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诊断与治疗 AL 型淀粉样变。

Diagnosis and Treatment of AL Amyloidosis.

机构信息

Department of Molecular Medicine, University of Pavia, Pavia, Italy.

Amyloidosis Research and Treatment Center, Foundation "Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Policlinico San Matteo", Viale Golgi, 19, 27100, Pavia, Italy.

出版信息

Drugs. 2023 Feb;83(3):203-216. doi: 10.1007/s40265-022-01830-z. Epub 2023 Jan 18.

Abstract

Systemic light chain (AL) amyloidosis is caused by an usually small B cell clone that produces a toxic light chain forming amyloid deposits in tissue. The heart and kidney are the major organs affected, but all others, with the exception of the CNS, can be involved. The disease is rapidly progressive, and it is still diagnosed late. Screening programs in patients followed by hematologists for plasma cell dyscrasias should be considered. The diagnosis requires demonstration in a tissue biopsy of amyloid deposits formed by immunoglobulin light chains. The workup of patients with AL amyloidosis requires adequate technology and expertise, and patients should be referred to specialized centers whenever possible. Stagings are based on cardiac and renal biomarkers and guides the choice of treatment. The combination of daratumumab, cyclophosphamide, bortezomib and dexamethasone (dara-CyBorD) is the current standard of care. Autologous stem cell transplant is performed in eligible patients, especially those who do not attain a satisfactory response to dara-CyBorD. Passive immunotherapy targeting the amyloid deposits combined with chemo-/immune-therapy targeting the amyloid clone is currently being tested in controlled clinical trials. Response to therapy is assessed based on validated criteria. Profound hematologic response is the early goal of treatment and should be accompanied over time by deepening organ response. Many relapsed/refractory patients are also treated with daratumumab combination, but novel regimens will be needed to rescue daratumumab-exposed subjects. Immunomodulatory drugs are the current cornerstone of rescue therapy, while immunotherapy targeting B-cell maturation antigen and inhibitors of Bcl-2 are promising alternatives.

摘要

系统性轻链(AL)淀粉样变性是由通常较小的 B 细胞克隆引起的,该克隆产生有毒的轻链,在组织中形成淀粉样沉积物。心脏和肾脏是主要受影响的器官,但所有其他器官(除中枢神经系统外)都可能受累。该疾病进展迅速,目前仍诊断较晚。应考虑对接受血液科浆细胞异常检查的患者进行筛查计划。诊断需要在组织活检中证明由免疫球蛋白轻链形成的淀粉样沉积物。AL 淀粉样变性患者的检查需要足够的技术和专业知识,并且应尽可能将患者转介至专门中心。分期基于心脏和肾脏生物标志物,并指导治疗选择。达雷木单抗、环磷酰胺、硼替佐米和地塞米松(dara-CyBorD)联合是目前的标准治疗方法。在有资格的患者中进行自体干细胞移植,特别是那些对 dara-CyBorD 治疗未达到满意反应的患者。针对淀粉样沉积物的被动免疫疗法与针对淀粉样克隆的化疗/免疫疗法联合目前正在对照临床试验中进行测试。根据经过验证的标准评估对治疗的反应。深度血液学反应是治疗的早期目标,并且随着时间的推移,应伴随着器官反应的加深。许多复发/难治性患者也接受达雷木单抗联合治疗,但需要新的方案来挽救达雷木单抗暴露的患者。免疫调节药物是目前挽救治疗的基石,而针对 B 细胞成熟抗原的免疫疗法和 Bcl-2 抑制剂是很有前途的替代方法。

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