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:Case report: CAR-T therapy demonstrated safety and efficacy in relapsed/refractory diffuse large B-cell lymphoma patients complicated with hepatitis B-related cirrhosis.
Case report: CAR-T therapy demonstrated safety and efficacy in relapsed/refractory diffuse large B-cell lymphoma patients complicated with hepatitis B-related cirrhosis.
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CAR-T 细胞疗法对感染乙型肝炎病毒(HBV)的复发/难治性弥漫性大B细胞淋巴瘤(DLBCL)患者已显示疗效和安全性。
然而,由于可能出现难以预测的并发症,该疗法对合并肝硬化患者的适用性仍鲜有研究。本文报告了3例接受CAR-T 细胞输注的HBV相关肝硬化复发/难治性DLBCL病例(P1、P2和P3)。P1和P2接受氟达拉滨联合环磷酰胺(FC)预处理以清除淋巴细胞,随后输注CAR-T 细胞;P3则接受SEAM方案(司莫司汀、依托泊苷、阿糖胞苷和美法仑)及自体干细胞移植,作为CAR-T 输注的桥接治疗。P1和P2迅速达到完全缓解(CR);P3在CAR-T 输注1个月后最初表现为疾病稳定,随后经局部挽救性放疗和来那度胺维持治疗达到CR。CAR-T 治疗后中位随访42个月时,无进展生存率为100%。
值得注意的是,随访期间患者出现了肝硬化相关并发症,包括内镜下曲张静脉出血、HBV再激活或确诊肝脏恶性肿瘤。我们的研究结果提示,CAR-T 疗法适用于HBV相关肝硬化DLBCL患者且具有疗效,但仍需监测潜在肝脏并发症。
Chimeric antigen receptor T-cell (CAR-T) therapy has demonstrated both efficacy and safety in relapsed/refractory diffuse large B-cell lymphoma (DLBCL) patients infected with hepatitis B virus (HBV).
However, its applicability in individuals with liver cirrhosis remains largely unexplored due to the potential for unpredictable complications.
Here, we report three cases (P1, P2, and P3) of relapsed/refractory DLBCL with HBV-related cirrhosis treated with CAR-T cell infusion. P1 and P2 received CAR-T cell infusion following a conditioning regimen of fludarabine and cyclophosphamide (FC) for lymphodepletion, while P3 received the SEAM (semustine, etoposide, cytarabine, and melphalan) regimen and autologous stem cell transplantation bridging CAR-T cell infusion.
P1 and P2 achieved rapid complete remission (CR), whereas P3 initially exhibited stable disease a month after CAR-T infusion and subsequently achieved CR after local radiation salvage therapy and lenalidomide maintenance. With a median follow-up of 42 months after CAR-T, the progression-free survival rate was 100%.
Notably, during follow-up, these patients experienced complications associated with cirrhosis, including endoscopic variceal bleeding, HBV reactivation, or the diagnosis of hepatic malignancy.
Our findings suggest that CAR-T therapy is applicable and effective for the treatment of DLBCL patients with HBV-related cirrhosis, albeit necessitating monitoring for potential hepatic complications.
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