Dolastatin 10 in Treating Patients With Indolent Lymphoma, Waldenstrom's Macroglobulinemia, or Chronic Lymphocytic Leukemia

NCT ID: NCT00005579

Last Updated: 2013-06-26

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 1998-06-30
• Study Completion Date: 2003-02-28

Brief Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die.

PURPOSE: Phase II trial to study the effectiveness of dolastatin 10 in treating patients with indolent lymphoma, Waldenstrom's macroglobulinemia, or chronic lymphocytic leukemia.

Detailed Description

OBJECTIVES:

• Estimate the efficacy of dolastatin 10 in patients with indolent lymphoma, Waldenstrom's macroglobulinemia, or chronic lymphocytic leukemia.
• Evaluate the qualitative and quantitative toxicities of dolastatin 10 in this patient population.
• Investigate the mechanism of action of dolastatin 10 in regards to apoptosis and effects of microtubules.

OUTLINE: This is an open-label, multicenter study. Patients are stratified by disease (chronic lymphocytic leukemia vs indolent lymphoma vs Waldenstrom's macroglobulinemia).

All patients receive dolastatin 10 IV bolus every 3 weeks. Patients continue treatment until disease progression, unacceptable toxicity, or patient's withdrawal from the study.

PROJECTED ACCRUAL: A maximum of 74 patients will be accrued for this study over 15 months.

Conditions

Leukemia; Lymphoma

Study Design

• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

dolastatin 10

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

DISEASE CHARACTERISTICS:

• Histologic or cytologic diagnosis of indolent lymphoma as defined by International Working Formulation categories A-C or diagnosis of Waldenstrom's macroglobulinemia, or chronic lymphocytic leukemia
• Lymphoma must be stage III, IV, or recurrent (no primary CNS lymphoma or lymphomatous meningitis)
• Waldenstrom's macroglobulinemia must have at least one of the following:

• IGM greater than 3,000 mg/dL
• Hemoglobin less than 10.0 g/dL
• Bone marrow involvement greater than 30% lymphocytes
• At least 2 cm lymphadenopathy
• Serum viscosity greater than 3.0
• Chronic lymphocytic leukemia must be intermediate or high risk stages I-IV and have progressed on fludarabine therapy unless patient cannot tolerate fludarabine

• Intermediate risk group must have at least one indication of active disease:

• Presence of any one of the disease related B symptoms: 10% or more loss of body weight over the preceding 6 month period, extreme fatigue, fever above 100 degrees F without evidence of infection, or night sweats
• Massive (greater than 6 cm below left costal margin) or progressive splenomegaly
• Massive (greater than 10 cm in longest diameter) or progressive lymphadenopathy
• Progressive lymphocytosis with an increase of 50% over a 2 month period or anticipated doubling time of less than 12 months
• Evidence of progressive marrow failure as manifested by the development or worsening of anemia and/or thrombocytopenia
• Autoimmune anemia and/or thrombocytopenia poorly responsive to corticosteroid therapy
• Intolerance, relapse, or failure following prior fludarabine allowed
• Measurable or evaluable disease
• No untreated immediate life threatening tumor complications

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• CALGB 0-2

Life expectancy:

• Not specified

Hematopoietic:

• See Disease Characteristics
• WBC at least 4,000/mm^3*
• Absolute granulocyte count at least 1,500/mm^3*
• Platelet count at least 100,000/mm^3*
• Hemoglobin at least 9 g/dL* NOTE: *Unless documented bone marrow involvement

Hepatic:

• Bilirubin no greater than 1.5 mg/dL
• SGOT no greater than 2.5 times upper limit of normal

Renal:

• Creatinine no greater than 1.5 mg/dL OR
• Creatinine clearance at least 60 mL/min

Other:

• No prior malignancy except adequately treated basal or squamous cell skin cancer, carcinoma in situ of the cervix, well differentiated stage IA prostate cancer, or any other cancer from which the patient has been disease free for five years
• Not pregnant or nursing
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• No prior autologous bone marrow or stem cell transplantation

Chemotherapy:

• See Disease Characteristics
• No more than 2 prior systemic regimens for treatment of lymphoma
• No chemotherapy for treatment of any other prior malignancy
• At least 4 weeks since chemotherapy and recovered
• Prior fludarabine therapy allowed

Endocrine therapy:

• See Disease Characteristics

Radiotherapy:

• Prior radiotherapy allowed (index lesion cannot be within prior radiotherapy field)

Surgery:

• Recovered from prior surgery

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

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: collaborator

University of Vermont

OTHER

Sponsor Role: lead

Principal Investigators

Steven M. Grunberg, MD

Role: STUDY_CHAIR

University of Vermont

Locations

Marlene and Stewart Greenebaum Cancer Center, University of Maryland

Baltimore, Maryland, United States

Barbara Ann Karmanos Cancer Institute

Detroit, Michigan, United States

Arthur G. James Cancer Hospital - Ohio State University

Columbus, Ohio, United States

Vermont Cancer Center

Burlington, Vermont, United States

Countries

United States

Other Identifiers

CDR0000066360

Identifier Type: REGISTRY

Identifier Source: secondary_id

NCI-T98-0007

Identifier Type: -

Identifier Source: secondary_id

VCC-9802

Identifier Type: -

Identifier Source: org_study_id