We studied the outcome of allo-SCT after reduced-intensity conditioning in relapsed or refractory indolent and aggressive lymphoid
malignancies. All 54 patients (diagnosis: B-CLL n=13, indolent
lymphoma n=12, aggressive
lymphoma n=13, transformed
lymphoma n=16) received conditioning with
fludarabine and CY between July 2001 and November 2010. They underwent allo-SCT because of relapse after auto-SCT or because no other
therapy could lead to a meaningful remission. Patients received an unmanipulated peripheral blood stem-cell graft. Median follow-up was 67 months. Thirty-two patients had received
rituximab. Immediately after
transplantation, remission status had improved in 21 patients, all without DLI. During the follow-up six additional patients achieved CR without further
therapy. Four-year OS (EFS) was 46% (46%) for B-CLL, 83% (75%) for indolent
lymphoma, 69% (55%) for aggressive
lymphoma and 74% (67%) for transformed
lymphoma (P=0.28 (P=0.54)). Forty two percent developed acute GVHD, 68% chronic GVHD (16% limited, 52% extensive). Previous auto-SCT did not influence OS, while acute GVHD did. Two-year non-relapse mortality was 16%. In conclusion, reduced-intensity conditioning with
fludarabine-CY is feasible and effective for both indolent and aggressive lymphoid
malignancies, even after previous auto-SCT. Because of the excellent anti-
B-cell/lymphoma activity
fludarabine-CY decreases
tumor load, gaining time for the development of a graft versus
lymphoma effect.