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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Epcoritamab for Relapsed/Refractory EBV+ Post-Transplant Lymphoproliferative Disorder of DLBCL-Type.
Epcoritamab for Relapsed/Refractory EBV+ Post-Transplant Lymphoproliferative Disorder of DLBCL-Type.
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。
背景:实体器官移植(SOT)或造血干细胞移植(HSCT)后发生的移植后淋巴增殖性疾病(PTLD),若经一线化学免疫治疗后仍复发/难治(R/R),患者结局极差。该类患者尚无标准治疗,且通常被排除在临床试验之外或不符合入组条件。近年来,多种治疗弥漫大B细胞淋巴瘤(DLBCL)的有效新药获批,包括CD19 CAR-T 细胞疗法和CD3×CD20双特异性抗体。病例报告:鉴于相关数据有限,且参考DLBCL临床试验的证据,本文报告一例R/R PTLD患者接受CD3×CD20双特异性抗体epcoritamab治疗后获得良好耐受性和长期应答。试验注册:作者确认本病例报告无需进行临床试验注册。
BACKGROUND: Patients with relapsed/refractory post-transplant lymphoproliferative disorder (R/R PTLD) following solid-organ transplants (SOT) or hematopoietic stem cell transplants (HSCT) after frontline chemoimmunotherapy have dismal outcomes. There is no standard of care for this group of patients, and they are generally excluded or ineligible for clinical trials. Several effective novel agents have been licensed in recent years for the treatment of diffuse large b-cell lymphoma (DLBCL), including CD19 CAR-T cell therapy and CD3xCD20 bispecific antibody. CASE REPORT: Acknowledging the limited data and extrapolating the evidence from trials in DLBCL, we report a case of R/R PTLD successfully treated with CD3xCD20 bispecific antibody, Epcoritamab, with good tolerability and long-term response. TRIAL REGISTRATION: The authors have confirmed clinical trial registration is not needed for this submission.
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