Donor lymphocyte infusions for relapsed multiple myeloma after allogeneic stem-cell transplantation: Predictive factors for response and long-term outcome
Hm. Lokhorst et al., Donor lymphocyte infusions for relapsed multiple myeloma after allogeneic stem-cell transplantation: Predictive factors for response and long-term outcome, J CL ONCOL, 18(16), 2000, pp. 3031-3037
Purpose: To determine the efficacy, toxicity, and long-term outcome and pro
gnostic factors of donor lymphocyte infusions (DLI) in patients with relaps
ed multiple myeloma (MM) after allogeneic stem-cell transplantation (AlloSC
T).
Materials and Methods: Twenty-seven patients received 52 DLI courses at a m
edian of 30 months after the previous AlloSCT, Reinduction therapy was admi
nistered to 13 patients before DLI,
Results: Reinduction therapy wets successful in eight of 13 patients. Fourt
een patients (52%) responded to DLI, including six patients (22%) who achie
ved a complete remission (CR), Five patients responded after T-cell dose es
calation in subsequent DLIs. Four patients experienced relapse or disease p
rogression (three from partial response and one from CR). Five patients rem
ain in remission more than 30 months after DLI, Major toxicity was acute an
d chronic graft-versus-host disease (GVHD), which was present in 55% and 26
% of patients, respectively. Two patients died from bone marrow aplasia. Me
dian overall survival of all patients was 18 months. Overall survival was 1
1 months for DLI-resistant patients and has not been reached for the respon
ding patients. In two patients, sustained molecular remission wets observed
, The factors that were correlated with response to DLI were a T-cell dose
of more than 1.10(8) cells/kg, response to reinduction therapy, and chemoth
erapy-sensitive disease before AlloSCT.
Conclusion: These data confirm the potential and durable graft-versus-myelo
ma effect of DLI in patients with relapsed MM after AlloSCT, future studies
should be aimed at increasing response rates, especially in patients with
chemoresistant disease, and reducing toxicity by limiting GVHD. Adjuvant DL
I seems an attractive and promising approach for patients who do not achiev
e a molecular remission after AlloSCT. (C) 2000 by American Society of Clin
ical Oncology.