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:CD19 CAR-T therapy in solid organ transplant recipients: case report and systematic review.
CD19 CAR-T therapy in solid organ transplant recipients: case report and systematic review.
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移植后淋巴增殖性疾病(PTLD)是实体器官移植受者(SOTRs)癌症死亡的主要原因。复发/难治性(R/R)PTLD预示着高死亡风险,且有效的管理尚未确立。CD19靶向CAR-T 细胞疗法已被使用,但其风险和获益尚不明确。
我们报告了首例使用lisocabtagene maraleucel治疗弥漫性大B细胞淋巴瘤(DLBCL)PTLD的病例,并对接受CD19 CAR-T 治疗的PTLD SOTRs进行了系统性文献综述。
我们的患者获得了完全缓解(CR),毒性有限,但在输注后8个月出现了CD19+复发,尽管CAR-T 持续存在。文献综述揭示了14例DLBCL和2例Burkitt淋巴瘤PTLD病例接受了CD19 CAR-T 细胞治疗。分析了肾(n = 12)、肝(n = 2)、心脏(n = 2)和肾后胰腺(n = 1)移植受者。客观缓解率(ORR)为82.4%(14/17),其中58.5%(10/17)为CR,中位缓解持续时间为6.5个月。在肾移植受者中,ORR为91.7%(11/12)。移植物排斥反应发生率为23.5%(4/17)。未发生移植物衰竭。
我们的分析表明,CD19 CAR-T 疗法在伴有R/R PTLD的SOTRs中提供了短期有效性和可控的毒性。需要通过更大的数据集和前瞻性研究进行进一步调查。
Post-transplant lymphoproliferative disorder (PTLD) is a leading cause of cancer death in solid organ transplant recipients (SOTRs). Relapsed or refractory (R/R) PTLD portends a high risk of death and effective management is not well established. CD19-targeted CAR-T cell therapy has been utilized, but the risks and benefits are unknown.
We report the first case of diffuse large B-cell lymphoma (DLBCL) PTLD treated with lisocabtagene maraleucel and present a systematic literature review of SOTRs with PTLD treated with CD19 CAR-T therapy.
Our patient achieved a complete response (CR) with limited toxicity but experienced a CD19 + relapse 8 months after infusion despite CAR-T persistence. Literature review revealed 14 DLBCL and 2 Burkitt lymphoma PTLD cases treated with CD19 CAR-T cells. Kidney (n = 12), liver (n = 2), heart (n = 2), and pancreas after kidney (n = 1) transplant recipients were analyzed.
The objective response rate (ORR) was 82. 4% (14/17), with 58. 5% (10/17) CRs and a 6. 5-month median duration of response. Among kidney transplant recipients, the ORR was 91. 7% (11/12). Allograft rejection occurred in 23. 5% (4/17). No graft failure occurred.
Our analysis suggests that CD19 CAR-T therapy offers short-term effectiveness and manageable toxicity in SOTRs with R/R PTLD.
Further investigation through larger datasets and prospective study is needed.
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