Plasma thymus and activation-regulated chemokine as an early response marker in classical Hodgkin’s lymphoma
Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and r...
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Published in | Haematologica (Roma) Vol. 97; no. 3; pp. 410 - 415 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Pavia
Ferrata Storti Foundation
01.03.2012
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Online Access | Get full text |
ISSN | 0390-6078 1592-8721 1592-8721 |
DOI | 10.3324/haematol.2011.053199 |
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Abstract | Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and relapsed classical Hodgkin's lymphoma patients.
Plasma was collected from 60 (39 early stage and 21 advanced stage) newly diagnosed classical Hodgkin's lymphoma patients before, during, and after treatment, and from 12 relapsed patients before and after treatment. Plasma thymus and activation-regulated chemokine levels were determined by enzyme-linked immunosorbent assay and were related to pre-treatment metabolic tumor volume, as measured by quantification of 2-[18F]fluoro-2-deoxyglucose positron emission tomography images, and to treatment response.
Baseline plasma thymus and activation-regulated chemokine levels correlated with stage of disease and bulky disease, and more closely with metabolic tumor volume. Response to treatment was observed among 38 of 39 early stage and 19 of 21 advanced stage patients. Reduction in plasma thymus and activation-regulated chemokine to normal range levels could be observed as early as after one cycle of chemotherapy in all responsive patients, while plasma levels remained elevated during and after treatment in the 3 non-responsive patients. Plasma thymus and activation-regulated chemokine was elevated in all 12 relapsed patients at time of relapse and remained elevated after salvage treatment in the 4 non-responsive patients.
Baseline plasma thymus and activation-regulated chemokine levels correlate with classical Hodgkin's lymphoma tumor burden and serial levels correlate with response to treatment in patients with classical Hodgkin's lymphoma. |
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AbstractList | Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and relapsed classical Hodgkin's lymphoma patients.BACKGROUNDPlasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and relapsed classical Hodgkin's lymphoma patients.Plasma was collected from 60 (39 early stage and 21 advanced stage) newly diagnosed classical Hodgkin's lymphoma patients before, during, and after treatment, and from 12 relapsed patients before and after treatment. Plasma thymus and activation-regulated chemokine levels were determined by enzyme-linked immunosorbent assay and were related to pre-treatment metabolic tumor volume, as measured by quantification of 2-[18F]fluoro-2-deoxyglucose positron emission tomography images, and to treatment response.DESIGN AND METHODSPlasma was collected from 60 (39 early stage and 21 advanced stage) newly diagnosed classical Hodgkin's lymphoma patients before, during, and after treatment, and from 12 relapsed patients before and after treatment. Plasma thymus and activation-regulated chemokine levels were determined by enzyme-linked immunosorbent assay and were related to pre-treatment metabolic tumor volume, as measured by quantification of 2-[18F]fluoro-2-deoxyglucose positron emission tomography images, and to treatment response.Baseline plasma thymus and activation-regulated chemokine levels correlated with stage of disease and bulky disease, and more closely with metabolic tumor volume. Response to treatment was observed among 38 of 39 early stage and 19 of 21 advanced stage patients. Reduction in plasma thymus and activation-regulated chemokine to normal range levels could be observed as early as after one cycle of chemotherapy in all responsive patients, while plasma levels remained elevated during and after treatment in the 3 non-responsive patients. Plasma thymus and activation-regulated chemokine was elevated in all 12 relapsed patients at time of relapse and remained elevated after salvage treatment in the 4 non-responsive patients.RESULTSBaseline plasma thymus and activation-regulated chemokine levels correlated with stage of disease and bulky disease, and more closely with metabolic tumor volume. Response to treatment was observed among 38 of 39 early stage and 19 of 21 advanced stage patients. Reduction in plasma thymus and activation-regulated chemokine to normal range levels could be observed as early as after one cycle of chemotherapy in all responsive patients, while plasma levels remained elevated during and after treatment in the 3 non-responsive patients. Plasma thymus and activation-regulated