Hypofractionated Stereotactic Re-irradiation and Anti-PDL1 Durvalumab Combination in Recurrent Glioblastoma: STERIMGLI Phase I Results

Author:

Pouessel Damien1,Ken Soléakhéna23,Gouaze-Andersson Valérie34,Piram Lucie34,Mervoyer Augustin5,Larrieu-Ciron Delphine1,Cabarrou Bastien6,Lusque Amélie6,Robert Marie7,Frenel Jean-Sebastien7,Uro-Coste Emmanuelle38,Olivier Pascale9,Mounier Muriel10,Sabatini Umberto11,Sanchez Eduardo Hugo12,Zouitine Mehdi12,Berjaoui Ahmad312,Cohen-Jonathan Moyal Elizabeth34

Affiliation:

1. Department of Medical Oncology, Institut Universitaire du Cancer Toulouse Oncopole, Institut Claudius Re-gaud , Toulouse , France

2. Department of Engineering and Medical Physics, Institut Universitaire du Cancer Toulouse Oncopole, Institut Claudius Regaud , Toulouse , France

3. INSERM UMR1037, Centre de Recherche en Cancérologie de Toulouse (CRCT), Team Radiation Optimization “RADOPT” , Toulouse , France

4. Department of Radiation Oncology, Institut Universitaire du Cancer Toulouse Oncopole, Institut Claudius Regaud , Toulouse , France

5. Department of Radiation Oncology, Institut de Cancérologie de l’Ouest , Nantes , France

6. Department of Biostatistics, Institut Universitaire du Cancer Toulouse Oncopole, Institut Claudius Regaud , Toulouse , France

7. Department of Medical Oncology, Institut de Cancérologie de l’Ouest , Nantes , France

8. Department of Anatomopathology , CHU Toulouse, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse , France

9. Department of Medical and Clinical Pharmacology, Center of Pharmacovigilance and Pharmacoepidemiology, Toulouse University Hospital , Toulouse , France

10. Clinical Research Unit, Institut Universitaire du Cancer Toulouse Oncopole, Institut Claudius Regaud , Toulouse , France

11. Institute of Neuroradiology, University Magna Graecia , Catanzaro , Italy

12. Institut de Recherche Technologique Saint Exupéry , Toulouse , France

Abstract

Abstract Background Hypofractionated stereotactic radiotherapy (hFSRT) is a salvage option for recurrent glioblastoma (GB) which may synergize anti-PDL1 treatment. This phase I study evaluated the safety and the recommended phase II dose of anti-PDL1 durvalumab combined with hFSRT in patients with recurrent GB. Methods Patients were treated with 24 Gy, 8 Gy per fraction on days 1, 3, and 5 combined with the first 1500 mg Durvalumab dose on day 5, followed by infusions q4weeks until progression or for a maximum of 12 months. A standard 3 + 3 Durvalumab dose de-escalation design was used. Longitudinal lymphocytes count, cytokines analyses on plasma samples, and magnetic resonance imaging (MRI) were collected. Results Six patients were included. One dose limiting toxicity, an immune-related grade 3 vestibular neuritis related to Durvalumab, was reported. Median progression-free interval (PFI) and overall survival (OS) were 2.3 and 16.7 months, respectively. Multi-modal deep 
learning-based analysis including MRI, cytokines, and lymphocytes/neutrophil ratio isolated the patients presenting pseudoprogression, the longest PFI and those with the longest OS, but statistical significance cannot be established considering phase I data only. Conclusion Combination of hFSRT and Durvalumab in recurrent GB was well tolerated in this phase I study. These encouraging results led to an ongoing randomized phase II. (ClinicalTrials.gov Identifier: NCT02866747).

Funder

Institut Claudius Regaud

ARC Foundation

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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