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Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy

The value of the serum tumour marker CA 125 to date has been in the monitoring of ovarian cancer patients for response to therapy and for recurrence of disease. However, despite the availability of serial data on CA 125, the problem of interpreting a change over time is still unsolved. The aim of th...

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Autores principales: Tuxen, M K, Sölétormos, G, Dombernowsky, P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363637/
https://www.ncbi.nlm.nih.gov/pubmed/11355938
http://dx.doi.org/10.1054/bjoc.2001.1787
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author Tuxen, M K
Sölétormos, G
Dombernowsky, P
author_facet Tuxen, M K
Sölétormos, G
Dombernowsky, P
author_sort Tuxen, M K
collection PubMed
description The value of the serum tumour marker CA 125 to date has been in the monitoring of ovarian cancer patients for response to therapy and for recurrence of disease. However, despite the availability of serial data on CA 125, the problem of interpreting a change over time is still unsolved. The aim of this study was to assess the ability of CA 125 to monitor patients with ovarian cancer during postoperative chemotherapy. 255 patients with stage IC-IV ovarian cancer were allocated to the tumour marker monitoring study. The evaluation of CA 125 information was based on the analytical imprecision, the normal intra-individual biological variation, the sampling interval, and the cut-off value. Additionally, a new assessment criterion based upon an increment of 2.5 times the baseline CA 125 concentration confirmed by a third measurement was elaborated and the utility investigated. The efficiency of CA 125 for identifying progression and non-progression during first-line chemotherapy was 91.9%. The median lead time for true positive results was 41 days. Using the new elaborated criterion the efficiency of CA 125 for identifying progression and non-progression during first-line chemotherapy was 90.5%. The median lead time for true positive results was 35 days. CA 125 gave reliable prediction of progressive disease during postoperative chemotherapy. The results indicate a high applicability of the presented progression criteria during CA 125 monitoring of patients with changing activity of ovarian cancer. © 2001 Cancer Research Campaign www.bjcancer.com
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spelling pubmed-23636372009-09-10 Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy Tuxen, M K Sölétormos, G Dombernowsky, P Br J Cancer Regular Article The value of the serum tumour marker CA 125 to date has been in the monitoring of ovarian cancer patients for response to therapy and for recurrence of disease. However, despite the availability of serial data on CA 125, the problem of interpreting a change over time is still unsolved. The aim of this study was to assess the ability of CA 125 to monitor patients with ovarian cancer during postoperative chemotherapy. 255 patients with stage IC-IV ovarian cancer were allocated to the tumour marker monitoring study. The evaluation of CA 125 information was based on the analytical imprecision, the normal intra-individual biological variation, the sampling interval, and the cut-off value. Additionally, a new assessment criterion based upon an increment of 2.5 times the baseline CA 125 concentration confirmed by a third measurement was elaborated and the utility investigated. The efficiency of CA 125 for identifying progression and non-progression during first-line chemotherapy was 91.9%. The median lead time for true positive results was 41 days. Using the new elaborated criterion the efficiency of CA 125 for identifying progression and non-progression during first-line chemotherapy was 90.5%. The median lead time for true positive results was 35 days. CA 125 gave reliable prediction of progressive disease during postoperative chemotherapy. The results indicate a high applicability of the presented progression criteria during CA 125 monitoring of patients with changing activity of ovarian cancer. © 2001 Cancer Research Campaign www.bjcancer.com Nature Publishing Group 2001-05 /pmc/articles/PMC2363637/ /pubmed/11355938 http://dx.doi.org/10.1054/bjoc.2001.1787 Text en Copyright © 2001 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Regular Article
Tuxen, M K
Sölétormos, G
Dombernowsky, P
Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title_full Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title_fullStr Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title_full_unstemmed Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title_short Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy
title_sort serum tumour marker ca 125 in monitoring of ovarian cancer during first-line chemotherapy
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363637/
https://www.ncbi.nlm.nih.gov/pubmed/11355938
http://dx.doi.org/10.1054/bjoc.2001.1787
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