Literature DB >> 17988996

Comparison of myeloablative and nonmyeloablative hematopoietic stem cell transplantation for treatment of chronic myeloid leukemia.

Ming-Huang Chen1, Tzeon-Jye Chiou, Peng-Chan Lin, Jyh-Pyng Gau, Hui-Chi Hsu, Liang-Tsai Hsiao, Jin-Hwang Liu, Po-Min Chen.   

Abstract

This retrospective study compared outcomes for 81 chronic myeloid leukemia patients who underwent myeloablative or nonmyeloablative allogeneic hematopoietic stem cell transplantation (HSCT). Sixty-five patients received myeloablative HSCT, and 16 patients received fludarabine (Fd), low-dose busulfan (Bu), and antithymocyte globulin (ATG) in nonmyeloablative HSCT. We determined overall survival (OS) and disease-free survival (DFS), as well as the occurrence of acute and chronic graft-versus-host disease (GVHD). The incidences of acute GVHD of grades II to IV were 14.0% and 18.7% for the myeloablative and nonmyeloablative groups, respectively. The incidence of chronic GVHD was significantly higher in the nonmyeloablative group (80% versus 66%). Five-year OS and DFS rates were significantly higher in nonmyeloablative group (70% for both), compared with 56% and 54%, respectively, for the myeloablative group. A univariate analysis, however, revealed a strong but statistically insignificant trend for enhanced overall OS and DFS in the nonmyeloablative group (P = .1 and .07, respectively). A multivariate analysis with the factors of treatment, age, sex, acute and chronic GVHD, and disease status at the time of transplantation revealed that both OS and DFS were significantly higher in the nonmyeloablative group than in the myeloablative group. These findings suggest that nonmyeloablative Fd/Bu/ATG treatment is at least not inferior (and quite probably superior) in terms of patient outcome compared with standard myeloablative therapy. Further larger-scale randomized clinical trials are warranted to clarify the efficacy of this treatment regimen.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17988996     DOI: 10.1532/IJH97.A10701

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  27 in total

1.  2002 guidelines for the use of antimicrobial agents in neutropenic patients with cancer.

Authors:  Walter T Hughes; Donald Armstrong; Gerald P Bodey; Eric J Bow; Arthur E Brown; Thierry Calandra; Ronald Feld; Philip A Pizzo; Kenneth V I Rolston; Jerry L Shenep; Lowell S Young
Journal:  Clin Infect Dis       Date:  2002-02-13       Impact factor: 9.079

Review 2.  Chronic graft-versus-host disease and other late complications of bone marrow transplantation.

Authors:  K M Sullivan; E Agura; C Anasetti; F Appelbaum; C Badger; S Bearman; K Erickson; M Flowers; J Hansen; T Loughran
Journal:  Semin Hematol       Date:  1991-07       Impact factor: 3.851

3.  Marrow transplantation for CML: the Seattle experience.

Authors:  R A Clift; R Storb
Journal:  Bone Marrow Transplant       Date:  1996-05       Impact factor: 5.483

4.  Allogeneic bone marrow transplantation for CML: a report from the International Bone Marrow Transplant Registry.

Authors:  M M Horowitz; P A Rowlings; J R Passweg
Journal:  Bone Marrow Transplant       Date:  1996-05       Impact factor: 5.483

5.  Dose-reduced conditioning for allografting in 44 patients with chronic myeloid leukaemia: a retrospective analysis.

Authors:  M Bornhäuser; M Kiehl; W Siegert; J Schetelig; B Hertenstein; H Martin; R Schwerdtfeger; H G Sayer; V Runde; N Kröger; C Theuser; G Ehninger
Journal:  Br J Haematol       Date:  2001-10       Impact factor: 6.998

6.  Antileukemic effect of graft-versus-host disease in human recipients of allogeneic-marrow grafts.

Authors:  P L Weiden; N Flournoy; E D Thomas; R Prentice; A Fefer; C D Buckner; R Storb
Journal:  N Engl J Med       Date:  1979-05-10       Impact factor: 91.245

7.  Salvage immunotherapy using donor leukocyte infusions as treatment for relapsed chronic myelogenous leukemia after allogeneic bone marrow transplantation: efficacy and toxicity of a defined T-cell dose.

Authors:  W R Drobyski; C A Keever; M S Roth; S Koethe; G Hanson; P McFadden; J L Gottschall; R C Ash; P van Tuinen; M M Horowitz
Journal:  Blood       Date:  1993-10-15       Impact factor: 22.113

8.  Kinetics of minimal residual disease and chimerism in patients with chronic myeloid leukemia after nonmyeloablative conditioning and allogeneic stem cell transplantation.

Authors:  Mehmet Uzunel; Jonas Mattsson; Mats Brune; Jan-Erik Johansson; Johan Aschan; Olle Ringdén
Journal:  Blood       Date:  2002-08-29       Impact factor: 22.113

9.  In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants.

Authors:  Thomas O'Hare; Denise K Walters; Eric P Stoffregen; Taiping Jia; Paul W Manley; Jürgen Mestan; Sandra W Cowan-Jacob; Francis Y Lee; Michael C Heinrich; Michael W N Deininger; Brian J Druker
Journal:  Cancer Res       Date:  2005-06-01       Impact factor: 12.701

10.  Loss of response to imatinib: mechanisms and management.

Authors:  Neil P Shah
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2005
View more
  3 in total

1.  Comparison of Wilms' tumor antigen 1-specific T lymphocyte generation soon after nonmyeloablative allergenic stem-cell transplantation in acute and chronic leukemia patients.

Authors:  Li Wei; HongLi Zuo; XueDong Sun; TieQiang Liu; Mei Guo; GuangXian Liu; QiYun Sun; JianHui Qiao; DanHong Wang; ChangLin Yu; KaiXun Hu; Zheng Dong; HuiSheng Ai
Journal:  Int J Hematol       Date:  2010-04-08       Impact factor: 2.490

Review 2.  Indications and outcomes of reduced-toxicity hematopoietic stem cell transplantation in adult patients with hematological malignancies.

Authors:  S Fadilah Abdul Wahid
Journal:  Int J Hematol       Date:  2013-04-13       Impact factor: 2.490

3.  Pediatric chronic myeloid leukemia is a unique disease that requires a different approach.

Authors:  Nobuko Hijiya; Kirk R Schultz; Markus Metzler; Frederic Millot; Meinolf Suttorp
Journal:  Blood       Date:  2015-10-28       Impact factor: 22.113

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.