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Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement

The objective of this study was to investigate whether metabolic tumor volume (MTV) by positron emission tomography (PET) can be a potential prognostic tool when compared with Ann Arbor stage, in stages II and III nodal diffuse large B cell lymphoma (DLBCL). We evaluated 169 patients with nodal stag...

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Autores principales: Song, Moo-Kon, Chung, Joo-Seop, Shin, Ho-Jin, Lee, Sang-Min, Lee, Su-Ee, Lee, Ho-Sup, Lee, Gyeong-Won, Kim, Seong-Jang, Lee, Seok-Mo, Chung, Dong-Seop
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319905/
https://www.ncbi.nlm.nih.gov/pubmed/22071570
http://dx.doi.org/10.1007/s00277-011-1357-2
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author Song, Moo-Kon
Chung, Joo-Seop
Shin, Ho-Jin
Lee, Sang-Min
Lee, Su-Ee
Lee, Ho-Sup
Lee, Gyeong-Won
Kim, Seong-Jang
Lee, Seok-Mo
Chung, Dong-Seop
author_facet Song, Moo-Kon
Chung, Joo-Seop
Shin, Ho-Jin
Lee, Sang-Min
Lee, Su-Ee
Lee, Ho-Sup
Lee, Gyeong-Won
Kim, Seong-Jang
Lee, Seok-Mo
Chung, Dong-Seop
author_sort Song, Moo-Kon
collection PubMed
description The objective of this study was to investigate whether metabolic tumor volume (MTV) by positron emission tomography (PET) can be a potential prognostic tool when compared with Ann Arbor stage, in stages II and III nodal diffuse large B cell lymphoma (DLBCL). We evaluated 169 patients with nodal stages II and III DLBCL who underwent measurements with PET prior to rituximab combined with cyclophosphamide, adriamycin, vincristine, and prednisone (R-CHOP). Cutoff point of MTV was measured using the receiver operating characteristic (ROC) curve. During a median period of 36 months, stage II was 59.2% and III was 40.8%. Using the ROC curve, the MTV of 220 cm(3) was the cutoff value. The low MTV group (<220 cm(3)) had longer progression-free survival (PFS) and overall survival (OS), compared with the high MTV group (≥220 cm(3)) (p < 0.001, p < 0.001). Stage II patients had longer survival than those in stage III (PFS, p = 0.011; OS, p = 0.001). The high MTV group had lower PFS and OS patterns, regardless of stage, compared with the low MTV group (p < 0.001, p < 0.001). Multivariate analysis revealed an association of the high MTV group with lower PFS and OS (PFS, hazard ratio (HR) = 5.300, p < 0.001; OS, HR = 7.009, p < 0.001), but not stage III (PFS, p = 0.187; OS, p = 0.054). Assessment of MTV by PET had more potential predictive power than Ann Arbor stage in the patients that received R-CHOP.
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spelling pubmed-33199052012-04-05 Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement Song, Moo-Kon Chung, Joo-Seop Shin, Ho-Jin Lee, Sang-Min Lee, Su-Ee Lee, Ho-Sup Lee, Gyeong-Won Kim, Seong-Jang Lee, Seok-Mo Chung, Dong-Seop Ann Hematol Original Article The objective of this study was to investigate whether metabolic tumor volume (MTV) by positron emission tomography (PET) can be a potential prognostic tool when compared with Ann Arbor stage, in stages II and III nodal diffuse large B cell lymphoma (DLBCL). We evaluated 169 patients with nodal stages II and III DLBCL who underwent measurements with PET prior to rituximab combined with cyclophosphamide, adriamycin, vincristine, and prednisone (R-CHOP). Cutoff point of MTV was measured using the receiver operating characteristic (ROC) curve. During a median period of 36 months, stage II was 59.2% and III was 40.8%. Using the ROC curve, the MTV of 220 cm(3) was the cutoff value. The low MTV group (<220 cm(3)) had longer progression-free survival (PFS) and overall survival (OS), compared with the high MTV group (≥220 cm(3)) (p < 0.001, p < 0.001). Stage II patients had longer survival than those in stage III (PFS, p = 0.011; OS, p = 0.001). The high MTV group had lower PFS and OS patterns, regardless of stage, compared with the low MTV group (p < 0.001, p < 0.001). Multivariate analysis revealed an association of the high MTV group with lower PFS and OS (PFS, hazard ratio (HR) = 5.300, p < 0.001; OS, HR = 7.009, p < 0.001), but not stage III (PFS, p = 0.187; OS, p = 0.054). Assessment of MTV by PET had more potential predictive power than Ann Arbor stage in the patients that received R-CHOP. Springer-Verlag 2011-11-11 2012 /pmc/articles/PMC3319905/ /pubmed/22071570 http://dx.doi.org/10.1007/s00277-011-1357-2 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Article
Song, Moo-Kon
Chung, Joo-Seop
Shin, Ho-Jin
Lee, Sang-Min
Lee, Su-Ee
Lee, Ho-Sup
Lee, Gyeong-Won
Kim, Seong-Jang
Lee, Seok-Mo
Chung, Dong-Seop
Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title_full Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title_fullStr Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title_full_unstemmed Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title_short Clinical significance of metabolic tumor volume by PET/CT in stages II and III of diffuse large B cell lymphoma without extranodal site involvement
title_sort clinical significance of metabolic tumor volume by pet/ct in stages ii and iii of diffuse large b cell lymphoma without extranodal site involvement
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3319905/
https://www.ncbi.nlm.nih.gov/pubmed/22071570
http://dx.doi.org/10.1007/s00277-011-1357-2
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