TY - JOUR
T1 - Effect of acute and chronic GVHD on relapse and survival after reduced-intensity conditioning allogeneic transplantation for myeloma
AU - Ringdén, O.
AU - Shrestha, Smriti
AU - Da Silva, G. T.
AU - Zhang, Mei Jie
AU - Dispenzieri, Angela
AU - Remberger, M.
AU - Kamble, R.
AU - Freytes, Cesar O.
AU - Gale, Robert Peter
AU - Gibson, John
AU - Gupta, V.
AU - Holmberg, L.
AU - Lazarus, Hillard M.
AU - McCarthy, Philip L.
AU - Meehan, K.
AU - Schouten, H.
AU - Milone, Gustavo A.
AU - Lonial, S.
AU - Hari, Parameswaran N.
PY - 2012/6/1
Y1 - 2012/6/1
N2 - We evaluated the effect of acute and chronic GVHD on relapse and survival after allogeneic hematopoietic SCT (HSCT) for multiple myeloma using non-myeloablative conditioning (NMA) and reduced-intensity conditioning (RIC). The outcomes of 177 HLA-identical sibling HSCT recipients between 1997 and 2005, following NMA (n=98) or RIC (n=79) were analyzed. In 105 patients, autografting was followed by planned NMA/RIC allogeneic transplantation. The impact of GVHD was assessed as a time-dependent covariate using Cox models. The incidence of acute GVHD (aGVHD; grades I-IV) was 42% (95% confidence interval (CI), 35-49%) and of chronic GVHD (cGVHD) at 5 years was 59% (95% CI, 49-69%), with 70% developing extensive cGVHD. In multivariate analysis, aGVHD (≥grade I) was associated with an increased risk of TRM (relative risk (RR)=2.42, P=0.016), whereas limited cGVHD significantly decreased the risk of myeloma relapse (RR=0.35, P=0.035) and was associated with superior EFS (RR=0.40, P=0.027). aGVHD had a detrimental effect on survival, especially in those receiving autologous followed by allogeneic HSCT (RR=3.52, P=0.001). The reduction in relapse risk associated with cGVHD is consistent with a beneficial graft-vs-myeloma effect, but this did not translate into a survival advantage. © 2012 Macmillan Publishers Limited All rights reserved.
AB - We evaluated the effect of acute and chronic GVHD on relapse and survival after allogeneic hematopoietic SCT (HSCT) for multiple myeloma using non-myeloablative conditioning (NMA) and reduced-intensity conditioning (RIC). The outcomes of 177 HLA-identical sibling HSCT recipients between 1997 and 2005, following NMA (n=98) or RIC (n=79) were analyzed. In 105 patients, autografting was followed by planned NMA/RIC allogeneic transplantation. The impact of GVHD was assessed as a time-dependent covariate using Cox models. The incidence of acute GVHD (aGVHD; grades I-IV) was 42% (95% confidence interval (CI), 35-49%) and of chronic GVHD (cGVHD) at 5 years was 59% (95% CI, 49-69%), with 70% developing extensive cGVHD. In multivariate analysis, aGVHD (≥grade I) was associated with an increased risk of TRM (relative risk (RR)=2.42, P=0.016), whereas limited cGVHD significantly decreased the risk of myeloma relapse (RR=0.35, P=0.035) and was associated with superior EFS (RR=0.40, P=0.027). aGVHD had a detrimental effect on survival, especially in those receiving autologous followed by allogeneic HSCT (RR=3.52, P=0.001). The reduction in relapse risk associated with cGVHD is consistent with a beneficial graft-vs-myeloma effect, but this did not translate into a survival advantage. © 2012 Macmillan Publishers Limited All rights reserved.
KW - allogeneic
KW - graft-vs-host disease
KW - myeloma
KW - reduced intensity
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U2 - 10.1038/bmt.2011.192
DO - 10.1038/bmt.2011.192
M3 - Article
C2 - 21946381
SN - 0268-3369
VL - 47
SP - 831
EP - 837
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 6
ER -