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PD-L1、PD-L2、CD30、CD23和BCL-6在原发纵隔大B细胞淋巴瘤诊断和预后评估中的应用价值
引用本文:袁婷,曹铮,刘秀云,郑波,冯晓莉.PD-L1、PD-L2、CD30、CD23和BCL-6在原发纵隔大B细胞淋巴瘤诊断和预后评估中的应用价值[J].肿瘤防治研究,2021,48(10):941-946.
作者姓名:袁婷  曹铮  刘秀云  郑波  冯晓莉
作者单位:100021 北京,国家癌症中心/国家肿瘤临床医学研究中心/中国医学科学院北京协和医学院肿瘤医院病理科
摘    要:目的 探讨治疗相关标志物PD-L1、PD-L2、CD30、CD23、BCL-2、BCL-6、MUM1和GATA3在原发纵隔大B细胞淋巴瘤(PMBL)诊断和预后评估中的应用价值。方法 收集PMBL的34例患者进行回顾性研究,31例非纵隔原发的非特指型弥漫性大B细胞淋巴瘤(DLBCL-NOS)作为对照组,免疫组织化学染色方法检测8种蛋白的表达情况。结果 PD-L1、PD-L2和CD30在PMBL组阳性肿瘤细胞百分比的中位数分别为70%(30%, 90%)、25%(0, 70%)和17.5%(0, 60%),显著高于DLBCL-NOS组,差异有统计学意义(P<0.05);CD30和CD23在PMBL组的阳性率分别为61.76%(21/34)和76.47%(26/34),与DLBCL-NOS组之间差异有统计学意义(P=0.000)。伴有CD30或BCL-6表达的PMBL患者生存曲线尽管P>0.05,仍显示出预后差的趋势。结论 PMBL中PD-L1、PD-L2和CD30的表达水平较高,有助于精准识别更多可能对免疫或靶向治疗有反应的患者。免疫组织化学标记PD-L1、PD-L2、CD30和CD23有助于PMBL与DLBCL-NOS鉴别诊断。CD30和BCL-6作为PMBL的候选预后指标应该在更大量的样本中进一步研究。

关 键 词:淋巴瘤  纵隔  免疫组织化学  PD-L1  PD-L2  CD30  CD23  BCL-6  
收稿时间:2021-03-19

Application of PD-L1, PD-L2, CD30, CD23 and BCL-6 in Diagnosis and PrognosticEvaluation of Primary Mediastinal Large B-cell Lymphoma
YUAN Ting,CAO Zheng,LIU Xiuyun,ZHENG Bo,FENG Xiaoli.Application of PD-L1, PD-L2, CD30, CD23 and BCL-6 in Diagnosis and PrognosticEvaluation of Primary Mediastinal Large B-cell Lymphoma[J].Cancer Research on Prevention and Treatment,2021,48(10):941-946.
Authors:YUAN Ting  CAO Zheng  LIU Xiuyun  ZHENG Bo  FENG Xiaoli
Affiliation:Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China
Abstract:Objective To explore the application value of treatment-related markers PD-L1, PD-L2, CD30, CD23, BCL-2, BCL-6, MUM1 and GATA3 in the diagnosis and prognostic evaluation of primary mediastinal B-cell lymphoma(PMBL). Methods A retrospective study was conducted on 34 patients diagnosed with PMBL, and 31 patients with DLBCL-NOS which was not primary in the mediastinum were taken as control group. The expressions of 8 proteins were detected by IHC staining. Results The median percentages of tumor cells with PD-L1, PD-L2 and CD30 expression in PMBL group were 70% (30%, 90%), 25% (0, 70%) and 17.5% (0, 60%) respectively, which were significantly higher than those in the DLBCL-NOS group (P<0.05). The positive rates of CD30 and CD23 in PMBL group were 61.76% (21/34) and 76.47% (26/34) respectively, significantly different with those in the DLBCL-NOS group (P=0.000). The survival curve of PMBL patients with CD30 or BCL-6 expression showed a trend of poor prognosis, despite the P value was >0.05. Conclusion The high expression levels of PD-L1, PD-L2 and CD30 in PMBL are helpful to accurately identify more patients who may respond to immune or targeted therapy. Immunohistochemical staining of PD-L1, PD-L2, CD30 and CD23 is helpful for the differential diagnosis of PMBL and DLBCL-NOS. As candidate prognostic indicators of PMBL, CD30 and BCL-6 should be further studied in a larger number of samples.
Keywords:Lymphoma  Mediastinum  Immunohistochemistry  PD-L1  PD-L2  CD30  CD23  BCL-6  
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