Department of Radiotherapy, University Hospital Son Espases, Palma de Mallorca, Balearic Islands, Spain.
Blood. 2012 Jun 21;119(25):6072-9. doi: 10.1182/blood-2011-11-394627. Epub 2012 Apr 30.
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.
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。