School of Biomedical Sciences, Faculty of Health & Medical Sciences, The University of Western Australia, Crawley, Western Australia, Australia.
PathWest Laboratory Medicine WA, Nedlands, Western Australia, Australia.
J Clin Pathol. 2022 Jan;75(1):50-57. doi: 10.1136/jclinpath-2020-207066. Epub 2020 Nov 24.
Determination of the number of plasma cells in bone marrow biopsies is required for the diagnosis and ongoing evaluation of plasma cell neoplasms. We developed an automated digital enumeration platform to assess plasma cells identified by antigen expression in whole bone marrow sections in multiple myeloma, and compared it with manual assessments.
Bone marrow trephine biopsy specimens from 91 patients with multiple myeloma at diagnosis, remission and relapse were stained for CD138 and multiple myeloma oncogene 1 (MUM1). Manual assessment and digital quantification were performed for plasma cells in the entire trephine section. Concordance rates between manual and digital methods were evaluated for each antigen by intraclass correlation analyses (ICC) with associated Spearman's correlations.
The digital platform counted 16 484-1 118 868 cells and the per cent CD138 and MUM1-positive plasma cells ranged from 0.05% to 93.5%. Overall concordance between digital and manual methods was 0.63 for CD138 and 0.89 for MUM1. Concordance was highest with diffuse plasma cell infiltrates (MUM1: ICC=0.90) and lowest when in microaggregates (CD138: ICC=0.13). Manual counts exceeded digital quantifications for both antigens (CD138: mean=26.4%; MUM1: mean=9.7%). Diagnostic or relapse threshold counts, as determined by CD138 manual assessments, were not reached with digital counting for 16 cases (18%).
Automated digital enumeration of the entire, immunohistochemically stained bone marrow biopsy section can accurately determine plasma cell burden, irrespective of pattern and extent of disease (as low as 0.05%). This increases precision over manual visual assessments which tend to overestimate plasma burden, especially for CD138, and when plasma cells are in clusters.
骨髓活检中浆细胞数量的测定是浆细胞肿瘤诊断和病情评估的必需条件。我们开发了一种自动数字化计数平台,用于评估多发性骨髓瘤患者全骨髓切片中抗原表达所鉴定的浆细胞,并与手动评估进行了比较。
对 91 例初诊、缓解和复发的多发性骨髓瘤患者的骨髓活检标本进行 CD138 和多发性骨髓瘤癌基因 1(MUM1)染色。对整个骨髓活检切片中的浆细胞进行手动评估和数字定量。采用 ICC 分析和 Spearman 相关分析评估两种方法对每种抗原的一致性。
数字平台计数了 16484-1118868 个细胞,CD138 和 MUM1 阳性浆细胞的百分比范围为 0.05%-93.5%。数字和手动方法之间的总体一致性为 CD138 为 0.63,MUM1 为 0.89。弥漫性浆细胞浸润时一致性最高(MUM1:ICC=0.90),微聚集时最低(CD138:ICC=0.13)。两种抗原的手动计数均高于数字定量(CD138:平均 26.4%;MUM1:平均 9.7%)。通过 CD138 手动评估确定的诊断或复发阈值计数,有 16 例(18%)未达到数字计数。
自动数字化计数整个免疫组化染色的骨髓活检切片可以准确地确定浆细胞负担,而与疾病的形态和程度无关(低至 0.05%)。这比手动视觉评估更精确,因为手动评估往往会高估浆细胞负担,尤其是对于 CD138 而言,并且当浆细胞成簇时更是如此。