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采用多参数流式细胞术评估 AL 淀粉样变性患者的微小残留病。

Assessment of minimal residual disease using multiparametric flow cytometry in patients with AL amyloidosis.

作者信息

Staron Andrew, Burks Eric J, Lee John C, Sarosiek Shayna, Sloan J Mark, Sanchorawala Vaishali

机构信息

Amyloidosis Center and.

Department of Pathology and Laboratory Medicine, Boston Medical Center, Boston University School of Medicine, Boston, MA.

出版信息

Blood Adv. 2020 Mar 10;4(5):880-884. doi: 10.1182/bloodadvances.2019001331.

Abstract

Despite achieving a hematologic complete response after treatment, many patients with AL amyloidosis do not attain recovery of organ function and/or experience hematologic relapse. A persistent plasma cell clone producing amyloidogenic light chains at levels below the detection threshold of traditional serologic methods is hypothesized to impede organ response in some patients. Assessment of minimal residual disease (MRD) may therefore have clinical importance as a more stringent treatment response tool for patients in a hematologic complete response. We used 2-tube, 10-color combination multiparametric flow cytometry to assess for MRD at a minimum sensitivity of 1 in 105 nucleated cells. Of 65 patients in hematologic complete response, 36 (55%) were found to have a residual clonal plasma cell population in the bone marrow. Comparing the MRD-negative and MRD-positive groups, renal response was observed in 88% vs 64% (P = .06), cardiac response in 75% vs 59% (P = .45), and any organ response in 90% vs 75% (P = .20) of patients. Depth of organ response as measured by the percent decrease in 24-hour proteinuria and brain natriuretic peptide was 96% vs 91% (P = .16) and 55% vs 46% (P = .66), respectively. These data suggest a possible correlation between MRD negativity and higher probability of organ response after treatment in AL amyloidosis. Future prospective studies with a larger cohort are needed to determine the clinical relevance of these improvements. This trial was registered at www.clinicaltrials.gov as #NCT00898235.

摘要

尽管治疗后实现了血液学完全缓解,但许多AL淀粉样变性患者并未实现器官功能恢复和/或经历血液学复发。据推测,持续产生淀粉样轻链的浆细胞克隆,其水平低于传统血清学方法的检测阈值,会阻碍一些患者的器官反应。因此,作为一种更严格的治疗反应工具,评估微小残留病(MRD)对于处于血液学完全缓解的患者可能具有临床重要性。我们使用两管10色组合多参数流式细胞术,以至少1/105有核细胞的灵敏度评估MRD。在65例血液学完全缓解的患者中,36例(55%)被发现骨髓中存在残留的克隆性浆细胞群。比较MRD阴性和阳性组,患者的肾脏反应率分别为88%和64%(P = 0.06),心脏反应率分别为75%和59%(P = 0.45),任何器官反应率分别为90%和75%(P = 0.20)。通过24小时蛋白尿和脑钠肽降低百分比衡量的器官反应深度分别为96%和91%(P = 0.16)以及55%和46%(P = 0.66)。这些数据表明,AL淀粉样变性患者治疗后MRD阴性与更高的器官反应概率之间可能存在相关性。需要更大队列的未来前瞻性研究来确定这些改善的临床相关性。该试验已在www.clinicaltrials.gov上注册,编号为#NCT00898235。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5930/7065470/48cb7f1467b5/advancesADV2019001331absf1.jpg

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