Tipifarnib in Treating Patients With Advanced Hematologic Cancer

National Cancer Institute (NCI)

Status and phase: Completed; Phase 1

Conditions: Multiple Myeloma and Plasma Cell Neoplasm; Chronic Myeloproliferative Disorders; Lymphoma; Leukemia; Myelodysplastic Syndromes

Treatments: Drug: tipifarnib

Study type: Interventional

Funder types: NIH

Identifiers

NCT00005967

NCI-42

UCCRC-10294

CDR0000067950 (Registry Identifier)

NCI-2012-02342

Details and patient eligibility

About

Randomized phase I trial to study the effectiveness of tipifarnib in treating patients who have advanced hematologic cancer. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die.

Full description

OBJECTIVES:

I. Determine the relationship between tipifarnib dose and inhibition of farnesylation in malignant cells of patients with advanced hematologic malignancies.

II. Determine the safety profile of this drug in this patient population. III. Determine the clinical activity of this drug in these patients.

OUTLINE: This is a randomized study. Patients are randomized to 1 of 4 dose levels.

Patients receive oral tipifarnib twice daily for 21 days. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After 1 course of therapy, patients may receive subsequent therapy at the maximum tolerated dose at the investigator's discretion.

Enrollment: 36 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed hematologic malignancy refractory to standard therapy or for which no known effective therapy exists

  • Hodgkin's or non-Hodgkin's lymphoma

    • Known bone marrow involvement

  • Acute myeloid leukemia

  • Chronic myelogenous leukemia

    • Chronic phase

      • No significant symptoms after treatment
      • No features of accelerated phase or blastic phase

    • Accelerated phase

      • WBC difficult to control with conventional busulfan or hydroxyurea in terms of dose requirement or shortening of intervals between courses
      • Rapid doubling of WBC (less than 5 days)
      • At least 10% blasts in blood or marrow
      • At least 20% blasts plus promyelocytes in blood or marrow
      • At least 20% basophils plus eosinophils in blood
      • Anemia or thrombocytopenia unresponsive to busulfan or hydroxyurea
      • Persistent thrombocytosis
      • Additional chromosome changes
      • Increasing splenomegaly
      • Development of chloromas or myelofibrosis

    • Blastic phase

      • At least 30% blasts plus promyelocytes in blood or bone marrow

  • Acute lymphoblastic leukemia

  • Chronic lymphocytic leukemia

  • Myelodysplastic syndromes

    • Refractory anemia with excess blasts (RAEB)
    • Chronic myelomonocytic leukemia
    • RAEB in transformation

  • Multiple myeloma

  • Chronic myeloproliferative diseases including, but not limited to, myelofibrosis with myeloid metaplasia

• Measurable or evaluable disease documented by radiographic, hematologic, bone marrow, or clinical examination parameters

• Refusal of allogeneic bone marrow transplantation allowed

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• Karnofsky 60-100%

Hepatic:

• Bilirubin no greater than 1.5 mg/dL
• Albumin at least 2.5 g/dL

Renal:

• Creatinine less than 2.0 mg/dL

Other:

• No other uncontrolled medical disorder
• No active inflammatory bowel disease, ileus, or other chronic malabsorption syndromes
• Not pregnant or nursing
• Fertile patients must use effective contraception during and for 2 months after study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• At least 4 weeks since prior immunotherapy

Chemotherapy:

• At least 4 weeks since prior chemotherapy (6 weeks for mitomycin or nitrosoureas)
• At least 3 days since prior hydroxyurea

Endocrine therapy:

• At least 4 weeks since prior systemic steroids for multiple myeloma

Radiotherapy:

• At least 4 weeks since prior radiotherapy

Surgery:

• No prior total gastrectomy or total ileocolectomy

Other:

• No prior tipifarnib
• No concurrent proton pump inhibitors (e.g., omeprazole)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

---

36 participants in 1 patient group

Arm I

Experimental group

Description:

Patients receive oral tipifarnib twice daily for 21 days. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After 1 course of therapy, patients may receive subsequent therapy at the maximum tolerated dose at the investigator's discretion.

Treatment:

Drug: tipifarnib