Source:http://linkedlifedata.com/resource/pubmed/id/11699220
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rdf:type | |
lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0023449,
umls-concept:C0035647,
umls-concept:C0185117,
umls-concept:C0332466,
umls-concept:C0531832,
umls-concept:C0600558,
umls-concept:C0871261,
umls-concept:C1442989,
umls-concept:C1519595,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911684,
umls-concept:C2911692
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pubmed:issue |
1-2
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pubmed:dateCreated |
2001-11-8
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pubmed:abstractText |
We prospectively examined the frequency of the t(12;21)TEL-AML1 fusion in 504 children with newly diagnosed standard risk ALL using RT-PCR assays. Cells from 95 patients (18.8%) were TEL-AML1+. There was a significantly higher frequency of pseudodiploidy among the TEL-AML1+ cases (39.4% versus 14.1%, P = 0.001), primarily because structural abnormalities involving 12p and del(6q) occurred more frequently in the TEL-AML1+ group. TEL-AML1+ ALL was more sensitive to the induction chemotherapy than TEL-AML1- ALL. The percentage of "rapid early responders", i.e., patients who achieved an M1 (< 5% blasts) or M2 (5-25% blasts) marrow status on day 7 of induction chemotherapy, was significantly higher among TEL-AML1+ cases. The quality of remission of RT-PCR positive cases was excellent, as evidenced by the very low to absent MRD burden of their end-of-induction bone marrow specimens. TEL-AML1+ patients also had an excellent early EFS outcome. The probability of EFS at 30 months from study entry were 98.9 +/- 1.0% for the TEL-AML1+ group and 92.1 +/- 1.5% for the TEL-AML1- group (P = 0.0001). This prospective study significantly expands the knowledge gained from previous studies regarding the prognostic significance of t(12;21)TEL-AML1 fusion in pediatric ALL.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Core Binding Factor Alpha 2 Subunit,
http://linkedlifedata.com/resource/pubmed/chemical/Oncogene Proteins, Fusion,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/TEL-AML1 fusion protein
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1042-8194
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
41-56
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:11699220-Bone Marrow,
pubmed-meshheading:11699220-Child,
pubmed-meshheading:11699220-Core Binding Factor Alpha 2 Subunit,
pubmed-meshheading:11699220-Cytogenetic Analysis,
pubmed-meshheading:11699220-Disease-Free Survival,
pubmed-meshheading:11699220-Humans,
pubmed-meshheading:11699220-Neoplasm, Residual,
pubmed-meshheading:11699220-Oncogene Proteins, Fusion,
pubmed-meshheading:11699220-Precursor Cell Lymphoblastic Leukemia-Lymphoma,
pubmed-meshheading:11699220-Prospective Studies,
pubmed-meshheading:11699220-RNA, Messenger,
pubmed-meshheading:11699220-Remission Induction,
pubmed-meshheading:11699220-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:11699220-Risk Factors
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pubmed:year |
2001
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pubmed:articleTitle |
Expression of TEL-AML1 fusion transcripts and response to induction therapy in standard risk acute lymphoblastic leukemia.
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pubmed:affiliation |
Children's Cancer Group ALL Biology Reference Laboratory, Parker Hughes Institute, 2665 Long Lake Road, Suite 300, St. Paul, MN 55113, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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