Panobinostat, Etoposide, and Cisplatin as First-Line Therapy in Treating Patients With Extensive-Stage Small Cell Lung Cancer

NCT ID: NCT01160731

Last Updated: 2014-12-31

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-11-30

Brief Summary

RATIONALE: Panobinostat 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 etoposide and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving panobinostat together with etoposide and cisplatin may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of panobinostat when given together with etoposide and cisplatin as first-line therapy in treating patients with extensive-stage small cell lung cancer.

Detailed Description

OBJECTIVES:

Primary

• To determine the maximum-tolerated dose, the recommended dose, and the activity of panobinostat when given in combination with etoposide and cisplatin to patients with extensive-stage small cell lung cancer.

Secondary

• To estimate the time-to-progression, the duration of response, and disease stabilization in these patients.
• To estimate the overall survival of these patients.
• To determine the pharmacokinetic profile of panobinostat in combination with etoposide and cisplatin.
• To assess the overall safety profile of panobinostat in these patients.
• To determine the adverse events in these patients treated with this regimen.
• To assess the quality of life of these patients.

OUTLINE: This is a multicenter, dose-escalation study of panobinostat.

Patients receive chemotherapy comprising cisplatin IV on day 1, etoposide IV on days 1-3, and panobinostat IV over 30 minutes on days 1 and 8. Treatment repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline and then periodically during study treatment and follow up, using questionnaire EQ-5D (Euro QoL).

Blood samples may be collected at baseline and periodically during and after study treatment for pharmacokinetic assessment and biomarker translational studies.

After completion of study treatment, patients are followed up at 4 weeks and then every 3 months.

Conditions

Lung Cancer

Keywords

extensive stage small cell lung cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cisplatin, Etoposide & Panobinostat

Group Type: EXPERIMENTAL

cisplatin

Intervention Type: DRUG

etoposide phosphate

Intervention Type: DRUG

panobinostat

Intervention Type: DRUG

laboratory biomarker analysis

Intervention Type: OTHER

pharmacological study

Intervention Type: OTHER

Interventions

cisplatin

Intervention Type: DRUG

etoposide phosphate

Intervention Type: DRUG

panobinostat

Intervention Type: DRUG

laboratory biomarker analysis

Intervention Type: OTHER

pharmacological study

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed small cell lung cancer

• Extensive-stage disease
• Measurable disease according to RECIST criteria
• No symptomatic brain metastasis or meningeal tumors

PATIENT CHARACTERISTICS:

• ECOG performance status 0-1
• Life expectancy ≥ 6 months
• Absolute neutrophil count > 1,500/mm^3
• Platelet count ≥ 100,000/mm^3
• Hemoglobin ≥ 10.0 g/dL
• Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR 24-hour creatinine clearance ≥ to 60 mL/min
• Magnesium, potassium, and phosphorus ≥ the lower limit of normal OR correctable with supplements prior to study treatment
• AST/ALT ≤ 2.5 x ULN (≤ 5.0 x ULN if hepatic metastases are present)
• Serum bilirubin ≤ 1.5 x ULN
• Alkaline phosphatase ≤ 2.5 x ULN OR liver fraction ≤ 2.5 x ULN
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective double contraception (at least 1 barrier method) during and for at least 30 days after completion of study treatment
• No impaired cardiac function, including any one of the following:

• LVEF < 45% as determined by ECHO
• Complete left bundle branch block, obligate use of a cardiac pacemaker, congenital long QT syndrome, history or presence of atrial or ventricular tachyarrhythmias, clinically significant resting bradycardia (< 50 beats per minute), QTcF > 480 msec on screening ECG, or right bundle branch block and left anterior hemiblock (bifascicular block)
• Uncontrolled angina pectoris or acute myocardial infarction within the past 3 months
• Other clinically significant heart disease (e.g., congestive heart failure, uncontrolled hypertension, history of labile hypertension, or history of poor compliance with an antihypertensive regimen)
• No history of HIV or AIDS-related illness
• No acute or chronic liver or renal disease
• No other concurrent severe and/or uncontrolled medical conditions that could cause unacceptable safety risks or compromise compliance with the protocol, including any of the following:

• Uncontrolled diabetes
• Chronic obstructive or chronic restrictive pulmonary disease
• Active or uncontrolled infection
• No known immediate or delayed hypersensitivity reaction or idiosyncrasy to drugs chemically related to panobinostat, cisplatin, or etoposide
• No hearing impairment that would be a contraindication to the use of cisplatin

PRIOR CONCURRENT THERAPY:

• No prior chemotherapy
• No investigational drug or experimental medications or treatments within the past 30 days or 5 half-lives, whichever is longer

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cancer Trials Ireland

NETWORK

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Paul Donnellan

Role: PRINCIPAL_INVESTIGATOR

Galway University Hospital

Countries

Ireland; United Kingdom

Other Identifiers

ICORG-07-09

Identifier Type: -

Identifier Source: secondary_id

EUDRACT-2008-003634-21

Identifier Type: -

Identifier Source: secondary_id

EU-21047

Identifier Type: -

Identifier Source: secondary_id

07-09 ICORG

Identifier Type: -

Identifier Source: org_study_id