Malignant Pleural Mesothelioma
Conditions
Keywords
MPM, Unresectable, Phase II, Randomized, Maintenance
Brief summary
This is a multicenter, randomized, 1:1, double blinded phase II trial. Patients with unresectable malignant pleural mesothelioma (MPM) will be randomized between arm A: nintedanib and arm B:placebo
Detailed description
This is a multicenter, prospective, double blinded, randomized, two-arm phase II trial aiming to evaluate nintedanib treatment as switch maintenance in patients with unresectable MPM. After signing of the informed consent and upon confirmation of all eligibility criteria, patients will be randomized 1:1 to: * Arm A: twice daily nintedanib at a dose of 200 mg until progression or unacceptable toxicities. * Arm B: matched placebo. Response evaluation will be performed through CT scans every 8 weeks.
Interventions
DRUGNintedanib
Nintedanib 200 mg administered twice daily
DRUGPlacebo
Matching placebo administered twice daily
Sponsors
European Organisation for Research and Treatment of Cancer - EORTC
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
* Histological diagnosis of unresectable Malignant Pleural Mesothelioma (MPM); * Response or Stable disease according to modified RECIST criteria \[48\] after first line platinum-pemetrexed chemotherapy for 4-6 cycles; * Last platinum chemotherapy dose administered within 60 days (i.e. randomization must occur within 60 days from the last dose of the last cycle of platinum-pemetrexed chemotherapy); * Age \>18 years; * ECOG performance status (PS) 0-2; * Life expectancy of at least 12 weeks in the opinion of the investigator; * Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements to be conducted within 7 days prior to start of first dose
Exclusion criteria
* prior systemic anticancer therapy including cytotoxic therapy or immune-checkpoint inhibitor, for MPM, other than first line platinum-based doublet chemotherapy; * previous extra-pleural pneumonectomy (other forms of previous surgery eg pleurectomy are acceptable); * previous Vascular Endothelial Growth Factor (VEGF) inhibitors (eg bevacizumab, sorafenib, etc); * treatment with other investigational drugs or treatment in another clinical interventional trial within the past 4 weeks before start of therapy or concomitantly with the trial; * patients that, in the opinion of the investigator, have reduced performance status by 2 ECOG levels (e.g. PS 0 to 2 or PS 1 to 3) from beginning to completion of 1st line chemotherapy; * radiotherapy (with the exception of palliative radiotherapy) during study or within 4 weeks of start of study drug; * known brain metastasis or lepto-meningeal disease. Patients with suspicious neurological symptoms should undergo a CT scan/MRI of the brain to exclude brain metastasisNo active brain metastases (e.g. stable for \< 4 weeks;, no adequate previous treatment with radiotherapy;, symptomatic, requiring treatment with anti-convulsants; dexamethasone therapy will be allowed if administered as stable dose for at least one month before randomization); patients with suspicious neurological symptoms should undergo a CT scan/MRI of the brain to assess brain metastasis; * leptomeningeal metastases; * significant weight loss (\> 10 %) within the past 6 weeks prior to treatment in the present trial; * pre-existing clinically significant ascites and/or clinically significant pleural effusion; * active or history of bleeding complications that would prevent anti-angiogenic therapy * centrally located tumors with radiographic evidence (CT or MRI) of local invasion of major blood vessels; typical mediastinal pleural involvement with mesothelioma remains eligible; * clinically active cancer other than mesothelioma within 5 years prior to start of study treatment; * radiographic evidence of cavitatory or necrotic tumors; * unstoppable use of therapeutic anticoagulation (except low dose heparin and/or heparin flush as needed for maintenance of an indwelling intravenous device) or antiplatelet therapy (except for chronic low-dose therapy with acetylsalicylic acid =325mg per day); * clinically significant cardiovascular diseases (i.e. hypertension not controlled by medical therapy, unstable angina, history of myocardial infarction within the past 6 months, congestive New York Heart Association (NYHA) II, serious cardiac arrhythmia, clinically significant pericardial effusion)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Progression-free survival | 6 months | From randomization until progression or death |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Overall survival | 12 months | From randomization until progression or death |
| Overall Response Rate | 6 months | Response according to modified RECIST |
Countries
Belgium, Italy, United Kingdom
Outcome results
None listed