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:Tandem autologous hematopoietic stem cell transplantation in multiple myeloma: A historical perspective and current challenges.
Tandem autologous hematopoietic stem cell transplantation in multiple myeloma: A historical perspective and current challenges.
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多发性骨髓瘤(MM)是一种异质性高、易复发且尚无法治愈的血液系统恶性肿瘤。对于70岁及以下、符合移植条件的新诊断患者,自体造血干细胞移植(auto-HSCT)是一线首选治疗。对于高危多发性骨髓瘤(HRMM),部分研究显示,与单次auto-HSCT相比,序贯双次auto-HSCT可带来显著获益,尤其能延长无进展生存期(PFS)和总生存期(OS)。目前,尽管异基因造血干细胞移植(allo-HSCT)是MM唯一可能实现长期治愈的疗法,其应用受移植相关死亡率(TRM)高和移植物抗宿主病(GVHD)风险限制。近年来,蛋白酶体抑制剂、免疫调节药物、单克隆抗体和CAR-T 细胞疗法等新疗法出现,对序贯双次auto-HSCT在MM治疗中的作用提出了新挑战。本综述旨在批判性评估双次与单次auto-HSCT的疗效差异,以及auto-HSCT后序贯allo-HSCT的作用,并严格评价不断演进的治疗格局中序贯双次auto-HSCT的价值和挑战。
Multiple myeloma (MM) is a heterogeneous and relapse-prone hematologic malignancy that remains incurable. For newly diagnosed patients aged 70 years or younger, who are eligible for transplantation, autologous hematopoietic stem cell transplantation (auto-HSCT) is the preferred first-line treatment. In patients with high-risk multiple myeloma (HRMM), some studies have demonstrated that tandem auto-HSCT provides notable benefits over single auto-HSCT, particularly in extending progression-free survival (PFS) and overall survival (OS).
Although allogeneic hematopoietic stem cell transplantation (allo-HSCT) currently offers the only potential for long-term cure in MM, its application is limited by high transplant-related mortality (TRM) and the risk of graft-versus-host disease (GVHD).
In recent years, the emergence of novel therapies, including proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, and chimeric antigen receptor T-cell (CAR-T) therapy, has posed new challenges to the role of tandem auto-HSCT in MM treatment. This review aims to critically examine the efficacy differences between tandem and single auto-HSCT, and sequential allo-HSCT following auto-HSCT.
Furthermore, it will rigorously evaluate the role and challenges of tandem auto-HSCT within the evolving therapeutic landscape.
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