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SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析
OBJECTIVE: To assess the clinical characteristics and prognosis of patients with SIL-TAL1-positive T-cell acute lymphoblastic leukemia(T-ALL). METHODS: The clinical data of 19 SIL-TAL1-positive T-ALL patients admitted to the First Affiliated Hospital of Soochow University between January 2014 and Fe...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033260/ https://www.ncbi.nlm.nih.gov/pubmed/36948867 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.02.008 |
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collection | PubMed |
description | OBJECTIVE: To assess the clinical characteristics and prognosis of patients with SIL-TAL1-positive T-cell acute lymphoblastic leukemia(T-ALL). METHODS: The clinical data of 19 SIL-TAL1-positive T-ALL patients admitted to the First Affiliated Hospital of Soochow University between January 2014 and February 2022 were retrospectively computed and contrasted with SIL-TAL1-negative T-ALL patients. RESULTS: The median age of the 19 SIL-TAL1-positive T-ALL patients was 15(7 to 41 years), including 16 males(84.2%). SIL-TAL1-positive T-ALL patients had younger age, higher WBC, and hemoglobin compared with SIL-TAL1-negative T-ALL patients. There was no discrepancy in gender distribution, PLT, chromosome abnormality distribution, immunophenotyping, and complete remission(CR)rate. The 3-year overall survival(OS)was 60.9% and 74.4%, respectively(HR=2.070, P=0.071). The 3-year relapse-free survival(RFS)was 49.2% and 70.6%, respectively(HR=2.275, P=0.040). The 3-year RFS rate of SIL-TAL1-positive T-ALL patients was considerably lower than SIL-TAL1-negative T-ALL patients. CONCLUSION: SIL-TAL1-positive T-ALL patients were connected to younger age, higher WBC, higher HGB, and poor outcome. |
format | Online Article Text |
id | pubmed-10033260 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-100332602023-03-24 SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To assess the clinical characteristics and prognosis of patients with SIL-TAL1-positive T-cell acute lymphoblastic leukemia(T-ALL). METHODS: The clinical data of 19 SIL-TAL1-positive T-ALL patients admitted to the First Affiliated Hospital of Soochow University between January 2014 and February 2022 were retrospectively computed and contrasted with SIL-TAL1-negative T-ALL patients. RESULTS: The median age of the 19 SIL-TAL1-positive T-ALL patients was 15(7 to 41 years), including 16 males(84.2%). SIL-TAL1-positive T-ALL patients had younger age, higher WBC, and hemoglobin compared with SIL-TAL1-negative T-ALL patients. There was no discrepancy in gender distribution, PLT, chromosome abnormality distribution, immunophenotyping, and complete remission(CR)rate. The 3-year overall survival(OS)was 60.9% and 74.4%, respectively(HR=2.070, P=0.071). The 3-year relapse-free survival(RFS)was 49.2% and 70.6%, respectively(HR=2.275, P=0.040). The 3-year RFS rate of SIL-TAL1-positive T-ALL patients was considerably lower than SIL-TAL1-negative T-ALL patients. CONCLUSION: SIL-TAL1-positive T-ALL patients were connected to younger age, higher WBC, higher HGB, and poor outcome. Editorial office of Chinese Journal of Hematology 2023-02 /pmc/articles/PMC10033260/ /pubmed/36948867 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.02.008 Text en 2023年版权归中华医学会所有 https://creativecommons.org/licenses/by/3.0/This work is licensed under a Creative Commons Attribution 3.0 License. |
spellingShingle | 论著 SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title | SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title_full | SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title_fullStr | SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title_full_unstemmed | SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title_short | SIL-TAL1融合基因阳性急性T淋巴细胞白血病19例临床分析 |
title_sort | sil-tal1融合基因阳性急性t淋巴细胞白血病19例临床分析 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033260/ https://www.ncbi.nlm.nih.gov/pubmed/36948867 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2023.02.008 |
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