Management of acute promyelocytic leukemia.

被引:18
作者
Tallman M.S. [1 ]
Nabhan C. [1 ]
机构
[1] Division of Hematology/Oncology, Northwestern University Medical School, Robert H. Lurie Comprehensive Cancer Center, 676 N. St. Clair Street, Chicago, 60611, IL
关键词
Acute Promyelocytic Leukemia; Minimal Residual Disease; Idarubicin; Allogeneic Hematopoietic Stem Cell Transplant; Arsenic Trioxide;
D O I
10.1007/s11912-002-0031-1
中图分类号
学科分类号
摘要
Acute promyelocytic leukemia (APL) has become the most potentially curable subtype of acute myeloid leukemia (AML) in adults. With current treatment strategies that incorporate all-trans retinoic acid (ATRA), long-term disease-free survival and potential cure rates of 70% to 80% can be expected. Such progress reflects what can be accomplished with insights into the molecular pathogenesis of leukemia, identification of a molecular target, and rapid accrual to a series of clinical trials. The leukemic promyelocytes from patients with APL are uniquely susceptible to a variety of novel agents in addition to ATRA, including arsenic trioxide, and in preliminary studies, gemtuzumab ozogamicin, the immunoconjugate comprised of an anti-CD33 monoclonal antibody linked to the potent cytotoxic agent calicheamicin. Incorporation of such agents into the treatment of patients with high-risk disease may be an important future direction to pursue.
引用
收藏
页码:381 / 389
页数:8
相关论文
共 253 条
[1]  
Paietta E(1994)Significantly lower P-glycoprotein expression in acute promyelocytic leukemia than in other types of acute myeloid leukemia: immunological, molecular and functional analyses Leukemia 8 968-973
[2]  
Andersen J(2000)P-glycoprotein (PGP), lung resistance-related protein (LRP) and multidrug resistance-associated protein (MRP) expression in acute promyelocytic leukaemia Br J Haematol 108 703-709
[3]  
Racevskis J(2000)Role of P-glycoprotein in all-trans retinoic acid (ATRA) resistance in acute promyelocytic leukaemia cells: analysis of intracellular concentration of ATRA Br J Haematol 108 90-92
[4]  
Michieli M(1973)Acute promyelocytic leukemia: results of treatment by daunorubicin Blood 41 489-496
[5]  
Damiani D(1978)Acute promyelocytic leukemia: management of the coagulopathy during daunorubicin-prednisone remission induction Arch Intern Med 138 1677-1680
[6]  
Ermacora A(1984)Acute promyelocytic leukemia: retrospective study of 119 patients treated with daunorubicin Nouv Rev Fr Hematol 26 371-387
[7]  
Takeshita A(1987)Acute promyelocytic leukemia: clinical aspects and results of treatment in 62 patients Haematologica 72 151-155
[8]  
Shinjo K(1988)Acute promyelocytic leukemia: therapy results and prognostic factors Cancer 61 7-13
[9]  
Naito K(1990)Idarubicin (4-demethoxydaunorubicin) as single agent for remission induction of previously untreated acute promyelocytic leukemia: a pilot study of the Italian cooperative group GIMEMA Eur J Haematol 44 257-260
[10]  
Bernard J(1999)Event-free survival (EFS) duration in newly diagnosed acute promyelocytic leukemia (APL) is favorably influenced by induction treatment with idarubicin alone: final results of the GIMEMA randomized study (LAP389) comparing idarubicin+Ara-C in newly diagnosed APL [abstract] Blood 94 2259a-2259a