Lomustine With and Without Reirradiation for First Progression of Glioblastoma: a Randomized Phase III Study

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorEuropean Organisation for Research and Treatment of Cancer - EORTC

About this trial

Despite comprehensive multimodal treatment of newly diagnosed glioblastoma, almost all patients suffer from tumour relapse. Currently, no standard of care exists to treat these tumour relapses. Treatment options include repeated surgery (if feasible), systemic therapy (bevacizumab, lomustine, temozolomide re-challenge), reirradiation and best supportive care. Currently, the superiority of combined chemoradiation versus chemotherapy alone remains unproven. Given that lomustine is the standard chemotherapeutic agent for the treatment of recurrent glioblastoma in Europe and the unclear efficacy of reirradiation, we want to explore whether combining lomustine and reirradiation may be a better treatment than lomustine alone. The results of the prospective randomized trial proposed here should demonstrate a significant improvement in overall survival when lomustine is combined with reirradiation in patients with recurrent glioblastoma compared to lomustine alone without adversely affecting quality of survival. The trial will be stopped based on overall survival in a preplanned futility and efficacy interim analysis.

Eligibility criteria

Qualifiers

Before patient's enrolment, written informed consent must be given according to ICH/GCP, and national/local regulations.

Patients with first progression or recurrent glioblastoma after standard chemoradiotherapy (any treatment other than use of nitroureas) having occurred at least 6 months after the end of prior radiotherapy

Measurable disease according to RANO criteria with a maximum tumour diameter of 5 cm (local investigator assessment)

In case of surgery for recurrence: fully recovered from surgery, confirmation of recurrence by histology, and patient fit for treatment as per local investigator assessment.

Disqualifiers

Any prior anticancer treatment for recurrent glioblastoma (except surgery)

Significant reduction in thrombocyte and/or leukocyte counts as well as severe renal impairment according to investigator's opinion

History or present acute leukaemia or any myeloid disease

Known hypersensitivity to the active components or excipients of lomustine

Trial design

Treatments tested in this trial

  • Lomustine
  • Reirradiation

Treatment groups

411 Participants
are divided into 2 treatment groups

Sponsors and collaborators