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Active, not recruiting Phase 1/2

Phase I/IIa Study of Concomitant Radiotherapy With Olaparib and Temozolomide in Unresectable High Grade Gliomas Patients

NCT03212742 · tracked via the Priya Life Science France tracker
Phase
Phase 1/2
Started
2017-09-04
Last updated
2025-12-04

Condition(s) studied

Malignant GliomasRadiotherapyPARP Inhibitor

Investigational drug(s) / intervention(s)

Olaparib →Temozolomide (TMZ) →IMRT (Intensity Modulated Radiation Therapy)

Olaparib: We propose 7 dose levels to reach the target dose of 400 mg per day (200 mg twice daily) of olaparib continuously DL1 (starting dose level) : Olaparib 50 mg Q12H Monday to wednesday DL2 : Olaparib 100mg Q12H Monday to wednesday DL3: Olaparib 100mg Q12H Monday to friday DL4 : Olaparib 200mg Q12H Monday to wednesday DL5: Olaparib 200mg Q12H Monday to friday DL6: Olaparib 200mg Q12H, continously

Temozolomide (TMZ): TMZ will be given at the dose of 75mg/m²/day during radiotherapy period. TMZ will be re-introduced 4 weeks after the end of radiotherapy at the dose of 150mg/m²/day on days 1 to 5 every 28 days, for a total of 6 cycles.

IMRT (Intensity Modulated Radiation Therapy): Radiotherapy consists of fractionated focal irradiation at a dose of 2 Gy per fraction given once daily five days per week over 6 weeks, for a total dose of 60 Gy by 3D- Intensity-Modulated RT (IMRT)

Study summary

The Stupp protocol is the standard treatment of glioblastoma multiform (GBM) which prognosis remains poor.

The non-dividing nature of normal brain cells provides an opportunity to enhance the therapeutic ratio by combining radiation with inhibitors of replication-specific DNA repair pathways such poly(ADP-ribose) polymerase (PARP) inhibitors, thus inducing more cytotoxic effects of DNA-damage related to treatment modalities, including alkylating reagents like temozolomide (TMZ).

Olaparib, a potent PARP inhibitor, overcomes apoptotic resistance and sensitizes GBM cells for death receptor-mediated apoptosis induced by TRAIL (Tumor necrosis factor-Related Apoptosis Inducing Ligand). Moreover, inhibition of PARP activity increases cellular sensitivity to ionizing radiation: it was even suggested to be more pronounced in tumors than in normal tissue.

