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SCH 66336 With or Without Gemcitabine Followed by Surgery Compared With Surgery Alone in Treating Patients With Primary Liver Cancer

Primary Purpose

Liver Cancer

Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
gemcitabine hydrochloride
lonafarnib
conventional surgery
Sponsored by
Jonsson Comprehensive Cancer Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Liver Cancer focused on measuring localized resectable adult primary liver cancer, recurrent adult primary liver cancer, adult primary hepatocellular carcinoma, adult primary cholangiocellular carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Histologically or cytologically confirmed resectable primary hepatocellular carcinoma or cholangiocarcinoma 18 and over Karnofsky 70-100% Hematopoietic: Absolute neutrophil count greater than 1,500/mm3 Platelet count at least 100,000/mm3 Hemoglobin at least 9 g/dL Hepatic: Bilirubin no greater than 2 times upper limit of normal (ULN) SGOT or SGPT no greater than 5 times ULN Albumin at least 2.5 g/dL INR less than 1.3 Renal: Creatinine no greater than 1.5 mg/dL Cardiovascular: QTc prolongation no greater than 440 msec Other: Negative pregnancy test Fertile patients must use effective barrier contraception At least 6 weeks since prior radiotherapy and recovered At least 6 weeks since prior surgery and recovered At least 6 weeks since prior systemic therapy and recovered Exclusion Criteria: metastatic disease outside of the liver pregnant or nursing malabsorption or other gastrointestinal (GI) condition that would preclude ability to take oral medication and/or GI absorption (e.g., partial small bowel obstruction) non-malignant systemic disease that would preclude study active uncontrolled infection No grade II nausea or grade I vomiting despite antiemetic medication concurrent immunotherapy Chemotherapy: No other concurrent chemotherapy concurrent hormonal therapy including estrogen therapy concurrent oral contraceptives or other hormonal methods Concurrent megestrol acetate allowed concurrent corticosteroids (except for nausea/vomiting during gemcitabine administration) concurrent CYP3A4 inhibitors or inducers including: Azoles (e.g., itraconazole, clotrimazole, fluconazole, or ketoconazole) Macrolide antibiotics (e.g., azithromycin, clarithromycin, or erythromycin) Cyclosporine Grapefruit Antiepileptic medication (e.g., phenytoin, carbamazepine, or phenobarbital) Antibiotics for tuberculosis (e.g., rifampin or isoniazid) concurrent HIV protease inhibitors (e.g., amprenavir, ritonavir, or saquinavir mesylate) concurrent cisapride other concurrent investigational therapy

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Secondary Outcome Measures

    Full Information

    First Posted
    July 11, 2001
    Last Updated
    July 29, 2020
    Sponsor
    Jonsson Comprehensive Cancer Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00020774
    Brief Title
    SCH 66336 With or Without Gemcitabine Followed by Surgery Compared With Surgery Alone in Treating Patients With Primary Liver Cancer
    Official Title
    A Phase IB Clinical Study Of The Farnesyltransferase Inhibitor SCH 66336 And Gemcitabine In Patients With Resectable Primary Liver Neoplasms
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2012
    Overall Recruitment Status
    Withdrawn
    Study Start Date
    October 1998 (undefined)
    Primary Completion Date
    January 2003 (Actual)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Jonsson Comprehensive Cancer Center

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Randomized phase II trial to compare the effectiveness of SCH 66336 with or without gemcitabine followed by surgery with that of surgery alone in treating patients who have primary liver cancer.
    Detailed Description
    OBJECTIVES: I. Determine the biologic activity and toxicity of neoadjuvant SCH 66336 with or without gemcitabine followed by surgical resection vs surgical resection alone in patients with resectable primary liver cancer. OUTLINE: This is a randomized, open-label study. Patients are randomized to one of three treatment arms. Arm I: Patients receive neoadjuvant oral SCH 66336 twice daily for 14 days followed by surgical resection. Arm II: Patients receive neoadjuvant oral SCH 66336 twice daily for 14 days and gemcitabine IV over 30 minutes once weekly for 2 weeks followed by surgical resection. Arm III: Patients undergo surgical resection. Patients receive no neoadjuvant therapy prior to resection. PROJECTED ACCRUAL: Approximately 30 patients (10 per treatment arm) will be accrued for this study.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Liver Cancer
    Keywords
    localized resectable adult primary liver cancer, recurrent adult primary liver cancer, adult primary hepatocellular carcinoma, adult primary cholangiocellular carcinoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    gemcitabine hydrochloride
    Intervention Type
    Drug
    Intervention Name(s)
    lonafarnib
    Intervention Type
    Procedure
    Intervention Name(s)
    conventional surgery

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Histologically or cytologically confirmed resectable primary hepatocellular carcinoma or cholangiocarcinoma 18 and over Karnofsky 70-100% Hematopoietic: Absolute neutrophil count greater than 1,500/mm3 Platelet count at least 100,000/mm3 Hemoglobin at least 9 g/dL Hepatic: Bilirubin no greater than 2 times upper limit of normal (ULN) SGOT or SGPT no greater than 5 times ULN Albumin at least 2.5 g/dL INR less than 1.3 Renal: Creatinine no greater than 1.5 mg/dL Cardiovascular: QTc prolongation no greater than 440 msec Other: Negative pregnancy test Fertile patients must use effective barrier contraception At least 6 weeks since prior radiotherapy and recovered At least 6 weeks since prior surgery and recovered At least 6 weeks since prior systemic therapy and recovered Exclusion Criteria: metastatic disease outside of the liver pregnant or nursing malabsorption or other gastrointestinal (GI) condition that would preclude ability to take oral medication and/or GI absorption (e.g., partial small bowel obstruction) non-malignant systemic disease that would preclude study active uncontrolled infection No grade II nausea or grade I vomiting despite antiemetic medication concurrent immunotherapy Chemotherapy: No other concurrent chemotherapy concurrent hormonal therapy including estrogen therapy concurrent oral contraceptives or other hormonal methods Concurrent megestrol acetate allowed concurrent corticosteroids (except for nausea/vomiting during gemcitabine administration) concurrent CYP3A4 inhibitors or inducers including: Azoles (e.g., itraconazole, clotrimazole, fluconazole, or ketoconazole) Macrolide antibiotics (e.g., azithromycin, clarithromycin, or erythromycin) Cyclosporine Grapefruit Antiepileptic medication (e.g., phenytoin, carbamazepine, or phenobarbital) Antibiotics for tuberculosis (e.g., rifampin or isoniazid) concurrent HIV protease inhibitors (e.g., amprenavir, ritonavir, or saquinavir mesylate) concurrent cisapride other concurrent investigational therapy
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Rafael G. Amado, MD
    Organizational Affiliation
    Jonsson Comprehensive Cancer Center
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Learn more about this trial

    SCH 66336 With or Without Gemcitabine Followed by Surgery Compared With Surgery Alone in Treating Patients With Primary Liver Cancer

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