Intravoxel incoherent motion (IVIM) modeling of diffusion MRI during chemoradiation predicts therapeutic response in IDH wildtype glioblastoma. (March 2021)
- Record Type:
- Journal Article
- Title:
- Intravoxel incoherent motion (IVIM) modeling of diffusion MRI during chemoradiation predicts therapeutic response in IDH wildtype glioblastoma. (March 2021)
- Main Title:
- Intravoxel incoherent motion (IVIM) modeling of diffusion MRI during chemoradiation predicts therapeutic response in IDH wildtype glioblastoma
- Authors:
- Jabehdar Maralani, Pejman
Myrehaug, Sten
Mehrabian, Hatef
Chan, Aimee K.M.
Wintermark, Max
Heyn, Chris
Conklin, John
Ellingson, Benjamin M.
Rahimi, Saba
Lau, Angus Z
Tseng, Chia-Lin
Soliman, Hany
Detsky, Jay
Daghighi, Shadi
Keith, Julia
Munoz, David G.
Das, Sunit
Atenafu, Eshetu G.
Lipsman, Nir
Perry, James
Stanisz, Greg
Sahgal, Arjun - Abstract:
- Highlights: Simplified IVIM metrics from MRIs taken during chemoradiation have prognostic value. Nonenhancing T2-FLAIR regions have important prognostic value. Abstract: Background: Prediction of early progression in glioblastoma may provide an opportunity to personalize treatment. Simplified intravoxel incoherent motion (IVIM) MRI offers quantitative estimates of diffusion and perfusion metrics. We investigated whether these metrics, during chemoradiation, could predict treatment outcome. Methods: 38 patients with newly diagnosed IDH-wildtype glioblastoma undergoing 6-week/30-fraction chemoradiation had standardized post-operative MRIs at baseline (radiation planning), and at the 10th and 20th fractions. Non-overlapping T1-enhancing (T1C) and non-enhancing T2-FLAIR hyperintense regions were independently segmented. Apparent diffusion coefficient (ADCT1C, ADCT2-FLAIR ) and perfusion fraction ( f T1C, f T2-FLAIR ) maps were generated with simplified IVIM modelling. Parameters associated with progression before or after 6.9 months (early vs late progression, respectively), overall survival (OS) and progression-free survival (PFS) were investigated. Results: Higher ADCT2-FLAIR at baseline [Odds Ratio (OR) = 1.06, 95% CI 1.01–1.15, p = 0.025], lower f T2-FLAIR at fraction 10 (OR = 2.11, 95% CI 1.04–4.27, p = 0.018), and lack of increase in ADCT2-FLAIR at fraction 20 compared to baseline (OR = 1.12, 95% CI 1.02–1.22, p = 0.02) were associated with early progression. CombiningHighlights: Simplified IVIM metrics from MRIs taken during chemoradiation have prognostic value. Nonenhancing T2-FLAIR regions have important prognostic value. Abstract: Background: Prediction of early progression in glioblastoma may provide an opportunity to personalize treatment. Simplified intravoxel incoherent motion (IVIM) MRI offers quantitative estimates of diffusion and perfusion metrics. We investigated whether these metrics, during chemoradiation, could predict treatment outcome. Methods: 38 patients with newly diagnosed IDH-wildtype glioblastoma undergoing 6-week/30-fraction chemoradiation had standardized post-operative MRIs at baseline (radiation planning), and at the 10th and 20th fractions. Non-overlapping T1-enhancing (T1C) and non-enhancing T2-FLAIR hyperintense regions were independently segmented. Apparent diffusion coefficient (ADCT1C, ADCT2-FLAIR ) and perfusion fraction ( f T1C, f T2-FLAIR ) maps were generated with simplified IVIM modelling. Parameters associated with progression before or after 6.9 months (early vs late progression, respectively), overall survival (OS) and progression-free survival (PFS) were investigated. Results: Higher ADCT2-FLAIR at baseline [Odds Ratio (OR) = 1.06, 95% CI 1.01–1.15, p = 0.025], lower f T2-FLAIR at fraction 10 (OR = 2.11, 95% CI 1.04–4.27, p = 0.018), and lack of increase in ADCT2-FLAIR at fraction 20 compared to baseline (OR = 1.12, 95% CI 1.02–1.22, p = 0.02) were associated with early progression. Combining ADCT2-FLAIR at baseline, f T2-FLAIR at fraction 10, ECOG and MGMT promoter methylation status significantly improved AUC to 90.3% compared to a model with only ECOG and MGMT promoter methylation status ( p = 0.001). Using multivariable analysis, neither IVIM metrics were associated with OS but higher f T2-FLAIR at fraction 10 (HR = 0.72, 95% CI 0.56–0.95, p = 0.018) was associated with longer PFS. Conclusion: ADCT2-FLAIR at baseline, its lack of increase from baseline to fraction 20, or f T2-FLAIR at fraction 10 significantly predicted early progression. f T2-FLAIR at fraction 10 was associated with PFS. … (more)
- Is Part Of:
- Radiotherapy and oncology. Volume 156(2021)
- Journal:
- Radiotherapy and oncology
- Issue:
- Volume 156(2021)
- Issue Display:
- Volume 156, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 156
- Issue:
- 2021
- Issue Sort Value:
- 2021-0156-2021-0000
- Page Start:
- 258
- Page End:
- 265
- Publication Date:
- 2021-03
- Subjects:
- DWI diffusion-weighted imaging -- T2-FLAIR T2-weighted fluid-level attenuated inversion recovery -- IVIM intravoxel incoherent motion -- IDH isocitrate dehydrogenase 1 -- IDHwt wildtype IDH -- ECOG Eastern Cooperative Oncology Group -- MGMT O6-methylguanine-DNA methyltransferase -- VOI volume of interest -- cNAWM contralateral normal appearing white matter -- cNAGM contralateral normal appearing grey matter -- ADC apparent diffusion coefficient -- RANO response assessment in neuro-oncology -- AUC area under the receiver operating characteristic curve -- aOR adjusted odds ratio
Glioblastoma -- Survival -- Progression-free Survival -- Diffusion MRI -- Intravoxel incoherent motion imaging -- Radiotherapy
Oncology -- Periodicals
Radiotherapy -- Periodicals
Tumors -- Periodicals
Medical Oncology -- Periodicals
Neoplasms -- radiotherapy -- Periodicals
Radiotherapy -- Periodicals
Radiothérapie -- Périodiques
Cancérologie -- Périodiques
Tumeurs -- Périodiques
Electronic journals
616.9940642 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01678140 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01678140 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01678140 ↗
http://www.estro.org/ ↗
http://www.elsevier.com/journals ↗
http://www.journals.elsevier.com/radiotherapy-and-oncology/ ↗ - DOI:
- 10.1016/j.radonc.2020.12.037 ↗
- Languages:
- English
- ISSNs:
- 0167-8140
- Deposit Type:
- Legaldeposit
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