Evaluation Of The Efficacy Of The Combination Of Axitinib With Pemetrexed And Cisplatin In The Treatment Of Non-Squamous Non-Small Cell Lung Cancer



Status:Completed
Conditions:Lung Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:January 2009
End Date:March 2012

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Randomized Phase 2 Study Of Cisplatin/Pemetrexed With Or Without Axitinib (AG-013736) As First-Line Treatment For Patients With Non-Squamous Non-Small Cell Lung Cancer

AG-013736 (axitinib) in combination with cisplatin and pemetrexed will be evaluated as
first-line treatment of patients with locally advanced, recurrent, or metastatic
non-squamous, non small cell lung cancer (NSCLC).


Inclusion Criteria:

- Histologically or cytologically confirmed diagnosis of adeno-, large cell or
bronchioalveolar non-small cell lung cancer

- Cytologic specimens for diagnosis or for cell type classification must have been
obtained from bronchial brushings or washings or from needle aspiration of a defined
lesion. Sputum cytology alone will not be acceptable for diagnosis or for cell type
classification.

- Patients with mixed NSCLC with predominantly squamous cell carcinoma should be
classified as squamous and thus do not qualify for this study.

- Stage IIIB with malignant effusion (with cytologic confirmation of malignant pleural
or pericardial effusion), Stage IV, or recurrent disease after definitive
loco-regional therapy.

- Candidate for primary treatment with cisplatin and pemetrexed

Exclusion Criteria:

- Any histological/cytological evidence of predominantly squamous NSCLC.

- Small cell or carcinoid lung cancer patients are also ineligible.

- NSCLC that cannot be classified as one of the eligible histologies (adenocarcinoma,
large cell or bronchioalveolar).

- Prior systemic therapy for Stage IIIB (with malignant effusion), Stage IV, or
recurrent NSCLC. (Prior treatment with systemic therapy as adjuvant chemotherapy or
in conjunction with radiotherapy for Stage II or III NSCLC is permitted if the last
dose of chemotherapy was completed 12 months or more prior to randomization).

- Prior treatment with a VEGF or VEGFR inhibitor.
We found this trial at
12
sites
Marietta, Georgia 30060
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Marietta, GA
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Atlanta, Georgia 30309
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Atlanta, GA
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Bloomington, Illinois 61701
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Bloomington, IL
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Decatur, Georgia 30033
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Decatur, GA
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East Providence, Rhode Island 02915
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East Providence, RI
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Genova,
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Hershey, Pennsylvania 17033
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Hershey, PA
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Huntsville, Alabama 35801
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Huntsville, AL
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Macon, Georgia 31201
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Macon, GA
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Peoria, Illinois 61614
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Peoria, IL
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Sandy Springs, Georgia 30342
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Sandy Springs, GA
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West Reading, Pennsylvania 19611
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West Reading, PA
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