Chemotherapy Followed by Zevalin for Relapsed Mantle Cell Lymphoma

NCT ID: NCT00119730

Last Updated: 2014-04-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-02-28
• Study Completion Date: 2013-12-31

Brief Summary

• The purpose of this study is to find out whether combining a short course of chemotherapy (Fludarabine, Mitoxantrone and Rituximab) followed by Zevalin will be effective in treating relapsed mantle cell lymphoma.
• The secondary purposes of the study are to determine the safety and to evaluate whether there is additional benefit from Zevalin therapy following the chemotherapy.

Detailed Description

• Patients receive fludarabine (days 1-3), mitoxantrone (day 1), and rituximab (day 1) of each 28-day cycle.
• Patients undergo a CT scan and bone marrow biopsy after two cycles. Unless the cancer has progressed, the patient will then receive Zevalin study treatment.
• Blood counts are taken every week for 12 weeks. After 12 weeks, a CT scan and bone marrow biopsy are performed.
• Long-term followup is 4 years. Physical exam and blood work is performed every 3 months for the first two years. Following that, physical exams and blood work is every 6 months for another two years. CT scans and bone marrow biopsies are every 6 months during this 4 year followup period.

Conditions

Mantle Cell Lymphoma

Study Design

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

Study Groups

Fludarabine, Mitoxantrone, Rituximab, Zevalin

Drug: Fludarabine Given on days 1-3 of each 28-day cycle Drug: Mitoxantrone Given on day 1 of each 28-day cycle Drug: Rituximab Given on day 1 of each 28-day cycle Drug: Zevalin Given after two cycles if there is no disease progression.

Group Type: EXPERIMENTAL

Fludarabine

Intervention Type: DRUG

Given on days 1-3 of each 28-day cycle

Mitoxantrone

Intervention Type: DRUG

Given on day 1 of each 28-day cycle

Rituximab

Intervention Type: DRUG

Given on day 1 of each 28-day cycle

Zevalin

Intervention Type: DRUG

After two cycles if there is no disease progression, zevalin treatment will be given. Rituximab will be given followed by an imaging dose of zevalin. Two or three scans will be performed over a week to determine if it is safe to give the full treatment dose of zevalin. The treatment dose is given with the second infusion or rituximab, seven days after the first dose.

Interventions

Fludarabine

Given on days 1-3 of each 28-day cycle

Intervention Type: DRUG

Mitoxantrone

Given on day 1 of each 28-day cycle

Intervention Type: DRUG

Rituximab

Given on day 1 of each 28-day cycle

Intervention Type: DRUG

Zevalin

After two cycles if there is no disease progression, zevalin treatment will be given. Rituximab will be given followed by an imaging dose of zevalin. Two or three scans will be performed over a week to determine if it is safe to give the full treatment dose of zevalin. The treatment dose is given with the second infusion or rituximab, seven days after the first dose.

Intervention Type: DRUG

Other Intervention Names

Fludara; Mitozantrone; Rituxan, MabThera and Zytux; Ibritumomab tiuxetan

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed mantle cell lymphoma in 1st or 2nd relapse, or with persistent disease following induction therapy.
• Measurable disease (lymph node > 1.5 cm)
• No anti-cancer therapy for three weeks (six weeks if Rituximab, nitrosourea or Mitomycin C) prior to study initiation, and fully recovered from all toxicities associated with prior surgery, radiation treatments, chemotherapy, or immunotherapy
• An IRB-approved signed informed consent
• Age >/= 18 years
• Expected survival >/= 3 months
• ECOG performance status 0, 1, or 2
• Acceptable hematologic status within two weeks prior to registration, including: * Absolute neutrophil count ([segmented neutrophils + bands] x total WBC) ≥ 1,500/mm3; * Platelet counts ≥ 100,000/mm3
• Female patients who are not pregnant or lactating
• Men and women of reproductive potential who are following accepted birth control methods (as determined by the treating physician, however abstinence is not an acceptable method)
• Patients previously on Phase II drugs if no long-term toxicity is expected, and the patient has been off the drug for eight or more weeks with no significant post treatment toxicities observed

• Hematologic recovery from FMR (ANC >1500, platelets > 100,000)
• Stable or responding disease on restaging following two cycles of FMR
• < 25% of bone marrow cellularity involved with lymphoma on restaging bone marrow biopsy
• Bone marrow cellularity at least 20% (including lymphoma and normal cells)
• Total bilirubin < 2.0 mg/dL (if total bilirubin is >75% indirect, then may use direct bilirubin < 0.8 mg/dL)
• Serum creatinine < 2.0 mg/dL
• No G-CSF or GM-CSF therapy within two weeks prior to Zevalin treatment, or neulasta within four weeks prior to Zevalin treatment
• No evidence of altered biodistribution of 111-In-Zevalin as indicated by:

1. Absent cardiac blood pool on day 1, with high liver / spleen uptake

2. Lung uptake greater than blood pool on day 1 or greater than liver on day 2-3

3. Kidney (in posterior view) or bowel uptake greater than liver on day 2-3

Exclusion Criteria

• Patients with impaired bone marrow reserve, as indicated by one or more of the following: * Prior myeloablative therapies with allogeneic or autologous bone marrow transplantation (ABMT) or peripheral blood stem cell (PBSC) rescue; * Platelet count < 100,000 cells/mm3; * Prior external beam radiation to >25% of active bone marrow; * History of failed stem cell collection
• Prior radioimmunotherapy
• Known cardiac ejection fraction < 40%. In patients with prior adriamycin exposure >= 300 mg/m2, echocardiogram must be obtained within three months prior to registration
• Known CNS lymphoma (lumbar puncture only required if symptomatic)
• Chronic lymphocytic leukemia (CLL)
• HIV or AIDS-related lymphoma
• Pleural effusion or ascites
• Abnormal liver function: total bilirubin > 2.0 mg/dL (if total bilirubin is >75% indirect, then may use direct bilirubin > 0.8 mg/dL)
• Abnormal renal function: serum creatinine > 2.0 mg/dL
• G-CSF or GM-CSF therapy within two weeks prior to treatment, or neulasta within four weeks
• Positive direct antiglobulin test
• Major surgery, other than diagnostic surgery, within four weeks
• Serious nonmalignant disease or infection which in the opinion of the investigator would compromise protocol objectives

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

Sponsors

Massachusetts General Hospital

OTHER

Sponsor Role: collaborator

Biogen

INDUSTRY

Sponsor Role: collaborator

Dana-Farber Cancer Institute

OTHER

Sponsor Role: lead

Responsible Party

Jennifer R. Brown, MD, PhD

Assistant Professor of Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jennifer R Brown, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Dana-Farber Cancer Institute

Locations

Massachusetts General Hospital

Boston, Massachusetts, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Countries

United States

Other Identifiers

04-251

Identifier Type: -

Identifier Source: org_study_id