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.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Does presence of complex translocations involving BCR::ABL1 in chronic myeloid leukemia affect the response rate to tyrosine kinase inhibitors? A systematic review of the literature
    Sharma, Diwakar
    Wilson, Christine
    Kumar, Sachin
    Ghose, Sampa
    Sahoo, Ranjit
    Sharawat, Surender K.
    ANNALS OF DIAGNOSTIC PATHOLOGY, 2024, 71
  • [42] ABL1 tyrosine kinase domain mutations in chronic myeloid leukemia treatment resistance
    Irina Cezara Vacarean-Trandafir
    Iuliu Cristian Ivanov
    Loredana Mihaiela Dragos
    Angela Smaranda Dascalescu
    Amalia Andrea Titieanu
    Dumitru Cojocaru
    Molecular Biology Reports, 2019, 46 : 3747 - 3754
  • [43] Molecular biology of bcr-abl1-positive chronic myeloid leukemia
    Quintas-Cardama, Alfonso
    Cortes, Jorge
    BLOOD, 2009, 113 (08) : 1619 - 1630
  • [44] A T315I mutation in e19a2 BCR/ABL1 chronic myeloid leukemia responding to dasatinib
    Cea, Michele
    Cirmena, Gabriella
    Garuti, Anna
    Rocco, Ilaria
    Palermo, Claudia
    Cagnetta, Antonia
    Moran, Eva
    Colombo, Nicoletta
    Grasso, Raffaella
    Fugazza, Giuseppina
    Gobbi, Marco
    Nencioni, Alessio
    Ballestrero, Alberto
    Patrone, Franco
    LEUKEMIA RESEARCH, 2010, 34 (09) : E240 - E242
  • [45] BCR/ABL1ΔE7-8-9 isoform contributes to tyrosine kinase inhibitor resistance in chronic myeloid leukemia
    Tan, Yanhong
    Zhang, Lingli
    Zhu, Guiyang
    Yang, Yuchao
    Guo, Wenzheng
    Chen, Lanhui
    Chang, Jianmei
    Xu, Yang
    Muyey, Daniel Muteb
    Wang, Hongwei
    HEMATOLOGICAL ONCOLOGY, 2022, 40 (05) : 1067 - 1075
  • [46] Ultra-deep sequencing mutation analysis of the BCR/ABL1 kinase domain in newly diagnosed chronic myeloid leukemia patients
    Park, Hyunkyung
    Kim, Inho
    Kim, Hyeong-Joon
    Shin, Dong-Yeop
    Lee, Sung-Yeoun
    Kwon, Oh-Hyung
    Kim, Dae-Young
    Lee, Kyoo-Hyung
    Ahn, Jae-Sook
    Park, Jinny
    Sohn, Sang-Kyun
    Lee, Jeong-Ok
    Cheong, June-Won
    Kim, Kyoung Ha
    Kim, Hoon-Gu
    Kim, Hawk
    Lee, Yoo Jin
    Nam, Seung-Hyun
    Do, Young Rok
    Park, Sang-Gon
    Park, Seong Kyu
    Bae, Sung Hwa
    Song, Hun Ho
    Oh, Doyeun
    Jung, Chul Won
    Park, Seonyang
    LEUKEMIA RESEARCH, 2021, 111
  • [47] Cytogenetic, fluorescence in situ hybridization, and molecular characterization of chronic myeloid leukemia in chronic phase with four BCR/ABL1 fusion signals: a case report
    Teresa Vargas, Maria
    Angeles Portero, Maria
    Rodriguez, Alicia
    Reyes, Juana
    Fernandez-Novoa, Carmen
    CANCER GENETICS AND CYTOGENETICS, 2009, 195 (01) : 71 - 74
  • [48] Monitoring patients with chronic myeloid leukemia receiving Abl tyrosine kinase inhibitor therapy
    Oehler, Vivian
    Radich, Jerald P.
    CLINICAL LYMPHOMA & MYELOMA, 2007, 7 : S58 - S63
  • [49] A review on characterization of BCR - ABL transcript variants for molecular monitoring of chronic myeloid leukemia phenotypes
    Zenebe, Benyam
    Nigussie, Helen
    Belay, Gurja
    Seboka, Nigussie
    HEMATOLOGY, 2023, 28 (01)
  • [50] BCR-ABL1-induced downregulation of WASP in chronic myeloid leukemia involves epigenetic modification and contributes to malignancy
    Pereira, Welbert O.
    De Carvalho, Daniel D.
    Zenteno, Maria Emilia
    Ribeiro, Beatriz F.
    Jacysyn, Jacqueline F.
    Sardinha, Luiz R.
    Zanichelli, Maria A.
    Hamerschlak, Nelson
    Jones, Gareth E.
    Pagnano, Katia B.
    Castro, Fabiola A.
    Calle, Yolanda
    Amarante-Mendes, Gustavo P.
    CELL DEATH & DISEASE, 2017, 8 : e3114 - e3114