A Multicenter Retrospective Chart Review Study of Treatment and Disease Patterns and Clinical Outcomes of Patients with Chronic-Phase Chronic Myeloid Leukemia in Third-Line Treatment or with T315I Mutation

被引:3
作者
Nicolini, Franck-Emmanuel [1 ,2 ]
Huguet, Francoise [2 ,3 ]
Huynh, Lynn [4 ]
Xu, Churong [5 ]
Bouvier, Christophe [1 ,2 ]
Yocolly, Aurore [6 ]
Etienne, Gabriel [2 ,7 ]
机构
[1] Ctr Leon Berard, F-69373 Lyon, France
[2] Fi LMC Grp, F-69437 Lyon, France
[3] Inst Univ Canc Toulose Oncopole, Hematol, F-31100 Toulouse, France
[4] Anal Grp Inc, Boston, MA 02199 USA
[5] Anal Grp Inc, Los Angeles, CA 90071 USA
[6] Novartis Serv Inc, E Hanover, NJ 07936 USA
[7] Inst Bergonie, F-33076 Bordeaux, France
关键词
chronic-phase chronic myeloid leukemia (CML-CP); tyrosine kinase inhibitor (TKI); treatment patterns; overall survival; T315I mutation; CHRONIC MYELOGENOUS LEUKEMIA; TYROSINE KINASE INHIBITORS; CML PATIENTS; IMATINIB; BOSUTINIB; RESISTANT; SURVIVAL; THERAPY; FAILURE; TKIS;
D O I
10.3390/cancers15164161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This retrospective chart review study investigated the clinical burden of adult patients with chronic-phase chronic myeloid leukemia (CP-CML) treated at three centers in France (2006-2021) who failed on two or more tyrosine kinase inhibitors (TKIs; third-line [3L]+ cohort) or harbored the BCR::ABL1 T315I mutation (T315I cohort). In the 3L+ cohort (N = 157; median age at diagnosis, 56 years), TKIs received in 3L (median duration: 17 months) were dasatinib (32%), nilotinib (19%), imatinib (18%), ponatinib (17%), and bosutinib (14%). Of the 145 patients with documented responses in 3L, 42% experienced major molecular response (MMR) at 12 months. Median event-free survival [95% confidence interval] was 53.6 [44.0, 67.5] months, and median progression-free survival and overall survival (OS) were not reached. Achieving MMR in 3L was associated with a decreased mortality risk. In the T315I cohort (N = 17; 52 years), 41% of patients received five or more lines of therapy. Following identification of the T315I mutation, ponatinib was the most common TKI used (59%); the median [interquartile range] OS was 5 [3-10] years. The most common adverse events were infections (3L+ cohort) and thrombocytopenia (T315I cohort) (both 18%). Well-tolerated therapies that achieve durable responses are needed in 3L or earlier to improve CP-CML prognosis.
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页数:14
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