Overview

BEAM vs. 90-Yttrium Ibritumomab Tiuxetan (Zevalin®)/BEAM With ASCT for Relapsed DLBCL

Status:
Terminated
Trial end date:
2016-10-01
Target enrollment:
0
Participant gender:
All
Summary
This randomized phase III trial studies 90-yttrium ibritumomab tiuxetan and combination chemotherapy compared with combination chemotherapy alone before stem cell transplant in treating patients with diffuse large b-cell non-Hodgkin lymphoma that has returned after a period of improvement. Radioactive substances linked to monoclonal antibodies, such as 90-yttrium ibritumomab tiuxetan, can bind to cancer cells and give off radiation which may help kill cancer cells. Drugs used in chemotherapy, such as carmustine, etoposide phosphate, cytarabine, and melphalan (BEAM), work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. It is not yet known whether 90-yttrium ibritumomab tiuxetan and BEAM before a stem cell transplant are more effective than BEAM alone in treating patients with diffuse large b-cell non-Hodgkin lymphoma.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
City of Hope Medical Center
Collaborator:
National Cancer Institute (NCI)
Treatments:
Antibodies, Monoclonal
Carmustine
Cytarabine
Etoposide
Etoposide phosphate
Melphalan
Rituximab
Criteria
Inclusion Criteria:

1. Patients with CD20 positive diffuse large B-cell lymphoma as confirmed by a
pathological biopsy report.

2. Patients who are candidates for autologous stem-cell transplantation due to primary
refractory or first relapse of disease.

3. Patients must have chemo-sensitive disease achieving at least partial response (Cheson
2007 criteria) to last chemotherapy.

4. Patients with adequate autologous stem cell collection for transplantation (target >=
2.5 x 10^6 CD34+ cells/kg).

5. Patients must sign written informed consent.

6. Adequate birth control in fertile patients.

7. All prior chemotherapy completed at least three weeks before study treatment.

8. Marrow involvement less than 25% at transplantation, no limitation on blood counts
(low platelet count allowed).

9. Negative HIV antibody.

Exclusion Criteria:

1. Chemo-refractory disease as determined by less than partial response (Cheson 2007
Criteria) to last chemotherapy.

2. Two or more relapses after initial response to induction chemotherapy.

3. High-grade transformation from earlier diagnosis of low-grade lymphoma. Patients with
"De Novo" Transformed DLBCL, defined as DLBCL only on lymph node biopsy and a
discordant marrow with para-trabecular small cells at first diagnosis of lymphoma, are
eligible if adherent to all other selection criteria.

4. Bilirubin > 3.0 mg/dl, transaminases > 3 times upper normal limit.

5. Creatinine > 2.0 mg/dl.

6. KPS < 70.

7. Uncontrolled infection.

8. Pregnancy or lactation.

9. Abnormal lung diffusion capacity (DLCO < 40% predicted).

10. Severe cardiovascular disease; New York Heart Association (NYHA) Functional
Classification ≥2.

11. Active CNS disease involvement.

12. Presence of any other malignancy or history of prior malignancy within 5 years of
study entry. Within 5 years, patients treated for Stage I or II cancers are eligible
provided they have a life expectancy > 5 years in relation to this prior malignance.
The 5-year exclusion rule does not apply to-non melanoma skin tumors and in situ
cervical cancer.

13. Pleural effusion or ascites > 1 liter.

14. Known hypersensitivity to rituximab.

15. Psychiatric conditions/disease that impair the ability to give informed consent or to
adequately co-operate.

16. Prior radioimmunotherapy.

17. Prior autologous or allogeneic HSCT.

18. Active evidence of Hepatitis B or C infection; Hepatitis B surface antigen positive.

19. Patients who have had prior radiation to the lung will be excluded from the study,
although mediastinal irradiation will be permitted if minimal lung is in the treatment
volume.

20. Patients who have received >500cGy radiation to the kidneys will be excluded from the
study.