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:Cilta-cel, a BCMA-targeting CAR-T therapy for patients with multiple myeloma.
Cilta-cel, a BCMA-targeting CAR-T therapy for patients with multiple myeloma.
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。
CAR-T 疗法可改善不同 LOT 的 MM 患者结局。
引言:靶向 BCMA 的 CAR-T 疗法 ciltacabtagene autoleucel(cilta-cel)已在美国和欧洲获批,用于既往接受一线治疗(包含蛋白酶体抑制剂和免疫调节药物)且对来那度胺耐药的复发/难治性多发性骨髓瘤(RRMM)患者。综述范围:本文考察在经多线治疗的 RRMM 患者中开展的近期长期数据(LEGEND-2、CARTITUDE-1),以及较早治疗线患者数据(CARTITUDE-4),并与标准治疗对比;同时讨论对适合和不适合移植患者开展 cilta-cel 一线治疗研究(CARTITUDE-5、CARTITUDE-6)的依据。
专家意见:CAR-T 可改善不同治疗线 MM 患者结局。CARTITUDE-1 和 CARTITUDE-4 树立了新的疗效标杆:重度经治患者(CARTITUDE-1)中位 PFS 为 34.9 个月;既往接受 1–3 线治疗患者(CARTITUDE-4)与标准治疗相比,疾病进展或死亡相对风险降低 74%,且安全性可管理。两项研究缓解率相近:CARTITUDE-1 为 98%,CARTITUDE-4 中接受输注者接近 100%。Cilta-cel 可成为 RRMM 患者一线治疗后的关键选择。针对一线 cilta-cel 的临床试验将提供宝贵见解,帮助优化治疗路径并以潜在治愈 MM 为目标。
INTRODUCTION: Ciltacabtagene autoleucel (cilta-cel), a BCMA-targeting CAR-T therapy, is approved in the United States and Europe for patients with relapsed/refractory multiple myeloma (RRMM) and 1 prior line of therapy (LOT), including a proteasome inhibitor and an immunomodulatory drug, and are lenalidomide refractory. AREAS COVERED: We examine recent long-term data in heavily pretreated RRMM (LEGEND-2, CARTITUDE-1) and earlier LOTs (CARTITUDE-4) compared with standard therapy and discuss the rationale for investigating cilta-cel as frontline therapy for transplant-eligible and transplant-ineligible patients (CARTITUDE-5, CARTITUDE-6). EXPERT OPINION: CAR-T therapies can improve outcomes for patients with MM across different LOTs.
CARTITUDE-1 and CARTITUDE-4 have set a new bar for efficacy, with median PFS of 34. 9 months in heavily pretreated patients (CARTITUDE-1) and a 74% relative risk reduction for progression/death versus standard care in patients with 1-3 prior LOTs (CARTITUDE-4), with manageable safety.
Response rates were consistent between the two studies: 98% in CARTITUDE-1 and approaching 100% for infused patients in CARTITUDE-4. Cilta-cel could be a key treatment choice for patients with RRMM after first LOT. Clinical trials investigating frontline cilta-cel therapy will provide valuable insights into optimizing treatment pathways with the aim to potentially cure MM.
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