Non Hodgkin Lymphoma Clinical Trial

Irinotecan in Treating Patients With Recurrent or Refractory Non-Hodgkin’s Lymphoma

Summary

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

PURPOSE: Phase II trial to study the effectiveness of irinotecan in treating patients with recurrent or refractory non-Hodgkin's lymphoma.

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Full Description

OBJECTIVES:

Determine the objective response rate and toxicity of irinotecan when administered to patients with recurrent or refractory non-Hodgkin's lymphoma.

OUTLINE: Patients are stratified by disease category (aggressive vs indolent vs mantle cell lymphoma). Patients with aggressive and indolent lymphoma are further stratified as to being refractory (no complete response (CR) or partial response (PR) to initial therapy) vs recurrent (CR or PR to initial therapy); i.e, the following subcategories are used:

Stratum I:Refractory aggressive non-Hodgkin's lymphoma (NHL)
Stratum II:Recurrent aggressive NHL
Stratum III: Refractory indolent NHL
Stratum IV: Recurrent indolent NHL
Stratum V: Mantle cell NHL All patients receive irinotecan intravenously every 21 days. Patients achieving CR or PR receive 6 courses. Patients may receive bone marrow transplantation after at least 2 courses.

Patients are followed every 3 months for survival.

PROJECTED ACCRUAL: This study will accrue 18 patients per stratum; if at least three patients respond, an additional 25 patients will be accrued for a total of 43 evaluable patients per stratum. The total number accrued will be 90-215 over a period of approximately 3 years.

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Eligibility Criteria

DISEASE CHARACTERISTICS:

Histologically confirmed recurrent or refractory non-Hodgkin's lymphoma

First relapse requires histologic confirmation of relapse
No CNS metastases
No lymphomatous meningitis
Measurable disease

PATIENT CHARACTERISTICS:

Age:

15-75

Performance status:

Zubrod 0-2

Life expectancy:

At least 12 weeks

Hematopoietic:

Unless due to lymphoma:

Platelet count at least 100,000/mm^3
Absolute granulocyte count at least 1,500/mm^3
Hemoglobin at least 9 g/dL

Hepatic:

Bilirubin no greater than 1.5 mg/dL
SGOT no greater than 3 times upper limit of normal (ULN) (no greater than 5 times ULN if liver involvement)

Renal:

Creatinine no greater than 2.0 mg/dL
Baseline calcium less than 12 mg/dL

Cardiovascular:

No myocardial infarction within 6 months
No congestive heart failure requiring therapy

Other:

No history of seizures
No uncontrolled diabetes mellitus (i.e., random blood sugar of at least 250 mg)
No other concurrent severe disease
No uncontrolled infection
HIV negative
No psychoses
No prior malignancy except for adequately treated basal cell or squamous cell skin cancer or in situ cancer of the cervix unless surgically treated and disease free for at least 5 years
Not pregnant or lactating
Effective contraception required of fertile patients

PRIOR CONCURRENT THERAPY:

Biologic therapy:

No prior bone marrow transplantation

Chemotherapy:

No more than 2 prior chemotherapy regimens for treatment of lymphoma
No prior irinotecan, topotecan or aminocamptothecin
At least 3 weeks since prior chemotherapy

Endocrine therapy:

Not specified

Radiotherapy:

At least 3 weeks since prior radiotherapy
Radiotherapy that is not a part of a combined-modality therapy is counted as a regimen (see Chemotherapy)

Surgery:

Not specified

Other:

No phenytoin, phenobarbital, or other antiepileptic prophylaxis

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

50

Study ID:

NCT00003245

Recruitment Status:

Completed

Sponsor:

M.D. Anderson Cancer Center

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There is 1 Location for this study

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University of Texas - MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Non Hodgkin Lymphoma

Phase:

Phase 2

Estimated Enrollment:

50

Study ID:

NCT00003245

Recruitment Status:

Completed

Sponsor:


M.D. Anderson Cancer Center

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