← 返回

自体、异基因造血细胞移植和 CAR-T/NK 疗法:它们在 PTCL 中的真正重要性是什么?

英文原题:Autologous, allogeneic hematopoietic cell transplantation and CAR-T/NK therapy: what is their real importance in PTCL?

查看英文原题

Autologous, allogeneic hematopoietic cell transplantation and CAR-T/NK therapy: what is their real importance in PTCL?

PubMed 2023/08/30(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

外周T细胞淋巴瘤(PTCL)是一种罕见且侵袭性强的非霍奇金淋巴瘤,累及成熟T细胞。异常增殖的T细胞可聚集于淋巴结、脾脏、骨髓及其他器官,引起多种症状。PTCL通常较难诊断和治疗,预后也差于其他类型淋巴瘤。不过,靶向治疗等近期疗法进展为改善患者结局带来了希望。本文讨论自体和异基因造血细胞移植(HCT)作为PTCL治疗策略的应用,并综述近期先进细胞疗法。由于PTCL发病率低且组织学亚型异质性较高,随机试验有限,目前关于HCT治疗PTCL的证据主要来自登记数据、回顾性研究和专家意见。

展开英文摘要原文

Peripheral T cell lymphoma (PTCL) is a rare and aggressive type of non-Hodgkin's lymphoma that affects mature T cells. This type of cancer is characterized by the abnormal growth of T cells, which can accumulate in the lymph nodes, spleen, bone marrow, and other organs, leading to a variety of symptoms. PTCLs are often difficult to diagnose and treat, and they have a poorer prognosis than other types of lymphoma.

However, recent advancements in treatment options, such as targeted therapies have shown promise in improving outcomes for patients with PTCL.

Here, we discuss the use of autologous and allogeneic hematopoietic cell transplantation (HCT) as a treatment strategy for patients with PTCL, as well as the recent treatment approaches based on advanced cellular therapy. The current evidence for the use of HCT in PTCL is mainly derived from registry data, retrospective studies, and expert opinion, as randomized trials are limited due to the low incidence and histological heterogeneity of PTCL subtypes.

论文信息

作者
Couto SCF、Kowes A、Aurabi CS、Oliveira TGM、Klinger P、Rocha V
单位
Laboratory of Medical Investigation in Pathogenesis and Directed Therapy in Onco-Immuno-Hematology (LIM-31), Department of Hematology and Cell Therapy, Hospital das Clínicas HCFMUSP, Faculdade de Medicina, University of São Paulo, São Paulo, Brazil.Brazil
文献类型
综述
期刊
Frontiers in oncology2023
原文标识
PubMed 37711206 · DOI 10.3389/fonc.2023.1195759