Molecular responses at 3 and 6 months after switching to a second-generation tyrosine kinase inhibitor are complementary and predictive of long-term outcomes in patients with chronic myeloid leukemia who fail imatinib

被引:8
作者
Boquimpani, Carla [1 ,2 ]
Schaffel, Rony [2 ]
Biasoli, Irene [2 ]
Bendit, Israel [3 ]
Spector, Nelson [2 ]
机构
[1] HEMORIO, Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Sch Med, Div Hematol, BR-21941 Rio De Janeiro, Brazil
[3] Univ Sao Paulo, Sch Med, Div Hematol & Hemotherapy, BR-05508 Sao Paulo, Brazil
关键词
Chronic myeloid leukemia; early molecular response; predictive factor; tyrosine kinase inhibitor; BCR-ABL1 TRANSCRIPT LEVELS; CHRONIC-PHASE; EUROPEAN LEUKEMIANET; CYTOGENETIC RESPONSE; INTOLERANT PATIENTS; CLINICAL-TRIALS; COMPETING RISK; FOLLOW-UP; NILOTINIB; SURVIVAL;
D O I
10.3109/10428194.2014.974047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Early molecular response (MR) defined by BCR-ABL(IS) levels has prognostic impact in chronic myeloid leukemia (CML). MR was evaluated at 3 and 6 months after switching to nilotinib or dasatinib in 115 patients with resistance to imatinib. Three groups were delineated at 3 months (<1%, 1-10% or >10% BCR-ABL(IS) levels) with different outcomes at 3 years regarding major molecular response (MMR, 91%, 47%, 22%, p<0.001), failure-free survival (FFS), progression-free survival (PFS, 96%, 89% and 78%, p = 0.05) and overall survival (OS). After 6 months, patients with MR < 1% had higher 3-year MMR (83% vs. 16%, p < 0.001), FFS, PFS (94% vs. 84%, p = 0.05) and OS. Four patients had 3-month and 6-month MR > 10% and <1%, respectively (3-year FFS 50%). Thirteen had 3-month and 6-month MR < 10% and >= 1%, respectively (3-year FFS 38%). These findings confirm the strong predictive value of 3-month and 6-month BCR-ABL(IS) levels in imatinib-resistant patients.
引用
收藏
页码:1787 / 1792
页数:6
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