Surgery for Recurrent Glioblastoma
- Conditions
- Glioblastoma
- Interventions
- Procedure: Surgery followed by adjuvant second-line therapyProcedure: Second-line therapy alone
- Registration Number
- NCT02394626
- Lead Sponsor
- Insel Gruppe AG, University Hospital Bern
- Brief 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.
- Detailed Description
Background
Glioblastoma is a malignant, locally invasive brain tumor whose prognosis remains grim despite various intense treatment modalities. In the past, radical surgery was met with skepticism due to the aggressive infiltrative character of the tumor. However, an increasing number of retrospective studies over the last decade suggest a survival benefit for surgery. A recent post-hoc analysis of a randomized controlled trial on the use of the surgical adjunct 5-ALA reported a prolonged overall survival from 11.9 to 16.7 months (evidence level 2a) after more extensive resection. Thus, maximal safe resection has become a mainstay of treatment for newly diagnosed glioblastoma, followed by adjuvant radio-chemotherapy.
Glioblastoma almost invariably recurs after a median of 6.9 months, leaving but few options for further treatment. Recurrence of glioblastoma after surgery and concomitant adjuvant therapy represents an additional therapeutic challenge and may be treated with second-line pharmacotherapy. In addition, a second surgery may also be considered in highly selected patients.
The rationale for surgery - maximum safe resection - is to prolong survival through reduction of tumor load, and, maybe due to an increased efficacy of adjuvant treatment. However, surgery carries risks of complications, that may result in a decreased functional and survival outcome. The crucial question therefore is whether, to what extent, and at what costs in terms of neurological risks a second resection prolongs survival.
Objective
The primary objective of this randomized trial is to compare survival outcome after surgery followed by adjuvant second-line therapy to no surgery followed by second-line therapy in recurrent glioblastoma. An auxiliary objective to primary objective is to compare the survival outcomes of operated patients to control in the subgroups stratified by extent of resection: incomplete resection (non-CRET) vs complete resection (CRET).
Secondary objectives are: assessment of recruitment for all screened patients, comparison of progression-free survival between treatment arms, evaluation of crossover and comparison of patient quality of life between treatment arms.
Safety objectives are: to assess neurological deficits, local infections and morbidity associated to surgery and hospital stay after surgery and during follow-up.
Methods
All patients (≥18 years) with a radiological suspicion of first recurrence of glioblastoma are screened for this trial. Patients eligible for study participation are informed on the treatment options for recurrent glioblastoma (surgery followed by adjuvant second-line therapy, second-line therapy, or palliative therapy alone) by the center investigators. Patients randomized to the control group will receive second-line therapy according to local guidelines. Patients randomized to the interventional group will receive a craniotomy and resection of the tumor followed by adjuvant second-line therapy. Outcome will be measured at 3 months intervals.
Recruitment rate and reason for non-inclusion will be monitored.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 120
- 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)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Surgery followed by adjuvant second-line therapy Surgery followed by adjuvant second-line therapy Surgery followed by adjuvant second-line therapy Second-line therapy alone Second-line therapy alone Second-line therapy alone
- Primary Outcome Measures
Name Time Method Overall survival from the date of inclusion From the date of inclusion until death/end of study, assessed up to 5.7 years
- Secondary Outcome Measures
Name Time Method Recruitment rate for all screened patients Screening and inclusion Total number of days spent at home after recurrence From the date of inclusion until death/end of study, assessed up to 5.7 years Morbidity of surgery Every 3 months up to 2 years or until death, assessed up to 5.7 years Total number of days spent outside home after recurrence From the date of inclusion until death/end of study, assessed up to 5.7 years Progression-free survival From the date of inclusion until the date of objective progression or the date of patient's death, whichever occurs first, assessed up to 5.7 years
Trial Locations
- Locations (26)
Universitätsklinikum Innsbruck
🇦🇹Innsbruck, Austria
Helios Klinikum Erfurt
🇩🇪Erfurt, Germany
Department of Neurosurgery, Universitätsklinikum Frankfurt
🇩🇪Frankfurt, Germany
Dep. of Neurosurgery, Universitätsklinikum Freiburg
🇩🇪Freiburg, Germany
Universitätsklinikum Gießen und Marburg
🇩🇪Giessen, Germany
Universitätsmedizin der Johannes Gutenberg-Universität Mainz
🇩🇪Mainz, Germany
Universitätsklinikum Münster
🇩🇪Münster, Germany
Department of Neurosurgery, Hospital of Larissa & General Hospital of Larissa
🇬🇷Larissa, Greece
Department of Neurosurgery, AHEPA University Hospital
🇬🇷Thessaloníki, Greece
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta
🇮🇹Milano, Italy
Department of Neurosurgery, Amsterdam University Medical Center
🇳🇱Amsterdam, Netherlands
Department of Neurosurgery, Radboud University Medical Center, Nijmegen
🇳🇱Nijmegen, Netherlands
Department of Neurosurgery, Haaglanden Medical Center, The Hague
🇳🇱The Hague, Netherlands
Department of Neurosurgery, Centro Hospitalar Universitário Lisboa Norte - Hospital de Santa Maria
🇵🇹Lisboa, Portugal
Department of Neurosurgery, Spitalul Clinic De Urgență "Bagdasar-Arseni"
🇷🇴Bucharest, Romania
Department of Neurosurgery, L'Hospitalet de Llobregat, Barcelona
🇪🇸Barcelona, Spain
Department of Neurosurgery, Puerta de Hierro University Hospital, Madrid
🇪🇸Madrid, Spain
Kantonsspital Aarau
🇨🇭Aarau, Switzerland
Universitätsspital Basel
🇨🇭Basel, Switzerland
Dep. of Neurosurgery, Bern University Hospital
🇨🇭Bern, Switzerland
Dep. of Neurosurger, Hôpitaux Universitaires de Genève
🇨🇭Geneva, Switzerland
Dep. of Neurosurgery, Centre hospitalier universitaire vaudois
🇨🇭Lausanne, Switzerland
Ospedale Regionale di Lugano
🇨🇭Lugano, Switzerland
Kantonsspital Luzern
🇨🇭Luzern, Switzerland
Department of Neurosurgery, Kantonsspital St. Gallen
🇨🇭Saint Gallen, Switzerland
Dep. of Neurosurgery, University Hospital of Zurich
🇨🇭Zurich, Switzerland