Non-small Cell Lung Cancer Stage IV
Conditions
Brief summary
Primary Objective: * to assess the objective response rate (ORR) of Iniparib (SAR240550) administered as a 60-min intravenous infusion twice weekly, when combined to gemcitabine/cisplatin chemotherapy regimen (GCS) as well as with the standard regimen of gemcitabine/cisplatin (GC) in patients with stage IV non small cell lung cancer. Secondary objectives are: * to assess the safety profiles of the study combination GCS and of the standard regimen GC; * to assess the progression free survival and the overall survival in both arms; * to assess the relationship between DNA repair pathway characteristics of tumors at baseline and clinical outcome of disease. * to assess the effect of Iniparib on PAR level in peripheral blood mononuclear cells (PBMC). (As of 10 September 2010, the collection of PBMC is temporarily discontinued.)
Detailed description
The duration of the study for a patient will include a period for inclusion of up to 3 weeks. The patients may continue treatment up to a maximum of 6 cycles or until disease progression, unacceptable toxicity or consent withdrawal, followed by a minimum of 30-day follow-up after the last study treatment administration. Patients will be followed for at least 30 days after the last administration of study treatment for safety purpose. In case of study treatment discontinuation without disease progression, efficacy data will be collected every 6 weeks until disease progression, death or end of study whatever comes first. After disease progression, the patient will be followed-up every 12 weeks (3 months) for overall survival (OS) until death or end of study whatever comes first. The end of the study will be one year after the first dose of the last treated patient.
Interventions
DRUGIniparib
Pharmaceutical form: solution for infusion Route of administration: 60-minute IV infusion
DRUGgemcitabine
Pharmaceutical form: solution for infusion Route of administration: 30-minute IV infusion
DRUGcisplatin
Pharmaceutical form: solution for infusion Route of administration: 1- to 4-hour IV infusion, according to the local standard
Sponsors
Sanofi
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Stage IV disease (including stage IIIB with pleural effusion) with no prior systemic therapy. Adjuvant therapy is allowed if ended more than 1 year before inclusion in the study. * Histologically confirmed squamous cell bronchogenic carcinoma OR non squamous cell carcinoma. * Patients with previous radiotherapy as definitive therapy for locally advanced non-small cell lung cancer are eligible, as long as the selected measurable lesions are outside the original radiation therapy port. Radiation therapy must have been completed \>4 weeks prior to study entry. * Palliative radiotherapy must have been completed \> 2 weeks prior to study entry. Irradiated lesions may not serve as measurable lesions. * At least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1. * Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1. * Adequate bone marrow reserve. * Adequate liver and renal function. * Women of childbearing potential must have a negative serum or urine pregnancy test performed within 7 days prior to start of treatment.
Exclusion criteria
* Prior treatment with gemcitabine, platinum salts or any PARP inhibitor class compound. * Past or current history of neoplasm other than the entry diagnosis, with the exception of treated non-melanoma skin cancer or carcinoma in-situ of the cervix, or other cancers cured by local therapy alone and with an expected disease-free survival of \> or = 5 years. * Major medical conditions that might affect study participation e.g. cardiac disease, uncontrolled infection (\>Grade 2). * Presence of active brain metastases. * A major surgical procedure, open biopsy, or significant traumatic injury within 28 days of beginning treatment, or anticipation of the need for major surgery during the course of the study. * Any history of medical or psychiatric condition or laboratory abnormality that, in the opinion of the investigator, may increase the risks associated with the study participation or administration of the investigational products, or that may interfere with the interpretation of the results * Grade 2 or higher ear and labyrinth disorders. * Known or suspected allergy/hypersensitivity to any agent given in the course of this trial. The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| overall response rate (ORR) that is defined in the RECIST 1.1 version, as: complete response rate + partial response rate | up to a maximum follow-up of 25 weeks |
Secondary
| Measure | Time frame |
|---|---|
| progression free survival | up to a maximum of 2 years |
| overall survival | up to a maximum of 2 years |
Countries
France, Germany, Italy, Spain, United Kingdom
Outcome results
None listed