platinum sensitivity. Galenos Publishing 2018-09 2018-09-03 /pmc/articles/PMC6127478/ /pubmed/30202628 http://dx.doi.org/10.4274/tjod.28459 Text en ©Copyright 2018 by Turkish Society of Obstetrics and Gynecology Turkish Journal of Obstetrics and Gynecology published by Galenos Publishing House. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Investigation
Kahramanoğlu, İlker
Tokgözoğlu, Nedim
Turan, Hasan
Şal, Veysel
Şimşek, Gönül
Gelişgen, Remise
Beşe, Tugan
Demirkıran, Fuat
Arvas, Macit
Uzun, Hafize
YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title_full YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title_fullStr YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title_full_unstemmed YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title_short YKL-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
title_sort ykl-40 in the diagnosis, prediction of prognosis, and platinum sensitivity in serous epithelial ovarian cancer
topic Clinical Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127478/
https://www.ncbi.nlm.nih.gov/pubmed/30202628
http://dx.doi.org/10.4274/tjod.28459
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