TP53突变髓细胞肿瘤中胚泡计数的预后作用--明尼苏达州的经验。

IF 2.2 4区 医学 Q3 HEMATOLOGY Leukemia & Lymphoma Pub Date : 2024-09-10 DOI:10.1080/10428194.2024.2400213
Mehrnoosh Tashakori,Sophia Yohe,Michael A Linden,Robert W McKenna
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引用次数: 0

摘要

2022 年,世界卫生组织(WHO)和国际共识分类(ICC)将 TP53 视为髓样肿瘤中的实体定义改变,但标准不一,可能导致诊断不一致并影响临床试验资格。我们对 67 例 TP53 突变髓样肿瘤患者进行了研究,使用这两种标准对他们进行了重新分类。虽然大多数病例符合TP53突变定义实体的标准,但大多数差异出现在囊胚细胞≥20%的病例中。根据囊泡计数将患者分为三组(<10%、10-19% 和 ≥20%),结果显示临床病理特征、遗传特征和预后具有可比性。值得注意的是,与囊泡数<10%的患者相比,囊泡数≥10%的患者总生存期较短(8.1个月对12.4个月;P = 0.03)。这项研究是为数不多的将TP53突变髓细胞瘤作为单一实体进行研究的研究之一,它表明10%的囊泡计数阈值可以作为对这些患者进行更统一分类的入口。
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The prognostic effect of blast count in TP53 mutant myeloid neoplasms -the Minnesota experience.
In 2022, the World Health Organization (WHO) and International Consensus Classification (ICC) recognized TP53 as an entity-defining alteration in myeloid neoplasms, yet with differing criteria that could lead to discrepant diagnoses and affect clinical trial eligibility. We studied 67 patients with TP53 mutant myeloid neoplasms, reclassifying them using both criteria. While most cases fulfill the criteria for TP53 mutant defined entities, most discrepancies were found in cases with ≥20% blasts. Patients were stratified into three groups based on blast count (<10%, 10-19%, and ≥20%) which revealed comparable clinicopathologic features, genetic characteristics, and outcomes. Notably, patients with ≥10% blasts had shorter overall survival compared to those with <10% blasts (8.1 vs. 12.4 months; p = 0.03). This study is among the few to examine TP53 mutant myeloid neoplasms as a single entity and suggests that the 10% blast count threshold could serve as a gateway to a more harmonized classification for these patients.
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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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