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.).

Retinoic acid and arsenic trioxide for acute promyelocytic leukemia / Lo Coco, F; Avvisati, G; Vignetti, M; Thiede, C; Orlando, Sm; Iacobelli, S; Ferrara, F; Fazi, P; Cicconi, L; Di Bona, E; Specchia, G; Sica, S; Divona, M; Levis, A; Fiedler, W; Cerqui, E; Breccia, M; Fioritoni, G; Salih, Hr; Cazzola, M; Melillo, L; Carella, Am; Brandts, Ch; Morra, E; von Lilienfeld Toal, M; Hertenstein, B; Wattad, M; Lübbert, M; Hänel, M; Schmitz, N; Link, H; Kropp, Mg; Rambaldi, A; La Nasa, G; Luppi, Mario; Ciceri, F; Finizio, O; Venditti, A; Fabbiano, F; Döhner, K; Sauer, M; Ganser, A; Amadori, S; Mandelli, F; Döhner, H; Ehninger, G; Schlenk, Rf; Platzbecker, U; Gruppo Italiano Malattie Ematologiche, Dell'Adulto; German Austrian Acute Myeloid Leukemia Study, Group; Study Alliance, Leukemia. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - STAMPA. - 369:2(2013), pp. 111-121. [10.1056/NEJMoa1300874]

Retinoic acid and arsenic trioxide for acute promyelocytic leukemia.

LUPPI, Mario;
2013

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.).
2013
369
2
111
121
Retinoic acid and arsenic trioxide for acute promyelocytic leukemia / Lo Coco, F; Avvisati, G; Vignetti, M; Thiede, C; Orlando, Sm; Iacobelli, S; Ferrara, F; Fazi, P; Cicconi, L; Di Bona, E; Specchia, G; Sica, S; Divona, M; Levis, A; Fiedler, W; Cerqui, E; Breccia, M; Fioritoni, G; Salih, Hr; Cazzola, M; Melillo, L; Carella, Am; Brandts, Ch; Morra, E; von Lilienfeld Toal, M; Hertenstein, B; Wattad, M; Lübbert, M; Hänel, M; Schmitz, N; Link, H; Kropp, Mg; Rambaldi, A; La Nasa, G; Luppi, Mario; Ciceri, F; Finizio, O; Venditti, A; Fabbiano, F; Döhner, K; Sauer, M; Ganser, A; Amadori, S; Mandelli, F; Döhner, H; Ehninger, G; Schlenk, Rf; Platzbecker, U; Gruppo Italiano Malattie Ematologiche, Dell'Adulto; German Austrian Acute Myeloid Leukemia Study, Group; Study Alliance, Leukemia. - In: THE NEW ENGLAND JOURNAL OF MEDICINE. - ISSN 0028-4793. - STAMPA. - 369:2(2013), pp. 111-121. [10.1056/NEJMoa1300874]
Lo Coco, F; Avvisati, G; Vignetti, M; Thiede, C; Orlando, Sm; Iacobelli, S; Ferrara, F; Fazi, P; Cicconi, L; Di Bona, E; Specchia, G; Sica, S; Divona,...espandi
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