Multiplex Reverse Transcription-Polymerase Chain Reaction as Diagnostic Molecular Screening of 4 Common Fusion Chimeric Genes in Taiwanese Children With Acute Lymphoblastic Leukemia

被引:8
|
作者
Yang, Yung-Li [1 ,2 ,4 ]
Lin, Shu-Rung [6 ]
Chen, Jiann-Shiuh [7 ]
Hsiao, Chih-Cheng [8 ]
Lin, Kai-Hsin [2 ]
Sheen, Jiunn-Ming [8 ]
Cheng, Chao-Neng [7 ]
Wu, Kang-Hsi [9 ]
Lin, Shu-Wha [3 ]
Yu, Sung-Liang [3 ]
Chen, Hsuan-Yu [5 ]
Lu, Meng-Yao [2 ]
Chang, Hsiu-Hao [2 ,3 ]
Yen, Ching-Tzu [3 ]
Lin, Jing-Fang [3 ]
Su, Ying-Hui [3 ]
Li, Ya-Ping
Lin, Chien-Yu [5 ]
Jou, Shiann-Tarng [2 ]
Lin, Dong-Tsamn [1 ,2 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Lab Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Pediat, Taipei, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Clin Lab Sci & Med Biotechnol, Taipei 100, Taiwan
[4] Natl Taiwan Univ, Coll Med, Grad Inst Clin Med, Taipei 100, Taiwan
[5] Acad Sinica, Inst Stat Sci, Taipei 11529, Taiwan
[6] Chung Yuan Christian Univ, Coll Sci, Dept Biosci Technol, Tao Yuan, Taiwan
[7] Natl Cheng Kung Univ Hosp, Dept Pediat, Tainan 70428, Taiwan
[8] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp, Kaohsiung Med Ctr,Dept Pediat, Kaohsiung, Taiwan
[9] China Med Univ Hosp, Dept Pediat, Taichung, Taiwan
关键词
childhood acute lymphoblastic leukemia (ALL); multiplex PCR; ETV6-RUNX1; RT-PCR ASSAY; TEL/AML1; FUSION; PROGNOSTIC-SIGNIFICANCE; TREATMENT RESPONSE; ONCOLOGY GROUP; TRIALS; REARRANGEMENT; PROTOCOL; THERAPY; GERMAN;
D O I
10.1097/MPH.0b013e3181ed1655
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The classification of B-lineage acute lymphoblastic leukemia (ALL) by specific chromosomal translocations has prognostic implications for risk-directed therapy. Reverse transcription-polymerase chain reaction (RT-PCR) assay is a useful tool for detecting fusion transcripts from common chromosomal translocations of ALL cells. Methods: Multiplex RT-PCR and nested-PCR assays were used to detect ALL-type BCR-ABL1 transcripts of the t(9; 22), TCF-PBX1 transcripts of t(1; 19), the MLL-AF4 transcripts of t(4; 11), and 2 variants of ETV6-RUNX1 of the cryptic t(12; 21) in 148 leukemic samples upon diagnosis. The patients received risk-directed protocols of the Taiwan Pediatric Oncology Group-ALL-2002 that consisted of multiple chemotherapeutic agents of different intensities. Event-free survival (EFS) and overall survival (OS) rates were analyzed for genetic abnormalities detected by multiplex PCR and conventional cytogenetic analysis by the Kaplan-Meier method, and compared with the Mantel-Haenszel test. The Cox proportional hazards model was implemented to identify independent prognostic factors for EFS and OS. Results: In this cohort of Taiwanese children, the relative frequencies of the 4 translocations of B-lineage ALL were 8% with ALL-type t(9; 22)/BCR-ABL1, 4% with (1; 19)/TCF-PBX1, 2% with t(4; 11)/MLL-AF4, and 17.6% with t(12; 21)/ETV6-RUNX1. Patients with t(12; 21)/ETV6-RUNX1 fusion, hyperdiploidy, and t(1; 19)/TCF-PBX1 fusion had the most favorable outcomes, whereas those with the t(9; 22)/BCR-ABL1 fusion or t(4; 11) and other MLL gene rearrangement had poor prognosis (P<0.001 for EFS and OS). BCR-ABL1, MLL gene rearrangement, and very high-risk group were independent prognostic factors after Cox regression analysis. Conclusions: The biological factors of leukemia cells are associated with treatment outcomes in childhood ALL. Multiplex RT-PCR assay is an efficient and sensitive diagnostic tool that may improve the ability to accurately and rapidly risk-stratify children with ALL.
引用
收藏
页码:E323 / E330
页数:8
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