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Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care

Purpose. The aims were to correlate individual marrow metabolic changes after chemotherapy with bone marrow biopsy (BMBx) for its potential value of personalized care in lymphoma. Methods. 26 patients (mean age, 58 ± 15 y; 13 female, 13 male) with follicular lymphoma or diffuse large B-cell lymphoma...

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Autores principales: Tang, Bingfeng, Patel, Malaykumar M., Wong, Regina H., Wood, Daniel, Wong, Christiana O., Wu, Dafang, Khong, Pek Lan, Wong, Ching Yee Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182335/
https://www.ncbi.nlm.nih.gov/pubmed/21966591
http://dx.doi.org/10.1155/2011/942063
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author Tang, Bingfeng
Patel, Malaykumar M.
Wong, Regina H.
Wood, Daniel
Wong, Christiana O.
Wu, Dafang
Khong, Pek Lan
Wong, Ching Yee Oliver
author_facet Tang, Bingfeng
Patel, Malaykumar M.
Wong, Regina H.
Wood, Daniel
Wong, Christiana O.
Wu, Dafang
Khong, Pek Lan
Wong, Ching Yee Oliver
author_sort Tang, Bingfeng
collection PubMed
description Purpose. The aims were to correlate individual marrow metabolic changes after chemotherapy with bone marrow biopsy (BMBx) for its potential value of personalized care in lymphoma. Methods. 26 patients (mean age, 58 ± 15 y; 13 female, 13 male) with follicular lymphoma or diffuse large B-cell lymphoma, referred to FDG-PET/CT imaging, who had BMBx from unilateral or bilateral iliac crest(s) before chemotherapy, were studied retrospectively. The maximal standardized uptake value (SUV) was measured from BMBx site over the same area on both initial staging and first available restaging FDG-PET/CT scan. Results. 35 BMBx sites in 26 patients were evaluated. 12 of 35 sites were BMBx positive with interval decrease in SUV in 11 of 12 sites (92%). The remaining 23 of 35 sites were BMBx negative with interval increase in SUV in 21 of 23 sites (91%). The correlation between SUV change over the BMBx site before and after chemotherapy and BMBx result was significant (P < 0.0001). Conclusions. This preliminary result demonstrates a strong correlation between marrow metabolic changes (as determined by FDG PET) after chemotherapy and bone marrow involvement proven by biopsy. This may provide a retrospective means of personalized management of marrow involvement in deciding whether to deliver more extended therapy or closer followup of lymphoma patients.
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spelling pubmed-31823352011-09-30 Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care Tang, Bingfeng Patel, Malaykumar M. Wong, Regina H. Wood, Daniel Wong, Christiana O. Wu, Dafang Khong, Pek Lan Wong, Ching Yee Oliver Int J Mol Imaging Research Article Purpose. The aims were to correlate individual marrow metabolic changes after chemotherapy with bone marrow biopsy (BMBx) for its potential value of personalized care in lymphoma. Methods. 26 patients (mean age, 58 ± 15 y; 13 female, 13 male) with follicular lymphoma or diffuse large B-cell lymphoma, referred to FDG-PET/CT imaging, who had BMBx from unilateral or bilateral iliac crest(s) before chemotherapy, were studied retrospectively. The maximal standardized uptake value (SUV) was measured from BMBx site over the same area on both initial staging and first available restaging FDG-PET/CT scan. Results. 35 BMBx sites in 26 patients were evaluated. 12 of 35 sites were BMBx positive with interval decrease in SUV in 11 of 12 sites (92%). The remaining 23 of 35 sites were BMBx negative with interval increase in SUV in 21 of 23 sites (91%). The correlation between SUV change over the BMBx site before and after chemotherapy and BMBx result was significant (P < 0.0001). Conclusions. This preliminary result demonstrates a strong correlation between marrow metabolic changes (as determined by FDG PET) after chemotherapy and bone marrow involvement proven by biopsy. This may provide a retrospective means of personalized management of marrow involvement in deciding whether to deliver more extended therapy or closer followup of lymphoma patients. Hindawi Publishing Corporation 2011 2011-09-28 /pmc/articles/PMC3182335/ /pubmed/21966591 http://dx.doi.org/10.1155/2011/942063 Text en Copyright © 2011 Bingfeng Tang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tang, Bingfeng
Patel, Malaykumar M.
Wong, Regina H.
Wood, Daniel
Wong, Christiana O.
Wu, Dafang
Khong, Pek Lan
Wong, Ching Yee Oliver
Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title_full Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title_fullStr Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title_full_unstemmed Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title_short Revisiting the Marrow Metabolic Changes after Chemotherapy in Lymphoma: A Step towards Personalized Care
title_sort revisiting the marrow metabolic changes after chemotherapy in lymphoma: a step towards personalized care
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182335/
https://www.ncbi.nlm.nih.gov/pubmed/21966591
http://dx.doi.org/10.1155/2011/942063
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