Retinoic acid and arsenic trioxide for acute promyelocytic leukemia
- PMID: 23841729
- DOI: 10.1056/NEJMoa1300874
Retinoic acid and arsenic trioxide for acute promyelocytic leukemia
Abstract
Background: All-trans retinoic acid (ATRA) with chemotherapy is the standard of care for acute promyelocytic leukemia (APL), resulting in cure rates exceeding 80%. Pilot studies of treatment with arsenic trioxide with or without ATRA have shown high efficacy and reduced hematologic toxicity.
Methods: We conducted a phase 3, multicenter trial comparing ATRA plus chemotherapy with ATRA plus arsenic trioxide in patients with APL classified as low-to-intermediate risk (white-cell count, ≤10×10(9) per liter). Patients were randomly assigned to receive either ATRA plus arsenic trioxide for induction and consolidation therapy or standard ATRA-idarubicin induction therapy followed by three cycles of consolidation therapy with ATRA plus chemotherapy and maintenance therapy with low-dose chemotherapy and ATRA. The study was designed as a noninferiority trial to show that the difference between the rates of event-free survival at 2 years in the two groups was not greater than 5%.
Results: Complete remission was achieved in all 77 patients in the ATRA-arsenic trioxide group who could be evaluated (100%) and in 75 of 79 patients in the ATRA-chemotherapy group (95%) (P=0.12). The median follow-up was 34.4 months. Two-year event-free survival rates were 97% in the ATRA-arsenic trioxide group and 86% in the ATRA-chemotherapy group (95% confidence interval for the difference, 2 to 22 percentage points; P<0.001 for noninferiority and P=0.02 for superiority of ATRA-arsenic trioxide). Overall survival was also better with ATRA-arsenic trioxide (P=0.02). As compared with ATRA-chemotherapy, ATRA-arsenic trioxide was associated with less hematologic toxicity and fewer infections but with more hepatic toxicity.
Conclusions: ATRA plus arsenic trioxide is at least not inferior and may be superior to ATRA plus chemotherapy in the treatment of patients with low-to-intermediate-risk APL. (Funded by Associazione Italiana contro le Leucemie and others; ClinicalTrials.gov number, NCT00482833.).
Comment in
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Targeting agents alone to cure acute promyelocytic leukemia.N Engl J Med. 2013 Jul 11;369(2):186-7. doi: 10.1056/NEJMe1304762. N Engl J Med. 2013. PMID: 23841735 No abstract available.
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Treatment of acute promyelocytic leukemia.N Engl J Med. 2013 Oct 10;369(15):1472. doi: 10.1056/NEJMc1309895. N Engl J Med. 2013. PMID: 24106948 No abstract available.
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Treatment of acute promyelocytic leukemia.N Engl J Med. 2013 Oct 10;369(15):1471-2. doi: 10.1056/NEJMc1309895. N Engl J Med. 2013. PMID: 24106949 No abstract available.
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