Status and phase
Conditions
Treatments
Study type
Funder types
Identifiers
About
This is a multicentre randomised double-blind phase II trial, sponsored by Gustave Roussy and involving one French center as well as the Spanish Lung Cancer Group (≈20 centers of the SLCG).
Six hundred patients with diagnosis of stage IIIB/IV NSCLC will initially be registered prior to receiving the first line platinum-based chemotherapy or during or at the end of the first 6 cycles of inducation platinium based chemotherapy and provide consent for retrieving archival tissue collection and providing translational blood samples and tumor biopsies.
Patients displaying progressive disease or stable disease after induction chemotherapy will be withdrawn and further optimally managed according to local practice. For them, an optional tumour biopsy will be performed at the end of the induction treatment.
Treatment will be administered at a dose of 600 mg daily (2 doses of 300 mg [2 tablets of 150 mg] taken approximately 12 hours apart) and cycle duration will be 28 days. Disease will be assessed every 2 cycles by CTscan (MRI or PET-scan if the scan is not contributive) and treatment will be administered until disease progression or unacceptable toxicity. Patients will then be optimally managed according to local practice. Follow-up will be for a minimum of 15 months from the time of randomization, and until last venue. All randomised patients will be asked to provide translational blood samples at randomization, on treatment and at the end of the treatment. Optional tumour biopsies will be performed at randomization, at the end of the treatment (or at disease progression if available).
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
For inclusion in the study subjects should fulfill the following criteria:
Provision of written informed consent to treatment and companion translational studies prior to any study specific procedures
Patients must be > 18 years of age.
Affiliation to an health insurance
Histological diagnosis of NSCLC
Advanced or metastatic disease (stage IIIB/IV)
Access to the original tumor biopsy or planning of a fresh tumor biopsy before start the platinium based chemotherapy
Chemonaive for NSCLC or patient having received adjuvant chemotherapy at least 2 years before trial enrolment or patient currently receiving his/her first platinum-based chemotherapy for advanced NSCLC (first line or second line only if the first line was an anti-PD-1 or anti-PD-L1 agent monotherapy)
No other cancer in the previous 3 years, except cervical cancer or cutaneous cancer
Absence of EGFR-sensitising mutation or ALK translocation
ECOG Performance Status of 0-1
Fit to receive 6 cycles or currently receiving of platinum-based induction chemotherapy
At the start of the platinium based induction chemotherapy measurable lesions by RECIST v1.1 criteria, i.e. at least one lesion, not previously irradiated, that can be accurately measured at baseline as ≥ 10mm in the longest diameter (except lymph nodes that must have short axis ≥ 15mm) with computed tomography (CT), magnetic resonance imaging (MRI) or clinical examination and which is suitable for accurate repeated measurements.
Inclusion criteria 13 is only for patients registered before starting the platinum-based induction chemotherapy:
Patients must have normal organ and bone marrow function measured within 14 days prior to administration of the platinum based treatment
Evidence of non-childbearing status for women of childbearing potential: negative serum pregnancy test within 14 days of study treatment.
Postmenopausal is defined as:
Both men and women (of childbearing potential) who are sexually active should accept to use adequate contraception, during and for at least 6 months post-treatment
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.
Previous surgery (in the adjuvant setting) for NSCLC, radiotherapy (with a curative intent for local or locally-advanced disease) or immunotherapy by anti- PD-1 or anti-PD-L1 agent in the metastatic setting are allowed
Non-inclusion criteria:
Uncontrolled or symptomatic brain metastases. Controlled brain metastases are defined as stable for 1 month. A scan to confirm the absence of brain metastases is not required. Corticosteroids therapy will be allowed if administered at a stable dose for at least one month before entering the trial.
Previous enrolment (or randomisation) in the present study Any previous systemic treatment for cancer in the previous 3 years.
Any previous systemic treatment for cancer in the previous 3 years except for NSCLC.
Patients receiving any radiotherapy or considering to require radiotherapy to the lung at the time of study entry or in the near future, except for palliative reasons. 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 inclusion.
Patients receiving the following classes of inhibitors of CYP3A4 (see Section 6.5 for guidelines and wash out periods).
Major surgery within 14 days before to start the induction chemotherapy and patients who have not 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, coronary artery disease, cardiomyopathy, uncontrolled hypertension, myocardial infarction in the last 3 months, unstable spinal cord compression (untreated and unstable for at least 28 days prior to start the induction chemotherapy), superior vena cava syndrome, extensive bilateral lung disease on HRCT scan or any psychiatric disorder that prohibits obtaining informed consent.
Pregnant and/or breast-feeding women.
Patients who are known to be serologically positive for human immunodeficiency virus (HIV) and/or are receiving antiviral therapy. Systematic serologies to confirm the absence of this disease are not required.
Patients with known active hepatic disease (i.e., Hepatitis B or C) Systematic serologies to confirm the absence of these diseases are not required.
Patients with a known hypersensitivity to olaparib/placebo, cisplatin, carboplatin, or other platinum containing compounds, or any of the excipients of the product.
Concomitant yellow fever vaccine
Patients unable to swallow orally administered medication and patients with gastrointestinal disorders likely to interfere with absorption of olaparib/placebo.
Symptomatic peripheral neuropathy ≥ grade 2
Patients with uncontrolled seizures
Patients with myelodysplastic syndrome/acute myeloid leukaemia.
Enrolment in another clinical trial (except observational study).
Primary purpose
Allocation
Interventional model
Masking
600 participants in 2 patient groups, including a placebo group
Loading...
Central trial contact
Valérie Mairot; Sophie Postel-Vinay, MD
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal