Carboplatin, Gemcitabine, and Thalidomide in Patients Undergoing Surgery for Stage II or III Non-Small Cell Lung Cancer

Stopped early · Phase 2

Conditions studied: Lung Cancer

In brief

RATIONALE: Drugs used in chemotherapy, such as carboplatin and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Thalidomide may stop the growth of tumor cells by blocking blood flow to the tumor. Giving carboplatin and gemcitabine together with thalidomide before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This phase II trial is studying how well giving carboplatin and gemcitabine together with thalidomide works in treating patients who are undergoing surgery for stage II or stage III non-small cell lung cancer.

Key facts

Study ID

NCT00281827

Run by

Masonic Cancer Center, University of Minnesota

People needed

22

Starts

2002-05-01

Expected to finish

2008-07-01

Last updated by the study team

2017-12-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically or cytologically confirmed non-small cell lung cancer (NSCLC), including any of the following histologic subtypes:
• Squamous cell carcinoma
• Adenocarcinoma
• Large cell undifferentiated carcinoma
• Stage II or IIIA disease
• Measurable disease, defined as ≥ 1 unidimensionally measurable lesion ≥ 20 mm by conventional techniques OR ≥ 10 mm by spiral Computerized Axial Tomography (CT) scan
• No tumor involving the superior sulcus (e.g., Pancoast tumor)
• Karnofsky performance status 70-100%
• Absolute neutrophil count ≥ 1,500/mm\^3
• Platelet count ≥ 100,000/mm\^3
• Creatinine ≤ 2 mg/dL
• Bilirubin < 2 mg/dL
• Aspartate aminotransferase (AST) < 3 times upper limit of normal

You may not qualify if…

• Pregnant or nursing
• No nursing during and for ≥ 4 weeks after completion of study treatment
• Positive pregnancy test
• Fertile female patients must use 2 effective methods of contraception 4 weeks before, during, and for 4 weeks after completion of study treatment
• Fertile male patients must use effective barrier contraception during and for 4 weeks after completion of study treatment
• Blood, sperm, or ova donation during study treatment
• Post obstructive pneumonia
• Other serious infection or medical illness that would preclude study participation
• Other malignancy within the past 5 years except adequately treated basal cell or squamous cell skin cancer, carcinoma in situ of the cervix, or other malignancy that is unlikely to affect survival for the next 3 years
• Less than 5 years since prior resection of lung disease
• Prior systemic chemotherapy or radiotherapy for non-small cell lung cancer (NSCLC)
• Other concurrent chemotherapy or radiotherapy
• Concurrent hormonal therapy or immunotherapy
• Other concurrent anticancer therapy
• Other concurrent investigational agents
• Concurrent participation in another clinical study

Where it is running

• University of Minnesota Cancer Center — Minneapolis, Minnesota, United States
• Hubert H. Humphrey Cancer Center at North Memorial Outpatient Center — Robbinsdale, Minnesota, United States
• Norris Cotton Cancer Center at Dartmouth-Hitchcock Medical Center — Lebanon, New Hampshire, United States

Full record on ClinicalTrials.gov

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