TY - JOUR
T1 - Autologous transplantation for transformed non-hodgkin lymphoma using an yttrium-90 ibritumomab tiuxetan conditioning regimen
AU - Mei, Matthew
AU - Wondergem, Marielle J.
AU - Palmer, Joycelynne M.
AU - Shimoni, Avichai
AU - Hasenkamp, Justin
AU - Tsai, Ni Chun
AU - Simpson, Jennifer
AU - Nademanee, Auayporn
AU - Raubitschek, Andrew
AU - Forman, Stephen J.
AU - Krishnan, Amrita Y.
N1 - Publisher Copyright:
© 2014 American Society for Blood and Marrow Transplantation.
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Transformation from indolent non-Hodgkin lymphoma (NHL) to diffuse large Bcell lymphoma (DLBCL) has historically been associated with a poor prognosis. A small series of autologous stem cell transplantation (ASCT) studies using conventional conditioning regimens has demonstrated durable progression-free survival (PFS) rates ranging from 25% to 47%, but data in the rituximab era are lacking. Here we report the results of a multicenter retrospective trial evaluating ASCT in patients with transformed lymphoma using the Z-BEAM conditioning regimen, which combines yttrium-90-labeled ibritumomab tiuxetan (Zevalin) with high-dose BEAM (carmustine, etoposide, cytarabine, melphalan) chemotherapy. Sixty-three patients from 4 institutions were treated between 2003 and 2011. Histological confirmation of transformation was required and defined as a diagnosis of DLBCL in patients with either a prior history or concomitant diagnosis of low-grade Bcell NHL. Median patient age at ASCT was 59.5years, median number of prior regimens was 2, and all patients were exposed to rituximab. Disease status at ASCT was as follows: first complete remission (CR) (n=30), first partial remission (n=11), first relapse (n=14), and at least second CR (n=8). The median time from diagnosis of histological transformation to ASCT was 7.5months (range, 2.8 to 116). Two-year nonrelapse mortality was 0%. Median follow-up for living patients was 28months (range, 5 to 103). Two-year PFS was 68% (95% confidence interval, 58% to 75%), and overall survival was 90% (95% confidence interval, 80% to 95%). In conclusion, the Z-BEAM conditioning regimen for ASCT is well tolerated by patients with transformed lymphoma and demonstrates encouraging clinical outcomes.
AB - Transformation from indolent non-Hodgkin lymphoma (NHL) to diffuse large Bcell lymphoma (DLBCL) has historically been associated with a poor prognosis. A small series of autologous stem cell transplantation (ASCT) studies using conventional conditioning regimens has demonstrated durable progression-free survival (PFS) rates ranging from 25% to 47%, but data in the rituximab era are lacking. Here we report the results of a multicenter retrospective trial evaluating ASCT in patients with transformed lymphoma using the Z-BEAM conditioning regimen, which combines yttrium-90-labeled ibritumomab tiuxetan (Zevalin) with high-dose BEAM (carmustine, etoposide, cytarabine, melphalan) chemotherapy. Sixty-three patients from 4 institutions were treated between 2003 and 2011. Histological confirmation of transformation was required and defined as a diagnosis of DLBCL in patients with either a prior history or concomitant diagnosis of low-grade Bcell NHL. Median patient age at ASCT was 59.5years, median number of prior regimens was 2, and all patients were exposed to rituximab. Disease status at ASCT was as follows: first complete remission (CR) (n=30), first partial remission (n=11), first relapse (n=14), and at least second CR (n=8). The median time from diagnosis of histological transformation to ASCT was 7.5months (range, 2.8 to 116). Two-year nonrelapse mortality was 0%. Median follow-up for living patients was 28months (range, 5 to 103). Two-year PFS was 68% (95% confidence interval, 58% to 75%), and overall survival was 90% (95% confidence interval, 80% to 95%). In conclusion, the Z-BEAM conditioning regimen for ASCT is well tolerated by patients with transformed lymphoma and demonstrates encouraging clinical outcomes.
KW - Radioimmunotherapy
KW - Z-BEAM
KW - Zevalin
UR - http://www.scopus.com/inward/record.url?scp=84912122473&partnerID=8YFLogxK
U2 - 10.1016/j.bbmt.2014.07.028
DO - 10.1016/j.bbmt.2014.07.028
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C2 - 25079874
AN - SCOPUS:84912122473
SN - 1083-8791
VL - 20
SP - 2072
EP - 2075
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
IS - 12
ER -