决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Daratumumab-based salvage therapy enables umbilical cord blood transplantation in multiline refractory, elderly T-lymphoblastic lymphoma: a case report.
虽然T淋巴母细胞淋巴瘤(T-LBL)患者目前总体预后良好,3年无事件生存率接近69.2%,但老年难治性T-LBL几乎无一例外地致命,5年总生存率仅为4%。
尽管T淋巴母细胞淋巴瘤(T-LBL)患者目前总体预后良好,3年无事件生存率接近69.2%,但老年难治性T-LBL几乎无一例外地致命,5年总生存率仅为4%。由于常被排除在CD7 CAR T细胞试验等细胞疗法之外,这一不良预后进一步加剧。我们报告一例60岁男性多线难治性T-LBL患者,对hyper-CVAD呈部分缓解,随后在venetoclax联合azacitidine治疗下进展。该患者在接受一个周期的DMPD挽救治疗(包括daratumumab、脂质体米托蒽醌、培门冬酶和地塞米松)后达到完全缓解。这一易于获得的方案规避了CAR T细胞平台相关的生产延迟和高昂费用。它成功地将患者桥接至双份脐血移植,在移植后第+21天实现完全供者嵌合,且尽管出现移植后并发症,仍维持持续缓解。该难治性T-LBL病例中观察到的显著疗效与历史治疗结局形成鲜明对比,提示DMPD方案可能既可作为不适合造血干细胞移植的老年患者可立即实施的治疗方法,也可能成为其潜在的决定性治疗手段。
While patients with T-lymphoblastic lymphoma (T-LBL) now generally have a favorable prognosis, with 3-year event-free survival rate approaching 69.2%, refractory T-LBL in older adults is almost invariably fatal, exhibiting a dismal 5-year overall survival rate of only 4%. This poor prognosis is exacerbated by frequent exclusion from cellular therapies like CD7 CAR T-cell trials. We report a case of a 60-year-old man with multi-refractory T-LBL exhibiting a partial response to hyper-CVAD followed by progression on venetoclax plus azacitidine. This patient achieved complete remission after a single cycle of DMPD salvage therapy comprising daratumumab, liposomal mitoxantrone, pegaspargase and dexamethasone. This readily accessible regimen circumvented the manufacturing delays and prohibitive costs associated with CAR T-cell platforms. It successfully bridged the patient to double umbilical cord blood transplantation, resulting in full donor chimerism by day +21 and sustained remission despite post-transplant complications. The remarkable efficacy observed in this refractory T-LBL case, contrasting sharply with historical treatment outcomes, suggests that the DMPD regimen may serve as both an immediately actionable and potentially definitive therapeutic approach for elderly patients who are ineligible for hematopoietic stem cell transplantation.
MEMBER ACCOUNT
登录成功会直接打开下一页。