Cargando…
Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients
BACKGROUND: As cancer cachexia (CC) is associated with cancer progression, early identification would be beneficial. The aim of this study was to establish a workflow for automated MRI-based segmentation of visceral (VAT) and subcutaneous adipose tissue (SCAT) and lean tissue water (LTW) in a B16 me...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053172/ https://www.ncbi.nlm.nih.gov/pubmed/33130917 http://dx.doi.org/10.1007/s00262-020-02765-8 |
_version_ | 1783680068172644352 |
---|---|
author | Thaiss, Wolfgang M. Gatidis, Sergios Sartorius, Tina Machann, Jürgen Peter, Andreas Eigentler, Thomas K. Nikolaou, Konstantin Pichler, Bernd J. Kneilling, Manfred |
author_facet | Thaiss, Wolfgang M. Gatidis, Sergios Sartorius, Tina Machann, Jürgen Peter, Andreas Eigentler, Thomas K. Nikolaou, Konstantin Pichler, Bernd J. Kneilling, Manfred |
author_sort | Thaiss, Wolfgang M. |
collection | PubMed |
description | BACKGROUND: As cancer cachexia (CC) is associated with cancer progression, early identification would be beneficial. The aim of this study was to establish a workflow for automated MRI-based segmentation of visceral (VAT) and subcutaneous adipose tissue (SCAT) and lean tissue water (LTW) in a B16 melanoma animal model, monitor diseases progression and transfer the protocol to human melanoma patients for therapy assessment. METHODS: For in vivo monitoring of CC B16 melanoma-bearing and healthy mice underwent longitudinal three-point DIXON MRI (days 3, 12, 17 after subcutaneous tumor inoculation). In a prospective clinical study, 18 metastatic melanoma patients underwent MRI before, 2 and 12 weeks after onset of checkpoint inhibitor therapy (CIT; n = 16). We employed an in-house MATLAB script for automated whole-body segmentation for detection of VAT, SCAT and LTW. RESULTS: B16 mice exhibited a CC phenotype and developed a reduced VAT volume compared to baseline (B16 − 249.8 µl, − 25%; controls + 85.3 µl, + 10%, p = 0.003) and to healthy controls. LTW was increased in controls compared to melanoma mice. Five melanoma patients responded to CIT, 7 progressed, and 6 displayed a mixed response. Responding patients exhibited a very limited variability in VAT and SCAT in contrast to others. Interestingly, the LTW was decreased in CIT responding patients (− 3.02% ± 2.67%; p = 0.0034) but increased in patients with progressive disease (+ 1.97% ± 2.19%) and mixed response (+ 4.59% ± 3.71%). CONCLUSION: MRI-based segmentation of fat and water contents adds essential additional information for monitoring the development of CC in mice and metastatic melanoma patients during CIT or other treatment approaches. |
format | Online Article Text |
id | pubmed-8053172 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-80531722021-04-29 Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients Thaiss, Wolfgang M. Gatidis, Sergios Sartorius, Tina Machann, Jürgen Peter, Andreas Eigentler, Thomas K. Nikolaou, Konstantin Pichler, Bernd J. Kneilling, Manfred Cancer Immunol Immunother Original Article BACKGROUND: As cancer cachexia (CC) is associated with cancer progression, early identification would be beneficial. The aim of this study was to establish a workflow for automated MRI-based segmentation of visceral (VAT) and subcutaneous adipose tissue (SCAT) and lean tissue water (LTW) in a B16 melanoma animal model, monitor diseases progression and transfer the protocol to human melanoma patients for therapy assessment. METHODS: For in vivo monitoring of CC B16 melanoma-bearing and healthy mice underwent longitudinal three-point DIXON MRI (days 3, 12, 17 after subcutaneous tumor inoculation). In a prospective clinical study, 18 metastatic melanoma patients underwent MRI before, 2 and 12 weeks after onset of checkpoint inhibitor therapy (CIT; n = 16). We employed an in-house MATLAB script for automated whole-body segmentation for detection of VAT, SCAT and LTW. RESULTS: B16 mice exhibited a CC phenotype and developed a reduced VAT volume compared to baseline (B16 − 249.8 µl, − 25%; controls + 85.3 µl, + 10%, p = 0.003) and to healthy controls. LTW was increased in controls compared to melanoma mice. Five melanoma patients responded to CIT, 7 progressed, and 6 displayed a mixed response. Responding patients exhibited a very limited variability in VAT and SCAT in contrast to others. Interestingly, the LTW was decreased in CIT responding patients (− 3.02% ± 2.67%; p = 0.0034) but increased in patients with progressive disease (+ 1.97% ± 2.19%) and mixed response (+ 4.59% ± 3.71%). CONCLUSION: MRI-based segmentation of fat and water contents adds essential additional information for monitoring the development of CC in mice and metastatic melanoma patients during CIT or other treatment approaches. Springer Berlin Heidelberg 2020-11-01 2021 /pmc/articles/PMC8053172/ /pubmed/33130917 http://dx.doi.org/10.1007/s00262-020-02765-8 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Thaiss, Wolfgang M. Gatidis, Sergios Sartorius, Tina Machann, Jürgen Peter, Andreas Eigentler, Thomas K. Nikolaou, Konstantin Pichler, Bernd J. Kneilling, Manfred Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title | Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title_full | Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title_fullStr | Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title_full_unstemmed | Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title_short | Noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
title_sort | noninvasive, longitudinal imaging-based analysis of body adipose tissue and water composition in a melanoma mouse model and in immune checkpoint inhibitor-treated metastatic melanoma patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053172/ https://www.ncbi.nlm.nih.gov/pubmed/33130917 http://dx.doi.org/10.1007/s00262-020-02765-8 |
work_keys_str_mv | AT thaisswolfgangm noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT gatidissergios noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT sartoriustina noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT machannjurgen noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT peterandreas noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT eigentlerthomask noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT nikolaoukonstantin noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT pichlerberndj noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients AT kneillingmanfred noninvasivelongitudinalimagingbasedanalysisofbodyadiposetissueandwatercompositioninamelanomamousemodelandinimmunecheckpointinhibitortreatedmetastaticmelanomapatients |