Comprehensive Assessment of CD19 Immunohistochemical Staining in Classic Hodgkin Lymphoma.

IF 4.2 1区 医学 Q1 PATHOLOGY
American Journal of Surgical Pathology Pub Date : 2026-05-01 Epub Date: 2026-03-10 DOI:10.1097/PAS.0000000000002519
Sarah R Helman, Fikru Merechi, Hanan Alharthy, Rima Koka, Seung Tae Lee, Aaron P Rapoport, Jennie Y Law, Michael E Kallen
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引用次数: 0

Abstract

Classic Hodgkin Lymphoma (CHL) remains difficult to treat in patients with relapsed and refractory disease. The utility of immunotherapies, many of which target B-cell markers, is still under investigation. Although the neoplastic Hodgkin and Reed-Sternberg (HRS) cells are thought to lose most B-cell markers, studies have shown retention of these markers, mainly CD20, in some cases. However, the CD19 staining profile of HRS cells has not been thoroughly assessed and warrants exploration in the era of CD19-directed immunotherapies. We assessed CD19 immunohistochemical staining in 41 cases of CHL and correlated with histologic subtype, other markers, and clinical parameters. 13/41 cases (31.7%) demonstrated CD19 staining in HRS cells, with variation in staining pattern and intensity. When compared with CD19-negative cases, CD19 positivity correlated significantly with mixed-cellularity subtype (53.8% vs. 7.1%, P =0.002), CD20 (46.2% vs. 14.3%, P =0.0485), CD79a (53.8% vs. 9.1%, P =0.006), Epstein-Barr Virus (EBV) positivity (53.8% vs. 7.1%, P =0.002), and older age (median age 52 vs. 28.5 y, P =0.0006). 7/9 (77.8%) EBV+ cases demonstrated CD19 expression on HRS cells. By Kaplan-Meier analysis, CD19+ cases demonstrated worse overall survival compared with CD19- cases ( P =0.011), with EBV-, CD19- cases demonstrating the best overall survival. On the basis of these findings, CD19 expression on HRS cells should not preclude the pathologic diagnosis of CHL, particularly in the context of mixed-cellularity or EBV+ disease. In addition, older patients with mixed-cellularity and/or EBV+ disease may represent a subgroup of patients with CHL who could benefit from CD19-directed therapies.

CD19免疫组化染色在经典霍奇金淋巴瘤中的综合评价。
经典霍奇金淋巴瘤(CHL)在复发和难治性疾病患者中仍然难以治疗。免疫疗法的效用,其中许多靶向b细胞标记物,仍在研究中。虽然肿瘤霍奇金和里德-斯特恩伯格(HRS)细胞被认为失去了大多数b细胞标记物,但研究表明,在某些情况下,这些标记物主要是CD20。然而,HRS细胞的CD19染色谱尚未被彻底评估,在CD19定向免疫治疗时代值得探索。我们评估了41例CHL患者的CD19免疫组织化学染色,并将其与组织学亚型、其他标志物和临床参数相关联。13/41例(31.7%)HRS细胞CD19染色,染色模式和染色强度不同。与CD19阴性病例相比,CD19阳性与混合细胞亚型(53.8% vs. 7.1%, P=0.002)、CD20 (46.2% vs. 14.3%, P=0.0485)、CD79a (53.8% vs. 9.1%, P=0.006)、eb病毒(EBV)阳性(53.8% vs. 7.1%, P=0.002)和年龄(中位年龄52 vs. 28.5岁,P=0.0006)显著相关。7/9 (77.8%) EBV+病例在HRS细胞上表达CD19。Kaplan-Meier分析显示,CD19+患者的总生存期较CD19-患者差(P=0.011), EBV-、CD19-患者的总生存期最佳。基于这些发现,CD19在HRS细胞上的表达不应排除CHL的病理诊断,特别是在混合细胞性或EBV+疾病的背景下。此外,患有混合细胞性和/或EBV+疾病的老年患者可能代表可以从cd19定向治疗中获益的CHL患者亚组。
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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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