Axitinib in Malignant Mesothelioma (N08CPA)
Recruitment status was Recruiting
Malignant Pleural Mesothelioma
|Study Design:||Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Randomized Phase I/II Study of Standard Chemotherapy (Cisplatin and Pemetrexed) With or Without Axitinib in Patients With Malignant Mesothelioma: Interim Biopsy Analysis to Determine Efficacy|
- To test the impact of the addition of axitinib to standaard chemotherapy treatment on histology samples [ Time Frame: micro-vessel density;expression of VEGF and PDGF receptor; extent of necrosis and apoptosis ] [ Designated as safety issue: No ]To determine the effects of the addition of axitinib to standard chemotherapy on tissue samples with respect to micro-vessel density (MVD); expression of VEGF-Receptor; PDGF receptor expression; extent of necrosis and apoptosis
- the side effects of the standard chemotherapy and the additional risks related to axitinib use [ Time Frame: AE;SAE;SUSAR ] [ Designated as safety issue: Yes ]hypertension, fatigue, abdominal discomfort
|Study Start Date:||May 2009|
|Estimated Study Completion Date:||September 2010|
|Estimated Primary Completion Date:||September 2010 (Final data collection date for primary outcome measure)|
Experimental: arm 2
axitinib + cisplatin + premetrexed
axitinib: 5 mg BID, day 2 until day 21 of each cycle; cisplatin: 75 mg/m2 day 1, every 3 weeks; pemetrexed: 500 mg/m2 day 1, every 3 weeks.
Active Comparator: arm 1
cisplatin + premetrexed
cisplatin: 75 mg/m2 day 1, every 3 weeks; pemetrexed: 500 mg/m2 day 1, every 3 weeks.
To determine the effects of the addition of axitinib to standard chemotherapy on tissue samples with respect to micro-vessel density (MVD): expression of VEGF-Receptor; PDGF receptor expression; extent of necrosis and apoptosis.
To determine the safety of the addition of axitinib (to a maximum of the recommended dose of maximally 2 x 10 mg per day) to the standard treatment with cisplatin and pemetrexed.
To determine the feasibility of performing a (second) thoracoscopy after 10 weeks of the combination treatment with cisplatin, pemetrexed and axitinib.
Serum samples will be collected and tested for inhibiting effects in a tube formation and spheroid sprouting assay.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01211275
|Contact: P. Baas, Dr.||+31 (0)email@example.com|
|Contact: W. A. Buikhuisen, MD||+31 (0)firstname.lastname@example.org|
|Antoni van Leeuwenhoekziekenhuis (NKI-AVL)||Recruiting|
|Amsterdam, Noord-Holland, Netherlands, 1066 CX|
|Contact: P Baas, Dr. +31 (0)20-5122958 email@example.com|
|Contact: W. A. Buikhuisen, MD +31 (0)20-5122958 firstname.lastname@example.org|
|Principal Investigator: P Baas, Dr.|
|Principal Investigator:||P Baas, Dr.||NKI-AvL|