CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Clonal hematopoiesis of indeterminate potential and clonal cytopenias of undetermined significance: 2023 update on clinical associations and management recommendations.
Clonal hematopoiesis of indeterminate potential and clonal cytopenias of undetermined significance: 2023 update on clinical associations and management recommendations.
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病情概述:克隆性造血(CH)是指随年龄增长,造血干/祖细胞(HSPC)中体细胞变异克隆扩增。诊断:操作性定义的意义未明克隆性造血(CHIP),是指HSPC中存在致病性变异且变异等位基因频率≥2%。临床关联:CH与多种血液系统疾病发生率升高相关,包括血细胞减少(亦称意义未明克隆性血细胞减少)、血液系统肿瘤(主要是髓系,也包括淋巴系肿瘤)以及血细胞增多(包括单核细胞增多)。CH还与非血液系统疾病相关,如动脉粥样硬化性心脑血管疾病、缺血性充血性心力衰竭、静脉血栓栓塞、2型糖尿病、慢性阻塞性肺病、骨质疏松症和痛风;其对阿尔茨海默病(AD)可能具有保护作用。管理建议:目前CH检测的前瞻性数据有限,但由于体细胞和胚系新一代测序(NGS)检测已广泛应用,CH检出日益普遍。
此外,有数据显示,许多治疗相关髓系肿瘤(tMN)病例在发病前已检测到CH克隆,促使多家机构建立CH门诊。本机构目前在研究层面建议以下人群接受CH检测:持续≥4个月的无法解释性血细胞减少患者;接受辅助细胞毒化疗和/或放疗或放射性核素治疗前的恶性肿瘤患者;自体造血干细胞移植和CAR-T 细胞治疗前筛查者;以及需判断潜在胚系嵌合变异是否实际代表CH者。
CONDITION OVERVIEW: Clonal hematopoiesis (CH) refers to age-associated expansion of somatic variants in hematopoietic stem and progenitor cells (HSPC). DIAGNOSIS: CH of indeterminate potential (CHIP) is operationally defined as pathogenic variants in HSPCs at a variant allele frequency 2%. CLINICAL ASSOCIATIONS: CH is associated with increased occurrence of several hematological conditions such as cytopenias (also called clonal cytopenia of undetermined significance), hematological (predominantly myeloid but also lymphoid) neoplasms, cytosis (including monocytosis), and non-hematological conditions such as atherosclerotic cardiovascular and cerebrovascular disease, ischemic congestive heart failure, venous thromboembolism, type 2 diabetes mellitus, chronic obstructive pulmonary disease, osteoporosis, gout, with a potential protective effect in Alzheimer's disease (AD).
MANAGEMENT RECOMMENDATIONS: As of now, there is limited prospective data for CH testing; however, CH detection is becoming increasingly prevalent due to ubiquitous use of somatic and germline NGS testing. This in addition to data suggesting that therapy related myeloid neoplasm (tMN) in many cases is preceded by the detection of CH clones, has led to the establishment of CH clinics at several institutions.
At our institution, on a research basis, we currently recommend testing for CH for individuals with persistent ( 4 months) unexplained cytopenias, in patients with malignancies prior to adjuvant cytotoxic chemotherapy and/or radiation or radionuclide therapy, screening prior to autologous hematopoietic stem cell transplantation and chimeric antigen receptor T cell (CAR-T) therapy and to assess as to whether or not, potential germline mosaic variants actually represent CH.
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