Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors

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Standard

Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors. / Jensen, Kenneth Højsgaard; Hilsted, Linda; Jensen, Claus Verner; Mynster, Tommie; Rehfeld, Jens F; Knigge, Ulrich.

In: Scandinavian Journal of Gastroenterology, Vol. 48, No. 1, 2013, p. 70-77.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jensen, KH, Hilsted, L, Jensen, CV, Mynster, T, Rehfeld, JF & Knigge, U 2013, 'Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors', Scandinavian Journal of Gastroenterology, vol. 48, no. 1, pp. 70-77. https://doi.org/10.3109/00365521.2012.733953

APA

Jensen, K. H., Hilsted, L., Jensen, C. V., Mynster, T., Rehfeld, J. F., & Knigge, U. (2013). Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors. Scandinavian Journal of Gastroenterology, 48(1), 70-77. https://doi.org/10.3109/00365521.2012.733953

Vancouver

Jensen KH, Hilsted L, Jensen CV, Mynster T, Rehfeld JF, Knigge U. Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors. Scandinavian Journal of Gastroenterology. 2013;48(1):70-77. https://doi.org/10.3109/00365521.2012.733953

Author

Jensen, Kenneth Højsgaard ; Hilsted, Linda ; Jensen, Claus Verner ; Mynster, Tommie ; Rehfeld, Jens F ; Knigge, Ulrich. / Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors. In: Scandinavian Journal of Gastroenterology. 2013 ; Vol. 48, No. 1. pp. 70-77.

Bibtex

@article{400c67f5fa354a3eb065e48aba798735,
title = "Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors",
abstract = "Abstract Objective. The correlation between plasma Chromogranin A concentrations and changes in tumor size evaluated by computed tomography (CT) - as a gold standard - was evaluated. Material and methods. One hundred and sixteen patients with CgA-producing ileo-cecal neuroendocrine tumors were evaluated by events, which were recorded when a CT was followed by another CT 1 - 12 months later. Change in tumor size was defined as regression, progression, or stable disease using RECIST criteria 1.1. Of 426 events, there were 97 with progression, 279 with stable disease, and 50 with regression. Based on the ROC curves a cutoff value of 25% change was selected to discriminate between increased, decreased, or unchanged CgA concentrations in plasma, using a sensitive radioimmunoassay with well-defined epitope specificity. Results. In the 97 events showing tumor progression diagnostic sensitivity and specificity of an increased CgA concentration were 86% and 86%, respectively. The positive and negative predictive values were 64% and 85%, respectively. In the 279 events with unchanged tumor size the diagnostic sensitivity and specificity of an unchanged CgA concentration were 73% and 86%, and the positive and negative predictive values were 91% and 63%, respectively. In the 50 events showing tumor regression, diagnostic sensitivity and specificity of a decrease in CgA concentration were 78% and 91%, the positive and negative predictive values being 55% and 97%. Conclusions. CgA concentrations in plasma have a high diagnostic accuracy in monitoring patients with ileo-cecal neuroendocrine tumors. In particular, an increase in plasma CgA concentration was useful to indicate tumor progression.",
author = "Jensen, {Kenneth H{\o}jsgaard} and Linda Hilsted and Jensen, {Claus Verner} and Tommie Mynster and Rehfeld, {Jens F} and Ulrich Knigge",
year = "2013",
doi = "10.3109/00365521.2012.733953",
language = "English",
volume = "48",
pages = "70--77",
journal = "Scandinavian Journal of Gastroenterology",
issn = "0036-5521",
publisher = "Taylor & Francis",
number = "1",

}

RIS

TY - JOUR

T1 - Chromogranin A is a sensitive marker of progression or regression in ileo-cecal neuroendocrine tumors

AU - Jensen, Kenneth Højsgaard

AU - Hilsted, Linda

AU - Jensen, Claus Verner

AU - Mynster, Tommie

AU - Rehfeld, Jens F

AU - Knigge, Ulrich

PY - 2013

Y1 - 2013

N2 - Abstract Objective. The correlation between plasma Chromogranin A concentrations and changes in tumor size evaluated by computed tomography (CT) - as a gold standard - was evaluated. Material and methods. One hundred and sixteen patients with CgA-producing ileo-cecal neuroendocrine tumors were evaluated by events, which were recorded when a CT was followed by another CT 1 - 12 months later. Change in tumor size was defined as regression, progression, or stable disease using RECIST criteria 1.1. Of 426 events, there were 97 with progression, 279 with stable disease, and 50 with regression. Based on the ROC curves a cutoff value of 25% change was selected to discriminate between increased, decreased, or unchanged CgA concentrations in plasma, using a sensitive radioimmunoassay with well-defined epitope specificity. Results. In the 97 events showing tumor progression diagnostic sensitivity and specificity of an increased CgA concentration were 86% and 86%, respectively. The positive and negative predictive values were 64% and 85%, respectively. In the 279 events with unchanged tumor size the diagnostic sensitivity and specificity of an unchanged CgA concentration were 73% and 86%, and the positive and negative predictive values were 91% and 63%, respectively. In the 50 events showing tumor regression, diagnostic sensitivity and specificity of a decrease in CgA concentration were 78% and 91%, the positive and negative predictive values being 55% and 97%. Conclusions. CgA concentrations in plasma have a high diagnostic accuracy in monitoring patients with ileo-cecal neuroendocrine tumors. In particular, an increase in plasma CgA concentration was useful to indicate tumor progression.

AB - Abstract Objective. The correlation between plasma Chromogranin A concentrations and changes in tumor size evaluated by computed tomography (CT) - as a gold standard - was evaluated. Material and methods. One hundred and sixteen patients with CgA-producing ileo-cecal neuroendocrine tumors were evaluated by events, which were recorded when a CT was followed by another CT 1 - 12 months later. Change in tumor size was defined as regression, progression, or stable disease using RECIST criteria 1.1. Of 426 events, there were 97 with progression, 279 with stable disease, and 50 with regression. Based on the ROC curves a cutoff value of 25% change was selected to discriminate between increased, decreased, or unchanged CgA concentrations in plasma, using a sensitive radioimmunoassay with well-defined epitope specificity. Results. In the 97 events showing tumor progression diagnostic sensitivity and specificity of an increased CgA concentration were 86% and 86%, respectively. The positive and negative predictive values were 64% and 85%, respectively. In the 279 events with unchanged tumor size the diagnostic sensitivity and specificity of an unchanged CgA concentration were 73% and 86%, and the positive and negative predictive values were 91% and 63%, respectively. In the 50 events showing tumor regression, diagnostic sensitivity and specificity of a decrease in CgA concentration were 78% and 91%, the positive and negative predictive values being 55% and 97%. Conclusions. CgA concentrations in plasma have a high diagnostic accuracy in monitoring patients with ileo-cecal neuroendocrine tumors. In particular, an increase in plasma CgA concentration was useful to indicate tumor progression.

U2 - 10.3109/00365521.2012.733953

DO - 10.3109/00365521.2012.733953

M3 - Journal article

C2 - 23094948

VL - 48

SP - 70

EP - 77

JO - Scandinavian Journal of Gastroenterology

JF - Scandinavian Journal of Gastroenterology

SN - 0036-5521

IS - 1

ER -

ID: 48501076