chemokine was elevated in all 12 relapsed patients at time of relapse and remained elevated after salvage treatment in the 4 non-responsive patients.Baseline plasma thymus and activation-regulated chemokine levels correlate with classical Hodgkin's lymphoma tumor burden and serial levels correlate with response to treatment in patients with classical Hodgkin's lymphoma.CONCLUSIONSBaseline plasma thymus and activation-regulated chemokine levels correlate with classical Hodgkin's lymphoma tumor burden and serial levels correlate with response to treatment in patients with classical Hodgkin's lymphoma. Background Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin’s lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and relapsed classical Hodgkin’s lymphoma patients.Design and Methods Plasma was collected from 60 (39 early stage and 21 advanced stage) newly diagnosed classical Hodgkin’s lymphoma patients before, during, and after treatment, and from 12 relapsed patients before and after treatment. Plasma thymus and activation-regulated chemokine levels were determined by enzyme-linked immunosorbent assay and were related to pre-treatment metabolic tumor volume, as measured by quantification of 2-[18F]fluoro-2-deoxyglucose positron emission tomography images, and to treatment response.Results Baseline plasma thymus and activation-regulated chemokine levels correlated with stage of disease and bulky disease, and more closely with metabolic tumor volume. Response to treatment was observed among 38 of 39 early stage and 19 of 21 advanced stage patients. Reduction in plasma thymus and activation-regulated chemokine to normal range levels could be observed as early as after one cycle of chemotherapy in all responsive patients, while plasma levels remained elevated during and after treatment in the 3 non-responsive patients. Plasma thymus and activation-regulated chemokine was elevated in all 12 relapsed patients at time of relapse and remained elevated after salvage treatment in the 4 non-responsive patients.Conclusions Baseline plasma thymus and activation-regulated chemokine levels correlate with classical Hodgkin’s lymphoma tumor burden and serial levels correlate with response to treatment in patients with classical Hodgkin’s lymphoma. Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor treatment response, we correlated serial plasma thymus and activation-regulated chemokine levels with clinical response in newly diagnosed and relapsed classical Hodgkin's lymphoma patients. Plasma was collected from 60 (39 early stage and 21 advanced stage) newly diagnosed classical Hodgkin's lymphoma patients before, during, and after treatment, and from 12 relapsed patients before and after treatment. Plasma thymus and activation-regulated chemokine levels were determined by enzyme-linked immunosorbent assay and were related to pre-treatment metabolic tumor volume, as measured by quantification of 2-[18F]fluoro-2-deoxyglucose positron emission tomography images, and to treatment response. Baseline plasma thymus and activation-regulated chemokine levels correlated with stage of disease and bulky disease, and more closely with metabolic tumor volume. Response to treatment was observed among 38 of 39 early stage and 19 of 21 advanced stage patients. Reduction in plasma thymus and activation-regulated chemokine to normal range levels could be observed as early as after one cycle of chemotherapy in all responsive patients, while plasma levels remained elevated during and after treatment in the 3 non-responsive patients. Plasma thymus and activation-regulated chemokine was elevated in all 12 relapsed patients at time of relapse and remained elevated after salvage treatment in the 4 non-responsive patients. Baseline plasma thymus and activation-regulated chemokine levels correlate with classical Hodgkin's lymphoma tumor burden and serial levels correlate with response to treatment in patients with classical Hodgkin's lymphoma. |
Author | Jan Pruim Bouke Hepkema Hans Vos Anne-Marijn van der Graaf Gustaaf W. van Imhoff Wouter J. Plattel Arjan Diepstra Lydia Visser Anke van den Berg |
AuthorAffiliation | 3 Department of Nuclear Medicine and Molecular Imaging, University of Groningen, University Medical Center Groningen, the Netherlands 4 Department of Laboratory Medicine, University of Groningen, University Medical Center Groningen, the Netherlands 2 Department of Pathology and Medical BIology, University of Groningen, University Medical Center Groningen, the Netherlands 1 Department of Hematology, University of Groningen, University Medical Center Groningen, the Netherlands |
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Keywords | chemokine Thymus gland Hematology Biological marker Hodgkin disease Malignant hemopathy Lymphoma Blood plasma plasma thymus serial plasma Thymus activation regulated chemokine Lymphoproliferative syndrome Early Tumor tumor burden Cancer Hodgkin's lymphoma |
