Overview

NOA-12: BIBF1120 and R-RT in Glioblastoma

Status:
Terminated
Trial end date:
2017-09-01
Target enrollment:
0
Participant gender:
All
Summary
Patients with glioblastoma at first or second progression who have failed standard treatment that must have included radiochemotherapy with temozolomide and who are a candidate for a reirradiation can be included into the trial. In the phase I part the minimal tolerated dose (MTD)of BIBF 1120 in combination with radiotherapy will be investigated. Subjects in phase II will be randomised to receive reirradiation alone or reirradiation + 2 x MTD BIBF1120.
Phase:
Phase 1/Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Prof. Dr. Wolfgang Wick
Treatments:
Nintedanib
Criteria
Inclusion Criteria:

- Male and female patients with a recurrence / progression of glioblastoma either not
being eligible for tumour resection or having macroscopic residual tumour after
resection of the recurrence

- Diagnosis of glioblastoma must be proven histologically and progress must be
documented by MRI. MRI images must not be older than 2 weeks before first dosing/start
of RT

- Not more than two prior therapy regimens including one or two resections, one or two
chemotherapies (one temozolomide containing concomitant to radiotherapy) and one
radiotherapy (RT) for the brain tumour

- Previous irradiation therapy of the primary tumour with a maximal dose of 60 Gy; at
least 8 months since the end of preirradiation

- Candidate for reirradiation with recurrent tumour visible on MRIT1 (Gd) and with the
largest diameter measuring 1 cm to 5 cm

- Informed consent

- Age ≥ 18 years, smoking or non-smoking, of any ethnic origin

- Karnofsky performance index (KPI) ≥ 60%

- Neutrophile counts > 1500/μl / Platelet counts > 80.000/μl /Haemoglobin > 10 g/dl /
Serum creatinine < 1.5-fold upper normal range / Bilirubin, AST or ALT < 2,5-fold
upper normal range unless attributed to anticonvulsants / Alkaline phosphatase <
2,5-fold upper normal range

- Adequate contraception

- If on steroids, stable or decreasing treatment with steroids within 5 days before
treatment start

Exclusion Criteria:

- More than one RT of brain, prior first radiotherapy with more than 60 Gy

- Cumulative total dose on the optical chiasm >54 Gy for 2 Gy/fraction, α/β=2

- Prior treatment with bevacizumab, iodine seeds and/or brachytherapy

- Unable to undergo MRI

- Past medical history of diseases with poor prognosis according to the judgement of the
Investigator, e.g. severe coronary heart disease, severe diabetes, immune deficiency,
residual deficits after stroke, severe mental retardation

- HIV or hepatitis infection

- Pregnancy or breast feeding

- Treatment within any other clinical trial parallel to the treatment phase of the
current study or within 30 days before inclusion

- Known coronary artery disease, significant cardiac arrhythmias or severe congestive
heart failure (NYHA class III - IV)