FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy
Abstract Our aim was to analyse whether biomarkers extracted from baseline 18F-FDG PET before anti-PD1 treatment contribute to prognostic survival information for early risk stratification in metastatic melanoma. Fifty-six patients, without prior systemic treatment, BRAF wild type, explored using 18...
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doaj-f670e00483354b05be876dfe62c9c6da2021-09-26T11:31:23ZengNature Publishing GroupScientific Reports2045-23222021-09-011111910.1038/s41598-021-98310-3FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapyA. Flaus0V. Habouzit1N. De Leiris2J. P. Vuillez3M. T. Leccia4J. L. Perrot5N. Prevot6F. Cachin7Nuclear Medecine Department, Saint-Etienne University Hospital, University of Saint-EtienneNuclear Medecine Department, Saint-Etienne University Hospital, University of Saint-EtienneNuclear Medecine Department, CHU Grenoble Alpes, University Grenoble AlpesNuclear Medecine Department, CHU Grenoble Alpes, University Grenoble AlpesDermatology Department, CHU Grenoble Alpes, University Grenoble AlpesDermatology Department, Saint-Etienne University Hospital, University of Saint-EtienneNuclear Medecine Department, Saint-Etienne University Hospital, University of Saint-EtienneNuclear Medicine Department, Jean Perrin Cancer Center of Clermont-FerrandAbstract Our aim was to analyse whether biomarkers extracted from baseline 18F-FDG PET before anti-PD1 treatment contribute to prognostic survival information for early risk stratification in metastatic melanoma. Fifty-six patients, without prior systemic treatment, BRAF wild type, explored using 18F-FDG PET were included retrospectively. Our primary endpoint was overall survival (OS). Total metabolic tumoral volume (MTV) and forty-one IBSI compliant parameters were extracted from PET. Parameters associated with outcome were evaluated by a cox regression model and when significant helped build a prognostic score. Median follow-up was 22.1 months and 21 patients died. Total MTV and long zone emphasis (LZE) correlated with shorter OS and served to define three risk categories for the prognostic score. For low, intermediate and high risk groups, survival rates were respectively 91.1% (IC 95 80–1), 56.1% (IC 95 37.1–85) and 19% (IC 95 0.06–60.2) and hazard ratios were respectively 0.11 (IC 95 0.025–0.46), P = 0.0028, 1.2 (IC 95 0.48–2.8), P = 0.74 and 5.9 (IC 95 2.5–14), P < 0.0001. To conclude, a prognostic score based on total MTV and LZE separated metastatic melanoma patients in 3 categories with dramatically different outcomes. Innovative therapies should be tested in the group with the lowest prognosis score for future clinical trials.https://doi.org/10.1038/s41598-021-98310-3 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
A. Flaus V. Habouzit N. De Leiris J. P. Vuillez M. T. Leccia J. L. Perrot N. Prevot F. Cachin |
spellingShingle |
A. Flaus V. Habouzit N. De Leiris J. P. Vuillez M. T. Leccia J. L. Perrot N. Prevot F. Cachin FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy Scientific Reports |
author_facet |
A. Flaus V. Habouzit N. De Leiris J. P. Vuillez M. T. Leccia J. L. Perrot N. Prevot F. Cachin |
author_sort |
A. Flaus |
title |
FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy |
title_short |
FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy |
title_full |
FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy |
title_fullStr |
FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy |
title_full_unstemmed |
FDG PET biomarkers for prediction of survival in metastatic melanoma prior to anti-PD1 immunotherapy |
title_sort |
fdg pet biomarkers for prediction of survival in metastatic melanoma prior to anti-pd1 immunotherapy |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-09-01 |
description |
Abstract Our aim was to analyse whether biomarkers extracted from baseline 18F-FDG PET before anti-PD1 treatment contribute to prognostic survival information for early risk stratification in metastatic melanoma. Fifty-six patients, without prior systemic treatment, BRAF wild type, explored using 18F-FDG PET were included retrospectively. Our primary endpoint was overall survival (OS). Total metabolic tumoral volume (MTV) and forty-one IBSI compliant parameters were extracted from PET. Parameters associated with outcome were evaluated by a cox regression model and when significant helped build a prognostic score. Median follow-up was 22.1 months and 21 patients died. Total MTV and long zone emphasis (LZE) correlated with shorter OS and served to define three risk categories for the prognostic score. For low, intermediate and high risk groups, survival rates were respectively 91.1% (IC 95 80–1), 56.1% (IC 95 37.1–85) and 19% (IC 95 0.06–60.2) and hazard ratios were respectively 0.11 (IC 95 0.025–0.46), P = 0.0028, 1.2 (IC 95 0.48–2.8), P = 0.74 and 5.9 (IC 95 2.5–14), P < 0.0001. To conclude, a prognostic score based on total MTV and LZE separated metastatic melanoma patients in 3 categories with dramatically different outcomes. Innovative therapies should be tested in the group with the lowest prognosis score for future clinical trials. |
url |
https://doi.org/10.1038/s41598-021-98310-3 |
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