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肿瘤相关巨噬细胞与经典型霍奇金淋巴瘤患者临床结局无关。

Lack of association of tumor-associated macrophages with clinical outcome in patients with classical Hodgkin's lymphoma.

机构信息

Department of Hematology, Postgraduate Program in Internal Medicine, School of Medicine, Federal University of Rio de Janeiro, Rio de Janeiro, Brazil.

Department of Pathology, Stanford University School of Medicine, Stanford, USA.

出版信息

Ann Oncol. 2012 Mar;23(3):736-742. doi: 10.1093/annonc/mdr157. Epub 2011 May 20.

DOI:10.1093/annonc/mdr157
PMID:21602260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3331732/
Abstract

BACKGROUND

A recent study demonstrated that an increased number of CD68+ macrophages were correlated with primary treatment failure, shortened progression-free survival (PFS) and disease-specific survival (DSS) in patients with classical Hodgkin's lymphoma (cHL).

PATIENTS AND METHODS

The aim of the present study was to verify the relationship between the number of CD68+ and CD163+ macrophages with clinical outcomes in a cohort of 265 well-characterized patients with cHL treated uniformly with the standard doxorubicin, bleomycin, vinblastine and dacarbazine chemotherapy regimen. Two pairs of hematopathologists carried out independent pathological evaluations of tissue microarray slides.

RESULTS

There were no associations between clinical characteristics and the expression of CD68 or CD163. However, higher levels of CD68 and CD163 expression were correlated with the presence of Epstein-Barr virus-positive Hodgkin tumor cells (P = 0.01 and 0.037, respectively). The expression of CD68 or CD163 was not associated with either the PFS or the DSS.

CONCLUSION

CD68 and CD163 expression require further evaluation before their use can be recommended for prognostic stratification of patients with cHL.

摘要

背景

最近的一项研究表明,在经典霍奇金淋巴瘤(cHL)患者中,CD68+巨噬细胞数量的增加与初次治疗失败、无进展生存期(PFS)和疾病特异性生存期(DSS)缩短相关。

患者和方法

本研究的目的是在 265 例经标准多柔比星、博来霉素、长春碱和达卡巴嗪化疗方案治疗的 cHL 患者队列中,验证 CD68+和 CD163+巨噬细胞数量与临床结局的关系。两名配对的血液病理学家对组织微阵列载玻片进行了独立的病理评估。

结果

CD68 或 CD163 的表达与临床特征之间没有关联。然而,CD68 和 CD163 的高表达与 EBV 阳性霍奇金肿瘤细胞的存在相关(P=0.01 和 0.037)。CD68 或 CD163 的表达与 PFS 或 DSS 均无相关性。

结论

CD68 和 CD163 的表达需要进一步评估,然后才能推荐其用于 cHL 患者的预后分层。

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本文引用的文献

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Tumor-infiltrating macrophages correlate with adverse prognosis and Epstein-Barr virus status in classical Hodgkin's lymphoma.肿瘤浸润巨噬细胞与经典型霍奇金淋巴瘤的不良预后和 Epstein-Barr 病毒状态相关。
Haematologica. 2011 Feb;96(2):269-76. doi: 10.3324/haematol.2010.031542. Epub 2010 Nov 11.
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Hematology. Are macrophages the bad guys in Hodgkin lymphoma?血液学。巨噬细胞是霍奇金淋巴瘤的“坏人”吗?
Nat Rev Clin Oncol. 2010 Jun;7(6):301-2. doi: 10.1038/nrclinonc.2010.71.
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Toward a personalized treatment of Hodgkin's disease.迈向霍奇金淋巴瘤的个性化治疗。
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Tumor-associated macrophages and survival in classic Hodgkin's lymphoma.肿瘤相关巨噬细胞与经典型霍奇金淋巴瘤患者的生存情况
N Engl J Med. 2010 Mar 11;362(10):875-85. doi: 10.1056/NEJMoa0905680.
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Human germinal center-associated lymphoma protein expression is associated with improved failure-free survival in Brazilian patients with classical Hodgkin lymphoma.人胚中心相关淋巴瘤蛋白表达与巴西经典型霍奇金淋巴瘤患者无失败生存改善相关。
Leuk Lymphoma. 2009 Nov;50(11):1830-6. doi: 10.3109/10428190903242628.
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Latent Epstein-Barr virus infection of tumor cells in classical Hodgkin's lymphoma predicts adverse outcome in older adult patients.经典型霍奇金淋巴瘤中肿瘤细胞的潜伏性EB病毒感染预示老年患者预后不良。
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Biologic features of Hodgkin lymphoma and the development of biologic prognostic factors in Hodgkin lymphoma: tumor and microenvironment.霍奇金淋巴瘤的生物学特征及霍奇金淋巴瘤生物学预后因素的发展:肿瘤与微环境
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Expression of the Epstein-Barr virus-encoded Epstein-Barr virus nuclear antigen 1 in Hodgkin's lymphoma cells mediates Up-regulation of CCL20 and the migration of regulatory T cells.爱泼斯坦-巴尔病毒编码的爱泼斯坦-巴尔病毒核抗原1在霍奇金淋巴瘤细胞中的表达介导CCL20的上调及调节性T细胞的迁移。
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Early, intermediate and advanced Hodgkin's lymphoma: modern treatment strategies.早期、中期和晚期霍奇金淋巴瘤:现代治疗策略
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Immunohistochemical prognostic markers in diffuse large B-cell lymphoma: validation of tissue microarray as a prerequisite for broad clinical applications--a study from the Lunenburg Lymphoma Biomarker Consortium.弥漫性大B细胞淋巴瘤中的免疫组织化学预后标志物:组织芯片作为广泛临床应用前提条件的验证——来自吕嫩堡淋巴瘤生物标志物联盟的一项研究
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