Validation of diffusion MRI phenotypes for predicting response to bevacizumab in recurrent glioblastoma: post-hoc analysis of the EORTC-26101 trial

Author:

Schell Marianne12,Pflüger Irada12,Brugnara Gianluca12,Isensee Fabian3,Neuberger Ulf132,Foltyn Martha12,Kessler Tobias45,Sahm Felix67,Wick Antje4,Nowosielski Martha478,Heiland Sabine1,Weller Michael9ORCID,Platten Michael10,Maier-Hein Klaus H310,Von Deimling Andreas67,Van Den Bent Martin J11,Gorlia Thierry12,Wick Wolfgang457,Bendszus Martin1,Kickingereder Philipp12

Affiliation:

1. Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany

2. Section for Computational Neuroimaging, Department of Neuroradiology, Heidelberg University Hospital, Heidelberg, Germany

3. Medical Image Computing, German Cancer Research Center, Heidelberg, Germany

4. Neurology Clinic, Heidelberg University Hospital, Heidelberg, Germany

5. Clinical Cooperation Unit Neurooncology, German Cancer Research Center, Heidelberg, Germany

6. Department of Neuropathology, Institute of Pathology, Heidelberg University Hospital, Heidelberg, Germany

7. Clinical Cooperation Unit Neuropathology, German Cancer Research Center, Heidelberg, Germany

8. Department of Neurology, Medical University, Innsbruck, Austria

9. Department of Neurology, University Hospital and University of Zurich, Zurich, Switzerland

10. Department of Neurology, Mannheim Medical Center, University of Heidelberg, Mannheim, Germany

11. Brain Tumor Center at Erasmus MC Cancer Institute, Rotterdam, Netherlands

12. European Organisation for Research and Treatment of Cancer, Brussels, Belgium

Abstract

Abstract Background This study validated a previously described diffusion MRI phenotype as a potential predictive imaging biomarker in patients with recurrent glioblastoma receiving bevacizumab (BEV). Methods A total of 396/596 patients (66%) from the prospective randomized phase II/III EORTC-26101 trial (with n = 242 in the BEV and n = 154 in the non-BEV arm) met the inclusion criteria with availability of anatomical and diffusion MRI sequences at baseline prior treatment. Apparent diffusion coefficient (ADC) histograms from the contrast-enhancing tumor volume were fitted to a double Gaussian distribution and the mean of the lower curve (ADClow) was used for further analysis. The predictive ability of ADClow was assessed with biomarker threshold models and multivariable Cox regression for overall survival (OS) and progression-free survival (PFS). Results ADClow was associated with PFS (hazard ratio [HR] = 0.625, P = 0.007) and OS (HR = 0.656, P = 0.031). However, no (predictive) interaction between ADClow and the treatment arm was present (P = 0.865 for PFS, P = 0.722 for OS). Independent (prognostic) significance of ADClow was retained after adjusting for epidemiological, clinical, and molecular characteristics (P ≤ 0.02 for OS, P ≤ 0.01 PFS). The biomarker threshold model revealed an optimal ADClow cutoff of 1241*10–6 mm2/s for OS. Thereby, median OS for BEV-patients with ADClow ≥ 1241 was 10.39 months versus 8.09 months for those with ADClow < 1241 (P = 0.004). Similarly, median OS for non-BEV patients with ADClow ≥ 1241 was 9.80 months versus 7.79 months for those with ADClow < 1241 (P = 0.054). Conclusions ADClow is an independent prognostic parameter for stratifying OS and PFS in patients with recurrent glioblastoma. Consequently, the previously suggested role of ADClow as predictive imaging biomarker could not be confirmed within this phase II/III trial.

Funder

Else-Kröner Memorial Scholarship of the Else Kröner-Fresenius Foundation

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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