Thalidomide and Chemoembolization With Doxorubicin in Treating Patients With Liver Cancer That Cannot be Removed by Surgery

NCT ID: NCT00006016

Last Updated: 2015-04-15

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 75 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2000-05-31
• Study Completion Date: 2005-04-30

Brief Summary

This phase II trial is studying the effectiveness of combining thalidomide and chemoembolization in treating patients who have liver cancer that cannot be removed by surgery. Thalidomide may stop the growth of liver cancer by stopping blood flow to the tumor. Chemoembolization kills tumor cells by blocking the blood flow to the tumor and keeping chemotherapy drugs near the tumor. Combining thalidomide with chemoembolization may kill more tumor cells.

Detailed Description

OBJECTIVES:

I. Determine the feasibility and potential activity of thalidomide in patients with unresectable hepatocellular carcinoma who are undergoing chemoembolization to predominant tumor masses.

II. Determine the toxicity of this regimen of these patients. III. Determine the overall survival of patients treated with this regimen. IV. Determine the serum levels of vascular endothelial growth factor, basic fibroblast growth factor, and tumor necrosis factor alpha in patients treated with this regimen.

OUTLINE:

Patients receive oral thalidomide daily beginning 4 weeks before the first planned chemoembolization procedure. Thalidomide administration is stopped 24 hours before each chemoembolization procedure, and then restarted at 24 hours after completion of each procedure OR when blood counts and levels of bilirubin and transaminases recover, whichever occurs later. Thalidomide treatment continues in the absence of disease progression or unacceptable toxicity.

Patients undergo placement of a visceral arterial catheter. Patients receive doxorubicin as a chemoemulsion via the arterial catheter into 1 hepatic lobe only under angiographic guidance. Immediately after delivery of the chemoemulsion, patients undergo particulate embolization. The opposite lobe, if involved, is treated within 3-5 weeks of treatment of the initial lobe. Patients are reevaluated for repeat chemoembolization within 8-12 weeks of the last chemoembolization. For eligible patients, each lobe is treated separately a second time, in the same sequence, in the absence of disease progression or unacceptable toxicity.

PROJECTED ACCRUAL: A total of 75 patients will be accrued for this study within 18 months.

Conditions

Adult Primary Hepatocellular Carcinoma; Advanced Adult Primary Liver Cancer; Localized Unresectable Adult Primary Liver Cancer

Study Design

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

Study Groups

Treatment (thalidomide, chemoembolization)

Patients receive oral thalidomide daily beginning 4 weeks before the first planned chemoembolization procedure. Thalidomide administration is stopped 24 hours before each chemoembolization procedure, and then restarted at 24 hours after completion of each procedure OR when blood counts and levels of bilirubin and transaminases recover, whichever occurs later. Thalidomide treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo placement of a visceral arterial catheter. Patients receive doxorubicin as a chemoemulsion via the arterial catheter into 1 hepatic lobe only under angiographic guidance. Immediately after delivery of the chemoemulsion, patients undergo particulate embolization. The opposite lobe, if involved, is treated within 3-5 weeks of treatment of the initial lobe. Patients are reevaluated for repeat chemoembolization within 8-12 weeks of the last chemoembolization.

Group Type: EXPERIMENTAL

thalidomide

Intervention Type: DRUG

Given orally

doxorubicin hydrochloride

Intervention Type: DRUG

Given transarterially (chemoembolization)

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

Interventions

thalidomide

Given orally

Intervention Type: DRUG

doxorubicin hydrochloride

Given transarterially (chemoembolization)

Intervention Type: DRUG

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

Other Intervention Names

Kevadon; Synovir; THAL; Thalomid; ADM; ADR; Adria; Adriamycin PFS; Adriamycin RDF

Eligibility Criteria

Inclusion Criteria

• Histologically proven hepatocellular carcinoma
• Ineligible for potentially curative surgical resection
• Must be a candidate for palliative chemoembolization

• MRI must show one or more discrete tumor nodules that can be targeted by angiography for chemoembolization

• No diffusely infiltrating tumor
• Lesions under consideration for chemoembolization must demonstrate substantial hypervascularity
• Performance status - ECOG 0-2
• Absolute neutrophil count at least 1,200/mm^3
• Hemoglobin at least 8.0 g/dL
• Platelet count at least 50,000/mm^3
• SGOT and SGPT no greater than 5 times normal
• Bilirubin less than 3 mg/dL
• Creatinine no greater than 1.5 mg/dL
• No other medical condition that would preclude study participation
• No other malignancy within the past 5 years except curatively resected basal cell skin cancer or carcinoma in situ of the cervix
• Not pregnant or nursing
• Negative pregnancy test
• Regardless of fertility status:

• All female patients (unless they have undergone a hysterectomy or have been amenorrheic or postmenopausal for at least 2 years) must use at least 1 highly active method of contraception AND 1 additional effective method of contraception at least 4 weeks before, during, and for at least 4 weeks after study participation
• All male patients (even if they have undergone a successful vasectomy) must use effective barrier contraception during and for at least 4 weeks after study participation
• Prior interferon for hepatitis allowed
• No prior biologic therapy for hepatocellular carcinoma (HCC)
• No prior chemotherapy for hepatocellular carcinoma (HCC)
• No concurrent barbiturates or alcohol

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

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Alec Goldenberg

Role: PRINCIPAL_INVESTIGATOR

NYU Langone Health

Locations

New York University Langone Medical Center

New York, New York, United States

Countries

United States

Other Identifiers

NCI-2012-02352

Identifier Type: REGISTRY

Identifier Source: secondary_id

NCI-99

Identifier Type: -

Identifier Source: secondary_id

CDR0000068025

Identifier Type: -

Identifier Source: secondary_id

NYU-9937

Identifier Type: OTHER

Identifier Source: secondary_id

99

Identifier Type: OTHER

Identifier Source: secondary_id

N01CM17103

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2012-02352

Identifier Type: -

Identifier Source: org_study_id