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:Strengths and Weaknesses of Different Therapeutic Strategies for the Treatment of Patients with Multiple Myeloma Who Progress After the Frontline Use of Lenalidomide: A Narrative Review.
Strengths and Weaknesses of Different Therapeutic Strategies for the Treatment of Patients with Multiple Myeloma Who Progress After the Frontline Use of Lenalidomide: A Narrative Review.
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。
在PubMed数据库中检索相关文献,使用的检索词包括:复发性多发性骨髓瘤、难治性多发性骨髓瘤、首次复发、二线治疗、来那度胺难治(Len-R)和来那度胺暴露(Len-Exp)。
总体而言,无论既往治疗次数多少,包含抗CD38抗体、卡非佐米和地塞米松的三药方案均取得了较有利的PFS。其他试验也显示,含泊马度胺的联合方案具有不可忽视的获益,尤其是在较早治疗线次中。然而,这些研究纳入的Len-Exp/Len-R患者人数不一,且对一线来那度胺治疗后进展患者进行分析的人数有限,因此难以为MM首次复发患者确定“最佳”治疗方案。近期,含贝兰他单抗莫福汀的联合疗法以及尤其是CAR-T 细胞免疫疗法取得了令人鼓舞的结果;正在进行的临床试验则在探索双特异性抗体和CELMoD药物在该患者群体中的作用。
目前尚无明确数据说明现有方案对一线含来那度胺治疗后复发或难治的MM患者所产生的特异性疗效;预计基于不同免疫策略的新型方法将进一步改善这些患者的临床结局。
Background/Objectives: Patients with multiple myeloma (MM) who relapse after exposure to lenalidomide in the context of their first-line therapy are becoming a growing and clinically relevant population.
We performed a systematic review of available clinical trials evaluating the efficacy and safety of different therapeutic strategies for the treatment of patients with MM at first relapse after the frontline use of lenalidomide. Methods: Publications of interest were searched on the PubMed database. The following search terms were employed: relapsed multiple myeloma, refractory multiple myeloma, first relapse, second-line therapy, lenalidomide-refractory (Len-R) and lenalidomide-exposed (Len-Exp).
Results: Overall, triplet regimens that included anti-CD38 antibodies, carfilzomib and dexamethasone achieved a more favorable PFS regardless of the number of prior therapies. Other trials also demonstrated a non-negligible benefit with combinations containing pomalidomide, particularly in early lines of therapy.
However, the variable number of patients with Len-Exp/Len-R disease enrolled in these studies and the limited number of those analyzed after progression following frontline lenalidomide make it difficult to select an "optimal" choice for the treatment of patients with MM at first relapse. Promising results have been more recently obtained by using combo therapies, including belantamab mafodotin and, above all, immunotherapies with CAR-T cells, and ongoing clinical trials are exploring the role of bispecific antibodies and CELMoDs in this population of patients.
Conclusions: In the absence of clear-cut data regarding the specific effects of available regimens on patients with MM who are refractory or have relapsed after first-line therapies including lenalidomide, novel approaches based on different types of immune strategies are expected to further improve the clinical outcome of these patients.
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