Ponatinib as second-line treatment in chronic phase chronic myeloid leukemia patients in real-life practice

被引:31
作者
Breccia, Massimo [1 ]
Abruzzese, Elisabetta [2 ]
Castagnetti, Fausto [3 ]
Bonifacio, Massimiliano [4 ]
Gangemi, Domenica [5 ]
Sora, Federica [6 ]
Iurlo, Alessandra [7 ]
Luciano, Luigiana [8 ]
Gozzini, Antonella [9 ]
Gentile, Massimo
Bocchia, Monica [10 ]
Luzi, Debora [11 ]
Maggi, Alessandro
Sgherza, Nicola [12 ]
Isidori, Alessandro
Crugnola, Monica [13 ]
Pregno, Patrizia [14 ]
Scortechini, Anna Rita
Capodanno, Isabella [15 ]
Pizzuti, Michele
Foa, Robin
机构
[1] Sapienza Univ, Policlin Umberto 1, Dept Cellular Biotechnol & Hematol, Hematol, Via Benevento 6, I-00161 Rome, Italy
[2] S Eugenio Hosp, Rome, Italy
[3] Univ Bologna, Univ Hosp, Inst Hematol L & A Seragnoli, Bologna, Italy
[4] Univ Verona, Sect Hematol, Dept Med, Verona, Italy
[5] Fabrizio Spaziani Hosp, Frosinone, Italy
[6] Cattolica Sacro Cuore Univ, Rome, Italy
[7] Univ Milan, IRCCS Ca Granda Maggiore Policlin Hosp Fdn, Hematol Div, Milan, Italy
[8] Federico II Univ Naples, Naples, Italy
[9] Univ Firenze, AOU Careggi, Florence, Italy
[10] Univ Siena, Hematol, Siena, Italy
[11] S Maria Hosp, Terni, Italy
[12] Casa Sollievo Sofferenza Hosp, Hematol, San Giovanni Rotondo, Italy
[13] Parma Univ, Hematol, Parma, Italy
[14] Azienda Osped Univ Citta Salute & Sci, Hematol, Turin, Italy
[15] Arcispedale Santa Maria Nuova IRCCS, Hematol, Reggio Emilia, Italy
关键词
Chronic myeloid leukemia; Ponatinib; Second line; Prognosis; TYROSINE KINASE INHIBITOR; MANAGEMENT; TRIAL;
D O I
10.1007/s00277-018-3337-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Scarce information is available on the use of ponatinib as second-line treatment in chronic phase chronic myeloid leukemia (CP-CML) patients resistant and/or intolerant to prior tyrosine kinase inhibitor (TKI) therapy. We collected data from 29 CML patients, with a median age of 54 years (range 32-72). Eleven patients had received dasatinib, 15 patients received nilotinib, and 3 patients received imatinib as first-line treatment. Forty-five percent of patients started ponatinib for secondary resistance, 38% for primary resistance, 7% for severe intolerance associated to a molecular warning, 7% due to the presence of a T315I mutation, and 3% for severe intolerance. Ponatinib was started at a dose of 45 mg in 60% of patients, 30 mg in 38%, and 15 mg in 2% of patients. Overall, at a median follow-up of 12 months, 85% of treated patients improved the level of response as compared to baseline, with 10 patients achieving a deep molecular response (MR4-4.5). No thrombotic events were recorded. The dose was reduced during treatment in 2 patients due to intolerance and in 8 patients in order to reduce the cardiovascular risk. Ponatinib seems a valid second-line treatment option for chronic phase CML, in particular for patients who failed a front-line second-generation TKI due to BCR-ABL-independent mechanisms of resistance.
引用
收藏
页码:1577 / 1580
页数:4
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