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:Allogeneic Hematopoietic Stem Cell Transplant for Diffuse Large B-Cell Lymphoma: Evolving Role in the Era of CAR T-Cell Therapy.
Allogeneic Hematopoietic Stem Cell Transplant for Diffuse Large B-Cell Lymphoma: Evolving Role in the Era of CAR T-Cell Therapy.
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弥漫大 B 细胞淋巴瘤(DLBCL)是成人最常见的侵袭性淋巴瘤。尽管多数病例可治愈,仍有相当一部分患者会复发并死于淋巴瘤。本综述旨在总结异基因造血干细胞移植(allo-HSCT)治疗复发性 DLBCL 的作用,重点关注 CAR-T 细胞疗法时代的应用价值。 最新进展:allo-HSCT 主要用于 CAR-T 细胞治疗后疾病进展或复发的患者,这很大程度上是因为该移植方式的非复发死亡率(NRM)较高。移植时疾病状态具有预后意义,完全缓解(CR)与较好结局相关。减低强度预处理(RIC)可能与清髓性预处理(MAC)疗效相当,但毒性更低。对于多次复发患者,包括自体 HSCT 和 CAR-T 细胞治疗后复发者,约三分之一可通过 allo-HSCT 治愈。对于体能良好、无重大合并症,且疾病可由新兴治疗方式(如双特异性抗体、抗体药物偶联物)控制的成人患者,应考虑 allo-HSCT。
Diffuse large B-cell lymphoma (DLBCL) is the most common aggressive lymphoma in adults. Although curable in the majority of cases, a substantial portion of patients will experience disease relapse and will die from their lymphoma. This review is aimed at summarizing the role of allogeneic hematopoietic stem cell transplant (allo-HSCT) in patients with relapsed DLBCL with a focus on its role in the era of CAR T-cell therapy RECENT FINDINGS: Allo-HSCT is primarily reserved for patients who experience disease progression or relapse after CAR T-cell therapy, largely due to the high non-relapse mortality (NRM) associated with the procedure.
Disease status at the time of allo-HSCT is prognostic with complete remission (CR) associated with better outcomes. Reduced-intensity conditioning (RIC) is likely as effective as myeloablative conditioning (MAC) with less toxicity.
In patients with multiply relapsed disease, including after auto-HSCT and CAR T-cell therapy, approximately one-third can be cured with allo-HSCT. Allo-HSCT should be considered a treatment modality for fit adults without major comorbid conditions whose disease can be controlled with emerging treatment modalities (e. g. , bispecifics, antibody-drug conjugates).
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