Treatment of amyloid light chain cardiac amyloidosis: systematic review and future directions.

医学 硼替佐米 心脏淀粉样变性 背景(考古学) 内科学 肿瘤科 梅尔法兰 达拉图穆马 系统回顾 淀粉样变性 淀粉样变性 重症监护医学 奇纳 梅德林 化疗 多发性骨髓瘤 免疫学 法学 政治学 抗体 古生物学 精神科 生物 免疫球蛋白轻链 心理干预
作者
Dunya Alsomali,Dania Mohty,Martha Grogan,Angela Dispenzieri,Mahmoud Aljurf,Shaji Kumar,Morie A. Gertz,Amr Hanbali,Shahrukh K. Hashmi
出处
期刊:PubMed 卷期号:20 (10): 609-618
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摘要

Several treatment strategies for amyloid light chain cardiac amyloidosis (AL-CA) have been described in the literature; however, there is no consensus about the optimal approach to AL-CA.We conducted this systematic review to summarize current evidence from published studies about the safety and efficacy of various treatment regimens for patients with AL-CA, mainly focusing on autologous stem cell transplant (ASCT) and heart transplant.An electronic literature search of PubMed, Web of Science, Scopus, EBSCO, and CINAHL Plus was conducted through December 2019 using the relevant keywords and prespecified MeSH terminology. Records were screened, and eligible studies were selected and narratively discussed. Data on the hematologic and cardiac responses as well as the safety of the treatment regimens were extracted and synthesized narratively in the context of the systematic review.Thirty published articles were included in this systematic review. The most commonly used first-line treatment in the included studies was bortezomib-based therapy followed by high-dose melphalan and ASCT, with recent evidence of improved outcome with the addition of daratumumab. Heart transplant was found to extend survival for selected patients who were not eligible for ASCT; however, it was found to affect the patients' tolerance of further chemotherapy in some studies. Published data on longterm outcomes with immunomodulatory agents were scarce.Current evidence suggests several possible regimens for the treatment of AL-CA. Effective treatment approaches for AL-CA include induction therapy with bortezomib-based or immunotherapy-based combinations in moderate/severe forms of cardiac involvement, followed by high-dose melphalan and ASCT in eligible patients, and heart transplant for selected severe cases. Therefore, we highlight the necessity of conducting well-designed, randomized controlled trials to provide evidence about the efficacy of these drugs with respect to ASCT.

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