Haematologica (Aug 2024)

Outcome of 421 adult patients with Philadelphia-negative acute lymphoblastic leukemia treated under an intensive program inspired by the GIMEMA LAL1913 clinical trial: a Campus ALL study

  • Davide Lazzarotto,
  • Marco Cerrano,
  • Cristina Papayannidis,
  • Sabina Chiaretti,
  • Federico Mosna,
  • Nicola Fracchiolla,
  • Patrizia Zappasodi,
  • Silvia Imbergamo,
  • Maria Ilaria Del Principe,
  • Monia Lunghi,
  • Federico Lussana,
  • Matteo Piccini,
  • Monica Fumagalli,
  • Michelina Dargenio,
  • Prassede Salutari,
  • Fabio Forghieri,
  • Teresa Giulia Da Molin,
  • Massimiliano Bonifacio,
  • Matteo Olivi,
  • Fabio Giglio,
  • Silvia Trappolini,
  • Matteo Leoncin,
  • Antonino Mule,
  • Mario Delia,
  • Crescenza Pasciolla,
  • Francesco Grimaldi,
  • Benedetta Cambo,
  • Lidia Santoro,
  • Fabio Guolo,
  • Paola Minetto,
  • Marzia Defina,
  • Patrizia Chiusolo,
  • Matteo Fanin,
  • Endri Mauro,
  • Lara Aprile,
  • Carla Mazzone,
  • Fabio Trastulli,
  • Maria Ciccone,
  • Marco De Gobbi,
  • Alessandro Cignetti,
  • Eleonora De Bellis,
  • Valentina Mancini,
  • Alfonso Piciocchi,
  • Marco Vignetti,
  • Giovanni Marsili,
  • Irene Della Starza,
  • Renato Fanin,
  • Mario Luppi,
  • Felicetto Ferrara,
  • Giovanni Pizzolo,
  • Renato Bassan,
  • Robin Foa,
  • Anna Candoni

DOI
https://doi.org/10.3324/haematol.2024.285638
Journal volume & issue
Vol. 999, no. 1

Abstract

Read online

The introduction of pediatric-inspired regimens in adult Philadelphia-negative acute lymphoblastic leukemia (Ph-ALL) has significantly improved patients’ prognosis. Within the Campus ALL network we analyzed the outcome of adult Ph-ALL patients treated according to the GIMEMA LAL1913 protocol outside the clinical trial, to compare the real-life data with the study results. We included 421 consecutive patients, with a median age of 42 years. The complete remission (CR) rate after the first course of chemotherapy was 94% and a measurable residual disease (MRD) negativity after the third course was achieved in 72% of patients. The 3-year overall survival (OS) and disease-free survival (DFS) were 67% and 57%, respectively. In a multivariate analysis, MRD positivity negatively influenced DFS. In a time-dependent analysis including only very high risk (VHR) and MRD positive cases, transplanted (HSCT) patients had a significantly better DFS than non-HSCT ones (P=0.0017). During induction, grade ≥2 pegaspargase-related hepato-toxicity was observed in 25% of patients (vs 12% in the GIMEMA LAL1913 trial, P=0.0003). In this large real-life cohort of Ph-ALL, we confirmed the very high CR rate and a superimposable OS and DFS compared to the GIMEMA LAL1913 clinical trial: CR rate after C1 94% vs 85%, P=0.0004; 3-year OS 67% vs 67%, P=0.94; 3-year DFS 57% vs 63%, P=0.17. HSCT confirms its important role in VHR and MRD-positive patients. The rate of pegaspargase-related toxicity was significantly higher in the real-life setting, emphasizing the importance of dose adjustment in the presence of risk factors to avoid excessive toxicity.