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      Single-agent arsenic trioxide in the treatment of newly diagnosed acute promyelocytic leukemia: long-term follow-up data.

      Journal of clinical oncology : official journal of the American Society of Clinical Oncology
      Adult, Aged, Antineoplastic Agents, administration & dosage, pharmacokinetics, therapeutic use, Arsenicals, Disease-Free Survival, Female, Follow-Up Studies, Hair, metabolism, Humans, Infusions, Intravenous, Kaplan-Meier Estimate, Leukemia, Promyelocytic, Acute, diagnosis, drug therapy, Male, Middle Aged, Nails, Oxides, Recurrence, Remission Induction, Time Factors, Treatment Outcome

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          Abstract

          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/RARalpha+ 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.

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