Haematologica (Oct 2017)

Prolonged versus standard native E. coli asparaginase therapy in childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma: final results of the EORTC-CLG randomized phase III trial 58951

  • Veerle Mondelaers,
  • Stefan Suciu,
  • Barbara De Moerloose,
  • Alina Ferster,
  • Françoise Mazingue,
  • Geneviève Plat,
  • Karima Yakouben,
  • Anne Uyttebroeck,
  • Patrick Lutz,
  • Vitor Costa,
  • Nicolas Sirvent,
  • Emmanuel Plouvier,
  • Martine Munzer,
  • Maryline Poirée,
  • Odile Minckes,
  • Frédéric Millot,
  • Dominique Plantaz,
  • Philip Maes,
  • Claire Hoyoux,
  • Hélène Cavé,
  • Pierre Rohrlich,
  • Yves Bertrand,
  • Yves Benoit

DOI
https://doi.org/10.3324/haematol.2017.165845
Journal volume & issue
Vol. 102, no. 10

Abstract

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Asparaginase is an essential component of combination chemotherapy for childhood acute lymphoblastic leukemia and non-Hodgkin lymphoma. The value of asparaginase was further addressed in a group of non-very high-risk patients by comparing prolonged (long-asparaginase) versus standard (short-asparaginase) native E. coli asparaginase treatment in a randomized part of the phase III 58951 trial of the European Organization for Research and Treatment of Cancer Children’s Leukemia Group. The main endpoint was disease-free survival. Overall, 1,552 patients were randomly assigned to long-asparaginase (775 patients) or short-asparaginase (777 patients). Patients with grade ≥2 allergy to native E. coli asparaginase were switched to equivalent doses of Erwinia or pegylated E. coli asparaginase. The 8-year disease-free survival rate (±standard error) was 87.0±1.3% in the long-asparaginase group and 84.4±1.4% in the short-asparaginase group (hazard ratio: 0.87; P=0.33) and the 8-year overall survival rate was 92.6±1.0% and 91.3±1.2% respectively (hazard ratio: 0.89; P=0.53). An exploratory analysis suggested that the impact of long-asparaginase was beneficial in the National Cancer Institute standard-risk group with regards to disease-free survival (hazard ratio: 0.70; P=0.057), but far less so with regards to overall survival (hazard ratio: 0.89). The incidences of grade 3–4 infection during consolidation (25.2% versus 14.4%) and late intensification (22.6% versus 15.9%) and the incidence of grade 2–4 allergy were higher in the long-asparaginase arm (30% versus 21%). Prolonged native E. coli asparaginase therapy in consolidation and late intensification for our non-very high-risk patients did not improve overall outcome but led to an increase in infections and allergy. This trial was registered at www.clinicaltrials.gov as #NCT00003728.