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BCMA CAR-T 用于淋巴浆细胞性淋巴瘤浆细胞复发后的 AL 淀粉样变性

英文原题:BCMA CAR T for AL Amyloidosis After Plasmacytic Relapse of Lymphoplasmacytic Lymphoma.

查看英文原题

BCMA CAR T for AL Amyloidosis After Plasmacytic Relapse of Lymphoplasmacytic Lymphoma.

PubMed 2026/06/16(内容时间) EJHaem Q4 · IF 1.3(JCR 2025)

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研究概要

该病例凸显了 LPL 相关 AL 淀粉样变性的生物学复杂性,并支持使用 BCMA 靶向治疗,尤其是当复发或残留病灶由浆细胞成分构成时。

中文摘要

本文报告一例LPL相关AL淀粉样变患者病例。患者既往接受多种靶向B细胞及浆细胞的治疗方案。复发时,病理显示浆细胞样组织学特征;免疫组化可见浆细胞表达BCMA,且未检出B细胞浸润。患者随后接受研究性靶向B细胞成熟抗原(BCMA)的嵌合抗原受体(CAR)T细胞治疗。

接受BCMA靶向CAR-T 治疗后,患者获得血液学完全缓解。

本病例凸显了LPL相关AL淀粉样变的生物学复杂性,并支持使用BCMA靶向治疗,尤其当复发或残留病变由浆细胞成分构成时。 试验注册:ClinicalTrials.gov注册号NCT06097832。

展开英文摘要原文

Here we describe the case of a patient with a history of LPL-associated AL amyloidosis who had previously been treated with multiple B-cell- and plasma-cell-directed regimens. At the time of relapse, pathology demonstrated plasmacytic histology, with BCMA-expressing plasma cells by immunohistochemistry and no detectable B-cell infiltrate. The patient subsequently received investigational B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T-cell therapy.

Following BCMA-directed CAR T-cell therapy, the patient achieved a complete hematologic response.

This case highlights the biologic complexity of LPL-associated AL amyloidosis and supports the use of BCMA-targeted therapy, especially when the relapsing or residual disease is comprised by the plasma cell component. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT06097832.

论文信息

作者
Al Haddad N、Brailovski E、Dela-Pena J、Cook M、Rosenzweig M、Jolie Landau H
第一作者单位
Division of Nephrology Memorial Sloan Kettering Cancer Center New York City New York USA.United States
通讯作者单位
Division of Hematology/Oncology Memorial Sloan Kettering Cancer Center New York City New York USA.United States
期刊
EJHaem2026 Jun
原文标识
PubMed 42312318 · DOI 10.1002/jha2.70329