AMG 102, Pemetrexed Disodium, and Cisplatin in Treating Patients With Malignant Pleural Mesothelioma

National Cancer Institute (NCI)

Status and phase

Withdrawn

Phase 2

Conditions

Epithelial Mesothelioma

Advanced Malignant Mesothelioma

Recurrent Malignant Mesothelioma

Sarcomatous Mesothelioma

Treatments

Biological: rilotumumab

Other: laboratory biomarker analysis

Drug: pemetrexed disodium

Drug: cisplatin

Study type

Interventional

Funder types

NIH

Identifiers

NCT01105390

E1B09

NCI-2011-02068 (Registry Identifier)

CDR0000670445 (Registry Identifier)

U10CA021115 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This phase II trial is studying how well giving AMG 102 together with pemetrexed disodium and cisplatin works in treating patients with malignant pleural mesothelioma. Monoclonal antibodies, such as AMG 102, can block tumor growth in different ways. Some block the ability of tumor cells to grow or spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy, such as pemetrexed disodium and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving AMG 102 together with pemetrexed disodium and cisplatin may kill more tumor cells

Full description

PRIMARY OBJECTIVES:

I. To evaluate the progression-free survival of patients with malignant pleural mesothelioma (MPM) treated with anti-HGF monoclonal antibody AMG 102 in combination with pemetrexed disodium and cisplatin.

SECONDARY OBJECTIVES:

I. To assess the toxicity associated with this regimen in these patients. II. To determine the response rate of patients treated with this regimen. III. To determine the overall survival of patients treated with this regimen. IV. To evaluate multiple potential correlative biomarkers in MPM that are relevant to this combined regimen, including serum HGF and mesothelin levels, c-met expression by IHC in tumor specimens, presence of c-met mutations in tumor, and the presence of thymidylate synthetase (TS) and excision repair cross complementing protein-1 (ERCC1) polymorphisms.

OUTLINE: This is a multicenter study.

Patients receive anti-HGF monoclonal antibody AMG 102 (AMG 102) IV over 1 hour, pemetrexed disodium IV over 10 minutes, and cisplatin IV over 1 hour on day 1. Treatment repeats every 21 days for 6 courses in the absence of disease progression or unacceptable toxicity. Patients without disease progression may continue AMG 102 IV over 1 hour on day 1, every 3 weeks, as maintenance therapy in the absence of disease progression. Some patients undergo blood sample collection at baseline and periodically during study for correlative biomarker studies. Tumor samples from diagnostic tissue may also be analyzed.

After completion of study therapy, patients are followed up periodically every 3 months for 2 years and then every 6 months for 1 year.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

Histologically and cytologically confirmed malignant mesothelioma of the pleura
- All subtypes allowed
- Disease not amenable to curative surgery
Measurable disease
- Patients with disease not measurable by standard RECIST criteria (i.e., pleural rinds/thickening only) allowed
- Pleural effusions or positive bone scans are not considered measurable
No prior radiotherapy to the target lesion or measurable lesion unless the site has subsequent evidence of progression
Patients who have undergone pleurodesis allowed
- Post-pleurodesis CT scan required
No known or suspected brain metastases
ECOG performance status 0-1
ANC ≥ 1,500/mm^3
Platelet count ≥ 100,000/mm^3
Total bilirubin ≤ 1.5 times upper limit of normal (ULN)
Alkaline phosphatase ≤ 1.5 times ULN
ALT and AST ≤ 1.5 times ULN
Albumin ≥ 2.5 g/dL
Creatinine clearance ≥ 45 mL/min OR serum creatinine ≤ 1.5 times ULN
Able to take folic acid and vitamin B12
Not pregnant or nursing
Negative pregnancy test
Fertile patients must agree to use effective contraception
No active infection or serious concomitant systemic disorder in compatible with the study
No thrombosis or vascular ischemic events within the last 12 months, including any of the following:
- Deep venous thrombosis
- Pulmonary embolism
- Transient ischemic attack
- Cerebral infarction
- Myocardial infarction
No peripheral edema ≥ grade 3
No serious or non-healing wounds
No second primary malignancy except in situ carcinoma of the cervix or breast, other in situ malignancies, adequately treated basal cell carcinoma of the skin, or other malignancy within the past 3 years with no evidence of recurrence
No concurrent antiretroviral therapy for HIV-positive patients
At least 4 weeks since prior radiotherapy
More than 30 days since major surgery procedures or > 14 days since any minor surgical procedure and recovered
- Central venous catheter placement, fine-needle aspiration, thoracentesis, or paracentesis are not considered major or minor surgical procedures
No prior systemic chemotherapy for mesothelioma
No prior intracavity cytotoxic drugs or immunomodulators (unless for the purpose of pleurodesis)
No prior anti-HGF monoclonal antibody AMG 102, other c-MET, or HGF inhibitors
No prior or concurrent anticoagulation therapy within the past 7 days
- Low-dose Coumadin-type anticoagulants or low-molecular weight heparin for prophylaxis against central venous catheter thrombosis allowed
No investigational agents within the past 4 weeks