Arsenic trioxide - An old drug rediscovered

被引:229
作者
Emadi, Ashkan [1 ]
Gore, Steven D. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD 21231 USA
关键词
Arsenic trioxide (As2O3); Acute promyelocytic leukemia (APL); Differentiation; Apoptosis; Reactive oxygen species; Induction and consolidation chemotherapy; Multiple myeloma; T-cell lymphotropic virus type I (HTLV-I)-associated adult T-cell leukemia-lymphoma (ATL); Myelodysplastic syndrome (MDS); ACUTE PROMYELOCYTIC LEUKEMIA; ACID COMBINATION THERAPY; PHASE-II TRIAL; CELL-CYCLE ARREST; ASCORBIC-ACID; MULTIPLE-MYELOMA; GROWTH-INHIBITION; MYELODYSPLASTIC SYNDROMES; INTERFERON-ALPHA; RETINOIC ACID;
D O I
10.1016/j.blre.2010.04.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the last 17 years, clinical trials conducted worldwide have demonstrated the efficacy of arsenic trioxide (As2O3) in the treatment of relapsed acute promyelocytic leukemia (APL). Currently, the role of As2O3 in front-line therapy is under investigation. Recent trials in the US have demonstrated that the addition of As2O3 to standard treatment regimens improves survival outcomes in patients with APL and may allow a reduction in cytotoxic chemotherapy exposure. As2O3 has also shown efficacy in other malignancies, particularly multiple myeloma and myelodysplastic syndromes. Therapeutic doses of As2O3 are well tolerated, with no evidence of long-term toxicity. Adverse events include APL differentiation syndrome, electrocardiographic abnormalities, and mild elevations in liver enzymes. This review highlights trials investigating the role of As2O3 in induction and consolidation for newly diagnosed APL, as well as its role in other hematologic malignancies. The chemistry, mechanisms of action, and clinical side effects of As2O3 are also discussed. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:191 / 199
页数:9
相关论文
共 90 条
[41]   A phase II trial of arsenic trioxide in patients with metastatic melanoma [J].
Kim, KB ;
Bedikian, AY ;
Camacho, LH ;
Papadopoulos, NE ;
McCullough, C .
CANCER, 2005, 104 (08) :1687-1692
[42]   The release of cytochrome c from mitochondria: A primary site for Bcl-2 regulation of apoptosis [J].
Kluck, RM ;
BossyWetzel, E ;
Green, DR ;
Newmeyer, DD .
SCIENCE, 1997, 275 (5303) :1132-1136
[43]   Arsenic in the cerebrospinal fluid of a patient receiving arsenic trioxide for relapsed acute promyelocytic leukemia with CNS involvement [J].
Knipp, Sabine ;
Gattermann, Norbert ;
Schapira, Marc ;
Kaeferstein, Herbert ;
Germing, Ulrich .
LEUKEMIA RESEARCH, 2007, 31 (11) :1585-1587
[44]   Delicious poison: Arsenic trioxide for the treatment of leukemia [J].
Kwong, YL ;
Todd, D .
BLOOD, 1997, 89 (09) :3487-3488
[45]   Arsenite induces apoptosis via a direct effect on the mitochondrial permeability transition pore [J].
Larochette, N ;
Decaudin, D ;
Jacotot, E ;
Brenner, C ;
Marzo, I ;
Susin, SA ;
Zamzami, N ;
Xie, ZH ;
Reed, J ;
Kroemer, G .
EXPERIMENTAL CELL RESEARCH, 1999, 249 (02) :413-421
[46]   Arsenic trioxide in patients with hepatocellular carcinoma: a phase II trial [J].
Lin, Chia-Chi ;
Hsu, Chiun ;
Hsu, Chih-Hung ;
Hsu, Wei-Ling ;
Cheng, Ann-Lii ;
Yang, Chih-Hsin .
INVESTIGATIONAL NEW DRUGS, 2007, 25 (01) :77-84
[47]   Opportunities for Trisenox® (arsenic trioxide) in the treatment of myelodysplastic syndromes [J].
List, A ;
Beran, M ;
DiPersio, J ;
Slack, J ;
Vey, N ;
Rosenfeld, CS ;
Greenberg, P .
LEUKEMIA, 2003, 17 (08) :1499-1507
[48]  
Litzow MR, 2006, HAEMATOLOGICA, V91, P1105
[49]   Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: durable remissions with minimal toxicity [J].
Mathews, V ;
George, B ;
Lakshmi, KM ;
Viswabandya, A ;
Bajel, A ;
Balasubramanian, P ;
Shaji, RV ;
Srivastava, VM ;
Srivastava, A ;
Chandy, M .
BLOOD, 2006, 107 (07) :2627-2632
[50]  
Miller WH, 2002, CANCER RES, V62, P3893