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