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:Relapsed/refractory diffuse large B cell lymphoma with cardiac involvement: A case report and literature review.
Relapsed/refractory diffuse large B cell lymphoma with cardiac involvement: A case report and literature review.
本例患者的应答凸显了早期诊断与及时治疗对改善 SCL 预后的重要性,并为 SCL 治疗策略提供了重要参考。
背景:心脏血液系统恶性肿瘤(CHM)极为罕见,包括白血病、淋巴瘤浸润及伴髓外表现的多发性骨髓瘤。心脏淋巴瘤可分为原发性心脏淋巴瘤(PCL)和继发性心脏淋巴瘤(SCL)。与PCL相比,SCL更常见。组织学上,最常见的SCL为弥漫大B细胞淋巴瘤(DLBCL)。心脏受累淋巴瘤患者预后极差。近年来,CAR T细胞免疫疗法已成为治疗复发或难治性DLBCL的高效方法。迄今尚无指南就继发心脏或心包受累患者管理达成明确共识。本文报告一例复发/难治性DLBCL继发累及心脏的病例。病例:一名男性患者根据纵隔和胰周肿块活检及荧光原位杂交结果,确诊双表达型DLBCL。患者接受一线化疗和抗CD19 CAR T细胞免疫疗法,但12个月后出现心脏转移。考虑到患者身体状况和经济情况,先给予两周期多线化疗,随后患者在另一家医院接受CAR-NK细胞免疫疗法和异基因造血干细胞移植(allo-HSCT)。患者生存6个月后死于重症肺炎。结论:本病例的治疗反应凸显早期诊断和及时治疗对改善SCL预后的重要性,也为SCL治疗策略提供重要参考。
BACKGROUND: Hematological malignancies of the heart (CHMs) are extremely rare, and include leukemia, lymphoma infiltration, and multiple myeloma with extramedullary manifestations. Cardiac lymphoma can be divided into primary cardiac lymphoma (PCL) and secondary cardiac lymphoma (SCL). Compared to PCL, SCL is relatively more common. Histologically, the most frequent SCL is diffuse large B-cell lymphoma (DLBCL). The prognosis of lymphoma in patients with cardiac involvement is extremely poor. CAR T-cell immunotherapy has been recently become a highly effective treatment for relapsed or refractory diffuse large B-cell lymphoma. To date, there are no guidelines that provide a clear consensus on the management of patients with secondary heart or pericardial involvement. We report a case of relapsed/refractory DLBCL that secondarily affected the heart. CASE PRESENTATION: A male patient was diagnosed with double-expressor DLBCL based on biopsies of mediastinal and peripancreatic masses and fluorescence in situ hybridization. The patient received first-line chemotherapy and anti-CD19 CAR T cell immunotherapy, but developed heart metastases after 12 months. Considering his physical condition and economic situation of the patient, two cycles of multiline chemotherapies were administered, followed by CAR-NK cell immunotherapy and allogeneic hematopoietic stem cell transplantation (allo-HSCT) at another hospital. After achieving a six-month survival, the patient died of severe pneumonia. CONCLUSION: The response of our patient emphasizes the importance of early diagnosis and timely treatment to improve the prognosis of SCL and serves as an important reference for SCL treatment strategies.
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