Second-line age-adjusted International Prognostic Index in patients with advanced non-Hodgkin lymphoma after T-cell depleted allogeneic hematopoietic SCT

被引:19
作者
Perales, M-A [1 ,2 ,3 ]
Jenq, R. [1 ,2 ,3 ]
Goldberg, J. D. [1 ,2 ,3 ]
Wilton, A. S.
Lee, S. S. E. [1 ,2 ]
Castro-Malaspina, H. R. [1 ,2 ,3 ]
Hsu, K. [1 ,2 ,3 ]
Papadopoulos, E. B. [1 ,2 ,3 ]
van den Brink, M. R. M. [1 ,2 ,3 ]
Boulad, F. [2 ,3 ,4 ]
Kernan, N. A. [2 ,3 ,4 ]
Small, T. N. [2 ,3 ,4 ]
Wolden, S. [3 ,5 ]
Collins, N. H. [6 ]
Chiu, M. [2 ,4 ]
Heller, G.
O'Reilly, R. J. [2 ,3 ,4 ]
Kewalramani, T. [1 ,3 ,7 ]
Young, J. W. [1 ,2 ,3 ]
Jakubowski, A. A. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Allogene Bone Marrow Transplantat Serv, New York, NY 10065 USA
[3] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10065 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, New York, NY 10065 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Clin Labs, New York, NY 10065 USA
[7] Mem Sloan Kettering Canc Ctr, Hematol Serv, New York, NY 10065 USA
关键词
non-Hodgkin lymphoma; allo-BMT; allogeneic T-cell depleted; GVHD; prognostic factors; BONE-MARROW-TRANSPLANTATION; VERSUS-HOST-DISEASE; TOXICITY; THERAPY; CHEMOTHERAPY; PREDICTS; LEUKEMIA; FAILURE; RELAPSE; ADULTS;
D O I
10.1038/bmt.2009.371
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
T-cell depleted allogeneic hematopoietic SCT (TCD-HSCT) have shown durable disease-free survival with a low risk of GVHD in patients with AML. We investigated this approach in 61 patients with primary refractory or relapsed non-Hodgkin lymphoma (NHL), who underwent TCD-HSCT from January 1992 through September 2004. Patients received myeloablative cytoreduction consisting of hyperfractionated total body irradiation, followed by either thiotepa and cyclophosphamide (45 patients) or thiotepa and fludarabine (16 patients). We determined the second-line age-adjusted International Prognostic Index score (sAAIPI) before transplant transplant. Median follow-up of surviving patients is 6 years. The 10-year OS and EFS were 50% and 43%, respectively. The relapse rate at 10 years was 21% in patients with chemosensitive disease and 52% in those with resistant disease at time of HSCT. Nine of the 18 patients who relapsed entered a subsequent CR. OS (P = 0.01) correlated with the sAAIPI. The incidence of grades II-IV acute GVHD was 18%. We conclude that allogeneic TCD-HSCT can induce high rates of OS and EFS in advanced NHL with a low incidence of GVHD. Furthermore, the sAAIPI can predict outcomes and may be used to select the most appropriate patients for this type of transplant. Bone Marrow Transplantation (2010) 45, 1408-1416; doi:10.1038/bmt.2009.371; published online 11 January 2010
引用
收藏
页码:1408 / 1416
页数:9
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