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:Combined Impact of Prior Polatuzumab Vedotin Plus Bendamustine and Rituximab Therapy and Myeloablative Conditioning on Early Post-Transplant BK Virus-Associated Hemorrhagic Cystitis.
Combined Impact of Prior Polatuzumab Vedotin Plus Bendamustine and Rituximab Therapy and Myeloablative Conditioning on Early Post-Transplant BK Virus-Associated Hemorrhagic Cystitis.
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复发/难治性弥漫大B细胞淋巴瘤(R/R DLBCL)预后极差,目前尚无确立的挽救性化疗方案。Polatuzumab、利妥昔单抗和苯达莫司汀联合治疗(Pola-BR)已被批准作为R/R DLBCL的新治疗选择。近年来,CAR-T 细胞治疗和双特异性抗体已使许多R/R DLBCL患者获得长期缓解。
然而,对于上述治疗无应答的患者,异基因移植仍具有潜在治愈性。虽然异基因移植也可引起各种不良事件,但出血性膀胱炎是特别严重的并发症,需要有效的预防策略。
在此,我们报告两例在接受清髓性预处理的连续脐血移植和Pola-BR治疗早期复发DLBCL后发生的严重BK病毒相关性出血性膀胱炎(BKV-HC)病例。两例患者在接受多种挽救性治疗后接受Pola-BR,并在移植后发生早发性BKV-HC,表明Pola-BR和清髓性预处理的影响。
我们分析了两例病例之间的共同特征,以区分触发BKV-HC发病的因素和导致其严重程度的因素。基于两例病例临床过程的差异,我们提出BKV-HC的预防策略,并确定接受异基因移植的R/R DLBCL患者中Pola-BR的治疗策略。
Relapsed/refractory diffuse large B-cell lymphomas (R/R DLBCLs) have an extremely poor prognosis, with no established salvage chemotherapy currently available. Polatuzumab, rituximab, and bendamustine combination therapy (Pola-BR) has been approved as a new therapeutic option for R/R DLBCL. Recently, chimeric antigen receptor T-cell therapy and bispecific antibodies have induced long-term remission in many patients with R/R DLBCL.
However, allogeneic transplantation remains potentially curative for patients unresponsive to the abovementioned treatments. While allogeneic transplantation can also cause various adverse events, hemorrhagic cystitis is a particularly severe complication that requires effective prevention strategies.
Here, we report two cases of severe BK virus-associated hemorrhagic cystitis (BKV-HC) that developed after successive cord blood transplantation with myeloablative conditioning and Pola-BR treatment for early-relapsed DLBCL. Both patients received Pola-BR after undergoing multiple salvage therapies and developed early-onset BKV-HC post-transplant, demonstrating the effects of Pola-BR and myeloablative conditioning.
We analyzed the shared characteristics between these two cases to distinguish between the factors that trigger the onset of BKV-HC and those that contribute to its severity. Based on the differences in the clinical course between the two cases, we propose prevention strategies for BKV-HC and identify treatment strategies for Pola-BR in patients with R/R DLBCL undergoing allogeneic transplantation.
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