Combination Chemotherapy Plus Rituximab in Treating Patients With Recurrent or Refractory Non-Hodgkin's Lymphoma

Lymphoma Clinical Trial

Official title:

A Phase II Trial of Ifosfamide, Carboplatin, and Etoposide (ICE) Chemotherapy in Combination With Rituximab as Salvage Therapy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00007865
• Other study ID #: 0032-00-FB
• Secondary ID: P30CA036727NCI-V
• Status: Completed
• Phase: Phase 2
• Start date: September 1, 2000
• Est. completion date: April 22, 2008

Study information

• Verified date: December 2023
• Source: University of Nebraska
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Monoclonal antibodies such as rituximab can locate cancer cells and either kill them or deliver cancer-killing substances to them without harming normal cells.

PURPOSE: Phase II trial to study the effectiveness of combination chemotherapy combined with rituximab in treating patients who have recurrent or refractory non-Hodgkin's lymphoma.

Description:

OBJECTIVES:

• Determine the chemosensitivity rate in patients with recurrent or refractory non-Hodgkin's lymphoma treated with ifosfamide, carboplatin, and etoposide (ICE) in combination with rituximab.

• Determine whether the addition of rituximab changes the toxicity profile of the ICE chemotherapy regimen in these patients.

OUTLINE: Patients receive rituximab IV on days 1, 8, and 15 and ifosfamide IV over 1 hour, etoposide IV over 2 hours, and carboplatin IV on days 2-4. Treatment continues every 21 days for 2 courses in the absence of disease progression or unacceptable toxicity. Patients who are not candidates for autologous stem cell transplantation may receive 1-4 more courses of chemotherapy without rituximab.

Patients are followed at 1 month.

PROJECTED ACCRUAL: A total of 19-39 patients will be accrued for this study within 2 years.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: April 22, 2008
• Est. primary completion date: March 1, 2004
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years to 120 Years

Eligibility

Inclusion Criteria:

• Histologically confirmed recurrent or refractory B-cell non-Hodgkin's lymphoma

o CD20 positive

• Bidimensionally measurable or evaluable disease

• 19 years old and over

• ECOG 0-2 or Karnofsky 70-100%

• Life expectancy at least 3 months

• WBC at least 3,000/mm3

• Granulocyte count at least 1,000/mm3

• Platelet count at least 100,000/mm3

• Bilirubin no greater than 1.5 times upper limit of normal(ULN)

• AST or ALT no greater than 2.5 times ULN

• Creatinine no greater than 1.5 mg/dL

• Fertile patients must use effective contraception

• Concurrent non-steroidal hormonal therapy allowed for non-disease related conditions (e.g., insulin for diabetes)

Exclusion Criteria:

• No myelodysplastic syndrome or chronic myeloid leukemia

• Not pregnant or nursing/negative pregnancy test

• No other prior malignancy except curatively treated basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ of the cervix

• No active serious infection

• No other concurrent serious medical condition that would preclude study

• No prior bone marrow or peripheral blood stem cell transplantation for non-Hodgkin's lymphoma

• No other concurrent chemotherapy

• No concurrent corticosteroids except transient administration as antiemetic

• No concurrent radiotherapy

• No other concurrent investigational therapy

• No other concurrent antitumor agents

Related Conditions & MeSH terms

• Lymphoma

Intervention

Biological:
• rituximab

Drug:
• carboplatin

• etoposide

• ifosfamide

Locations

Country	Name	City	State
United States	University of Nebraska Medical Center, Eppley Cancer Center	Omaha	Nebraska

Sponsors (2)

Lead Sponsor	Collaborator
University of Nebraska	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States,