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:Death from mantle cell lymphoma limits sequential therapy, particularly after first relapse: Patterns of care and outcomes in a series from Australia and the United Kingdom.
Death from mantle cell lymphoma limits sequential therapy, particularly after first relapse: Patterns of care and outcomes in a series from Australia and the United Kingdom.
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。
套细胞淋巴瘤(MCL)是一种B细胞非霍奇金淋巴瘤,其临床病程具有异质性。患者通常可以接受序贯治疗,但这些治疗往往导致疾病控制时间逐渐缩短,从而引发关于最佳治疗顺序的疑问。新型药物,如CAR-T 细胞疗法和双特异性抗体,在复发MCL中显示出前景,但通常被保留用于较晚的治疗线,这可能无法充分服务于那些具有侵袭性疾病表型、在治疗早期即死亡的患者。为了评估淋巴瘤相关死亡导致患者脱落从而限制序贯治疗的问题,我们对10年期间在澳大利亚和英国中心接受治疗的389例患者进行了多中心回顾性队列分析。MCL导致的死亡在每个治疗线后均增加,分别有7%、23%和26%的患者在第一、第二和第三线治疗后死于未控制的MCL。诊断时年龄较大和诱导治疗后早期复发的患者在第二线治疗后死亡风险尤其高。淋巴瘤相关死亡对序贯治疗的这一限制,为在更早治疗线中试验新型疗法提供了支持,尤其是在高危患者群体中。
Mantle cell lymphoma (MCL) is a B-cell non-Hodgkin lymphoma characterised by a heterogeneous clinical course. Patients can often receive sequential treatments, yet these typically yield diminishing periods of disease control, raising questions about optimal therapy sequencing. Novel agents, such as chimeric antigen receptor T-cell therapies and bispecific antibodies, show promise in relapsed MCL, but are often reserved for later treatment lines, which may underserve patients with aggressive disease phenotypes who die early in the treatment journey.
To assess the problem of patient attrition from lymphoma-related death limiting sequential treatment, we performed a multicentre retrospective cohort analysis of 389 patients treated at Australian and UK centres over a 10-year period. Deaths from MCL increased after each treatment line, with 7%, 23% and 26% of patients dying from uncontrolled MCL after first, second and third lines respectively.
Patients with older age at diagnosis and early relapse after induction therapy were at particular risk of death after second-line treatment. This limitation of sequential treatment by lymphoma-related death provides support for the trial of novel therapies in earlier treatment lines, particularly in high-risk patient populations.
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