Expired Study
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Newark, New Jersey 07101


Purpose:

RATIONALE: Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays and other types of radiation to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue. Poly ICLC may stop the growth of liver cancer by blocking blood flow to the tumor. Giving the drug directly into the arteries around the tumor may kill more tumor cells. Giving cyclophosphamide and radiation therapy together with poly ICLC may be an effective treatment for liver cancer. PURPOSE: This phase I/II trial is studying the side effects of giving cyclophosphamide, radiation therapy, and poly ICLC together and to see how well they work in treating patients with unresectable, recurrent, primary, or metastatic liver cancer.


Study summary:

OBJECTIVES: - To study the safety and effectiveness of a strategy to establish robust anticancer immunologic body defenses by using low-dose radiation therapy to the liver cancer in order to increase tumor targetability; inject a body defense activator, polyinosinic-polycytidylic acid polylysine carboxymethylcellulose (poly ICLC, hiltonol, oncovir), into and around the cancer to activate sentinel dendritic cells to alarm body defenses; and shut down local production of factors that suppress the body's natural anticancer defenses by starving the cancer of its blood supply within the liver. OUTLINE: Patients receive low-dose oral cyclophosphamide once daily on days 1-21 and undergo 3-dimensional conformal radiotherapy on days 21-23. On day 24, patients undergo an intra- or peri-tumoral polyinosinic-polycytidylic acid polylysine carboxymethylcellulose (poly ICLC) injection directly into the tumor followed by trans-hepatic artery embolization to the designated tumor. Patients receive poly ICLC subcutaneously on days 26, 35, 37, 42, 44, 49, and 51. Treatment repeats every 57 days for up to 3 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 3 months for 1 year and then every 6 months thereafter.


Criteria:

DISEASE CHARACTERISTICS: - Radiologically or histologically confirmed hepatocellular carcinoma - Stage III or IV primary disease - Recurrent, unresectable, or metastatic disease meeting any of the following criteria: - Pancreatic cancer that underwent prior surgical resection and progressed with recurrent metastatic disease to the liver - Gastric, colon, breast, or ovarian cancer or melanoma with metastatic disease to the liver - Primary or recurrent disease that cannot be surgically resected leaving the patient disease-free - Radiologically measurable disease - Ineligible for liver transplantation according to University of San Francisco listing criteria: - Single lesion > 6.5 cm - Three or more tumors > 4.5 cm - Cumulative tumor diameter > 8 cm PATIENT CHARACTERISTICS: - Karnofsky performance status 60-100% - ANC ≥ 1,500/mm³ - Platelets ≥ 75,000/mm³ - Creatinine ≤ 1.7 mg/dL - Total bilirubin ≤ 1.5 mg/dL - AST and ALT ≤ 3 times the upper limit of normal - INR < 1.5 - LVEF ≥ 50% - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception - No serious concurrent infection or medical illness that would render the protocol treatment unsafe - LVEF ≥ 50% PRIOR CONCURRENT THERAPY: - See Disease Characteristics - No concurrent steroids


NCT ID:

NCT00553683


Primary Contact:

Study Chair
Andrew N. de la Torre, MD
UMDNJ University Hospital / St Joseph Medical Center


Backup Contact:

N/A


Location Contact:

Newark, New Jersey 07101
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 19, 2017

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