Is it appropriate to offer allogeneic hematopoietic stem cell transplantation to patients with primary refractory acute myeloid leukemia?

被引:34
作者
Song, KW
Lipton, J
机构
[1] Univ British Columbia, British Columbia Canc Agcy, Vancouver Hosp & Hlth Sci Ctr, Leukemia Bone Marrow Transplantat Program British, Vancouver, BC V5Z 1M9, Canada
[2] Univ Toronto, Univ Hlth Network, Princess Margaret Hosp, Leukemia & Allogene Stem Cell Transplant Serv, Toronto, ON, Canada
关键词
acute myeloid leukemia; allogeneic transplantation; primary refractory AML;
D O I
10.1038/sj.bmt.1705038
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Although continued advances have been made in the treatment of acute myeloid leukemia (AML), approximately 20 - 30% of patients will never achieve a remission. For these patients with primary refractory AML, the only curative option remains an allogeneic stem cell transplant. Allogeneic transplantation provides the ability to administer myeloablative doses of chemotherapy or chemoradiotherapy, as well as the advantage of a possible graft-versus-leukemia effect. Difficulty in interpreting the literature is due to selection bias, in particular, the varying definitions of primary refractory disease with respect to the morphological criteria and the number of induction regimen required before being defined as being refractory. Regardless, it is a procedure with high treatment-related mortality and risk of relapse. Most studies demonstrate an event-free survival of 10 - 20% at 5 years. Predictive factors of outcome include blast cell count in the marrow, karyotype, the number of prior regimen, age, performance status and availability of a related donor. These prognostic factors should be considered prior to offering allogeneic transplantation for primary refractory AML. Those patients with many favorable prognostic factors and an HLA-matched related donor available would be the best candidate for the procedure. Those with many poor prognostic factors and only an unrelated donor available may be better served by being offered palliation or being enrolled in investigational studies.
引用
收藏
页码:183 / 191
页数:9
相关论文
共 47 条
  • [1] A urokinase-activated recombinant diphtheria toxin targeting the granulocyt-emacrophage colony-stimulating factor receptor is selectively cytotoxic to human acute myeloid leukemia blasts
    Abi-Habib, RJ
    Liu, SH
    Bugge, TH
    Leppla, SH
    Frankel, AE
    [J]. BLOOD, 2004, 104 (07) : 2143 - 2148
  • [2] Immunization of allogeneic bone marrow transplant recipients with tumor cell vaccines enhances graft-versus-tumor activity without exacerbating graft-versus-host disease
    Anderson, LD
    Savary, CA
    Mullen, CA
    [J]. BLOOD, 2000, 95 (07) : 2426 - 2433
  • [3] Transplantation of bone marrow as compared with peripheral-blood cells from HLA-identical relatives in patients with hematologic cancers.
    Bensinger, WI
    Martin, PJ
    Storer, B
    Clift, R
    Forman, SJ
    Negrin, R
    Kashyap, A
    Flowers, MED
    Lilleby, K
    Chauncey, TR
    Storb, R
    Appelbaum, FR
    Rowley, S
    Heimfeld, S
    Blume, K
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (03) : 175 - 181
  • [4] BONE-MARROW TRANSPLANTS MAY CURE PATIENTS WITH ACUTE-LEUKEMIA NEVER ACHIEVING REMISSION WITH CHEMOTHERAPY
    BIGGS, JC
    HOROWITZ, MM
    GALE, RP
    ASH, RC
    ATKINSON, K
    HELBIG, W
    JACOBSEN, N
    PHILLIPS, GL
    RIMM, AA
    RINGDEN, O
    ROZMAN, C
    SOBOCINSKI, KA
    VEUM, JA
    BORTIN, MM
    [J]. BLOOD, 1992, 80 (04) : 1090 - 1093
  • [5] Chemotherapy compared with autologous or allogeneic bone marrow transplantation in the management of acute myeloid leukemia in first remission
    Cassileth, PA
    Harrington, DP
    Appelbaum, FR
    Lazarus, HM
    Rowe, JM
    Paietta, E
    Willman, C
    Hurd, DD
    Bennett, JM
    Blume, KG
    Head, DR
    Wiernik, PH
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (23) : 1649 - 1656
  • [6] Prevention of graft-versus-host disease while preserving graft-versus-leukemia effect after selective depletion of host-reactive T cells by photodynamic cell purging process
    Chen, BJ
    Cui, XY
    Liu, CX
    Chao, NJ
    [J]. BLOOD, 2002, 99 (09) : 3083 - 3088
  • [7] REPORT OF THE NATIONAL CANCER INSTITUTE-SPONSORED WORKSHOP ON DEFINITIONS OF DIAGNOSIS AND RESPONSE IN ACUTE MYELOID-LEUKEMIA
    CHESON, BD
    CASSILETH, PA
    HEAD, DR
    SCHIFFER, CA
    BENNETT, JM
    BLOOMFIELD, CD
    BRUNNING, R
    GALE, RP
    GREVER, MR
    KEATING, MJ
    SAWITSKY, A
    STASS, S
    WEINSTEIN, H
    WOODS, WG
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (05) : 813 - 819
  • [8] Revised recommendations of the international working group for diagnosis, standardization of response criteria, treatment outcomes, and reporting standards for therapeutic trials in acute myeloid leukemia
    Cheson, BD
    Bennett, JM
    Kopecky, KJ
    Büchner, T
    Willman, CL
    Estey, EH
    Schiffer, CA
    Döhner, H
    Tallman, MS
    Lister, TA
    LoCocco, F
    Willemze, R
    Biondi, A
    Hiddemann, W
    Larson, RA
    Löwenberg, B
    Sanz, MA
    Head, DR
    Ohno, R
    Bloomfield, CD
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (24) : 4642 - 4649
  • [9] Donor leukocyte infusions in 140 patients with relapsed malignancy after allogeneic bone marrow transplantation
    Collins, RH
    Shpilberg, O
    Drobyski, WR
    Porter, DL
    Giralt, S
    Champlin, R
    Goodman, SA
    Wolff, SN
    Hu, W
    Verfaillie, C
    List, A
    Dalton, W
    Ognoskie, N
    Chetrit, A
    Antin, JH
    Nemunaitis, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (02) : 433 - 444
  • [10] The impact of donor KIR and patient HLA-C genotypes on outcome following HLA-identical sibling hematopoietic stem cell transplantation for myeloid leukemia
    Cook, MA
    Milligan, DW
    Fegan, CD
    Darbyshire, PJ
    Mahendra, P
    Craddock, CF
    Moss, PAH
    Briggs, DC
    [J]. BLOOD, 2004, 103 (04) : 1521 - 1526