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References | 15994922 - Cancer Res. 2005 Jul 1;65(13):5516-9 21077737 - Leuk Lymphoma. 2010 Dec;51(12):2171-80 16585014 - Haematologica. 2006 Apr;91(4):475-81 17242396 - J Clin Oncol. 2007 Feb 10;25(5):579-86 20410186 - Haematologica. 2010 Jul;95(7):1198-206 17063502 - Cancer. 2006 Dec 1;107(11):2678-87 11100882 - Semin Cancer Biol. 2000 Oct;10(5):345-50 16766583 - Ann Oncol. 2006 Aug;17(8):1296-300 19544140 - Leuk Lymphoma. 2009 Aug;50(8):1257-60 21482982 - J Clin Oncol. 2011 May 10;29(14):1844-54 11920617 - Int J Cancer. 2002 Apr 1;98(4):567-72 18070985 - Blood. 2008 Feb 15;111(4):2339-46 10362793 - Am J Pathol. 1999 Jun;154(6):1685-91 20505930 - Eur J Nucl Med Mol Imaging. 2010 Oct;37(10):1824-33 20595100 - Haematologica. 2010 Jul;95(7):1046-8 18275430 - Br J Haematol. 2008 Mar;140(5):527-36 12149227 - Blood. 2002 Aug 15;100(4):1425-9 18704407 - Eur J Nucl Med Mol Imaging. 2008 Dec;35(12):2320-33 11240957 - J Allergy Clin Immunol. 2001 Mar;107(3):535-41 17646666 - J Clin Oncol. 2007 Aug 20;25(24):3746-52 18398732 - Leuk Lymphoma. 2008 Apr;49(4):659-62 19228806 - Ann Oncol. 2009 Jul;20(7):1270-4 11420464 - Am J Surg Pathol. 2001 Jul;25(7):925-9 19380407 - J Nucl Med. 2009 May;50 Suppl 1:21S-30S 17242397 - J Clin Oncol. 2007 Feb 10;25(5):571-8 16150944 - Blood. 2006 Jan 1;107(1):52-9 19078975 - Nat Rev Cancer. 2009 Jan;9(1):15-27 19273713 - J Clin Oncol. 2009 Apr 10;27(11):1906-14 20652564 - Eur J Nucl Med Mol Imaging. 2010 Oct;37(10):1821-3 12078904 - Ann Oncol. 2002;13 Suppl 1:52-6 19273698 - J Clin Oncol. 2009 Apr 10;27(11):1742-3 15939713 - Ann Oncol. 2005 Jul;16(7):1160-8 |
References_xml | – reference: 18398732 - Leuk Lymphoma. 2008 Apr;49(4):659-62 – reference: 12149227 - Blood. 2002 Aug 15;100(4):1425-9 – reference: 11100882 - Semin Cancer Biol. 2000 Oct;10(5):345-50 – reference: 16150944 - Blood. 2006 Jan 1;107(1):52-9 – reference: 20595100 - Haematologica. 2010 Jul;95(7):1046-8 – reference: 19544140 - Leuk Lymphoma. 2009 Aug;50(8):1257-60 – reference: 15939713 - Ann Oncol. 2005 Jul;16(7):1160-8 – reference: 11420464 - Am J Surg Pathol. 2001 Jul;25(7):925-9 – reference: 12078904 - Ann Oncol. 2002;13 Suppl 1:52-6 – reference: 11920617 - Int J Cancer. 2002 Apr 1;98(4):567-72 – reference: 10362793 - Am J Pathol. 1999 Jun;154(6):1685-91 – reference: 16585014 - Haematologica. 2006 Apr;91(4):475-81 – reference: 17242396 - J Clin Oncol. 2007 Feb 10;25(5):579-86 – reference: 19273698 - J Clin Oncol. 2009 Apr 10;27(11):1742-3 – reference: 11240957 - J Allergy Clin Immunol. 2001 Mar;107(3):535-41 – reference: 21482982 - J Clin Oncol. 2011 May 10;29(14):1844-54 – reference: 20505930 - Eur J Nucl Med Mol Imaging. 2010 Oct;37(10):1824-33 – reference: 18070985 - Blood. 2008 Feb 15;111(4):2339-46 – reference: 19078975 - Nat Rev Cancer. 2009 Jan;9(1):15-27 – reference: 20410186 - Haematologica. 2010 Jul;95(7):1198-206 – reference: 17063502 - Cancer. 2006 Dec 1;107(11):2678-87 – reference: 19228806 - Ann Oncol. 2009 Jul;20(7):1270-4 – reference: 15994922 - Cancer Res. 2005 Jul 1;65(13):5516-9 – reference: 20652564 - Eur J Nucl Med Mol Imaging. 2010 Oct;37(10):1821-3 – reference: 19380407 - J Nucl Med. 2009 May;50 Suppl 1:21S-30S – reference: 16766583 - Ann Oncol. 2006 Aug;17(8):1296-300 – reference: 17242397 - J Clin Oncol. 2007 Feb 10;25(5):571-8 – reference: 18275430 - Br J Haematol. 2008 Mar;140(5):527-36 – reference: 21077737 - Leuk Lymphoma. 2010 Dec;51(12):2171-80 – reference: 18704407 - Eur J Nucl Med Mol Imaging. 2008 Dec;35(12):2320-33 – reference: 17646666 - J Clin Oncol. 2007 Aug 20;25(24):3746-52 – reference: 19273713 - J Clin Oncol. 2009 Apr 10;27(11):1906-14 |
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Snippet | Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin's lymphoma. To define its value as a marker to monitor... Background Plasma thymus and activation-regulated chemokine is a potential biomarker for classical Hodgkin’s lymphoma. To define its value as a marker to... |
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SubjectTerms | Adolescent Adult Aged Biological and medical sciences Biomarkers - blood Chemokine CCL17 - blood Female Hematologic and hematopoietic diseases Hodgkin Disease - diagnosis Hodgkin Disease - drug therapy Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Male Medical sciences Middle Aged Neoplasm Staging Original and Brief Reports Prognosis Recurrence Treatment Outcome Tumor Burden Young Adult |
Title | Plasma thymus and activation-regulated chemokine as an early response marker in classical Hodgkin’s lymphoma |
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