Ph II OSI-774 (Erlotinib,Tarceva) In Advanced Bronchioloalveolar Cell Lung Cancer

• Status: Completed
• Trial end date: 2013-02-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is:

• To measure the ability of OSI-774 to effectively treat bronchioloalveolar cell lung cancer.

• To see whether the use of OSI-774 provides meaningful symptomatic benefit in patients with advanced bronchioloalveolar cell lung cancer.

This study is a Phase II study. The first study of OSI-774 was done to evaluate what dose should be given to patients with cancer has been completed. The purpose of this research study is to see whether this experimental treatment, called OSI-774, can cause a type of non-small cell lung cancer to stop growing or shrink. This study is sponsored by a company called Genentech, and is being done at Memorial Hospital, as well as other cancer centers around the country interested in developing new drugs for the treatment of this type of cancer.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Memorial Sloan Kettering Cancer Center
• Collaborators: Dana-Farber Cancer Institute; Genentech, Inc.; M.D. Anderson Cancer Center; Northwestern University; Vanderbilt-Ingram Cancer Center
• Treatments: Erlotinib Hydrochloride

Criteria

Inclusion Criteria:

• Either bronchioloalveolar cell carcinoma or a variant thereof after review

• Clinical stage IIIB (malignant pleural or pericardial effusion) or IV or recurrent/medically inoperable disease

• Measurable or evaluable indicator lesions

• No prior or one chemotherapy regimen for NSCLC

• Three weeks since last chemotherapy, and three weeks since prior radiation therapy to a major bone-marrow containing area

• Karnofsky performance status > or = to 80% OR ECOG performance status ≤ or = to 1

• Life expectancy > or = to 8 weeks

• Adequate hematologic, renal and/or hepatic function: WBC > or = to 3,000/ul, hemoglobin > or = to 9.0 g/dl, platelet count > or = to 100,000/ul, total bilirubin < or = to 1.0 mg/dl, AST < than or = to 2.5 X UNL, creatinine < or = to 1.5 mg/dl or Clcr > or = to 55ml/min.

• Effective contraception

Exclusion Criteria:

• Prior exposure to OSI-774 or other treatments targeting the HER family axis (e.g.-trastuzumab, ZD1839, C225, etc.)

• Two or more prior chemotherapy regimens

• Concurrent active cancer

• Uncontrolled central nervous system metastases (i.e. any known CNS lesion which is radiographically unstable, symptomatic and/or requiring escalating doses of corticosteroids)

• Pregnant or lactating women

• Malignancies within the past 5 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skin

• Prior systemic cytotoxic chemotherapy for other malignant disease

• Significant medical history or unstable medical condition (unstable systemic disease:

congestive heart failure, recent MI, unstable angina, active infection, uncontrolled hypertension).