A Phase I/II Study of I-131 Tositumomab in Patients With Relapsed/Refractory Hodgkin's Lymphoma
18 Years
N/A
Both
Hodgkin's Disease
Trial Information
A Phase I/II Study of I-131 Tositumomab in Patients With Relapsed/Refractory Hodgkin's Lymphoma
One third of patients with Hodgkin's lymphoma (HL) do not respond to or have their disease
come back after their first therapy. These patients often then receive high-dose
chemotherapy and blood or marrow transplant. Despite high response rates after transplant, a
significant number, 26-65%, of these patients have their disease come back again. After
transplant, therapy options are limited and alternative therapies for patients with HL who
have relapsed post-transplant or who are ineligible for transplant are needed. Based on
recent studies about how HL develops and good results of patient studies evaluating the use
of the unlabeled anti-CD20 antibody Rituximab in HL, we think that radioimmunotherapy (RIT)
with I-131 Tositumomab(Bexxar®) will be an effective alternative therapy in patients with
relapsed/refractory HL who are post or ineligible for transplant.
The rationale for the use of RIT in cancer is that radiolabeled monoclonal antibodies will
specifically target and irradiate tumor cells but not normal tissues. The specific tumor
targeting of RIT theoretically allows higher doses of radiation to be delivered to tumor as
compared to external beam radiation because the effects of the radiation on normal tissues
is less with RIT. Iodine-131 Tositumomab (Bexxar®) was approved by the FDA for another type
of lymphoma in 2003. The antibody (Tositumomab) recognizes and attaches to a protein on
lymphoma cells and can kill these cells. The radioisotope (I-131) can help the antibody
kill cells better.
Iodine-131 Tositumomab (Bexxar®) is given through a vein in the arm. Iodine-131 Tositumomab
(Bexxar®) is given in an outpatient setting.
Inclusion Criteria:
- Biopsy-proven Hodgkin's lymphoma that is relapsed or refractory and the patient has
previously had a transplant or is ineligible for transplant
- All stages and histologic subtypes of Hodgkin's lymphoma
- Malignant cells may be CD20+ or CD20-
- May have previously had either a non-myeloablative or myeloablative allogeneic or
autologous stem cell transplant
- If prior history of greater than 1 transplant, eligible if other entry criteria are
met
- No upper limit on the amount of prior chemotherapy
- Must be at least 4 weeks out from their most recent chemotherapy or radiation
therapy, 6 weeks if the last regimen included BCNU, or mitomycin
- Age 18 or greater
- Karnofsky performance status ≥ 60
- Organ and marrow function within 4 weeks of registration on the protocol as defined
below:
- Leukocytes >2,000/mm3
- Absolute neutrophil count >1,000/ mm3
- Platelets >75,000/ mm3
- Hemoglobin >7 g/dL
- Creatinine <2.5 mg/dL
- Less than 25% bone marrow involvement with Hodgkin's lymphoma within 4 weeks of
registration on the protocol
- If female, not pregnant or breast feeding
- Ability to understand and the willingness to sign a written informed consent document
- At least one measurable target lesion, measuring 1.5 cm in at least one dimension by
standard CT imaging which is FDG -avid on PET/CT.
- 2-year expected survival from other diseases
Exclusion Criteria:
- Receiving any other investigational agents at the same time
- Hypocellular bone marrow (less than or equal to 10% cellularity) or marked decrease
in any one (or more) hematopoietic precursor within 4 weeks of registration on the
protocol
- Inability to follow basic radiation safety precautions
- Active infections requiring intravenous antibiotics until after resolution of the
infection
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
Non-myeloablative maximum tolerated dose of I-131 Tositumomab that can be given to patients with relapsed/refractory Hodgkin's lymphoma who are post or ineligible for transplant
Outcome Time Frame:
2 years
Safety Issue:
Yes
Principal Investigator
Richard L Wahl, MD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Johns Hopkins University
Authority:
United States: Institutional Review Board
Study ID:
J0703
NCT ID:
NCT00484874
Start Date:
June 2007
Completion Date:
Related Keywords:
- Hodgkin's Disease
- Hodgkin's lymphoma
- Radioimmunotherapy
- Bexxar
- I-131 Tositumomab
- Safety
- Efficacy
- Nuclear Medicine
- Monoclonal antibody
- Radiolabeled
- Hodgkin Disease
- Lymphoma
Name | Location |
|---|---|
| Johns Hopkins Medical Institutions | Baltimore, Maryland 21205 |
