High Dose, Absorbed Dose Adjusted 90Y-ibritumomab With Peripheral Blood Stem Cells (PBSC) Support in B-cell Lymphoma
Conditions
B-cell Lymphoma
Conditions: official terms
Lymphoma - Lymphoma, B-Cell
Conditions: Keywords
B-cell lymphoma, Refractory, Recurrent, 90Y-ibritumomab, Stem cells support, Dosimetry study
Study Type
Interventional
Study Phase
Phase 1/Phase 2
Study Design
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Intervention
Name: 90Y-ibritumomab
Type: Drug
Overall Status
Recruiting
Summary
90Y-ibritumomab given with stem cells support, based on absorbed dose escalation to the liver. Absorbed dose escalation starts at 12 Gy and is capped at 36 Gy to the liver.
Criteria for eligibility
Healthy Volunteers: No
Maximum Age: N/A
Minimum Age: 18 Years
Gender: Both
Criteria: Inclusion Criteria:

- Written informed concent

- Age at least 18 years

- WHO Performance status 0-3

- Histologically verified B-cell lymphoma

- Diffuse large B-cell lymphoma and follicular grade III, failing an anthracycline containing regimen and patients not found suitable for a second line chemotherapy consolidated by high dose chemotherapy (HDCT) with stem cell support or radiotherapy

- Transformed B-cell lymphoma, failing first line therapy and not suitable for high dose chemotherapy (HDCT) or with a history of HDCT with stem cell support

- Follicular lymphoma grade II and I, and other indolent lymphomas must have failed second line treatment.

- One of these treatments must have contained chemotherapy and rituximab, the latter either together with chemotherapy or as maintenance.

- The lymphoma must require treatment, Mantle cell lymphoma, failing first line treatment,treatment required

- Measurable disease and the tumor burden must be acceptable according to the investigator

- Radiological studies must be performed and a unilateral bone marrow biopsy within 4 weeks before start of treatment

- Bone marrow reserve likely to give a harvest of at least 2x10 6 peripheral CD34+ stemcells or the existence of such a harvest or a corresponding central harvest

- Total bilirubin should not exceed 40 micromole/L

- A GFR as measured by Cystatin C of 50 ml/min

- HIV, Hepatitis B and C status known

- Life expectancy of at least 3 months.

Exclusion Criteria:

- Known or clinical evidence of CNS involvement

- Bone marrow involvement at harvest as measured by biopsy and flow cytometry

- Subjects with prior radiation to a field that includes over or equal 25% of their red marrow, liver or lung or to both kidneys

- Prior chemotherapy or radiotherapy within 4 weeks

- Subjects who are pregnant or nursing

- Pulmonary involvement, that is not negligible at the discretion of the investigator

- Liver involvement of lymphoma

- History of hepatitis B or C.
Location
Lund University Hospital
Lund, Sweden
Status: Recruiting
Contact: Karin Fritz, RN - +46 46 17 10 00 - karin.fritz@skane.se
Start Date
April 2008
Sponsors
Lund University Hospital
Source
Lund University Hospital
Record processing date
ClinicalTrials.gov processed this data on July 28, 2015
ClinicalTrials.gov page