Bergstrom S K, Gillan E, Quinn J J, Altman A J
Department of Pediatrics, Connecticut Children's Medical Center, University of Connecticut School of Medicine, Hartford 06106, USA.
J Pediatr Hematol Oncol. 1998 Nov-Dec;20(6):545-7.
Little experience exists with the use of arsenic trioxide in the treatment of recurrent, all-trans retinoic acid (ATRA)-resistant, acute promyelocytic leukemia (APL). The authors report a patient with multiply recurrent APL treated with arsenic trioxide (As2O3), which was administered as recommended in the protocol from the People' s Republic of China. The results of this treatment and its toxicity are discussed. The available literature on arsenic therapy is reviewed.
The patient was a 15-year-old African-American girl with APL that had resisted conventional chemotherapy, ATRA therapy followed by autologous peripheral stem cell transplant, and a second course of ATRA induction therapy administered for relapse after transplant. The patient was treated with 10 mg As2O3 intravenously for 28 days. After a 4-week break, she received a second 28-day course of As2O3 therapy.
After completion of the first 28-day course of As2O3 treatment, morphologic and cytogenetic remission occurred. Reverse-transcription polymerase chain reaction demonstrated persistence of the PML-RARalpha fusion transcript. After the second course of As2O3, the patient had a complete remission by morphologic, cytogenetic, and molecular criteria. Approximately 6 months after the end of two courses of As2O3 therapy, the patient again underwent relapse. An additional course of As2O3 achieved a morphologic, although not a cytogenetic or molecular, remission.
As2O3 therapy produced remission in a patient with multiply relapsed, ATRA-resistant APL. Toxic side effects were minimal. The patient underwent relapse 6 months after this therapy. Further investigation will be necessary to determine the proper role of As2O3 therapy in patients with APL.
三氧化二砷用于治疗复发的、对全反式维甲酸(ATRA)耐药的急性早幼粒细胞白血病(APL)的经验较少。作者报告了一名多次复发的APL患者接受三氧化二砷(As2O3)治疗的情况,治疗按照中华人民共和国方案中的推荐进行。讨论了该治疗的结果及其毒性。并对砷治疗的现有文献进行了综述。
该患者是一名15岁的非裔美国女孩,患有APL,对传统化疗、ATRA治疗后进行自体外周干细胞移植以及移植后复发给予的第二疗程ATRA诱导治疗均耐药。患者接受10mg As2O3静脉注射,共28天。在休息4周后,她接受了第二个为期28天的As2O3治疗疗程。
在完成第一个为期28天的As2O3治疗疗程后,出现了形态学和细胞遗传学缓解。逆转录聚合酶链反应显示PML-RARα融合转录本持续存在。在第二个As2O3疗程后,患者在形态学、细胞遗传学和分子标准方面均达到完全缓解。在两个疗程的As2O3治疗结束后约6个月,患者再次复发。额外的一个As2O3疗程实现了形态学缓解,尽管未达到细胞遗传学或分子学缓解。
As2O3治疗使一名多次复发、对ATRA耐药的APL患者获得缓解。毒性副作用极小。该患者在此次治疗后6个月复发。有必要进行进一步研究以确定As2O3治疗在APL患者中的适当作用。