决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Antibody-Based and Cell Therapies for Advanced Mastocytosis: Established and Novel Concepts.
在过去 10 年中,改进的治疗方法使晚期 SM 患者的生活质量和生存期得到改善。
晚期系统性肥大细胞增多症(SM)是一组异质性髓系肿瘤,其特征为肥大细胞(MC)在一个或多个内脏器官中无控制地扩增、造成SM相关组织损伤且预后不良。晚期SM可分为侵袭性SM(ASM)、肥大细胞白血病(MCL)以及伴相关血液肿瘤的SM(SM-AHN)。绝大多数患者的肿瘤细胞存在KIT突变,主要为D816V,少数为其他KIT变异。尤其在伴AHN的患者中,还可能检出SRSF2、ASXL1或RUNX1等其他靶基因突变。过去10年间,治疗方法的改进提高了晚期SM患者的生活质量和生存率。然而,尽管已有针对KIT D816V的新型强效抑制剂,仍有患者未能缓解,另有患者复发;复发疾病常伴多基因突变,有时不再携带KIT D816V,并表现出多药耐药。对此类患者,联合化疗、抗体治疗及异基因造血干细胞移植可能是可行的替代方案。本文讨论耐药性晚期SM患者的治疗选择,包括新型KIT靶向药物、抗体类药物及清除干细胞的治疗。
Advanced systemic mastocytosis (SM) is a heterogeneous group of myeloid neoplasms characterized by an uncontrolled expansion of mast cells (MC) in one or more internal organs, SM-induced tissue damage, and poor prognosis. Advanced SM can be categorized into aggressive SM (ASM), MC leukemia (MCL), and SM with an associated hematologic neoplasm (SM-AHN). In a vast majority of all patients, neoplastic cells display a KIT mutation, mostly D816V and rarely other KIT variants. Additional mutations in other target genes, such as SRSF2 , ASXL1 , or RUNX1 , may also be identified, especially when an AHN is present. During the past 10 years, improved treatment approaches have led to a better quality of life and survival in patients with advanced SM. However, despite the availability of novel potent inhibitors of KIT D816V, not all patients enter remission and others relapse, often with a multi-mutated and sometimes KIT D816V-negative disease exhibiting multi-drug resistance. For these patients, (poly)chemotherapy, antibody-based therapies, and allogeneic hematopoietic stem cell transplantation may be viable treatment alternatives. In this article, we discuss treatment options for patients with drug-resistant advanced SM, including novel KIT-targeting drugs, antibody-based drugs, and stem cell-eradicating therapies.
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