Continuous therapy response references for BCR::ABL1 monitoring in pediatric chronic myeloid leukemia

被引:1
|
作者
Volz, Christian [1 ,2 ]
Zerjatke, Thomas [3 ]
Gottschalk, Andrea [3 ]
Semper, Sabine [1 ]
Suttorp, Meinolf [4 ]
Glauche, Ingmar [3 ]
Krumbholz, Manuela [1 ,5 ,6 ]
Metzler, Markus [1 ,5 ,6 ]
机构
[1] Univ Hosp Erlangen, Dept Pediat & Adolescent Med, Erlangen, Germany
[2] Friedrich Alexander Univ Erlangen Nurnberg, Erlangen, Germany
[3] Tech Univ Dresden, Inst Med Informat & Biometry, Fac Med Carl Gustav Carus, Dresden, Germany
[4] Tech Univ Dresden, Fac Med Carl Gustav Carus, Pediat Hematooncol, Dresden, Germany
[5] Comprehens Canc Ctr Erlangen EMN CCC ER EMN, Erlangen, Germany
[6] Bavarian Canc Res Ctr BZKF, Erlangen, Germany
关键词
CHRONIC MYELOGENOUS LEUKEMIA; TYROSINE KINASE INHIBITORS; IMATINIB CESSATION; MOLECULAR RESPONSE; CML PATIENTS; CHILDREN; PHASE; DISEASE; REMISSION; MESYLATE;
D O I
10.1038/s41598-023-45364-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Response to tyrosine kinase inhibitor (TKI) therapy in patients with chronic myeloid leukemia (CML) is monitored by quantification of BCR::ABL1 transcript levels. Milestones for assessing optimal treatment response have been defined in adult CML patients and are applied to children and adolescents although it is questionable whether transferability to pediatric patients is appropriate regarding genetic and clinical differences. Therefore, we analyzed the molecular response kinetics to TKI therapy in 129 pediatric CML patients and investigated whether response assessment based on continuous references can support an early individual therapy adjustment. We applied a moving quantiles approach to establish a high-resolution response target curve and contrasted the median responses in all patients with the median of the ideal target curve obtained from a subgroup of optimal responders. The high-resolution response target curve of the optimal responder group presents a valuable tool for continuous therapy monitoring of individual pediatric CML patients in addition to the fixed milestones. By further comparing BCR::ABL1 transcript levels with BCR::ABL1 fusion gene copy numbers, it is also possible to model the differential dynamics of BCR::ABL1 expression and cell number under therapy. The developed methodology can be transferred to other biomarkers for continuous therapy monitoring.
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页数:10
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