Hammersmith score application identifies chronic myeloid leukemia patients with poor prognosis before treatment with second-generation tyrosine kinase inhibitors

被引:6
|
作者
Breccia, Massimo [1 ]
Stagno, Fabio [2 ]
Gozzini, Antonella [3 ]
Abruzzese, Elisabetta [4 ]
Latagliata, Roberto [1 ]
Rossi, Antonella Russo [5 ]
Sora, Federica [6 ]
Porrini, Raffaele [7 ]
Vigneri, Paolo [2 ]
Trawinska, Malgorzata [4 ]
Montefusco, Enrico [7 ]
Sica, Simona [6 ]
Specchia, Giorgina [5 ]
Santini, Valeria [3 ]
Alimena, Giuliana [1 ]
机构
[1] Univ Roma La Sapienza, Dept Cellular Biotechnol & Hematol, Rome, Italy
[2] Univ Catania, Dept Biomed Sci, I-95124 Catania, Italy
[3] Univ Florence, AOU Careggi, Funct Unit Haematol, Florence, Italy
[4] Univ Roma Tor Vergata, S Eugenio Hosp, Dept Hematol, Rome, Italy
[5] Univ Bari, Dept Hematol, Bari, Italy
[6] Univ Cattolica Sacro Cuore, Policlin A Gemelli, Div Hematol, Rome, Italy
[7] S Andres Hosp, Rome, Italy
关键词
IMATINIB; FAILURE; TRANSCRIPTS; RESISTANCE; THERAPY;
D O I
10.1002/ajh.22020
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study, we confirm the validity of the proposed Hammersmith score, which identifies three risk categories of patients and establish its strength on a large group of 128 chronic myeloid leukemia patients treated with second-generation tyrosine kinase inhibitors (TKIs) after being resistant to imatinib. Sixty-one patients were identified as good risk group, 27 patients as intermediate risk group, and 40 patients as poor risk group. The 1-year cumulative incidence of complete cytogenetic response was 73% in good risk patients, 40% in intermediate risk patients, and 22% in poor risk patients (P = 0.0001). Event-free survival at 3-year was 89% in good risk group, 70% in intermediate group, and 54% in poor risk group (P = 0.0001); the estimated 3-year progression-free survival was 95% in good risk category, 93% in intermediate risk category, and 87% in poor risk category (P = 0.05). Kaplan-Meier estimated that the 3-year overall survival was 100% in good risk category, 93% in intermediate risk category, and 82% in poor risk category (P = 0.04). In conclusion, some prognostic factors before starting second-generation TKIs might predict cytogenetic response and outcome. The so-called Hammersmith score was not yet validated in large series of patients: we demonstrated that this score is able to discriminate patients at high risk of failure and consequent progression before treatment with second-generation TKIs.
引用
收藏
页码:523 / 525
页数:4
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