Description and prognostic significance of the kinetics of minimal residual disease status in adults with acute lymphoblastic leukemia treated with HyperCVAD

被引:19
作者
Cassaday, Ryan D. [1 ,2 ]
Stevenson, Philip A. [3 ]
Wood, Brent L. [4 ]
Becker, Pamela S. [1 ,2 ]
Hendrie, Paul C. [1 ]
Sandmaier, Brenda M. [1 ,2 ]
Radich, Jerald L. [1 ,2 ]
Shustov, Andrei R. [1 ,2 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA
[2] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA
[3] Fred Hutchinson Canc Res Ctr, Clin Stat Div, 1124 Columbia St, Seattle, WA 98104 USA
[4] Univ Washington, Sch Med, Dept Lab Med, Seattle, WA 98195 USA
关键词
ACUTE LYMPHOCYTIC-LEUKEMIA; POOR-PROGNOSIS; FLOW-CYTOMETRY; STANDARD-RISK; CVAD; THERAPY; MRD; TRANSPLANTATION; QUANTIFICATION; PHASE-2;
D O I
10.1002/ajh.25030
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
HyperCVAD is a commonly-used regimen for adults with newly-diagnosed acute lymphoblastic leukemia (ALL). However, relatively little is known about the application of minimal residual disease (MRD) detection with this treatment. To address this, we studied 142 adults with ALL treated with hyperCVAD over a 10-year period who had MRD assessed by either multi-parameter flow cytometry or (for patients with Philadelphia chromosome positive ALL) reverse transcriptase polymerase chain reaction for the BCR-ABL1 translocation. In a multivariate analysis, patients who achieved MRD negativity (MRDNeg) at any point had significantly better overall survival (OS; hazard ratio [HR] 0.43; P = .01) and event-free survival (EFS; HR 0.27; P < .01). Of 121 patients with MRD assessed at various points within 90 days of starting hyperCVAD, 50% (n = 61) had achieved MRDNeg. Among those that became MRDNeg, the median time to MRDNeg was 68 days. Time to MRDNeg was significantly associated with EFS (P = .009), but not OS (P = .19), implying increasingly better EFS the earlier MRDNeg is achieved. These data add to our understanding of MRD assessment during treatment with hyperCVAD, aide clinicians with predicting relapse risk, and provide additional historical data on which future clinical trials can be designed.
引用
收藏
页码:546 / 552
页数:7
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