Lastly, progress in technical imaging and intensity-modulated-radiotherapy (IMRT) techniques provide new possibilities for sparing healthy tissues.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Provision of signed informed consent prior to any study specific procedures * Histologically-confirmed diagnosis of glioblastoma (IDH-wildtype, IDH-mutant or NOS, except gliosarcoma), non resectable or partially resectable with a residual tumor on pre-radiotherapy MRI. The presence of a residual disease will be assessed by the radiologist on the pre-radiotherapy imaging as compared with initial imaging. * IMRT must start within 6 weeks after histological diagnosis * Age between 18 and 70 years ; * Neurologically asymptomatic or pauci-symptomatic patients. Patients with moderated neurological symptoms without systemic corticosteroids treatment or with a stable dose of corticosteroids during the study as long as these were started at least 4 weeks prior to treatment can be included. * Adequate bone marrow and organ function measured within 15 days prior to administration of study treatment as defined below: * Haemoglobin ≥ 10.0 g/dL with no blood transfusions (packed red blood cells and platelet transfusions) in the past 28 days before start of treatment * Absolute neutrophil count (ANC) ≥ 1.5 x 109/L o No features suggestive of MDS/AML on peripheral blood smear * Platelet count ≥ 100 x 109/L * White blood cells (WBC) \> 3x109/L * Total bilirubin ≤ 1.5 x institutional upper limit of normal * AST (SGOT)/ALT (SGPT) ≤ 2.5 x institutional upper limit of normal * Creatinine clearance estimated using the Cockcroft-Gault equation of ≥51 mL/min: Estimated creatinine clearance = \[(140-age(years)) x weight(kg) (x Fsex) \] / \[serum creatinine (mg/dL) x 72\] where Fsex=0.85 for females and Fsex=1 for males. * ECOG performance status 0-2 * Patients must have a life expectancy ≥ 16 weeks. * Women of childbearing potential (WOCBP) and men under efficient contraception during treatment and at least 6 months after the end of treatment. * Evidence of non-childbearing status for women of childbearing potential: negative urine or serum pregnancy test within 28 days of study treatment, confirmed prior to treatment on day 1. * Postmenopausal (if applicable) is defined as: * Amenorrheic for 1 year or more following cessation of exogenous hormonal treatments, * LH and FSH levels in the post-menopausal range for women under 50, * radiation-induced oophorectomy with last menses \>1 year ago, * chemotherapy-induced menopause with \>1 year interval since last menses, * or surgical sterilisation (bilateral oophorectomy or hysterectomy). * Male patients and their partners, who are sexually active and of childbearing potential, must agree to the use of two highly effective forms of contraception in, throughout the period of taking study treatment and for 3 months after last dose of study drug(s) to prevent pregnancy in a partner. * Patient is willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examinations including follow up. * Subjects affiliated to an appropriate social security system Exclusion Criteria: * Any prior radiotherapy to brain * Any prior chemotherapy or immunotherapy * Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site) * Candidate for a concomitant therapy with Tumor-Treating Fields during the maintenance treatment \[70\] * Previous enrolment in the present study * Participation in another clinical trial protocol within 30 days prior to enrolment; * Any previous treatment with a PARP inhibitor, including olaparib. * Patients with second primary cancer, except: adequately treated non-melanoma skin cancer, curatively treated in-situ cancer of the cervix, or other solid tumours curatively treated with no evidence of disease for ≥ 5 years * Gadolinium hypersensitivity, or any contraindication to undergo MRI examination (Pacemaker, brain aneurysms clips) * Patients who had no initial pre-surgery contrast enhanced MRI scan including the standard sequences (T1 non enhanced, T1 contrast enhanced, T2 FLAIR) * Patients receiving any systemic chemotherapy, radiotherapy (except for palliative reasons), within 2 weeks from the last dose prior to study treatment. The patient can receive a stable dose of bisphosphonates for bone metastases, before and during the study as long as these were started at least 4 weeks prior to treatment with study drug. * Concomitant use of known strong CYP3A inhibitors (eg. itraconazole, telithromycin, clarithromycin, protease inhibitors boosted) or moderate CYP3A inhibitors (eg. ciprofloxacin, erythromycin, diltiazem, fluconazole, verapamil). The required washout period prior to starting olaparib is 2 weeks. * Concomitant use of known strong (eg. phenobarbital, phenytoin, rifampicin, rifabutin, rifapentine, carbamazepine, and St John's Wort ) or moderate CYP3A inducers (eg. bosentan, modafinil). The required washout period prior to starting olaparib is 5 weeks for phenobarbital and 3 weeks for other agents. * Resting ECG with QTc \> 470 msec detected on 2 or more time points within a 24 hour period or family history of long QT syndrome. If ECG demonstrates QTc \> 470 msec, patient will be eligible only if repeat ECG demonstrates QTc ≤470 msec; * Blood transfusions within 1 month prior to study start * Previous allogenic bone marrow transplant or double umbilical cord blood transplantation (dUCBT) * Patients with myelodysplastic syndrome/acute myeloid leukaemia or with features suggestive of MDS/AML. * Major surgery within 14 days of starting study treatment and patients must have recovered from any effects of any major surgery. * Patients considered a poor medical risk due to a serious, uncontrolled medical disorder, non-malignant systemic disease or active, uncontrolled infection. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 3 months) myocardial infarction, uncontrolled major seizure disorder, unstable spinal cord compression (untreated and unstable for at least 28 days prior to study entry), superior vena cava syndrome, extensive bilateral lung disease on HRCT scan or any psychiatric disorder that prohibits obtaining informed consent. * Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of the study medication (inflammatory bowel disease, major bowel resection …) * Pregnant or breast feeding women. * Immunocompromised patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV) and are receiving antiviral therapy. * Patients with known active hepatitis (i.e., Hepatitis B or C) due to risk of transmitting the infection through blood or other body fluids. * Patients with a known hypersensitivity to olaparib or any of the excipients of the product. * For temozolomide treatment, patients with a known galactose intolerance, a Lapp lactase deficit or a glucose or galactose malabsorption syndrome (rare hereditary diseases) * Patients with uncontrolled epileptic seizures. * Neurological, addictive or psychiatric disorder; * Lack of availability for clinical follow-up assessments; * Persons protected by a legal regime (guardianship, trusteeship).

Primary outcome measure(s)

  • The Recommended Phase II Dose (RP2D) - Phase I — The RP2D will be evaluated 4 weeks after the end of radiotherapy
    The primary objective for the phase I is to determine the Recommended Phase II Dose (RP2D) of olaparib combined with the Stupp protocol (TMZ and concomitant fractionated radiotherapy: 60Gy/30 fractions/6 weeks) in first line treatment of patients with unresectable high-grade gliomas
  • Overall survival - Phase II — 12 months after the first administration of treatment
    The primary objective for the phase II is to assess the 12-month overall survival of the combination

Trial sites (15)

FacilityCityRegionStatus
CHU Amiens France
Institut de Cancérologie de l'Ouest Angers France
CHU Bordeaux France
Centre François Baclesse Caen France
Centre Guillaume le Conquérant Le Havre France
CH du Havre Le Havre France
GHBS Lorient France
Centre léon Bérard Lyon France
Hôpitaux universitaires La Pitié Salpétrière - Charles Foix Paris France
Institut Curie Paris France
Centre Hospitalier Lyon Sud Pierre-Bénite France
Centre Eugène Marquis Rennes France
Centre Henri Becquerel Rouen France
Institut de Cancérologie de l'Ouest Saint-Herblain France
Institut Claudius Regaud Toulouse France
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03212742 on ClinicalTrials.gov ↗ ← All trials in France