Retinoic acid and arsenic trioxide for acute promyelocytic leukemia.

نویسندگان

  • Francesco Lo-Coco
  • Giuseppe Avvisati
  • Marco Vignetti
  • Christian Thiede
  • Sonia Maria Orlando
  • Simona Iacobelli
  • Felicetto Ferrara
  • Paola Fazi
  • Laura Cicconi
  • Eros Di Bona
  • Giorgina Specchia
  • Simona Sica
  • Mariadomenica Divona
  • Alessandro Levis
  • Walter Fiedler
  • Elisa Cerqui
  • Massimo Breccia
  • Giuseppe Fioritoni
  • Helmut R Salih
  • Mario Cazzola
  • Lorella Melillo
  • Angelo M Carella
  • Christian H Brandts
  • Enrica Morra
  • Marie von Lilienfeld-Toal
  • Bernd Hertenstein
  • Mohammed Wattad
  • Michael Lübbert
  • Matthias Hänel
  • Norbert Schmitz
  • Hartmut Link
  • Maria Grazia Kropp
  • Alessandro Rambaldi
  • Giorgio La Nasa
  • Mario Luppi
  • Fabio Ciceri
  • Olimpia Finizio
  • Adriano Venditti
  • Francesco Fabbiano
  • Konstanze Döhner
  • Michaela Sauer
  • Arnold Ganser
  • Sergio Amadori
  • Franco Mandelli
  • Hartmut Döhner
  • Gerhard Ehninger
  • Richard F Schlenk
  • Uwe Platzbecker
چکیده

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.).

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منابع مشابه

Superiority of an arsenic trioxide-based regimen over a historic control combining all-trans retinoic acid plus intensive chemotherapy in the treatment of relapsed acute promyelocytic leukemia.

There is still no consensus on the best approach for the treatment of relapsing acute promyelocytic leukemia. All-trans retinoic acid plus chemotherapy is hampered by potential mechanisms of resistance, and the safety profile of chemotherapy may be considered as not acceptable before stem cell transplantation. Arsenic trioxide provides an option for these patients.

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عنوان ژورنال:
  • Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi

دوره 34 2  شماره 

صفحات  -

تاریخ انتشار 2013