Outcomes of second allogeneic hematopoietic stem cell transplantation for patients with acute lymphoblastic leukemia

被引:34
|
作者
Poon, L. M. [1 ]
Bassett, R., Jr. [2 ]
Rondon, G. [1 ]
Hamdi, A. [1 ]
Qazilbash, M. [1 ]
Hosing, C. [1 ]
Jones, R. B. [1 ]
Shpall, E. J. [1 ]
Popat, U. R. [1 ]
Nieto, Y. [1 ]
Worth, L. L. [3 ]
Cooper, L. [3 ]
De Lima, M. [1 ]
Champlin, R. E. [1 ]
Kebriaei, P. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Stem Cell Transplantat & Cellular Therapy, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pediat, Houston, TX 77030 USA
关键词
ALL; allogeneic transplant; second; BONE-MARROW-TRANSPLANTATION; RELAPSE; ANTIBODY; ADULTS;
D O I
10.1038/bmt.2012.195
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
For patients with ALL who relapse following allo-SCT, only a second SCT provides a realistic chance for long-term disease remission. We retrospectively analyzed the outcomes of 31 patients with relapsed ALL after a prior allo-SCT, who received a second SCT (SCT2) at our center. With a median follow-up of 3 years, 1- and 3-year PFS was 23 and 11% and 1- and 3 year OS rates were 23 and 11%. Twelve patients (39%) were transplanted with active disease, of whom 75% attained a CR. We found a significant relationship between the time to treatment failure following first allograft (SCT1) and PFS following SCT2 (P = 0.02, hazard ratio = 0.93/month). In summary, a second transplant remains a potential treatment option for achieving response in a highly refractory patient population. While long-term survival is limited, a significant proportion of patients remains disease-free for up to 1 year following SCT2, providing a window of time to administer preventive interventions. Notably, our four long-term survivors received novel therapies with their second transplant underscoring the need for a fundamental change in the methods for SCT2 to improve outcome.
引用
收藏
页码:666 / 670
页数:5
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