Zevalin (radioimmunotherapy) before stem cell transplant in treating patients with non-Hodgkin's lymphoma

Enter your info and the study team will contact you soon!
Your data is securely stored and only shared with the research team
Data is not saved in preview.
"Is radioimmunotherapy before a donor peripheral blood stem cell transplant an effective treatment for non-Hodgkin's Lymphoma?"
Age:
19 to 75 years old
Gender:
Any
Healthy Volunteers:
No
Keywords:
Non-Hodgkin's Lymphoma, radioimmunotherapy
Type:
Biological study, Phase 2
Investigator:
Description
This study is for patients with relapsed (returning) non-Hodgkin’s lymphoma (NHL) that is not felt to benefit from standard treatment, or refractory non-Hodgkin's lymphoma, (have not obtained a complete remission) after receiving standard chemotherapy.

Besides chemotherapy, other standard treatment options for relapsed or refractory NHL include radiation therapy used alone or in combination with other treatments, bone marrow transplant, and immunotherapy (therapy with monoclonal antibodies). A monoclonal antibody uses the body’s own immune cells to kill cancer cells. Patients remain at high risk of lymphoma returning if they do not receive any additional therapy. The best therapy at this point is not known.

The study drug, Zevalin (ibritumomab tiuxetan), has been approved by the Food and Drug Administration (FDA) for use in this type of cancer. Zevalin is a radioimmunotherapy. This involves treating lymphoma with a monoclonal antibody that has been attached to a radioactive atom (or molecule). A radioactive material called yttrium 90 is attached to an antibody. This allows radiation to be brought straight to cancer cells to which the antibody attaches. This type of therapy uses both the antibody’s and radioactive material’s good effects.

Rituximab will be given as part of the study drug treatment plan. Rituximab is also a monoclonal antibody therapy that comes in a liquid form that is given through a vein. Rituximab is approved by the FDA and is now used in the treatment of lymphoma.
This study requires
Please contact for details
Who can participate?
Inclusion Criteria:

- Histologically or cytologically confirmed relapsed cluster of differentiation (CD)20+ non-Hodgkin's lymphoma (NHL) (included in this category are follicular grade I, II, III, marginal zone, mantle cell, diffuse large B cell, small lymphocytic lymphoma) and CD20+ Hodgkin's disease for which standard curative therapy does not exist or is no longer effective

- Patients must have had at least one prior chemotherapeutic regimen; steroids alone and local radiation do not count as regimens; radiotherapy must have been completed at least 4 weeks prior to entry into the study; Rituxan alone does not count as a regimen; however, Bexxar or Zevalin (ibritumomab tiuxetan) do and patients must have completed radioimmunotherapy (RIT) > 12 months prior to enrollment

- Karnofsky performance status of ≥ 60%

- Life expectancy of greater than 3 months

- Total bilirubin within institutional normal limits

- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 2.5 times institutional upper limit of normal

- Creatinine within normal institutional limits OR creatinine clearance >= 60 ml/min/1.73 m^2 for patients with creatinine levels above institutional normal

- Blood counts no restrictions

- Patients who had anything less than a CR (PR, SD or progressive disease) to their last salvage regimen

- Ability to understand and the willingness to sign a written informed consent document

- Patients fit for non-myeloablative transplantation or best treatment that have an available matched (9/10 or better) related or unrelated donor

- Patients who are considered rituximab refractory (defined as progression within 6 months of their last rituximab-containing regimen)


Exclusion Criteria:

- Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study, rituximab within three months (unless there is evidence of progression), or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier are excluded; this does not include the use of steroids which may continue until two days prior to enrollment

- Patients may not be receiving any other investigational agents

- Failure to obtain insurance/payment authorization for Zevalin, unless the subject agrees to cover the cost

- Patients with known active brain metastases, other neurological disorders/dysfunction or a history of seizure disorder, or other neurological dysfunction should be excluded from this clinical trial because of their poor prognosis

- Patients who have an uncontrolled infection (presumed or documented) with progression after appropriate therapy for greater than one month

- Patients with symptomatic coronary artery disease, uncontrolled congestive heart failure; left ventricular ejection fraction is not required to be measured, however if it is measured, patient is excluded if ejection fraction is < 30%

- Patients requiring supplementary continuous oxygen; diffusion capacity of the lung of carbon monoxide (DLCO) is not required to be measured, however if it is measured, patient is excluded if DLCO < 35%

- Patients with clinical or laboratory evidence of liver disease will be evaluated for the cause of liver disease, its clinical severity in terms of liver function and histology, and for the degree of portal hypertension

- Patients with any of the following liver function abnormalities will be excluded:

- Fulminant liver failure

- Cirrhosis with evidence of portal hypertension or bridging fibrosis

- Alcoholic hepatitis

- Esophageal varices

- A history of bleeding esophageal varices

- Hepatic encephalopathy

- Uncorrectable hepatic synthetic dysfunction evidenced by prolongation of the prothrombin time

- Ascites related to portal hypertension

- Chronic viral hepatitis with total serum bilirubin > 3 mg/dL

- Symptomatic biliary disease

- Pregnant women are excluded from this study

- Human immunodeficiency virus (HIV)-positive patients
Resources
Schedule
Study duration and period
Variable
Recruitment period
From Nov. 10, 2012
Location
UC Davis Comprehensive Cancer Center
2279 45th Street
Sacramento, CA 95817
Contact
Christina Romo
Research Topic
Conditions:
  • Refractory Non Hodgkin Lymphoma
  • Relapsed Non Hodgkin Lymphoma

Have any questions or want to learn more? Leave your contact details below and the research team will reach out to you.


Sending

Send SMS with Study Info:

SMS Sent!

Share Study Info via Email:


E-mail Preview