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 (26) 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
Germany
Helios Klinikum Erfurt
RECRUITING
Erfurt
Department of Neurosurgery, Universitätsklinikum Frankfurt
RECRUITING
Frankfurt
Dep. of Neurosurgery, Universitätsklinikum Freiburg
RECRUITING
Freiburg Im Breisgau
Universitätsklinikum Gießen und Marburg
RECRUITING
Giessen
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
RECRUITING
Mainz
Universitätsklinikum Münster
RECRUITING
Münster
Greece
Department of Neurosurgery, Hospital of Larissa & General Hospital of Larissa
RECRUITING
Larissa
Department of Neurosurgery, AHEPA University Hospital
RECRUITING
Thessaloniki
Italy
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
RECRUITING
Milan
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
Romania
Department of Neurosurgery, Spitalul Clinic De Urgență Bagdasar-Arseni
RECRUITING
Bucharest
Spain
Department of Neurosurgery, L'Hospitalet de Llobregat, Barcelona
RECRUITING
Barcelona
Department of Neurosurgery, Puerta de Hierro University Hospital, Madrid
RECRUITING
Madrid
Switzerland
Kantonsspital Aarau
RECRUITING
Aarau
Universitätsspital Basel
RECRUITING
Basel
Dep. of Neurosurgery, Bern University Hospital
RECRUITING
Bern
Dep. of Neurosurger, Hôpitaux Universitaires de Genève
ACTIVE_NOT_RECRUITING
Geneva
Dep. of Neurosurgery, Centre hospitalier universitaire vaudois
RECRUITING
Lausanne
Kantonsspital Luzern
RECRUITING
Lucerne
Ospedale Regionale di Lugano
RECRUITING
Lugano
Department of Neurosurgery, Kantonsspital St. Gallen
RECRUITING
Sankt Gallen
Dep. of Neurosurgery, University Hospital of Zurich
RECRUITING
Zurich
Contact Information
Primary
Claire Descombes
claire.descombes@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: 2025-12
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
Torstein Mehling, Shahan Momjian, Philippe Schucht
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