Lung Cancer Clinical Trial
Vandetanib, Carboplatin, and Paclitaxel in Treating Patients With Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer That Can Be Removed by Surgery
Summary
RATIONALE: Vandetanib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as carboplatin and paclitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving vandetanib together with chemotherapy 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 vandetanib together with carboplatin and paclitaxel works in treating patients with stage I, stage II, or stage III non-small cell lung cancer that can be removed by surgery.
Full Description
OBJECTIVES:
Primary
Determine the feasibility of neoadjuvant vandetanib in combination with carboplatin and paclitaxel in patients with resectable stage IB, II, or IIIA non-small cell lung cancer.
Secondary
Assess the 30-day postoperative mortality rate in these patients.
Assess the toxicity of this regimen in these patients.
Determine the percentage of patients who complete all planned courses of therapy.
Assess the clinical response rate in patients treated with this regimen.
Assess the pathologic complete response rate in patients treated with this regimen.
OUTLINE: This is a multicenter study.
Patients receive oral vandetanib once daily on days 1-21. Patients also receive paclitaxel IV over 3 hours and carboplatin IV over 1 hour on day 1. Treatment repeats every 3 weeks for up to 3 courses.
Patients undergo surgery at least 3 weeks after the last course of chemotherapy.
PROJECTED ACCRUAL: A total of 15 patients will be accrued for this study.
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically or cytologically confirmed non-small cell lung cancer (NSCLC), meeting 1 of the following staging criteria:
Stage IB or II disease
T3, N0-1 disease (stage IIIA)
Deemed a surgical candidate
No prior lung cancer (NSCLC or small cell lung cancer)
PATIENT CHARACTERISTICS:
ECOG performance status (PS) 0-2 OR Karnofsky PS 60-100%
WBC ≥ 3,000/mm³
Absolute neutrophil count ≥ 1,500/mm³
Platelet count ≥ 100,000/mm³
Bilirubin normal
AST and ALT ≤ 2.5 times upper limit of normal (ULN)
Creatinine ≤ 1.5 times ULN
Not pregnant or nursing
Negative pregnancy test
Fertile patients must use effective contraception
No evidence of severe or uncontrolled systemic disease or any concurrent condition that, in the opinion of the investigator, would preclude study compliance
No peripheral neuropathy ≥ grade 2
No hemoptysis within the past 12 weeks
No spontaneous bleeding within the past 12 weeks
No clinically significant cardiac event (e.g., NYHA class II-IV heart disease, myocardial infarction) within the past 3 months
No history of asymptomatic sustained ventricular tachycardia or arrhythmia that is symptomatic or requires treatment, including any of the following:
Multifocal premature ventricular contractions
Bigeminy
Trigeminy
Ventricular tachycardia
Uncontrolled atrial fibrillation
Atrial fibrillation controlled with medication allowed
No history of QTc prolongation as a result from other medication that required discontinuation of that medication
No congenital long QT syndrome or first-degree family relative with an unexplained death before the age of 40
No left bundle branch block
No QTc with Bazett's correction that is unmeasurable or QTc ≥ 480 milliseconds on screening ECG
Patients with QTc ≥ 480 milliseconds on screening ECG may have ECG repeated twice
Average QTc from the 3 screening ECG's must be < 480 milliseconds
No uncontrolled hypertension (systolic BP > 160 mm Hg or diastolic BP > 100 mm Hg)
No active diarrhea or active gastrointestinal disease that may affect the absorption of study drugs or ability to tolerate study drugs
No other malignancy within the past 3 years except in situ cervical carcinoma or adequately treated basal cell or squamous cell carcinoma of the skin
PRIOR CONCURRENT THERAPY:
More than 4 weeks since major surgery and recovered
No prior carboplatin, paclitaxel, or vandetanib
More than 30 days since prior investigational agents
More than 2 weeks since prior and no concurrent drugs that induce CYP3A4 including, but not limited to, any of the following:
Rifampin
Phenytoin
Carbamazepine
Barbiturates
Hypericum perforatum (St. John's wort)
No medication that may cause QTc prolongation or induce torsades de pointes for 2 weeks prior to beginning study treatment, during, and for 2 weeks after completion of study treatment
No concurrent combination antiretroviral treatment for HIV-positive patients
No other concurrent investigational agents
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There is 1 Location for this study
Detroit Michigan, 48201, United States
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