FR901228 in Treating Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma

NCT ID: NCT00383565

Last Updated: 2014-05-20

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 9 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-09-30
• Study Completion Date: 2011-04-30

Brief Summary

FR901228 may stop the growth of cancer cells by blocking some of the enzymes needed for cell to grow and by blocking blood flow to the cancer. This phase II trial is studying how well FR901228 works in treating patients with relapsed or refractory non-Hodgkin's lymphoma.

Detailed Description

OBJECTIVES:

I. Determine the response rate (complete and partial) to FR901228 in patients with relapsed or refractory mantle cell or diffuse large cell non-Hodgkin's lymphoma.

II. Evaluate the safety and feasibility of FR901228, in terms of the incidence of toxicity and maximum grade observed and courses delayed or dose reductions, in these patients.

III. Determine 2-year progression-free and overall survival.

OUTLINE: Patients receive FR901228 IV over 4 hours on days 1, 8, and 15.

Treatment repeats every 28 days for at least 6 courses in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed every 3-6 months for up to 5 years.

Conditions

Recurrent Adult Diffuse Large Cell Lymphoma; Recurrent Mantle Cell Lymphoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive FR901228 IV over 4 hours on days 1, 8, and 15.

Group Type: EXPERIMENTAL

romidepsin

Intervention Type: DRUG

Given IV

Interventions

romidepsin

Given IV

Intervention Type: DRUG

Other Intervention Names

FK228; FR901228; Istodax

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed aggressive B-cell non-Hodgkin's lymphoma of 1 of the following subtypes:

• Mantle cell lymphoma
• Diffuse large cell lymphoma
• (Ineligible for or unwilling to undergo stem cell transplantation)
• Relapsed or refractory disease:

• Any number of prior therapies allowed for relapsed disease, including peripheral blood stem cell or bone marrow transplantation
• No more than 2 prior regimens, excluding monotherapy with monoclonal antibody or radiotherapy, for refractory disease
• Measurable disease, defined as >= 1 lesion >= 1.5 cm in the longest diameter
• No transformed lymphoma, defined as the transformation of a low-grade lymphoma, including follicular lymphoma or small lymphocytic lymphoma, to a high-grade lymphoma (e.g., diffuse large cell lymphoma)
• ECOG performance status 0-2
• Absolute neutrophil count >= 1,000/mm^3 OR >= 500/mm^3 if extensive bone marrow involvement (> 50%) or hypersplenism with palpable splenomegaly
• Platelet count >= 75,000/mm^3 OR >= 50,000/mm^3 if extensive bone marrow involvement (> 50%) or hypersplenism with palpable splenomegaly
• Bilirubin normal
• Alkaline phosphatase =< 2 times upper limit of normal (ULN)
• AST =< 2 times ULN
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• No significant cardiac disease, including New York Heart Association class III-IV congestive heart failure
• No history of serious ventricular arrhythmia
• QTc < 500 msec
• No evidence of cardiac hypertrophy on ECG
• No known HIV positivity
• No other uncontrolled serious medical condition or active infection (e.g., chronic obstructive pulmonary disease, diabetes)
• Recovered from prior therapy
• No prior doxorubicin hydrochloride >= 450 mg/m^2 or mitoxantrone >= 112 mg/m^2 (Patients who received both mitoxantrone and doxorubicin hydrochloride should have a "doxorubicin equivalent dose" < 450 mg/m^2
• No prior therapy with a histone deacetylase inhibitor
• No concurrent dexamethasone or prednisone except for refractory nausea/vomiting
• No concurrent drugs associated with QTc prolongation (e.g., dolasetron mesylate)
• Concurrent hydrochlorothiazide, furosemide, or other diuretics allowed provided patient is receiving potassium chloride supplementation (No supplementation needed if switched to a potassium-conserving diuretic)
• No CNS lymphoma
• Creatinine normal
• Cardiac function >= 50% by MUGA

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

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jorge Romaguera

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

M D Anderson Cancer Center

Houston, Texas, United States

Countries

United States

Other Identifiers

NCI-2009-00240

Identifier Type: REGISTRY

Identifier Source: secondary_id

2005-0579

Identifier Type: -

Identifier Source: secondary_id

CDR0000486326

Identifier Type: -

Identifier Source: secondary_id

2005-0579

Identifier Type: OTHER

Identifier Source: secondary_id

7869

Identifier Type: OTHER

Identifier Source: secondary_id

P30CA016672

Identifier Type: NIH

Identifier Source: secondary_id

View Link

N01CM62202

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2009-00240

Identifier Type: -

Identifier Source: org_study_id