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Prognostic significance of early molecular response in chronic myeloid leukemia patients treated with tyrosine kinase inhibitors
被引:3
|作者:
Yeung, David T.
[1
,2
]
Mauro, Michael J.
[3
]
机构:
[1] SA Pathol, Dept Haematol & Mol Pathol, Adelaide, SA, Australia
[2] Univ Adelaide, Sch Med, Discipline Med, Adelaide, SA, Australia
[3] Mem Sloan Kettering Canc Ctr, Myeloproliferat Neoplasms Program, New York, NY 10065 USA
基金:
英国医学研究理事会;
关键词:
BCR-ABL1 TRANSCRIPT LEVELS;
FOLLOW-UP;
IMATINIB;
CML;
PREDICT;
DISCONTINUATION;
RECOMMENDATIONS;
DASATINIB;
NILOTINIB;
SURVIVAL;
D O I:
10.1182/asheducation-2014.1.240
中图分类号:
G40 [教育学];
学科分类号:
040101 ;
120403 ;
摘要:
A 55-year-old man presented with splenomegaly (10 cm below left costal margin) and leucocytosis (145 x 10(9)/L). Differential showed neutrophilia with increased basophils (2%), eosinophils (1.5%), and left shift including myeloblasts (3%). A diagnosis of chronic myeloid leukemia in chronic phase was established after marrow cytogenetics demonstrated the Philadelphia chromosome. Molecular studies showed a BCR-ABL1 qPCR result of 65% on the International Scale. Imatinib therapy at 400 mg daily was initiated due to patient preference, with achievement of complete hematological response after 4 weeks of therapy. BCR-ABL1 at 1 and 3 months after starting therapy was 37% and 13%, respectively (all reported on International Scale). Is this considered an adequate molecular response?
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页码:240 / 243
页数:4
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