RESURGE - Randomized Controlled Comparative Phase II Trial on Surgery for Glioblastoma Recurrence

Who is this study for? Patients with Glioblastoma
Status: Recruiting
Location: See all (25) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Patients with glioblastoma face a grim prognosis. Despite recent advancement in neurosurgical technology and neuro-oncology glioblastomas almost invariably progress or recur after a median of 4-8 months. The strategy to repeat tumor resection at recurrence in order to minimize tumor load and thus to facilitate subsequent second-line therapy has been shown to be feasible and safe. However, evidence for a survival benefit of surgery for recurrent glioblastoma is scarce and relies entirely on retrospective analyses. While most retrospective analyses report an apparent survival benefit, an EORTC meta-analysis on second-line therapies found no survival difference in patients with or without surgery at recurrence. With regard to the risks and costs inherent to surgery for glioblastoma, a randomized controlled trial is required. The purpose of the study is to compare the effect of craniotomy and tumor resection followed by adjuvant second-line therapy to no surgery followed by second-line therapy on overall survival, neurological status, and quality of life. Analysis of overall survival will be used to improve sample size estimation of a subsequent phase III trial for craniotomy and tumor resection of glioblastoma recurrence in cooperation with the EORTC.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Written informed consent

• ≥18 years of age

• Prior resection of glioblastoma confirmed by histology

• Glioblastoma pretreated with standard radiotherapy without or with temozolomide

• First progression according to RANO criteria

• First progression not within 3 months after completion of radiation therapy

• Complete removal of contrast-enhancing lesion considered feasible without significant risk of permanent speech or motor function according to MRI as confirmed by study eligibility committee after screening and prior to recruitment

• No encroachment of the M1 or A1 segments of the medial and anterior cerebral artery on MRI

• No contrast enhancement in presumed speech and primary motor areas on MRI

• No midline shift on MRI

• No contrast enhancing ventricular spread, multifocal recurrence, meningeosis carcinomatosa or infiltration of the contra-lateral hemisphere on MRI

• No contra-indication for surgery

• Good functional status (KPS ≥ 70)

Locations
Other Locations
Austria
Universitätsklinikum Innsbruck
RECRUITING
Innsbruck
Johannes Kepler University Linz University, Clinic for Neurosurgery
RECRUITING
Linz
Medical University of Vienna, Department of Neurosurgery
RECRUITING
Vienna
France
Centre Hospitalier Universitaire Dijon Bourgogne, Department of Neurosurgery
RECRUITING
Dijon
Hospices Civils de Lyon - CHU de Lyon, Department of Neuro-Oncology
RECRUITING
Lyon
Assistance Publique - Hôpitaux de Marseille, Department of Neuro-Oncology
RECRUITING
Marseille
Centre Hospitalier Universitaire de Nice, Department of Neurosurgery
RECRUITING
Nice
Assistance Publique - Hôpitaux de Paris (AP-HP), Department of Neurosurgery
RECRUITING
Paris
Centre Hospitalier Universitaire de Saint-Étienne, Department of Neurosurgery
RECRUITING
Saint-etienne
Institut de Cancérologie Strasbourg Europe (ICANS), Department of Oncology
RECRUITING
Strasbourg
Centre Hospitalier Régional et Universitaire de Tours (CHRU Tours), Department of Neurosurgery
RECRUITING
Tours
Germany
Helios Klinikum Erfurt
RECRUITING
Erfurt
Universitätsklinikum Münster
RECRUITING
Münster
Greece
Department of Neurosurgery, Hospital of Larissa & General Hospital of Larissa
RECRUITING
Larissa
Netherlands
Department of Neurosurgery, Amsterdam University Medical Center
RECRUITING
Amsterdam
Department of Neurosurgery, Radboud University Medical Center, Nijmegen
RECRUITING
Nijmegen
Department of Neurosurgery, Haaglanden Medical Center, The Hague
RECRUITING
The Hague
Portugal
Department of Neurosurgery, Centro Hospitalar Universitário Lisboa Norte - Hospital de Santa Maria
RECRUITING
Lisbon
Spain
Department of Neurosurgery, L'Hospitalet de Llobregat, Barcelona
RECRUITING
Barcelona
Sweden
University of Gothenburg, Department of Clinical Neuroscience
NOT_YET_RECRUITING
Gothenburg
University Hospital of Umeå, Department of Diagnostics and Intervention
NOT_YET_RECRUITING
Umeå
Switzerland
Universitätsspital Basel
RECRUITING
Basel
Dep. of Neurosurgery, Bern University Hospital
RECRUITING
Bern
Dep. of Neurosurgery, Centre hospitalier universitaire vaudois
RECRUITING
Lausanne
Ospedale Regionale di Lugano
RECRUITING
Lugano
Contact Information
Primary
Philippe Schucht, MD
resurge@insel.ch
+41 31 66 4 28 65
Backup
David Hasler
david.hasler@insel.ch
+41 31 632 76 80
Time Frame
Start Date: 2015-05-01
Estimated Completion Date: 2028-12
Participants
Target number of participants: 120
Treatments
Experimental: Surgery followed by adjuvant second-line therapy
Surgery followed by adjuvant second-line therapy
Active_comparator: Second-line therapy alone
Second-line therapy alone
Authors
Sponsors
Collaborators: European Organisation for Research and Treatment of Cancer - EORTC
Leads: Insel Gruppe AG, University Hospital Bern

This content was sourced from clinicaltrials.gov