BMS-247550 in Treating Patients With Liver or Gallbladder Cancer

Phase 2TerminatedNCT00023946

National Cancer Institute (NCI)50 enrolled

Overview

Phase II trial to study the effectiveness of BMS-247550 in treating patients who have liver or gallbladder cancer. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die.

PRIMARY OBJECTIVES: I. Determine the objective response rate of patients with hepatobiliary cancer treated with BMS-247550. II. Determine the toxicity of this drug in these patients. III. Determine the duration of response, median and overall survival, and time to progression in patients treated with this drug. OUTLINE: This is a multicenter study. Patients receive BMS-247550 IV over 3 hours on day 1. Treatment repeats every 21 days for at least 2 courses in the absence of disease progression or unacceptable toxicity. Patients are followed every 6 weeks until disease progression

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Adult Primary Cholangiocellular Carcinoma Adult Primary Hepatocellular Carcinoma Advanced Adult Primary Liver Cancer

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Histologically or cytologically confirmed locally advanced, metastatic, or recurrent hepatobiliary cancer * Liver (hepatocellular) * Bile duct (cholangiocarcinoma) * Gallbladder * At least 1 unidimensionally measurable lesion * At least 20 mm by conventional techniques OR at least 10 mm by spiral CT scan * The following are not considered measurable lesions: * Lesions seen on colonoscopic examination or barium studies * Bone metastases * CNS lesions * Ascites * No brain metastases * Performance status - ECOG 0-2 * At least 3 months * WBC at least 3,000/mm\^3 * Absolute neutrophil count at least 1,500/mm\^3 * Platelet count at least 100,000/mm\^3 * Bilirubin no greater than 1.5 mg/dL * AST/ALT no greater than 2.5 times upper limit of normal * Creatinine no greater than 1.5 mg/dL * Creatinine clearance at least 60 mL/min * No symptomatic congestive heart failure * No unstable angina pectoris * No cardiac arrhythmia * No grade 2 or greater peripheral neuropathy * No other uncontrolled concurrent illness * No ongoing or active infection * No psychiatric illness or social situation that would preclude study compliance * No prior allergic hypersensitivity reaction attributed to compounds containing Cremophor EL (e.g., paclitaxel or compounds of similar chemical or biological composition to BMS-247550) * No other currently active malignancy except nonmelanoma skin cancer, carcinoma in situ of the cervix, or cancer for which patient has completed therapy and is at less than 30% risk of relapse * Not pregnant or nursing * Negative pregnancy test * Fertile patients must use effective contraception * No concurrent immunotherapy * No prior chemotherapy * No other concurrent chemotherapy * No concurrent hormonal therapy * No concurrent therapeutic radiotherapy * At least 30 days since prior investigational agents * At least 7 days since prior cimetidine * No concurrent cimetidine * No other concurrent commercial or investigational anticancer agents or therapies * No concurrent unconventional therapies, food, or vitamin supplements (e.g., St. John's Wort) * No concurrent combination antiretroviral therapy for HIV-positive patients

Outcomes

Primary Outcomes

Objective response rate (partial or complete response) evaluated by RECIST

A 10% response rate precludes further study whereas a 25% response rate would indicate that further study is warranted.

Time frame: Up to 8 years

Frequency and extent of cytotoxic activity graded according to the NCI CTC Version 2.0

Time frame: Up to 8 years

Time to disease progression

Will also be evaluated using the Kaplan-Meier estimator.

Time frame: From the first day of treatment until the date PD or death is first reported, assessed up to 8 years

Overall survival