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COX-2 在 Reed-Sternberg 细胞中的表达是 ABVD 方案治疗的霍奇金淋巴瘤的一个独立的不良预后因素。

Expression of COX-2 on Reed-Sternberg cells is an independent unfavorable prognostic factor in Hodgkin lymphoma treated with ABVD.

机构信息

Department of Radiotherapy, University Hospital Son Espases, Palma de Mallorca, Balearic Islands, Spain.

出版信息

Blood. 2012 Jun 21;119(25):6072-9. doi: 10.1182/blood-2011-11-394627. Epub 2012 Apr 30.

Abstract

Cyclooxygenase 2 (COX-2) is an inflammatory enzyme involved in the pathogenesis and prognosis of several malignancies. In the present study, we investigated the prognostic value of COX-2 expression in a large (N = 242), uniformly treated Hodgkin lymphoma (HL) population from the Spanish Network of HL using tissue microarrays. Univariate and multivariate analysis was done, including comparing the most recognized clinical variables: the early- and advanced-stage subgroups. COX-2 was expressed on Reed-Sternberg cells in 37% of patients. There were no differences in the distribution of clinical variables according to COX-2 expression. With a median follow-up time of 58 months, PFS at 5 years was 60% and 79% for COX-2(+) and COX-2(-) patients, respectively (P = .003). The overall survival was 73% and 91%, respectively (P < .001). The major impact on prognosis was observed in the early AA stage (I-II) group. In fact, in these low-risk groups the expression of COX-2 defined a group with significantly worse progression-free and overall survival. In conclusion, COX-2 was expressed on Reed-Sternberg cells in one-third of HL patients and was a major independent, unfavorable prognostic factor in early-stage HL. We conclude that COX-2 may be a major prognostic variable in HL and a potential therapeutic target.

摘要

环氧化酶 2(COX-2)是一种参与多种恶性肿瘤发病机制和预后的炎症酶。在本研究中,我们使用组织微阵列研究了来自西班牙霍奇金淋巴瘤网络的 242 例大型、统一治疗的霍奇金淋巴瘤(HL)患者中 COX-2 表达的预后价值。进行了单变量和多变量分析,包括比较最公认的临床变量:早期和晚期亚组。COX-2 在 37%的患者的 Reed-Sternberg 细胞上表达。根据 COX-2 表达,临床变量的分布没有差异。在中位随访时间为 58 个月时,COX-2(+)和 COX-2(-)患者的 5 年无进展生存率(PFS)分别为 60%和 79%(P =.003)。总生存率分别为 73%和 91%(P <.001)。预后的主要影响因素是早期 AA 期(I-II)组。事实上,在这些低危组中,COX-2 的表达定义了一组无进展生存和总生存明显较差的患者。总之,COX-2 在三分之一的 HL 患者的 Reed-Sternberg 细胞上表达,是早期 HL 的主要独立不良预后因素。我们得出结论,COX-2 可能是 HL 的主要预后变量和潜在的治疗靶点。

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