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Tipifarnib, Gemcitabine, and Cisplatin in Treating Patients With Stage III or Stage IV Non-Small Cell Lung Cancer

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Completed
CT.gov ID
NCT00055757
Collaborator
(none)
48
Enrollment
1
Location
1
Arm

Study Details

Study Description

Brief Summary

Phase II trial to study the effectiveness of combining tipifarnib with gemcitabine and cisplatin in treating patients who have stage III or stage IV non-small cell lung cancer. Drugs used in chemotherapy such as gemcitabine and cisplatin use different ways to stop tumor cells from dividing so they stop growing or die. Tipifarnib may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth. Combining tipifarnib with combination chemotherapy may kill more tumor cells.

Condition or Disease Intervention/Treatment Phase
Phase 2

Detailed Description

PRIMARY OBJECTIVES:
  1. To describe the response rate in non-small cell lung cancer (NSCLC) patients receiving combination therapy with R115777, gemcitabine, and cisplatin.
SECONDARY OBJECTIVES:

  1. To estimate the time to event efficacy variables including: time to progressive disease, time to treatment failure, time to death of any cause.

  2. To estimate the duration of response for responding patients. III. To characterize the toxicities of R115777, gemcitabine, and cisplatin in this patient population.

TERTIARY OBJECTIVES:
  1. To evaluate the association between polymorphism expression in candidate genes and clinical endpoints and toxicity to R115777, gemcitabine, and cisplatin.

OUTLINE: This is a multicenter study.

Patients receive oral tipifarnib twice daily on days 1-14, gemcitabine IV over 30 minutes on days 1 and 8, and cisplatin IV over 2 hours on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Patients with at least stable disease may continue to receive oral tipifarnib alone twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Patients are followed every 6 months for 2 years.

Study Design

Study Type:
Interventional
Actual Enrollment :
48 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Phase II Trial of R115777, a Farnesyl Transferase Inhibitor, in Combination With Gemcitabine and Cisplatin in Advanced Non-Small Cell Lung Cancer (NSCLC)
Study Start Date :
Oct 1, 2003
Actual Primary Completion Date :
Apr 1, 2004

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment (tipifarnib, gemcitabine, cisplatin)

Patients receive oral tipifarnib twice daily on days 1-14, gemcitabine IV over 30 minutes on days 1 and 8, and cisplatin IV over 2 hours on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients with at least stable disease may continue to receive oral tipifarnib alone twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity.

Drug: tipifarnib
Given orally
Other Names:
  • R115777
  • Zarnestra

    • Drug: cisplatin
    Given IV
    Other Names:
  • CACP
  • CDDP
  • CPDD
  • DDP

    • Drug: gemcitabine hydrochloride
    Given IV
    Other Names:
  • dFdC
  • difluorodeoxycytidine hydrochloride
  • gemcitabine
  • Gemzar

    • Other: laboratory biomarker analysis
    Correlative studies

    Outcome Measures

    Primary Outcome Measures

    1. Proportion of confirmed tumor responses, defined to be either a CR or PR noted as the objective status on 2 consecutive evaluations at least 4 weeks apart [Up to 18 weeks (6 courses)]

      Ninety-five percent confidence intervals for the true success proportion will be calculated.

    Secondary Outcome Measures

    1. Survival time [Time from registration to death due to any cause, assessed up to 2 years]

      The distribution of survival time will be estimated using the method of Kaplan-Meier.

    2. Time to disease progression [Time from registration to documentation of disease progression, assessed up to 2 years]

      The distribution of time to progression will be estimated using the method of Kaplan-Meier.

    3. Duration of response is defined for all evaluable patients who have achieved an objective response as the date at which the patient's objective status is first noted to be either a CR or PR to the date progression is documented [Up to 2 years]

    4. Time to treatment failure [Time from the date of registration to the date at which the patient is removed from treatment due to progression, toxicity, or refusal, assessed up to 2 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    • Histologically confirmed NSCLC with one of the following classifications:

    • Stage IIIB with pleural effusion

    • Stage IIIB and not a candidate for combined modality treatment with radiation therapy and chemotherapy

    • Stage IV

    • Measurable disease, defined as at least one lesion whose longest diameter can be accurately measured as >= 2.0 cm

    • Absolute neutrophil count (ANC) >= 1500/mm^3

    • PLT >= 100,000

    • Hgb > 10.0 g/dL

    • Direct bilirubin =< 1.5 x UNL

    • Alkaline phosphatase =< 5 x UNL

    • AST =< 3 x UNL

    • Creatinine =< 1.5 x UNL

    • ECOG Performance Status (PS) 0 or 1

    • Capable of understanding the investigational nature, potential risks and benefits of the study and able to provide valid informed consent

    Exclusion Criteria:

    • Any of the following as this regimen may be harmful to a developing fetus or nursing child:

    • Pregnant women

    • Breastfeeding women

    • Men or women of childbearing potential or their sexual partners who are unwilling to employ adequate contraception (condoms, diaphragm, birth control pills, injections, intrauterine device [IUD], surgical sterilization, subcutaneous implants, or abstinence, etc.)

    • Any of the following prior therapies:

    • Prior chemotherapy for NSCLC (exception: therapies used as a radiosensitizer such as low-dose weekly cisplatin and carbo/taxol with XRT)

    • Prior radiation > 25% of bone marrow

    • Prior immunotherapy, biologic or gene therapy

    • New York Heart Association classification III or IV

    • CNS metastases

    • Uncontrolled infection

    • Any other severe, underlying diseases that are, in the judgment of the investigator, inappropriate for entry into this study

    • Prior malignancy, except for adequately treated basal cell or squamous cell skin cancer, adequately treated noninvasive carcinomas, or other cancer from which the patient has been disease-free for at least five years

    • Pre-existing peripheral neuropathy (motor or sensory) > grade 1 per NCI Common Toxicity Criteria (CTC)

    • Known peripheral vascular disease or a history of deep vein thrombosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Mayo Clinic Rochester Minnesota United States 55905

    Sponsors and Collaborators

    • National Cancer Institute (NCI)

    Investigators

    • Principal Investigator: Alex Adjei, Mayo Clinic

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    National Cancer Institute (NCI)
    ClinicalTrials.gov Identifier:
    NCT00055757
    Other Study ID Numbers:
    • NCI-2012-02808
    • MC0123
    • N01CM17104
    • N01CM17102
    First Posted:
    Mar 7, 2003
    Last Update Posted:
    Jun 4, 2013
    Last Verified:
    Jun 1, 2013
    Additional relevant MeSH terms:
    Lung Neoplasms
    Carcinoma, Non-Small-Cell Lung
    Gemcitabine
    Tipifarnib

    Study Results

    No Results Posted as of Jun 4, 2013