Monitoring disease burden in chronic myeloid leukemia: Past, present, and future

被引:7
|
作者
Egan, Daniel [1 ]
Radich, Jerald [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
关键词
CHRONIC MYELOGENOUS LEUKEMIA; PATIENTS RECEIVING IMATINIB; TYROSINE KINASE INHIBITORS; MINIMAL RESIDUAL DISEASE; BCR-ABL; FOLLOW-UP; CML PATIENTS; CELL TRANSPLANTATION; DOMAIN MUTATIONS; INTERFERON-ALPHA;
D O I
10.1002/ajh.24381
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Tyrosine kinase inhibitor (TKI) therapy yields sustained cytogenetic remissions in most patients with chronic-phase chronic myeloid leukemia (CML). Peripheral blood quantitative reverse transcription polymerase chain reaction (qRT-PCR) monitoring of the chimeric BCR-ABL1 mRNA transcript levels is a very sensitive method to measure disease burden in patients with cytogenetic remission. qRT-PCR allows identification of patients (1) at high risk of progression early (3-6 months) after treatment initiation, (2) with no response to TKI therapy, (3) with undetectable disease who could be eligible for TKI discontinuation trials. Molecular monitoring is a minimally invasive method to optimize treatment and outcomes in CML. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:742 / 746
页数:5
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