Guidelines for non-transplant chemotherapy for treatment of systemic AL amyloidosis: EHA-ISA working group.

IF 5.2 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Ashutosh D Wechalekar, M Teresa Cibeira, Simon D Gibbs, Arnaud Jaccard, Shaji Kumar, Giampaolo Merlini, Giovanni Palladini, Vaishali Sanchorawala, Stefan Schönland, Christopher Venner, Mario Boccadoro, Efstathios Kastritis
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引用次数: 16

Abstract

Background: This guideline has been developed jointly by the European Society of Haematology and International Society of Amyloidosis recommending non-transplant chemotherapy treatment for patients with AL amyloidosis.

Methods: A review of literature and grading of evidence as well as expert recommendations by the ESH and ISA guideline committees.

Results and conclusions: The recommendations of this committee suggest that treatment follows the clinical presentation which determines treatment tolerance tempered by potential side effects to select and modify use of drugs in AL amyloidosis. All patients with AL amyloidosis should be considered for clinical trials where available. Daratumumab-VCD is recommended from most untreated patients (VCD or VMDex if daratumumab is unavailable). At relapse, the two guiding principles are the depth and duration of initial response, use of a class of agents not previously exposed as well as the limitation imposed by patients' fitness/frailty and end organ damage. Targeted agents like venetoclax need urgent prospective evaluation. Future prospective trials should include advanced stage patients to allow for evidence-based treatment decisions. Therapies targeting amyloid fibrils or those reducing the proteotoxicity of amyloidogenic light chains/oligomers are urgently needed.

治疗全身性AL淀粉样变性的非移植化疗指南:EHA-ISA工作组。
背景:本指南由欧洲血液学学会和国际淀粉样变性学会联合制定,推荐对AL淀粉样变性患者进行非移植化疗。方法:文献回顾和证据分级以及专家建议由ESH和ISA指南委员会。结果和结论:该委员会的建议建议,治疗应遵循临床表现,临床表现决定了治疗耐受性和潜在的副作用,以选择和修改AL淀粉样变性的药物使用。所有AL淀粉样变患者都应考虑进行临床试验。大多数未经治疗的患者推荐使用daratumumab -VCD(如果没有daratumumab,建议使用VCD或VMDex)。在复发时,两个指导原则是初始反应的深度和持续时间,使用以前未暴露的一类药物,以及患者的健康/虚弱和终末器官损伤所施加的限制。像venetoclax这样的靶向药物需要迫切的前瞻性评估。未来的前瞻性试验应包括晚期患者,以允许循证治疗决策。目前迫切需要针对淀粉样蛋白原纤维或降低淀粉样蛋白轻链/低聚物的蛋白质毒性的治疗方法。
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来源期刊
Amyloid-Journal of Protein Folding Disorders
Amyloid-Journal of Protein Folding Disorders 生物-生化与分子生物学
CiteScore
10.60
自引率
10.90%
发文量
48
审稿时长
6-12 weeks
期刊介绍: Amyloid: the Journal of Protein Folding Disorders is dedicated to the study of all aspects of the protein groups and associated disorders that are classified as the amyloidoses as well as other disorders associated with abnormal protein folding. The journals major focus points are: etiology, pathogenesis, histopathology, chemical structure, nature of fibrillogenesis; whilst also publishing papers on the basic and chemical genetic aspects of many of these disorders. Amyloid is recognised as one of the leading publications on amyloid protein classifications and the associated disorders, as well as clinical studies on all aspects of amyloid related neurodegenerative diseases and major clinical studies on inherited amyloidosis, especially those related to transthyretin. The Journal also publishes book reviews, meeting reports, editorials, thesis abstracts, review articles and symposia in the various areas listed above.
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