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Hematological oncology · 2025

Real-World Efficacy Profile of Compassionate Use of Asciminib in an Italian, Multi-Resistant Chronic-Phase Chronic Myeloid Leukemia (CML-CP) Patient Population.

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Breccia Massimo, Rossi Antonella Russo, Giai Valentina, Martino Bruno, Fava Carmen, Annunziata Mario, Abruzzese Elisabetta, Binotto Gianni, Baratè Claudia, Nardozza Aurelio Pio, Misto Alessandra, Coco Paola, Calafiore Valeria, Carraro Maria Cristina, Cattina Federica, Cavazzini Francesco, Corsetti Maria Teresa, Crucitti Lara, Crugnola Monica, Di Veroli Ambra, Ditonno Paolo, Ermacora Anna, Ferrara Felicetto, Genua Angelo, Gozzini Antonella, Impera Stefana, Iurlo Alessandra, Levato Luciano, Luciano Luigia, Miggiano Maria Cristina, De Gobbi Marco, Santoro Marco, Scappini Barbara, Scortechini Anna Rita, Patriarca Andrea, Rosati Serena, Russo Sabina, Sancetta Rosaria, Sanpaolo Grazia, Santeramo Teresa Maria, Sibilla Silvia, Sorà Federica, Sportoletti Paolo, Stagno Fabio, Trabacchi Elena, Castagnetti Fausto

Аннотация

Chronic myeloid leukemia (CML) patients who have experienced failure and/or intolerance to multiple lines of treatment have limited therapeutic possibilities. Asciminib is a first-in-class tyrosine kinase inhibitor (TKI) that inhibits the ABL Myristoyl Pocket (STAMP or Specifically Targeting the ABL Myristoyl Pocket) within the BCR::ABL1 oncoprotein. This retrospective Italian analysis reports the efficacy and safety outcomes of asciminib in treating 77 CML patients in chronic phase (CML-CP) within a compassionate use setting. Patients were heavily pretreated with a median of 3 TKIs (55.8% had prior ponatinib exposure). Overall, 57.1% and 42.9% patients switched to asciminib because of resistance and intolerance, respectively. Asciminib maintained or improved molecular responses (MRs) in most patients: as best response, 41 patients (53%) achieved a MR3 or better, with 25 patients (32.5%) reaching deep molecular response (DMR). Greater percentages of intolerant patients achieved MR compared with resistant patients, although the probability of reaching at least a MR3 was not significant between the two groups (p = 0.116). Patients with the T315I mutation responded to asciminib, while ponatinib pre-treated patients showed lower MR improvements compared to naïve patients and had a lower probability to reach a MR3 versus naïve patients (p = 0.0262). These results highlight asciminib remarkable tolerability and efficacy in real-world CML-CP patient population, including heavily pretreated patients, those intolerant and resistant to previous TKIs, and presenting several comorbidities. TRAIL REGISTRATION: The identification code for the MAP is CABL001AIT01M.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты