Systemic inflammatory markers and volume of enhancing tissue on post-contrast T1w MRI images in differentiating true tumor progression from pseudoprogression in high-grade glioma.

High-grade glioma Neutrophil-Lymphocyte Ratio Post-contrast T1-weighted volume Pseudoprogression Systemic Immune-Inflammation Index Volumetric analysis

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
Nov 2024
Historique:
received: 10 03 2024
revised: 31 05 2024
accepted: 03 07 2024
medline: 25 9 2024
pubmed: 25 9 2024
entrez: 25 9 2024
Statut: epublish

Résumé

High-grade glioma (HGG) patients post-radiotherapy often face challenges distinguishing true tumor progression (TTP) from pseudoprogression (PsP). This study evaluates the effectiveness of systemic inflammatory markers and volume of enhancing tissue on post-contrast T1 weighted (T1WCE) MRI images for this differentiation within the first six months after treatment. We conducted a retrospective analysis on a cohort of HGG patients from 2015 to 2021, categorized per WHO 2016 and 2021 criteria. We analyzed treatment responses using modified RANO criteria and conducted volumetry on T1WCE and T2W/FLAIR images.Blood parameters assessed included neutrophil/lymphocyte ratio (NLR), systemic immune-inflammation index (SII), and systemic inflammation response index (SIRI). We employed Chi-square, Fisher's exact test, and Mann-Whitney The cohort consisted of 39 patients, where 16 exhibited PsP and 23 showed TTP. Univariate analysis revealed significantly higher NLR and SII in the TTP group [NLR: 4.1 vs 7.3, p = 0.002; SII 546.5 vs 890.5p = 0.009]. T1WCE volume distinctly differentiated PsP from TTP [2.2 vs 11.7, p < 0.001]. In multivariate regression, significant predictors included NLR and T1WCE volume in the "NLR Model," and T1WCE volume and SII in the "SII Model." The study also found a significantly lower OS rate in TTP patients compared to those with PsP [HR 3.97, CI 1.59 to 9.93, p = 0.003]. Elevated both, SII and NLR, and increased T1WCE volume were effective in differentiating TTP from PsP in HGG patients post-radiotherapy. These results suggest the potential utility of incorporating these markers into clinical practice, though further research is necessary to confirm these findings in larger patient cohorts.

Sections du résumé

Background UNASSIGNED
High-grade glioma (HGG) patients post-radiotherapy often face challenges distinguishing true tumor progression (TTP) from pseudoprogression (PsP). This study evaluates the effectiveness of systemic inflammatory markers and volume of enhancing tissue on post-contrast T1 weighted (T1WCE) MRI images for this differentiation within the first six months after treatment.
Material and Methods UNASSIGNED
We conducted a retrospective analysis on a cohort of HGG patients from 2015 to 2021, categorized per WHO 2016 and 2021 criteria. We analyzed treatment responses using modified RANO criteria and conducted volumetry on T1WCE and T2W/FLAIR images.Blood parameters assessed included neutrophil/lymphocyte ratio (NLR), systemic immune-inflammation index (SII), and systemic inflammation response index (SIRI). We employed Chi-square, Fisher's exact test, and Mann-Whitney
Results UNASSIGNED
The cohort consisted of 39 patients, where 16 exhibited PsP and 23 showed TTP. Univariate analysis revealed significantly higher NLR and SII in the TTP group [NLR: 4.1 vs 7.3, p = 0.002; SII 546.5 vs 890.5p = 0.009]. T1WCE volume distinctly differentiated PsP from TTP [2.2 vs 11.7, p < 0.001]. In multivariate regression, significant predictors included NLR and T1WCE volume in the "NLR Model," and T1WCE volume and SII in the "SII Model." The study also found a significantly lower OS rate in TTP patients compared to those with PsP [HR 3.97, CI 1.59 to 9.93, p = 0.003].
Conclusion UNASSIGNED
Elevated both, SII and NLR, and increased T1WCE volume were effective in differentiating TTP from PsP in HGG patients post-radiotherapy. These results suggest the potential utility of incorporating these markers into clinical practice, though further research is necessary to confirm these findings in larger patient cohorts.

Identifiants

pubmed: 39318678
doi: 10.1016/j.ctro.2024.100849
pii: S2405-6308(24)00126-5
pmc: PMC11419878
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100849

Informations de copyright

© 2024 The Authors. Published by Elsevier B.V. on behalf of European Society for Radiotherapy and Oncology.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Camilla Satragno (C)

Dept. of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.

Irene Schiavetti (I)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.

Eugenia Cella (E)

U.O. Oncologia Medica 2, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Dept. of Internal Medicine and Medical Speciality (DIMI), University of Genoa, Genoa, Italy.

Federica Picichè (F)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.

Laura Falcitano (L)

U.O. Neuroradiologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Martina Resaz (M)

U.O. Neuroradiologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Monica Truffelli (M)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Stefano Caneva (S)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Department of Neuroscience Ophthalmological Rehabilitation Genetics and Mother and Child Health (DINOGMI), University of Genoa, Genoa, Italy.

Pietro Mattioli (P)

Department of Neuroscience Ophthalmological Rehabilitation Genetics and Mother and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
U.O. Neurofisiopatologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Daniela Esposito (D)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.

Alessio Ginulla (A)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.

Claudio Scaffidi (C)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.

Pietro Fiaschi (P)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Department of Neuroscience Ophthalmological Rehabilitation Genetics and Mother and Child Health (DINOGMI), University of Genoa, Genoa, Italy.

Alessandro D'Andrea (A)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Andrea Bianconi (A)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Gianluigi Zona (G)

U.O. Clinica Neurochirurgica e Neurotraumatologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Department of Neuroscience Ophthalmological Rehabilitation Genetics and Mother and Child Health (DINOGMI), University of Genoa, Genoa, Italy.

Laura Barletta (L)

U.O. Neuroradiologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Luca Roccatagliata (L)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.
U.O. Neuroradiologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Lucio Castellan (L)

U.O. Neuroradiologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Silvia Morbelli (S)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.
U.O. Medicina Nucleare, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Matteo Bauckneht (M)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.
U.O. Medicina Nucleare, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Isabella Donegani (I)

U.O. Medicina Nucleare, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Paolo Nozza (P)

U.O. Anatomia Patologica Ospedaliera, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Dario Arnaldi (D)

Department of Neuroscience Ophthalmological Rehabilitation Genetics and Mother and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
U.O. Neurofisiopatologia, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Giulia Vidano (G)

U.O. Radioterapia Oncologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Flavio Gianelli (F)

U.O. Radioterapia Oncologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Salvina Barra (S)

U.O. Radioterapia Oncologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Elisa Bennicelli (E)

U.O. Oncologia Medica 2, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Liliana Belgioia (L)

Dept. of Health Science (DISSAL), University of Genoa, Genoa, Italy.
U.O. Radioterapia Oncologica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.

Classifications MeSH