Effect of acute and chronic GVHD on relapse and survival after reduced-intensity conditioning allogeneic transplantation for myeloma


Autoria(s): Ringden, O.; Shrestha, S.; Silva, G. T. da; Zhang, M-J; Dispenzieri, A.; Remberger, M.; Kamble, R.; Freytes, C. O.; Gale, R. P.; Gibson, J.; Gupta, V.; Holmberg, L.; Lazarus, H.; McCarthy, P.; Meehan, K.; Schouten, H.; Milone, G. A.; Lonial, S.; Hari, P. N.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

06/11/2013

06/11/2013

2012

Resumo

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. Bone Marrow Transplantation (2012) 47, 831-837; doi:10.1038/bmt.2011.192; published online 26 September 2011

Public Health Service from the National Cancer Institute (NCI) [U24-CA76518]

National Heart, Lung and Blood Institute (NHLBI)

National Institute of Allergy and Infectious Diseases

Health Resources and Services Administration (HRSA/DHHS) [HHSH 234200637015C]

Office of Naval Research [N00014-06-1-0704, N00014-08-1-0058]

AABB

Aetna

American Society for Blood and Marrow Transplantation

Amgen Inc.

Swedish Cancer Society

Children's Cancer Foundation

Swedish Research Council

Cancer Society in Stockholm

Karolinska Institutet

Identificador

BONE MARROW TRANSPLANTATION, LONDON, v. 47, n. 6, pp. 831-837, JUN, 2012

0268-3369

http://www.producao.usp.br/handle/BDPI/42363

10.1038/bmt.2011.192

http://dx.doi.org/10.1038/bmt.2011.192

Idioma(s)

eng

Publicador

NATURE PUBLISHING GROUP

LONDON

Relação

BONE MARROW TRANSPLANTATION

Direitos

restrictedAccess

Copyright NATURE PUBLISHING GROUP

Palavras-Chave #GRAFT-VS-HOST DISEASE #REDUCED INTENSITY #ALLOGENEIC #MYELOMA #STEM-CELL TRANSPLANTATION #BONE-MARROW-TRANSPLANTATION #DIAGNOSED MULTIPLE-MYELOMA #VERSUS-HOST DISEASE #CHRONIC GRAFT #CHRONIC LEUKEMIA #EUROPEAN GROUP #RECIPIENTS #TRIAL #CYCLOSPORINE #BIOPHYSICS #ONCOLOGY #HEMATOLOGY #IMMUNOLOGY #TRANSPLANTATION
Tipo

article

original article

publishedVersion