Cargando…

Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements

OBJECTIVES: MYC gene rearrangements in diffuse large B cell lymphomas (DLBCLs) result in high proliferation rates and are associated with a poor prognosis. Strong proliferation is associated with high metabolic demand and tumour necrosis. The aim of this study was to investigate differences in the p...

Descripción completa

Detalles Bibliográficos
Autores principales: Kahle, Xaver U., Hovingh, Menno, Noordzij, Walter, Seitz, Annika, Diepstra, Arjan, Visser, Lydia, van den Berg, Anke, van Meerten, Tom, Huls, Gerwin, Boellaard, Ronald, Kwee, Thomas C., Nijland, Marcel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795618/
https://www.ncbi.nlm.nih.gov/pubmed/31028445
http://dx.doi.org/10.1007/s00330-019-06178-9
_version_ 1783459478522298368
author Kahle, Xaver U.
Hovingh, Menno
Noordzij, Walter
Seitz, Annika
Diepstra, Arjan
Visser, Lydia
van den Berg, Anke
van Meerten, Tom
Huls, Gerwin
Boellaard, Ronald
Kwee, Thomas C.
Nijland, Marcel
author_facet Kahle, Xaver U.
Hovingh, Menno
Noordzij, Walter
Seitz, Annika
Diepstra, Arjan
Visser, Lydia
van den Berg, Anke
van Meerten, Tom
Huls, Gerwin
Boellaard, Ronald
Kwee, Thomas C.
Nijland, Marcel
author_sort Kahle, Xaver U.
collection PubMed
description OBJECTIVES: MYC gene rearrangements in diffuse large B cell lymphomas (DLBCLs) result in high proliferation rates and are associated with a poor prognosis. Strong proliferation is associated with high metabolic demand and tumour necrosis. The aim of this study was to investigate differences in the presence of necrosis and semiquantitative (18)F-FDG PET metrics between DLBCL cases with or without a MYC rearrangement. The prognostic impact of necrosis and semiquantitative (18)F-FDG PET parameters was investigated in an explorative survival analysis. METHODS: Fluorescence in situ hybridisation analysis for MYC rearrangements, visual assesment, semiquantitative analysis of (18)F-FDG PET scans and patient survival analysis were performed in 61 DLBCL patients, treated at a single referral hospital between 2008 and 2015. RESULTS: Of 61 tumours, 21 (34%) had a MYC rearrangement (MYC(+)). MYC status was neither associated with the presence of necrosis on (18)F-FDG PET scans (necrosis(PET); p = 1.0) nor associated with the investigated semiquantitative parameters maximum standard uptake value (SUV(max); p = 0.43), single highest SUV(max) (p = 0.49), metabolic active tumour volume (MATV; p = 0.68) or total lesion glycolysis (TLG; p = 0.62). A multivariate patient survival analysis of the entire cohort showed necrosis(PET) as an independent prognostic marker for disease-specific survival (DSS) (HR = 13.9; 95% CI 3.0–65; p = 0.001). CONCLUSIONS: MYC rearrangements in DLBCL have no influence on the visual parameter necrosis(PET) or the semi-quantiative parameters SUV(max), MATV and TLG. Irrespective of MYC rearrangements, necrosis(PET) is an independent, adverse prognostic factor for DSS. KEY POINTS: • Retrospective analysis indicates that MYC rearrangement is not associated with necrosis on (18) F-FDG PET (necrosis (PET) ) scans or semiquantitative (18) F-FDG PET parameters. • Necrosis (PET) is a potential independent adverse prognostic factor for disease-specific survival in patients with DLBCL and is not influenced by the presence of MYC rearrangements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-019-06178-9) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6795618
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-67956182019-10-25 Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements Kahle, Xaver U. Hovingh, Menno Noordzij, Walter Seitz, Annika Diepstra, Arjan Visser, Lydia van den Berg, Anke van Meerten, Tom Huls, Gerwin Boellaard, Ronald Kwee, Thomas C. Nijland, Marcel Eur Radiol Molecular Imaging OBJECTIVES: MYC gene rearrangements in diffuse large B cell lymphomas (DLBCLs) result in high proliferation rates and are associated with a poor prognosis. Strong proliferation is associated with high metabolic demand and tumour necrosis. The aim of this study was to investigate differences in the presence of necrosis and semiquantitative (18)F-FDG PET metrics between DLBCL cases with or without a MYC rearrangement. The prognostic impact of necrosis and semiquantitative (18)F-FDG PET parameters was investigated in an explorative survival analysis. METHODS: Fluorescence in situ hybridisation analysis for MYC rearrangements, visual assesment, semiquantitative analysis of (18)F-FDG PET scans and patient survival analysis were performed in 61 DLBCL patients, treated at a single referral hospital between 2008 and 2015. RESULTS: Of 61 tumours, 21 (34%) had a MYC rearrangement (MYC(+)). MYC status was neither associated with the presence of necrosis on (18)F-FDG PET scans (necrosis(PET); p = 1.0) nor associated with the investigated semiquantitative parameters maximum standard uptake value (SUV(max); p = 0.43), single highest SUV(max) (p = 0.49), metabolic active tumour volume (MATV; p = 0.68) or total lesion glycolysis (TLG; p = 0.62). A multivariate patient survival analysis of the entire cohort showed necrosis(PET) as an independent prognostic marker for disease-specific survival (DSS) (HR = 13.9; 95% CI 3.0–65; p = 0.001). CONCLUSIONS: MYC rearrangements in DLBCL have no influence on the visual parameter necrosis(PET) or the semi-quantiative parameters SUV(max), MATV and TLG. Irrespective of MYC rearrangements, necrosis(PET) is an independent, adverse prognostic factor for DSS. KEY POINTS: • Retrospective analysis indicates that MYC rearrangement is not associated with necrosis on (18) F-FDG PET (necrosis (PET) ) scans or semiquantitative (18) F-FDG PET parameters. • Necrosis (PET) is a potential independent adverse prognostic factor for disease-specific survival in patients with DLBCL and is not influenced by the presence of MYC rearrangements. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00330-019-06178-9) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2019-04-26 2019 /pmc/articles/PMC6795618/ /pubmed/31028445 http://dx.doi.org/10.1007/s00330-019-06178-9 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Molecular Imaging
Kahle, Xaver U.
Hovingh, Menno
Noordzij, Walter
Seitz, Annika
Diepstra, Arjan
Visser, Lydia
van den Berg, Anke
van Meerten, Tom
Huls, Gerwin
Boellaard, Ronald
Kwee, Thomas C.
Nijland, Marcel
Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title_full Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title_fullStr Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title_full_unstemmed Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title_short Tumour necrosis as assessed with (18)F-FDG PET is a potential prognostic marker in diffuse large B cell lymphoma independent of MYC rearrangements
title_sort tumour necrosis as assessed with (18)f-fdg pet is a potential prognostic marker in diffuse large b cell lymphoma independent of myc rearrangements
topic Molecular Imaging
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6795618/
https://www.ncbi.nlm.nih.gov/pubmed/31028445
http://dx.doi.org/10.1007/s00330-019-06178-9
work_keys_str_mv AT kahlexaveru tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT hovinghmenno tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT noordzijwalter tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT seitzannika tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT diepstraarjan tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT visserlydia tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT vandenberganke tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT vanmeertentom tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT hulsgerwin tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT boellaardronald tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT kweethomasc tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements
AT nijlandmarcel tumournecrosisasassessedwith18ffdgpetisapotentialprognosticmarkerindiffuselargebcelllymphomaindependentofmycrearrangements