Paclitaxel Albumin-Stabilized Nanoparticle Formulation and Gemcitabine in Treating Patients With Advanced Metastatic Solid Tumors

NCT ID: NCT00307255

Last Updated: 2012-04-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-08-31
• Study Completion Date: 2008-10-31

Brief Summary

RATIONALE: Drugs used in chemotherapy, such as paclitaxel albumin-stabilized nanoparticle formulation and gemcitabine, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

PURPOSE: This phase I trial is studying the side effects and best dose of paclitaxel albumin-stabilized nanoparticle formulation when given together with gemcitabine in treating patients with advanced metastatic solid tumors.

Detailed Description

OBJECTIVES:

Primary

• Determine the dose-limiting toxicity and maximum tolerated dose of paclitaxel albumin-stabilized nanoparticle formulation (Abraxane) in combination with gemcitabine hydrochloride in patients with advanced metastatic solid tumors.

Secondary

• Evaluate the efficacy of this regimen in these patients.

OUTLINE: This is a dose-escalation study of paclitaxel albumin-stabilized nanoparticle formulation (Abraxane).

Patients receive paclitaxel albumin-stabilized nanoparticle formulation (Abraxane) IV over 30 minutes on day 1 followed by gemcitabine hydrochloride IV over 30 minutes on days 1 and 8. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Cohorts of 3-6 patients receive escalating doses of paclitaxel albumin-stabilized nanoparticle formulation (Abraxane) until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity. Up to 10 additional patients may be treated at the MTD.

After completion of study treatment, patients are followed at 30 days.

Conditions

Unspecified Adult Solid Tumor, Protocol Specific

Study Design

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

Interventions

gemcitabine hydrochloride

1000 mg/m2 on days 1 and 8 of each 21 day cycle

Intervention Type: DRUG

paclitaxel albumin-stabilized nanoparticle formulation

260 mg/m2 to 340 mg/m2 (dose will depend on when subject enters the study). Paclitaxel will be given on day 1 of each 21 day cycle (every 3 weeks)

Intervention Type: DRUG

Other Intervention Names

Gemzar; Abraxane

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed solid tumors

• Advanced metastatic disease
• Measurable or evaluable disease
• Must meet 1 of the following criteria:

• Failed prior standard therapy
• Not a candidate for standard therapy
• Has a disease for which there is no defined standard therapy
• No symptomatic brain metastases

PATIENT CHARACTERISTICS:

• ECOG functional status 0-2
• Life expectancy ≥ 8 weeks
• Absolute neutrophil count ≥ 1,500/mm^3
• Platelet count > 100,000/mm^3
• Hemoglobin ≥ 9.0 g/dL
• Bilirubin normal
• Creatinine ≤ 1.5 times upper limit of normal (ULN) OR creatinine clearance ≥ 60 mL/min
• AST and ALT ≤ 2.5 times ULN
• Not pregnant or nursing
• Negative pregnancy test
• No prior anaphylactic reaction or severe allergic reaction to paclitaxel, docetaxel, or gemcitabine hydrochloride
• No active infectious process that will require treatment with antibiotics for > 4 weeks
• No uncontrolled congestive heart failure
• No symptomatic coronary artery disease or heart block
• No myocardial infarction within the past 3 months
• No peripheral neuropathy ≥ grade 2 from any cause

PRIOR CONCURRENT THERAPY:

• More than 3 weeks since prior chemotherapy, radiotherapy, or any other treatment
• No prior radiotherapy to > 25% of bone marrow
• No prior nitrosoureas
• No more than 6 prior courses of alkylating agents
• No more than 2 prior courses of mitomycin C
• No more than 3 prior courses of cytotoxic therapy for metastatic disease
• No concurrent filgrastim (G-CSF), pegfilgrastim, or sargramostim (GM-CSF) during study course 1

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

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

UNC Lineberger Comprehensive Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thomas E. Stinchcombe, MD

Role: PRINCIPAL_INVESTIGATOR

UNC Lineberger Comprehensive Cancer Center

Locations

University of North Carolina Lineberger Comprehensive Cancer Center

Chapel Hill, North Carolina, United States

Countries

United States

Other Identifiers

CDR0000550136

Identifier Type: OTHER

Identifier Source: secondary_id

LCCC 0520

Identifier Type: -

Identifier Source: org_study_id