Bosutinib, an orally active, Src/Abl tyrosine kinase inhibitor, has demonstrated clinical activity and acceptable tolerability in chronic phase chronic myeloid leukemia (CP CML). This updated analysis of the BELA trial assessed the safety profile and management of toxicities of bosutinib versus imatinib in adults with newly diagnosed (≤6 months) CP CML after >30 months from accrual completion. Among patients randomized to bosutinib 500 mg/d (n=250) or imatinib 400 mg/d (n=252), 248 and 251, respectively, received ≥1 dose of study treatment. Adverse events (AEs; any grade) with bosutinib versus imatinib were significantly more common for certain gastrointestinal events (diarrhea, 70% vs 26%; P<0.001; vomiting, 33% vs 16%; P<0.001), alanine aminotransferase (33% vs 9%; P<0.001) and aspartate aminotransferase (28% vs 10%; P<0.001) elevations, and pyrexia (19% vs 12%; P=0.046). AEs significantly less common with bosutinib included edema (periorbital, 2% vs 14%; P<0.001; peripheral, 5% vs 12%; P=0.006), musculoskeletal (myalgia, 5% vs 12%; P=0.010; muscle cramps, 5% vs 22%; P<0.001; bone pain, 4% vs 11%; P=0.003), increased creatine phosphokinase (8% vs 20%; P<0.001), neutropenia (13% vs 30%; P<0.001), and leukopenia (9% vs 22%; P<0.001). Between-group differences in the incidence of cardiac and vascular AEs were not significant. Diarrhea was typically transient, mostly grade 1/2, occurring early during treatment, and was manageable with antidiarrheal medication. Despite higher rates of aminotransferase elevation with bosutinib, events were managed in most patients with dose modification and/or concomitant medication. Bosutinib had a manageable safety profile distinct from that of imatinib in patients with newly diagnosed CP CML.

Gambacorti Passerini, C., Cortes, J., Lipton, J., Dmoszynska, A., Wong, R., Rossiev, V., et al. (2014). Safety of bosutinib versus imatinib in the phase 3 BELA trial in newly diagnosed chronic phase chronic myeloid leukemia. AMERICAN JOURNAL OF HEMATOLOGY, 89(10), 947-953 [10.1002/ajh.23788].

Safety of bosutinib versus imatinib in the phase 3 BELA trial in newly diagnosed chronic phase chronic myeloid leukemia

GAMBACORTI PASSERINI, CARLO
;
2014

Abstract

Bosutinib, an orally active, Src/Abl tyrosine kinase inhibitor, has demonstrated clinical activity and acceptable tolerability in chronic phase chronic myeloid leukemia (CP CML). This updated analysis of the BELA trial assessed the safety profile and management of toxicities of bosutinib versus imatinib in adults with newly diagnosed (≤6 months) CP CML after >30 months from accrual completion. Among patients randomized to bosutinib 500 mg/d (n=250) or imatinib 400 mg/d (n=252), 248 and 251, respectively, received ≥1 dose of study treatment. Adverse events (AEs; any grade) with bosutinib versus imatinib were significantly more common for certain gastrointestinal events (diarrhea, 70% vs 26%; P<0.001; vomiting, 33% vs 16%; P<0.001), alanine aminotransferase (33% vs 9%; P<0.001) and aspartate aminotransferase (28% vs 10%; P<0.001) elevations, and pyrexia (19% vs 12%; P=0.046). AEs significantly less common with bosutinib included edema (periorbital, 2% vs 14%; P<0.001; peripheral, 5% vs 12%; P=0.006), musculoskeletal (myalgia, 5% vs 12%; P=0.010; muscle cramps, 5% vs 22%; P<0.001; bone pain, 4% vs 11%; P=0.003), increased creatine phosphokinase (8% vs 20%; P<0.001), neutropenia (13% vs 30%; P<0.001), and leukopenia (9% vs 22%; P<0.001). Between-group differences in the incidence of cardiac and vascular AEs were not significant. Diarrhea was typically transient, mostly grade 1/2, occurring early during treatment, and was manageable with antidiarrheal medication. Despite higher rates of aminotransferase elevation with bosutinib, events were managed in most patients with dose modification and/or concomitant medication. Bosutinib had a manageable safety profile distinct from that of imatinib in patients with newly diagnosed CP CML.
Articolo in rivista - Articolo scientifico
Scientifica
tyrosine kinase inhibitor; safety; bosutinib; chronic phase chronic myeloid leukemia; frontline therapy; BELA trial
English
Gambacorti Passerini, C., Cortes, J., Lipton, J., Dmoszynska, A., Wong, R., Rossiev, V., et al. (2014). Safety of bosutinib versus imatinib in the phase 3 BELA trial in newly diagnosed chronic phase chronic myeloid leukemia. AMERICAN JOURNAL OF HEMATOLOGY, 89(10), 947-953 [10.1002/ajh.23788].
GAMBACORTI PASSERINI, C; Cortes, J; Lipton, J; Dmoszynska, A; Wong, R; Rossiev, V; Pavlov, D; Gogat Marchant, K; Duvillié, L; Khattry, N; Kantarjian, H; Brümmendorf, T
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10281/52075
Citazioni
  • Scopus 75
  • ???jsp.display-item.citation.isi??? 65
Social impact