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Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study

BACKGROUND: The usage of immune checkpoint inhibitors (ICIs) is the standard practice for the treatment of metastatic melanoma. However, a significant amount of patients show no response to immunotherapy, while issues on its reliable response interpretation exist. Aim of this study was to investigat...

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Autores principales: Sachpekidis, Christos, Kopp-Schneider, Annette, Hassel, Jessica C., Dimitrakopoulou-Strauss, Antonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426446/
https://www.ncbi.nlm.nih.gov/pubmed/34495433
http://dx.doi.org/10.1186/s13550-021-00832-4
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author Sachpekidis, Christos
Kopp-Schneider, Annette
Hassel, Jessica C.
Dimitrakopoulou-Strauss, Antonia
author_facet Sachpekidis, Christos
Kopp-Schneider, Annette
Hassel, Jessica C.
Dimitrakopoulou-Strauss, Antonia
author_sort Sachpekidis, Christos
collection PubMed
description BACKGROUND: The usage of immune checkpoint inhibitors (ICIs) is the standard practice for the treatment of metastatic melanoma. However, a significant amount of patients show no response to immunotherapy, while issues on its reliable response interpretation exist. Aim of this study was to investigate the phenomenon of early disease progression in 2-deoxy-2-((18)F)fluoro-D-glucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) in melanoma patients treated with ICIs. METHODS: Thirty-one patients under ICIs serially monitored with (18)F-FDG PET/CT were enrolled. All patients exhibited progressive metabolic disease (PMD) after two ICIs’ cycles according to the European Organization for Research and Treatment of Cancer (EORTC) criteria, and were characterized as unconfirmed PMD (uPMD). They were further followed with at least one PET/CT for either confirmation of PMD (cPMD) or demonstration of pseudoprogression remission. Patients were also evaluated with the PET Response Evaluation Criteria for Immunotherapy (PERCIMT). Moreover, in an attempt to investigate immune activation, the spleen to liver ratios (SLR(mean), SLR(max)) of (18)F-FDG uptake were measured. RESULTS: Median follow up was 69.7 months [64.6–NA]. According to EORTC, 26/31 patients with uPMD eventually showed cPMD (83.9%) and 5/31 patients showed pseudoprogression (16.1%). Patients with cPMD (n = 26) had a median OS of 10.9 months [8.5–NA], while those with pseudoprogression (n = 5) did not reach a median OS [40.9–NA]. Respectively, after application of PERCIMT, 2/5 patients of the pseudoprogression group were correctly classified as non-PMD, reducing the uPMD cohort to 29 patients; eventually, 26/29 patients demonstrated cPMD (89.7%) and 3/29 pseudoprogression (10.3%). One further patient with pseudoprogression exhibited transient, sarcoid-like, mediastinal/hilar lymphadenopathy, a known immune-related adverse event (irAE). Finally, patients eventually showing cPMD exhibited a significantly higher SLR(mean) than those showing pseudoprogression after two ICIs’ cycles (p = 0.038). CONCLUSION: PET/CT, performed already after administration of two ICIs’ cycles, can identify the majority of non-responders in melanoma immunotherapy. In order to tackle however, the non-negligible phenomenon of pseudoprogression, another follow-up PET/CT, the usage of novel response criteria and vigilance over emergence of radiological irAEs are recommended. Moreover, the investigation of spleen glucose metabolism may offer further prognostic information in melanoma patients under ICIs.
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spelling pubmed-84264462021-09-29 Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study Sachpekidis, Christos Kopp-Schneider, Annette Hassel, Jessica C. Dimitrakopoulou-Strauss, Antonia EJNMMI Res Original Research BACKGROUND: The usage of immune checkpoint inhibitors (ICIs) is the standard practice for the treatment of metastatic melanoma. However, a significant amount of patients show no response to immunotherapy, while issues on its reliable response interpretation exist. Aim of this study was to investigate the phenomenon of early disease progression in 2-deoxy-2-((18)F)fluoro-D-glucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) in melanoma patients treated with ICIs. METHODS: Thirty-one patients under ICIs serially monitored with (18)F-FDG PET/CT were enrolled. All patients exhibited progressive metabolic disease (PMD) after two ICIs’ cycles according to the European Organization for Research and Treatment of Cancer (EORTC) criteria, and were characterized as unconfirmed PMD (uPMD). They were further followed with at least one PET/CT for either confirmation of PMD (cPMD) or demonstration of pseudoprogression remission. Patients were also evaluated with the PET Response Evaluation Criteria for Immunotherapy (PERCIMT). Moreover, in an attempt to investigate immune activation, the spleen to liver ratios (SLR(mean), SLR(max)) of (18)F-FDG uptake were measured. RESULTS: Median follow up was 69.7 months [64.6–NA]. According to EORTC, 26/31 patients with uPMD eventually showed cPMD (83.9%) and 5/31 patients showed pseudoprogression (16.1%). Patients with cPMD (n = 26) had a median OS of 10.9 months [8.5–NA], while those with pseudoprogression (n = 5) did not reach a median OS [40.9–NA]. Respectively, after application of PERCIMT, 2/5 patients of the pseudoprogression group were correctly classified as non-PMD, reducing the uPMD cohort to 29 patients; eventually, 26/29 patients demonstrated cPMD (89.7%) and 3/29 pseudoprogression (10.3%). One further patient with pseudoprogression exhibited transient, sarcoid-like, mediastinal/hilar lymphadenopathy, a known immune-related adverse event (irAE). Finally, patients eventually showing cPMD exhibited a significantly higher SLR(mean) than those showing pseudoprogression after two ICIs’ cycles (p = 0.038). CONCLUSION: PET/CT, performed already after administration of two ICIs’ cycles, can identify the majority of non-responders in melanoma immunotherapy. In order to tackle however, the non-negligible phenomenon of pseudoprogression, another follow-up PET/CT, the usage of novel response criteria and vigilance over emergence of radiological irAEs are recommended. Moreover, the investigation of spleen glucose metabolism may offer further prognostic information in melanoma patients under ICIs. Springer Berlin Heidelberg 2021-09-08 /pmc/articles/PMC8426446/ /pubmed/34495433 http://dx.doi.org/10.1186/s13550-021-00832-4 Text en © The Author(s) 2021 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 Research
Sachpekidis, Christos
Kopp-Schneider, Annette
Hassel, Jessica C.
Dimitrakopoulou-Strauss, Antonia
Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title_full Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title_fullStr Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title_full_unstemmed Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title_short Assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)F-FDG PET/CT study
title_sort assessment of early metabolic progression in melanoma patients under immunotherapy: an (18)f-fdg pet/ct study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426446/
https://www.ncbi.nlm.nih.gov/pubmed/34495433
http://dx.doi.org/10.1186/s13550-021-00832-4
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