Single-Agent Arsenic Trioxide in the Treatment of Newly Diagnosed Acute Promyelocytic Leukemia: Long-Term Follow-Up Data

被引:210
|
作者
Mathews, Vikram [1 ]
George, Biju [1 ]
Chendamarai, Ezhilarasi [1 ]
Lakshmi, Kavitha M. [1 ]
Desire, Salamun [1 ]
Balasubramanian, Poonkuzhali [1 ]
Viswabandya, Auro [1 ]
Thirugnanam, Rajashekar [1 ]
Abraham, Aby [1 ]
Shaji, Ramachandran Velayudhan [1 ]
Srivastava, Alok [1 ]
Chandy, Mammen [1 ]
机构
[1] Christian Med Coll & Hosp, Vellore, Tamil Nadu, India
关键词
TRANS-RETINOIC ACID; METHYLENETETRAHYDROFOLATE REDUCTASE; MAINTENANCE THERAPY; CHEMOTHERAPY; EFFICACY; CONSOLIDATION; POLYMORPHISMS; MULTICENTER; TOXICITY; RISK;
D O I
10.1200/JCO.2010.28.5031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose We previously reported our results with a single-agent arsenic trioxide (ATO) - based regimen in newly diagnosed cases of acute promyelocytic leukemia (APL). The concern remained about the long-term outcome of this well-tolerated regimen. We report our long-term follow-up data on the same cohort. Patients and Methods From January 1998 to December 2004, 72 patients with PML/RAR alpha+ APL were enrolled. All patients were treated with a single-agent ATO regimen. Results Overall 62 (86.1%) achieved a hematologic remission (complete remission). After the initial report, an additional seven patients have relapsed for a total of 13 relapses. There were no additional toxicities to report on follow-up. At a median follow-up 60 months, the 5-year Kaplan-Meier estimate (+/- SE) of event-free survival, disease-free survival, and overall survival (OS) was 69% +/- 5.5%, 80% +/- 5.2%, and 74.2% +/- 5.2%, respectively. The OS in the good risk group as defined by us remains 100% over this period. Conclusion Single-agent ATO as used in this study in the management of newly diagnosed cases of APL is safe and is associated with durable responses. Results in the low-risk group are comparable to that reported with conventional therapy while additional interventions would probably be required in high-risk cases.
引用
收藏
页码:3866 / 3871
页数:6
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