Characteristics of B-CLL patients treated with nonmyeloablative peripheral blood alloHSCT
Patient . | A . | B . |
---|---|---|
Indication | Relapse | Relapse |
Sex | Male | Female |
Age* | 52 | 48 |
Enrollment | 2003 | 2002 |
Clinical trial† | NCT00055744 | NCT00003838 |
Induction chemotherapy | EPOCH + FR | FC |
Donor‡ | Brother | Brother |
GVHD prophylaxis | CSP + MTX | CSP + MTX |
Acute GVHD | No | No |
Chronic GVHD | No | No |
Response | PR; CR after DLI | CR |
Current status§ | Molecular remission | Molecular remission |
Patient . | A . | B . |
---|---|---|
Indication | Relapse | Relapse |
Sex | Male | Female |
Age* | 52 | 48 |
Enrollment | 2003 | 2002 |
Clinical trial† | NCT00055744 | NCT00003838 |
Induction chemotherapy | EPOCH + FR | FC |
Donor‡ | Brother | Brother |
GVHD prophylaxis | CSP + MTX | CSP + MTX |
Acute GVHD | No | No |
Chronic GVHD | No | No |
Response | PR; CR after DLI | CR |
Current status§ | Molecular remission | Molecular remission |
EPOCH + FR indicates etoposide, prednisone, vincristine, cyclophosphamide, doxorubicin plus fludarabine, rituximab; FC indicates fludarabine, cyclophosphamide; CSP + MTX, cyclosporine plus methotrexate; PR, partial response; CR, complete response; and DLI, donor lymphocyte infusion
At enrollment.
ClinicalTrials.gov identifier.
HLA-matched (6/6; A, B, and DR).
May 2009.