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首页> 外文期刊>Blood: The Journal of the American Society of Hematology >NOTCH1, SF3B1, and TP53 mutations in fludarabine-refractory CLL patients treated with alemtuzumab: results from the CLL2H trial of the GCLLSG.
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NOTCH1, SF3B1, and TP53 mutations in fludarabine-refractory CLL patients treated with alemtuzumab: results from the CLL2H trial of the GCLLSG.

机译:阿仑单抗治疗的氟达拉滨难治性CLL患者的NOTCH1,SF3B1和TP53突变:来自GCLLSG的CLL2H试验结果。

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摘要

We studied the incidences, associations, and prognostic roles of NOTCH1 and SF3B1 mutations (NOTCH1(mut), SF3B1(mut)) as compared with TP53(mut) in fludarabine-refractory chronic lymphocytic leukemia (CLL) patients treated with alemtuzumab in the CLL2H trial. We found NOTCH1(mut), SF3B1(mut), and TP53(mut) in 13.4%, 17.5%, and 37.4% of patients, respectively. NOTCH1(mut) and SF3B1(mut) were mutually exclusive, whereas TP53(mut) were evenly distributed within both subgroups. Apart from correlation of SF3B1(mut) with 11q deletion (P = .029), there were no other significant associations of the mutations with any baseline characteristics or response rates. However, NOTCH1(mut) cases had a significantly longer progression-free survival (PFS) compared with wild-type cases (15.47 vs 6.74 months; P = .025), although there was no significant difference with overall survival (OS). SF3B1(mut) had no significant impact on PFS and OS. In multivariable analyses, NOTCH1(mut) was identified as an independent favorable marker for PFS. This clinical trial is registered at www.clinicaltrials.gov as #NCT00274976.
机译:我们研究了在CLL2H中用Alemtuzumab治疗的氟达拉滨难治性慢性淋巴细胞白血病(CLL)患者中NOTCH1和SF3B1突变(NOTCH1(mut),SF3B1(mut))与TP53(mut)相比的发生率,关联和预后作用试用。我们发现NOTCH1(mut),SF3B1(mut)和TP53(mut)分别占13.4%,17.5%和37.4%的患者。 NOTCH1(mut)和SF3B1(mut)是互斥的,而TP53(mut)则均匀地分布在两个子组中。除了SF3B1(mut)与11q缺失的相关性(P = .029)外,没有其他与基线特征或响应率相关的显着关联。然而,NOTCH1(mut)病例的无进展生存期(PFS)与野生型病例相比明显更长(15.47 vs 6.74个月; P = .025),尽管总生存期(OS)没有显着差异。 SF3B1(mut)对PFS和OS没有重大影响。在多变量分析中,NOTCH1(mut)被确定为PFS的独立有利标记。该临床试验已在www.clinicaltrials.gov上注册为#NCT00274976。

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