Second hematopoietic SCT for lymphoma patients who relapse after autotransplantation: another autograft or switch to allograft?

被引:6
作者
Freytes, C. O. [1 ,2 ]
Lazarus, H. M. [3 ,4 ]
机构
[1] Univ Texas Hlth Sci Ctr San Antonio, Dept Med Hematol & Med Oncol, BMTU 111, San Antonio, TX 78229 USA
[2] S Texas Vet Hlth Care Syst, San Antonio, TX USA
[3] Univ Hosp Case Med Ctr, Ireland Canc Ctr, Cleveland, OH USA
[4] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA
关键词
second transplants; lymphoma; relapse; STEM-CELL TRANSPLANTATION; NON-HODGKINS-LYMPHOMA; BONE-MARROW-TRANSPLANTATION; MONOCLONAL-ANTIBODY THERAPY; HIGH-DOSE CHEMOTHERAPY; AUTOLOGOUS TRANSPLANTATION; ALLOGENEIC TRANSPLANTATION; PROGRESSIVE DISEASE; FOLLICULAR LYMPHOMA; CLINICAL ACTIVITY;
D O I
10.1038/bmt.2009.214
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Although autologous hematopoietic SCT (auto-HSCT) is the only potentially curative treatment for lymphoma that has relapsed after conventional chemotherapy, the prognosis of patients with disease recurrence after auto-HSCT is poor. Some highly selected patients can benefit from second transplants. One-third with late recurrence after initial auto-HSCT may attain a prolonged remission after second auto-HSCT. Non-myeloablative or reduced-intensity conditioning (RIC) allogeneic hematopoietic SCT (allo-HSCT) has been used successfully after auto-HSCT failures, especially in subjects who have an HLA-compatible donor, chemosensitive disease and good performance status. Patients with chemosenstive disease recurrence who have completed at least 1 year after their first auto-HSCT should be considered for a second auto-HSCT. Patients who have chemoresistant disease are best served by participation in a well-designed clinical trial examining novel antitumor agents. Bone Marrow Transplantation (2009) 44, 559-569; doi:10.1038/bmt.2009.214; published online 24 August 2009
引用
收藏
页码:559 / 569
页数:11
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