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:SOHO State of the Art Updates and Next Questions | Contemporary Role of Autologous Stem Cell Transplantation for the Treatment of Relapsed/Refractory Diffuse Large B-Cell Lymphoma in the Era of Cellular Therapies.
SOHO State of the Art Updates and Next Questions | Contemporary Role of Autologous Stem Cell Transplantation for the Treatment of Relapsed/Refractory Diffuse Large B-Cell Lymphoma in the Era of Cellular Therapies.
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自20世纪90年代以来,复发/难治性弥漫大B细胞淋巴瘤(DLBCL)的标准治疗一直是挽救性化疗,随后对化疗敏感缓解的患者进行大剂量化疗和自体干细胞移植(HDT-ASCT)。
然而,近期评估CAR-T 细胞疗法对比HDT-ASCT用于二线复发/难治性DLBCL疗效的TRANSFORM和ZUMA-7试验取得了令人鼓舞的结果,试图挑战这一标准治疗。尽管这些研究为早期复发和原发难治性DLBCL的治疗建立了新标准,但这些研究之间在试验设计上的显著差异以及疾病进程中随机化时机的局限性,要求对结果进行审慎解读。
此外,CAR-T 细胞治疗的经济负担和后勤挑战以及这些疗法的可及性有限仍然是持续存在的问题。尽管这些试验结果令人鼓舞,HDT-ASCT在DLBCL治疗中仍有其作用,特别是在初始治疗后12个月复发的疾病中,以及对挽救性化疗反应良好的化疗敏感疾病中。正在进行的评估HDT-ASCT前新型挽救方案的研究,以及未来评估CAR-T 细胞疗法在化疗敏感疾病中作用的研究,将有助于确定HDT-ASCT在复发/难治性DLBCL中的持续作用。
Since the 1990s, the standard of care for the treatment of relapsed/refractory diffuse large B-cell lymphoma (DLBCL) had been salvage chemotherapy followed by high-dose chemotherapy and autologous stem cell transplantation (HDT-ASCT) in patients with a chemotherapy-sensitive remission.
However, promising results from the recent TRANSFORM and ZUMA-7 trials evaluating the efficacy of CAR T-cell therapy versus HDT-ASCT for second line relapsed/refractory DLBCL have sought to challenge this standard of care. While these studies have established a new standard for the treatment of early relapsed and primary refractory DLBCL, significant differences in the trial design between these studies and limitations with the timing of randomization during the disease course warrant a thoughtful interpretation of the results.
Additionally, the financial burden and logistic challenges of CAR T-cell administration and limited access to these therapies continue to be ongoing issues. Despite the encouraging results from these trials, HDT-ASCT continues to have a role in the treatment of DLBCL, especially in disease relapsing 12 months after initial therapy, and in chemo sensitive disease with a good response to salvage chemotherapy.
Ongoing studies evaluating novel salvage regimens for use prior to HDT-ASCT, and future studies evaluating the role of CAR T-cell therapy in chemo sensitive disease will help determine the continued role of HDT-ASCT for relapsed/refractory DLBCL.
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