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与定量检测 CD26- 或 CD7- CD4+ T 细胞相比,免疫表型异常的确定能更好地评估蕈样肉芽肿/赛泽里综合征外周血受累情况。

Determination of immunophenotypic aberrancies provides better assessment of peripheral blood involvement by mycosis fungoides/Sézary syndrome than quantification of CD26- or CD7- CD4+ T-cells.

机构信息

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

Department of Dermatology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.

出版信息

Cytometry B Clin Cytom. 2021 Mar;100(2):183-191. doi: 10.1002/cyto.b.21933. Epub 2020 Jul 15.

Abstract

BACKGROUND

Blood involvement by mycosis fungoides (MF)/Sézary syndrome (SS) influences prognosis and therapeutic decisions. MF/SS blood stage is currently determined by absolute CD4 + CD26- or CD4 + CD7-cell counts, which quantification method may overestimate MF/SS by including CD26- or CD7- normal CD4+ T-cells, or underestimate disease burden when MF/SS cells show incomplete loss of CD26 and/or CD7. Recently, through the standardization effort led by the International Clinical Cytometry Society (ICCS), recommendation was made to quantify MF/SS by enumerating immunophenotypically aberrant CD4+ T-cells, rather than CD26- or CD7- in isolation.

METHODS

We compared these two quantitation methods in 309 MF/SS patients who had blood samples analyzed by flow cytometry immunophenotyping (FCI) over a 1-year period.

RESULTS

Using the European Organization of Research and Treatment of Cancer (EORTC)/International Society for Cutaneous Lymphomas (ISCL) criteria, 221 (71.5%) patients had a blood stage corresponding to B0, 57 (18.4%) to B1, and 31 (10%) to B2. By FCI analysis, a total of 62 patients (20.0%) were found positive for MF/SS. Among EORTC B0 patients, 11/221 (5%) were positive by FCI (false negatives), and among EORTC Stage B1 patients, 35/57 (61%) were negative by FCI (false positives). Regarding patients positive for MF/SS cells by FCI, there was an overall excellent correlation (r = .999, p < .001) between the EORTC/ISCL method and FCI method; however, four (6.5%) patients would have an altered B stage between B0 and B1.

CONCLUSION

The MF/SS cell quantification method using immunophenotypic aberrancies, as recommended by the ICCS, allows to distinguish MF/SS cells from background benign T-cells and enables for more accurate staging, especially among patients currently being considered to have B0 and B1 stage diseases.

摘要

背景

蕈样真菌病(MF)/ Sézary 综合征(SS)的血液累及影响预后和治疗决策。MF/SS 血液分期目前通过绝对 CD4+CD26-或 CD4+CD7-细胞计数确定,其定量方法可能通过包括 CD26-或 CD7-正常 CD4+T 细胞而高估 MF/SS,或者当 MF/SS 细胞不完全丧失 CD26 和/或 CD7 时低估疾病负担。最近,通过国际临床细胞化学学会(ICCS)主导的标准化工作,建议通过计数免疫表型异常的 CD4+T 细胞,而不是单独计数 CD26-或 CD7-,来定量 MF/SS。

方法

我们在一年内通过流式细胞仪免疫表型分析(FCI)分析了 309 例 MF/SS 患者的血液样本,比较了这两种定量方法。

结果

使用欧洲癌症研究与治疗组织(EORTC)/国际皮肤淋巴瘤学会(ISCL)标准,221 例(71.5%)患者血液分期为 B0,57 例(18.4%)为 B1,31 例(10%)为 B2。通过 FCI 分析,共有 62 例(20.0%)患者 MF/SS 阳性。在 EORTC B0 患者中,11/221 例(5%)FCI 阳性(假阴性),在 EORTC B1 患者中,57/57 例(100%)FCI 阴性(假阳性)。对于 FCI 阳性的 MF/SS 细胞患者,EORTC/ISCL 方法与 FCI 方法之间存在总体极好的相关性(r = 0.999,p < 0.001);然而,有 4 例(6.5%)患者的 B 期会在 B0 和 B1 之间发生改变。

结论

ICCS 推荐的使用免疫表型异常的 MF/SS 细胞定量方法可以将 MF/SS 细胞与背景良性 T 细胞区分开来,并实现更准确的分期,特别是对于目前被认为患有 B0 和 B1 期疾病的患者。

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