Wood Brent L, Arroz Maria, Barnett David, DiGiuseppe Joseph, Greig Bruce, Kussick Steven J, Oldaker Teri, Shenkin Mark, Stone Elizabeth, Wallace Paul
Department of Laboratory Medicine, University of Washington Medical Center, Seattle, Washington 98195, USA.
Cytometry B Clin Cytom. 2007;72 Suppl 1:S14-22. doi: 10.1002/cyto.b.20363.
Immunophenotyping by flow cytometry has become standard practice in the evaluation and monitoring of patients with hematopoietic neoplasia. However, despite its widespread use, considerable variability continues to exist in the reagents used for evaluation and the format in which results are reported. As part of the 2006 Bethesda Consensus conference, a committee was formed to attempt to define a consensus set of reagents suitable for general use in the diagnosis and monitoring of hematopoietic neoplasms. The committee included laboratory professionals from private, public, and university hospitals as well as large reference laboratories that routinely operate clinical flow cytometry laboratories with an emphasis on lymphoma and leukemia immunophenotyping. A survey of participants successfully identified the cell lineage(s) to be evaluated for each of a variety of specific medical indications and defined a set of consensus reagents suitable for the initial evaluation of each cell lineage. Elements to be included in the reporting of clinical flow cytometric results for leukemia and lymphoma evaluation were also refined and are comprehensively listed. The 2006 Bethesda Consensus conference represents the first successful attempt to define a set of consensus reagents suitable for the initial evaluation of hematopoietic neoplasia.
通过流式细胞术进行免疫表型分析已成为评估和监测造血系统肿瘤患者的标准做法。然而,尽管其应用广泛,但用于评估的试剂以及报告结果的格式仍存在相当大的差异。作为2006年贝塞斯达共识会议的一部分,成立了一个委员会,试图确定一套适用于造血系统肿瘤诊断和监测的通用试剂。该委员会成员包括来自私立、公立和大学医院的实验室专业人员,以及大型参考实验室的人员,这些实验室常规开展临床流式细胞术实验室工作,重点是淋巴瘤和白血病的免疫表型分析。对参与者的一项调查成功确定了针对各种特定医学指征应评估的细胞谱系,并定义了一套适用于每个细胞谱系初始评估的共识试剂。用于白血病和淋巴瘤评估的临床流式细胞术结果报告中应包含的要素也得到了完善,并进行了全面列举。2006年贝塞斯达共识会议是首次成功尝试定义一套适用于造血系统肿瘤初始评估的共识试剂。