Evolution of the Heart Function When Monitoring Immunotherapies Anti-cancerous Inhibiting PD-1
- Conditions
- Non-small CellMelanomaLung Cancer
- Interventions
- Registration Number
- NCT03313544
- Lead Sponsor
- Assistance Publique Hopitaux De Marseille
- Brief Summary
Prospective, monocentric clinical study. Patients selected for nivolumab therapy in AP-HM for melanoma and non-small cell lung cancer will be eligible. Do not include patients with conditions that do not allow MRI, prior cardiovascular disease with LVEF\<50%, cardiomyopathy, history of cardiac arrhythmia, history of cardiovascular toxicity under anticancer therapy, coronary artery disease or stroke less than 3 months Therapeutic management will not be modified and treatment will be administrated as usual.
Cardiovascular follow up will be identical to that recommended and realized in current care in the Cardio-Oncology unit of AP-HM. It will include clinical, biological (BNP and troponin) and trans-thoracic echocardiography (TTE) at baseline and then at 1, 3 and 6 months. Auto-antibodies against troponin I assay will be performed to avoid false negatives of normal blood level of troponin I at baseline and then at 6 months. Cardiac MRI will be performed as well at baseline and at the end of the study (6 months). MRI is the gold standard for ventricular function evaluation.
Primary endpoint will be left ventricular function evolution evaluated by global longitudinal strain (GLS, 2D speckles tracking) in TTE. Secondary endpoints will be left and right ventricular function parameters: LEVF by TTE and MRI, left ventricular indexed volumes by TTE and MRI, right ejection ventricular function and indexed volumes by TTE and MRI, systolic pulmonary arterial pressure by TTE, serum troponin I and BNP, arrhythmias and conduction disorders on the electrocardiogram (ECG).
Number of required subjects: GLS is recommended for following up left ventricular function under anticancer treatments. Based on the hypothesis of a significant GLS decrease (15%) in 20% of cases with alpha risk of 0.05 and accuracy of 0.12 which means expected confidence interval of 0.08-0.32, then the number of required subjects is 50 patients.
The inclusion period will be 18 months with a follow up if 6 months, ie a total duration of the study of 24 months.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
patients treated with nivolumab
- Age <18 years
- Preliminary cardiac disease with FeVG <50%
- Cardiomyopathy dilated, hypertrophic or restrictive
- History of cardiac arrhythmia
- History of cardiac toxicity under another anti-cancer treatment
- Known coronary disease
- History of stroke less than 3 months old
- Patient not wishing to participate in the study
- Vulnerable persons (pregnant women, adults under guardianship or guardianship, persons deprived of their liberty)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description NIVOLUMAB PATIENTS MRI - NIVOLUMAB PATIENTS BLOOD SAMPLES - NIVOLUMAB PATIENTS trans-thoracic echocardiography - NIVOLUMAB PATIENTS Nivolumab -
- Primary Outcome Measures
Name Time Method systolic pulmonary arterial pressure 6 months trans-thoracic echocardiography
- Secondary Outcome Measures
Name Time Method Brain natriuretic peptide (BNP) 1,3, 6 months BLOOD SAMPLES
ventricular function evaluation. 6 MONTHS MRI
serum troponin I 1,3, 6 months BLOOD SAMPLES
Trial Locations
- Locations (1)
Assistance Publique Hopitaux de Marseille
🇫🇷Marseille, France