CHOP-Rituximab Augmented With GM-CSF in Patients With Previously Untreated Diffuse Large B Cell Non-Hodgkin's Lymphoma

Sponsor

Massachusetts General Hospital (Other)

Overall Status

Terminated

CT.gov ID

NCT00455897

Collaborator

Beth Israel Deaconess Medical Center (Other), Brigham and Women's Hospital (Other), Dana-Farber Cancer Institute (Other), Bayer (Industry)

Enrollment

Locations

Arm

Duration (Months)

Patient Per Site

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The primary goal of this study is to determine the effects (good and bad) of Granulocyte-macrophage colony stimulating factor (GM-CSF) in combination with Cytoxan, Adriamycin, Vincristine, Prednisone, Rituximab (CHOP-R) on diffuse Large B cell Non-Hodgkin's lymphoma (DLBCL). The standard of care for DLBCL is the combination of drugs known as CHOP-Rituximab (CHOP-R). The drugs that make up CHOP-R are the chemotherapy drugs cyclophosphamide, doxorubicin and vincristine, prednisone and rituximab. GM-CSF is a drug that stimulates the immune system by increasing the numbers of white blood cells. Previous research has shown that GM-CSF might help rituximab to be more effective in treating lymphoma.

Condition or Disease	Intervention/Treatment	Phase
Lymphoma, Non-Hodgkin Lymphoma, B-Cell Lymphoma, Diffuse	Drug: GM-CSF Drug: CHOP Drug: Rituximab	Phase 2

Detailed Description

Study treatment is divided into 21-day time periods called cycles. Almost all participants will be treated as outpatients unless they have an existing medical problem that requires them to be treated as in inpatient.
The drugs used in this study treatment are standard of care for this type of lymphoma and participants could receive these even if they are not taking part in the study.
Participants will start receiving GM-CSF 11 days before Day 1 of Cycle 1 for 10 days. They will receive the first dose of GM-CSF at the clinic. At least 1 1/2 days after the last GM-CSF injection (Day 1), they will receive chemotherapy (CHOP-R). Eleven days before they start the next cycle (Days 11-20), they will again start to receive GM-CSF injections for 10 days.
Participants will receive up to 6 cycles of study treatment if their disease is responding and they are tolerating the study treatment.
Additional medications may be given to prevent lung infection, return of brain and nervous system disease and tumor lysis syndrome.
Before beginning GM-CSF during each cycle of treatment blood will be drawn to monitor the participants health and to check for side effects.
On Day 1 of each cycle a physical examination and blood tests will be performed. On Day 7 and Day 14 of each cycle, routine blood tests will also be done.
After Cycle 2 and 4 CT scans of the neck, chest, abdomen and pelvis will be performed to check the status of the participants disease.
After 6 cycles of study treatment, the participant will return to the clinic for an End of Treatment Visit. At this visit a physical exam, routine blood tests, and CT scan of neck, chest, abdomen and pelvis will be performed.
The participant will be asked to return to the clinic every 3 months for the first year after study treatment and every 6 months up to 2 years after study treatment for the procedures outline in the End of Treatment Visit.

Study Design

Study Type:

Interventional

Actual Enrollment :

3 participants

Allocation:

Non-Randomized

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase II Trial of CHOP-Rituximab Augmented With Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) in Patients With Previously Untreated Diffuse Large B Cell Non-Hodgkin's Lymphoma

Study Start Date :

Dec 1, 2006

Actual Primary Completion Date :

Nov 1, 2007

Actual Study Completion Date :

Jul 1, 2011

Arms and Interventions

Arm	Intervention/Treatment
Experimental: GMCSF-RCHOP	Drug: GM-CSF Given 11 days before day 1 of cycle 1 for 10 days Drug: CHOP Administered as part of standard care Drug: Rituximab Administered as part of standard treatment

Arm

Intervention/Treatment

Experimental: GMCSF-RCHOP

Drug: GM-CSF

Given 11 days before day 1 of cycle 1 for 10 days

Drug: CHOP

Administered as part of standard care

Drug: Rituximab

Administered as part of standard treatment

Outcome Measures

Primary Outcome Measures

To determine the safety of GM-CSF when administered in combination with CHOP-R to patients with previously untreated diffuse large B cell non-Hodgkin's lymphoma. [2 years]

Secondary Outcome Measures

To assess the response rate, 2-year event-free survival and overall survival with CM-CSF and CHOP-R in this patient population []
to analyze the biologic activity of GM-CSF at this dosing schedule and timing. [2 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically confirmed diagnosis of diffuse large B cell Non-Hodgkin's lymphoma with characteristic immunophenotypic profile
Patient has not received any prior anti-cancer therapy for lymphoma
Tumor tissue confirmed to express the cluster of differentiation antigen 20 antigen by flow cytometry or immunohistochemistry
Measurable disease as defined by a tumor mass of 1cm or greater in one dimension
Stage II (abdominal-not radiotherapy appropriate), III, or IV disease
Age > 18 years
Performance Status of 0-2
Laboratory parameters as outlined in protocol
Patient agrees to use birth control

Exclusion Criteria:

Known central nervous system involvement by lymphoma
Serious uncontrolled concurrent illness such as active coronary artery disease, severe lung disease, heart failure, active alcohol abuse, active concurrent malignancy except non-melanoma skin cancer or carcinoma in situ of the cervix
Any evidence of prior natural exposure to Hepatitis B
Active rheumatologic disease which may be exacerbated by GM-CSF
Cardiac ejection fraction less than 45%
Known HIV disease
Patient is pregnant or nursing
Patient is receiving other investigational drugs

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Beth Israel Deaconess Medical Center	Boston	Massachusetts	United States	02115
2	Dana-Farber Cancer Institute	Boston	Massachusetts	United States	02115
3	Massachusetts General Hospital	Boston	Massachusetts	United States	02215