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(18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study

PURPOSE: To determine whether interim 3′-deoxy-3′-[(18)F]fluorothymidine (iFLT) PET/CT is a superior predictor of progression-free survival (PFS) compared with interim (18)F-fluorodeoxyglucose (iFDG) PET/CT in patients with diffuse large B cell lymphoma (DLBCL) treated with rituximab, cyclophosphami...

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Autores principales: Minamimoto, Ryogo, Fayad, Luis, Vose, Julie, Meza, Jane, Advani, Ranjana, Hankins, Jordan, Mottaghy, Felix, Macapinlac, Homer, Heinzel, Alexander, Juweid, Malik E., Quon, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263539/
https://www.ncbi.nlm.nih.gov/pubmed/33909086
http://dx.doi.org/10.1007/s00259-021-05353-9
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author Minamimoto, Ryogo
Fayad, Luis
Vose, Julie
Meza, Jane
Advani, Ranjana
Hankins, Jordan
Mottaghy, Felix
Macapinlac, Homer
Heinzel, Alexander
Juweid, Malik E.
Quon, Andrew
author_facet Minamimoto, Ryogo
Fayad, Luis
Vose, Julie
Meza, Jane
Advani, Ranjana
Hankins, Jordan
Mottaghy, Felix
Macapinlac, Homer
Heinzel, Alexander
Juweid, Malik E.
Quon, Andrew
author_sort Minamimoto, Ryogo
collection PubMed
description PURPOSE: To determine whether interim 3′-deoxy-3′-[(18)F]fluorothymidine (iFLT) PET/CT is a superior predictor of progression-free survival (PFS) compared with interim (18)F-fluorodeoxyglucose (iFDG) PET/CT in patients with diffuse large B cell lymphoma (DLBCL) treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) or rituximab, etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (R-EPOCH). METHODS: Ninety-two prospectively enrolled patients with DLBCL underwent both FLT-PET/CT and FDG-PET/CT 18–24 days after two cycles of R-CHOP/R-EPOCH. Deauville-criteria, PERCIST1.0, standardized uptake value (SUV), total lesion glycolysis (TLG), and metabolic tumor volume were used to interpret iFDG-PET/CT while dichotomous visual interpretation was used to interpret iFLT-PET/CT and the results were compared with the 3- and 5-year PFS. RESULTS: iFLT-PET/CT was negative in 67 (73%) and positive in 25 (27%) patients. iFDG-PET/CT by Deauville criteria was negative (Deauville scores [DS] of 1–3) in 53 (58%) and positive (DS = 4–5) in 39 (42%) patients. Of the 67 iFLT-PET/CT-negative patients, 7 (10.4%) progressed at a median of 14.1 months whereas 14/25 (56.0%) iFLT-PET/CT-positive patients progressed at a median of 7.8 months (P < .0001). Of the 53 Deauville-negative patients, 9 (17.0%) progressed at a median of 14.1 months whereas 12/39 (30.8%) Deauville-positive patients progressed at a median of 5.6 months (P = .11). In multivariate analysis, including iFLT-PET/CT, PERCIST, interim TLG, and interim SUV(max), only iFLT-PET/CT was an independent predictor for 3- and 5-year PFS (P < .0001 and P = .001, respectively). CONCLUSIONS: In patients with DLBCL given R-CHOP/R-EPOCH, iFLT-PET/CT is a superior independent predictor of outcome compared with iFDG-PET/CT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00259-021-05353-9.
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spelling pubmed-82635392021-07-20 (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study Minamimoto, Ryogo Fayad, Luis Vose, Julie Meza, Jane Advani, Ranjana Hankins, Jordan Mottaghy, Felix Macapinlac, Homer Heinzel, Alexander Juweid, Malik E. Quon, Andrew Eur J Nucl Med Mol Imaging Original Article PURPOSE: To determine whether interim 3′-deoxy-3′-[(18)F]fluorothymidine (iFLT) PET/CT is a superior predictor of progression-free survival (PFS) compared with interim (18)F-fluorodeoxyglucose (iFDG) PET/CT in patients with diffuse large B cell lymphoma (DLBCL) treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) or rituximab, etoposide, prednisone, vincristine, cyclophosphamide, and doxorubicin (R-EPOCH). METHODS: Ninety-two prospectively enrolled patients with DLBCL underwent both FLT-PET/CT and FDG-PET/CT 18–24 days after two cycles of R-CHOP/R-EPOCH. Deauville-criteria, PERCIST1.0, standardized uptake value (SUV), total lesion glycolysis (TLG), and metabolic tumor volume were used to interpret iFDG-PET/CT while dichotomous visual interpretation was used to interpret iFLT-PET/CT and the results were compared with the 3- and 5-year PFS. RESULTS: iFLT-PET/CT was negative in 67 (73%) and positive in 25 (27%) patients. iFDG-PET/CT by Deauville criteria was negative (Deauville scores [DS] of 1–3) in 53 (58%) and positive (DS = 4–5) in 39 (42%) patients. Of the 67 iFLT-PET/CT-negative patients, 7 (10.4%) progressed at a median of 14.1 months whereas 14/25 (56.0%) iFLT-PET/CT-positive patients progressed at a median of 7.8 months (P < .0001). Of the 53 Deauville-negative patients, 9 (17.0%) progressed at a median of 14.1 months whereas 12/39 (30.8%) Deauville-positive patients progressed at a median of 5.6 months (P = .11). In multivariate analysis, including iFLT-PET/CT, PERCIST, interim TLG, and interim SUV(max), only iFLT-PET/CT was an independent predictor for 3- and 5-year PFS (P < .0001 and P = .001, respectively). CONCLUSIONS: In patients with DLBCL given R-CHOP/R-EPOCH, iFLT-PET/CT is a superior independent predictor of outcome compared with iFDG-PET/CT. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00259-021-05353-9. Springer Berlin Heidelberg 2021-04-28 2021 /pmc/articles/PMC8263539/ /pubmed/33909086 http://dx.doi.org/10.1007/s00259-021-05353-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Minamimoto, Ryogo
Fayad, Luis
Vose, Julie
Meza, Jane
Advani, Ranjana
Hankins, Jordan
Mottaghy, Felix
Macapinlac, Homer
Heinzel, Alexander
Juweid, Malik E.
Quon, Andrew
(18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title_full (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title_fullStr (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title_full_unstemmed (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title_short (18)F-Fluorothymidine PET is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large B cell lymphoma: a multicenter study
title_sort (18)f-fluorothymidine pet is an early and superior predictor of progression-free survival following chemoimmunotherapy of diffuse large b cell lymphoma: a multicenter study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263539/
https://www.ncbi.nlm.nih.gov/pubmed/33909086
http://dx.doi.org/10.1007/s00259-021-05353-9
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