Treatment of acute promyelocytic leukemia and other hematologic malignancies with arsenic trioxide: Review of clinical and basic studies

被引:26
作者
Liu, P
Han, ZC
机构
[1] Chinese Acad Med Sci, Inst Hematol, State Key Lab Expt Hematol, Tianjin 300020, Peoples R China
[2] Chinese Acad Med Sci, Blood Dis Hosp, Tianjin 300020, Peoples R China
[3] Peking Union Med Coll, Tianjin, Peoples R China
关键词
arsenic trioxide; acute promyelocytic leukemia; hematologic malignancy; clinical trials; mechanisms of action;
D O I
10.1007/BF02983237
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Acute promyelocytic leukemia (APL) is now the most potentially curable subtype of acute myeloid leukemia in adults because of the introduction of novel approaches in the management of this disease. All-trans-retinoic acid (ATRA)-based therapy is now the first-choice treatment of patients presenting with de novo APL, and clinical studies have shown that nearly all patients who receive ATRA therapy achieve complete remission. However, approximately 20% to 30% of APL patients eventually have relapses with resistance to further ATRA treatment. Arsenic trioxide (As2O3 [ATO]) has been established as highly effective therapy for patients with APL, even for those with disease refractory to ATRA. Furthermore, results of recent studies have suggested a broad therapeutic potential for ATO in the treatment of hematologic malignancies beyond APL. In this review, we discuss the clinical activity and multiple mechanisms of ATO therapy in the management of APL and other hematologic neoplasms. (C) 2003 The Japanese Society of Hematology.
引用
收藏
页码:32 / 39
页数:8
相关论文
共 89 条
  • [1] ALEXANIAN R, 1992, BLOOD, V80, P887
  • [2] Introduction: The history of arsenic trioxide in cancer therapy
    Antman, KH
    [J]. ONCOLOGIST, 2001, 6 : 1 - 2
  • [3] A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma
    Attal, M
    Harousseau, JL
    Stoppa, AM
    Sotto, JJ
    Fuzibet, JG
    Rossi, JF
    Casassus, P
    Maisonneuve, H
    Facon, T
    Ifrah, N
    Payen, C
    Bataille, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (02) : 91 - 97
  • [4] Arsenic trioxide and ascorbic acid: synergy with potential implications for the treatment of acute myeloid leukaemia?
    Bachleitner-Hofmann, T
    Gisslinger, B
    Grumbeck, E
    Gisslinger, H
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2001, 112 (03) : 783 - 786
  • [5] Bahlis NJ, 2001, BLOOD, V98, p375A
  • [6] Barbey JT, 2000, BLOOD, V96, p318A
  • [7] Bellamy WT, 1999, CANCER RES, V59, P728
  • [8] The Myelodysplastic Syndromes: Morphology, risk assessment, and clinical management (2002)
    Bennett, JM
    Kouides, PA
    Forman, SJ
    [J]. INTERNATIONAL JOURNAL OF HEMATOLOGY, 2002, 76 (Suppl 2) : 228 - 238
  • [9] Hematopathologic and cytogenetic findings in imatinib mesylate-treated chronic myelogenous leukemia patients: 14 months' experience
    Braziel, RM
    Launder, TM
    Druker, BJ
    Olson, SB
    Magenis, RE
    Mauro, MJ
    Sawyers, CL
    Paquette, RL
    O'Dwyer, ME
    [J]. BLOOD, 2002, 100 (02) : 435 - 441
  • [10] Arsenic trioxide-induced apoptosis and differentiation are associated respectively with mitochondrial transmembrane potential collapse and retinoic acid signaling pathways in acute promyelocytic leukemia
    Cai, X
    Shen, YL
    Zhu, Q
    Jia, PM
    Yu, Y
    Zhou, L
    Huang, Y
    Zhang, JW
    Xiong, SM
    Chen, SJ
    Wang, ZY
    Chen, Z
    Chen, GQ
    [J]. LEUKEMIA, 2000, 14 (02) : 262 - 270