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:Loncastuximab tesirine for treatment of relapsed or refractory diffuse large B cell lymphoma.
Loncastuximab tesirine for treatment of relapsed or refractory diffuse large B cell lymphoma.
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Loncastuximab tesirine 是一种抗 CD19 抗体药物偶联物,具有新型细胞毒性载荷。早期研究显示该药物可耐受,其安全性特征不同于其他获批用于淋巴系统恶性肿瘤的抗体药物偶联物。疗效数据显示其在不同非霍奇金淋巴瘤类型中具有活性,一项在 DLBCL 中完成的 2 期研究显示持久缓解,包括在高危亚组中。Loncastuximab tesirine 将成为 DLBCL 治疗选择的重要补充。
大约三分之一的弥漫性大B细胞淋巴瘤(DLBCL)患者在初始治疗后出现难治或复发性疾病。尽管最近有几种新药获得监管批准,包括CAR-T 细胞疗法、polatuzumab vedotin和tafasitamab,但仍需要更多疗法来扩大治疗选择并改善一线治疗后进展的DLBCL患者的结局。涵盖领域:综述了最近获批用于复发性DLBCL的药物研究。CD19作为免疫治疗靶点的相关性。loncastuximab tesirine及其细胞毒性载荷(一种吡咯并苯二氮卓二聚体)的药理学组成。loncastuximab tesirine在非霍奇金淋巴瘤中的I期和2期数据,显示该药物的安全性特征以及DLBCL中正在显现的疗效结果。
INTRODUCTION: Approximately, a third of patients with diffuse large B-cell lymphoma (DLBCL) have refractory or relapsed disease after initial treatment. Despite recent regulatory approval of several new agents, including CAR-T cell therapy, polatuzumab vedotin and tafasitamab, there is still a need for additional therapies that expand the therapeutic alternatives and improve outcomes for patients with DLBCL that progresses after first line therapy. AREAS COVERED: Studies of recently approved agents for relapsed DLBCL are reviewed. The relevance of CD19 as an immunotherapeutic target. The pharmacologic composition of loncastuximab tesirine and its cytotoxic payload, a pyrrolobenzodiazepine dimer.
Phase I and phase 2 data for loncastuximab tesirine in non-Hodgkin lymphoma, showing the safety profile of this drug and the emerging efficacy results in DLBCL. EXPERT OPINION: Loncastuximab tesirine is an antiCD19 antibody drug conjugate with a novel cytotoxic payload. Early studies showed this drug is tolerable, with a safety profile that is different from other antibody drug conjugates approved for lymphoid malignancies.
Efficacy data shows activity in different non-Hodgkin lymphoma entities, and a phase 2 study has been completed in DLBCL showing durable responses, including in high-risk subgroups. Loncastuximab tesirine will be an important addition to the treatment alternatives for DLBCL.
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