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:Autologous hematopoietic stem cell transplantation for multiple myeloma in the age of CAR T cell therapy.
Autologous hematopoietic stem cell transplantation for multiple myeloma in the age of CAR T cell therapy.
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嵌合抗原受体(CAR)T细胞疗法显著改变了复发/难治性骨髓瘤的治疗,疗效优异且安全性可耐受。对于足够年轻且身体状况良好、能够耐受强化治疗的新诊断多发性骨髓瘤(NDMM)患者,大剂量化疗联合自体造血干细胞移植(AHCT)已成为主流治疗。该标准基于新型药物出现之前比较AHCT与化疗的随机试验。近期较大型研究主要显示前期AHCT可改善无进展生存期(PFS),而非总生存期(OS)。对于OS获益缺失的意义仍存在争论,同时需考虑疾病慢性病程、研究设计以及AHCT暴露的利弊等潜在混杂因素。事实上,前期AHCT可能并非如以往认为的那样具有独特获益,且并非没有风险。
新型四药方案活性高,可有效达到可测量残留病灶(MRD)评估的深度缓解。AHCT所用大剂量化疗会带来短期和长期不良反应,可能改变疾病病程及患者耐受未来治疗的能力。部分高危亚组可能从AHCT获得更多获益,但最终结局仍差。与CAR-T 疗法结局相比,AHCT能否或是否应推迟已成为重要议题。对于达到MRD阴性的患者,推迟AHCT可作为个体化决策;MRD阴性已充分确立为PFS和OS的重要预后因素。许多情况下,复发时保留或重新实施AHCT是可行的,并有望重置T细胞区室、开启免疫再激活治疗选择。未来治疗排序可能由个体化、MRD指导的决策塑造,但仍需更多研究明确何时推迟安全且适宜。
Chimeric antigen receptor (CAR) T cell therapy has revolutionized the management of relapsed and refractory myeloma, with excellent outcomes and a tolerable safety profile. High dose chemotherapy with autologous hematopoietic stem cell transplantation (AHCT) is established as a mainstream of newly diagnosed multiple myeloma (NDMM) management in patients who are young and fit enough to tolerate such intensity. This standard was developed based on randomized trials comparing AHCT to chemotherapy in the era prior to novel agents. More recently, larger studies have primarily shown a progression free survival (PFS) benefit of upfront AHCT, rather than overall survival (OS) benefit. There is debate about the significance of this lack of OS, acknowledging the potential confounders of the chronic nature of the disease, study design and competing harms and benefits of exposure to AHCT. Indeed upfront AHCT may not be as uniquely beneficial as we once thought, and is not without risk.
New quadruple-agent regimens are highly active and effective in achieving a deep response as quantified by measurable residual disease (MRD). The high dose chemotherapy administered with AHCT imposes a burden of short and long-term adverse effects, which may alter the disease course and patient's ability to tolerate future therapies. Some high-risk subgroups may have a more valuable benefit from AHCT, though still ultimately suffer poor outcomes. When compared to the outcomes of CAR T cell therapy, the question of whether AHCT can or indeed should be deferred has become an important topic in the field.
Deferring AHCT may be a personalized decision in patients who achieve MRD negativity, which is now well established as a key prognostic factor for PFS and OS. Reserving or re-administering AHCT at relapse is feasible in many cases and holds the promise of resetting the T cell compartment and opening up options for immune reengagement. It is likely that personalized MRD-guided decision making will shape how we sequence in the future, though more studies are required to delineate when this is safe and appropriate.
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