Myeloablative allogeneic hematopoietic stem cell transplantation in patients who experience relapse after autologous stem cell transplantation for lymphoma: a report of the International Bone Marrow Transplant Registry

被引:82
作者
Freytes, CO
Loberiza, FR
Rizzo, JD
Bashey, A
Bredeson, CN
Cairo, MS
Gale, RP
Horowitz, MM
Klumpp, TR
Martino, R
McCarthy, PPL
Molina, A
Pavlovsky, S
Pecora, AL
Serna, DS
Tsai, T
Zhang, MJ
Vose, JM
Lazarus, HM
van Besien, K
机构
[1] Univ Texas, Hlth Sci Ctr, San Antonio, TX 78229 USA
[2] Med Coll Wisconsin, Hlth Policy Inst, Milwaukee, WI 53226 USA
[3] Int Bone Marrow Transplant Registry, Lymphoma Working Comm, Milwaukee, WI USA
[4] Univ Calif San Diego, La Jolla, CA 92093 USA
[5] Columbia Univ, New York, NY USA
[6] Los Angeles Ctr Adv Studies Leukemia, Los Angeles, CA USA
[7] Univ Penn, Philadelphia, PA 19104 USA
[8] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[9] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
[10] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[11] Fundaleu Angelica Ocampo, Buenos Aires, DF, Argentina
[12] Univ Nebraska, Med Ctr, Omaha, NE 68182 USA
[13] Case Western Reserve Univ Hosp, Cleveland, OH 44106 USA
[14] Univ Chicago, Chicago, IL 60637 USA
关键词
D O I
10.1182/blood-2004-01-0231
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Myeloablative allogeneic hematopoietic stem cell transplantation (allo-HSCT) is increasingly used in patients with lymphoma who experience disease relapse after autologous hematopoietic stem cell transplantation (auto-HSCT) because the allograft is tumor free and may induce a graft-versus-tumor effect. We analyzed 114 patients treated with this approach from 1990 to 1999 to assess disease progression, progression-free survival (PFS), and overall survival (CS). Cumulative incidence of disease progression at 3 years was 52%, whereas treatment-related mortality was 22%, lower than previously reported. Three-year probabilities of OS and PFS were 33% and 25%, respectively. With prolonged follow-up, however, nearly all patients experienced disease progression, and 5-year probabilities were 24% and 5%, respectively. Complete remission at the time of allo-HSCT and use of total body irradiation (TBI) in patients with non-Hodgkin lymphoma (NHL) were associated with lower rates of disease progression and higher rates of OS. In summary, allo-HSCT is feasible for patients with lymphoma who have relapses after auto-HSCT and can result in prolonged survival for some, but it is usually not curative. Most likely to benefit are patients who have HLA-matched sibling donors, are in remission, and have good performance status.
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收藏
页码:3797 / 3803
页数:7
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