Official Title: “(NJ 1508) Modulation of Autophagy With Hydroxychloroquine in Combination With Carboplatin, Paclitaxel and Bevacizumab in Patients With Advanced/Recurrent Non-Small Cell Lung Cancer - A Phase I/II Study”

RATIONALE: Drugs used in chemotherapy, such as hydroxychloroquine, carboplatin, and paclitaxel and work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them.

Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor.

Giving hydroxychloroquine together with carboplatin, paclitaxel and bevacizumab may kill more tumor cells.

PURPOSE: This phase I/II trial is studying the side effects and best dose of hydroxychloroquine when given together with carboplatin, paclitaxel, and bevacizumab and to see how well they work in treating patients with recurrent advanced non-small cell lung cancer.

Study Type: Interventional

Study Design: Treatment, Open Label

Study Primary Completion Date: August 2011

OBJECTIVES:

Primary - To determine the recommended phase II dose of hydroxychloroquine and carboplatin in combination with paclitaxel and bevacizumab in patients with advanced recurrent non-small cell lung cancer. (Phase I) - To assess the antitumor activity, as measured by tumor response rate, of this regimen in these patients. (Phase II)

Secondary - To measure time to progression, progression-free survival, and overall survival of these patients. - To assess the incidence of toxicity of this regimen in these patients.

OUTLINE: This is a multicenter study. This is a phase I, dose-escalation study of carboplatin and hydroxychloroquine followed by a phase II study.

Patients receive paclitaxel IV over 3 hours, carboplatin IV over 15-30 minutes, and bevacizumab IV over 90 minutes on day 1 and oral hydroxychloroquine on days 1-21. Treatment repeats every 21 days for a total of 4 courses. Patients then receive bevacizumab IV over 30-90 minutes every 21 days and oral hydroxychloroquine daily for up to 1 year in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed every 6 months.

Intervention(s) in this Clinical Trial

• Biological: bevacizumab
• Drug: carboplatin
• Drug: hydroxychloroquine
• Drug: paclitaxel

Primary Measures

• Recommended phase II dose of hydroxychloroquine and carboplatin when administered with paclitaxel and bevacizumab (phase I)
  • Safety Issue?: No
• Overall response (phase II)
  • Safety Issue?: No

Secondary Measures

• Time to progression (phase II)
  • Safety Issue?: No
• Progression-free survival at 1 year (phase II)
  • Safety Issue?: No
• Overall survival (phase II)
  • Safety Issue?: No

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed advanced non-small cell lung cancer, meeting the following criteria:
• Recurrent disease
• No component of squamous cell carcinoma
• Mixed tumors will be categorized by predominant cell type
• No mixed histology with small cell component
• Diagnosis established on metastatic tumor aspirate or biopsy (not sputum cytology alone) and meets 1 of the following staging criteria:
• Stage IIIB disease with malignant pleural effusion
• Stage IV disease
• Measurable disease
• More than 1 year since post-operative adjuvant therapy for previously resected non-small cell lung cancer with evidence of disease progression
• No known CNS metastases by CT scan or brain MRI within the past 28 days

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1
• ANC ≥ 1,500/mm³
• Platelet count ≥ 100,000/mm³
• Hemoglobin ≥ 9 g/dL
• Total bilirubin ≤ 1.5 times upper limit of normal (ULN) (≤ 2 times ULN and no other liver function test abnormality in patients with Gilbert disease)
• AST/ALT ≤ 2.5 times ULN (≤ 5 times ULN in the presence of liver metastases)
• Alkaline phosphatase ≤ 2.5 times ULN
• Creatinine ≤ 1.5 times ULN OR creatinine clearance ≥ 60 mL/min
• INR ≤ 1.5 and aPTT normal
• Urine protein:creatinine ratio < 1.0 OR urine protein ratio < 1,000 mg by 24-hour urine collection
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No ongoing or active infection
• No psoriasis or porphyria
• No HIV positivity
• No significant traumatic injury within the past 28 days
• No serious non-healing wound, ulcer, or bone fracture
• No peripheral or sensory neuropathy > grade 1
• No hypertension that cannot be controlled by antihypertensive medication (i.e., blood pressure > 150/100 mm Hg despite optimal medical therapy)
• No cardiovascular disease, including any of the following:
• Unstable angina
• New York Heart Association class II-IV congestive heart failure
• History of significant vascular disease (e.g., aortic aneurysm)
• Symptomatic peripheral vascular disease within the past 6 months
• Myocardial infarction within the past 6 months
• Stroke within the past 6 months
• No other active malignancy within the past 3 years, except curatively treated basal cell or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, or ductal or lobular carcinoma in situ of the breast, or other curatively treated malignancy with no evidence of disease > 3 years
• No retinal or visual field changes from prior 4-aminoquinoline compound therapy
• No known hypersensitivity to 4-aminoquinoline compound
• No known glucose-6-phosphate (G-6P) deficiency
• No known bleeding diathesis or coagulopathy
• No known gastrointestinal pathology that would interfere with drug bioavailability
• No known prior hypersensitivity to carboplatin, paclitaxel, bevacizumab, hydroxychloroquine, or any of their components
• No history of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within the past 6 months
• No history of gross hemoptysis (i.e., bright red blood of a ½ teaspoon or more) within the past 3 months
• No history of any social or medical condition that, in the investigator's opinion, might interfere with the patient's ability to comply with the protocol or pose additional or unacceptable risk to the patient

PRIOR CONCURRENT THERAPY:

• See Disease Characteristics
• At least 2 weeks since prior radiation to sites other than the brain, and recovered to ≤ grade 1
• At least 28 days since prior and no concurrent full-dose anticoagulants or thrombolytic agents
• At least 28 days since prior major surgical procedure or open biopsy and no anticipated need for such during study therapy
• Vascular access device placement with wound recovery allowed before study
• No prior cytotoxic chemotherapy or targeted therapy in the advanced or metastatic setting
• No concurrent treatment for rheumatoid arthritis or systemic lupus erythematosus
• No concurrent combination antiretroviral therapy
• No concurrent hydroxychloroquine for treatment or prophylaxis of malaria
• No concurrent aurothioglucose
• No other concurrent investigational or commercial agent or therapy for this malignancy

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 18 Years

Maximum Age for this Clinical Trial: N/A

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: Cancer Institute of New Jersey

Overall Clinical Trial Officials and Contacts

Mika Sovak, MD, PhD Principal Investigator Cancer Institute of New Jersey  

Information obtained from ClinicalTrials.gov on July 02, 2009

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00728845

Study ID Number: CDR0000600241

ClinicalTrials.gov Identifier: NCT00728845

Health Authority: Unspecified

Clinical trial summary from the National Cancer Institute's PDQ® database