Winter Jane N, Li Shuli, Aurora Vikas, Variakojis Daina, Nelson Beverly, Krajewska Maryla, Zhang Lijun, Habermann Thomas M, Fisher Richard I, Macon William R, Chhanabhai Mukesh, Felgar Raymond E, Hsi Eric D, Medeiros L Jeffrey, Weick James K, Weller Edie A, Melnick Ari, Reed John C, Horning Sandra J, Gascoyne Randy D
Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Clin Cancer Res. 2010 Apr 15;16(8):2435-42. doi: 10.1158/1078-0432.CCR-09-1219. Epub 2010 Apr 6.
To prospectively investigate the prognostic significance of p21 and p53 expression in diffuse large B-cell lymphoma in the context of the U.S. Intergroup trial comparing conventional cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy to rituximab-CHOP (R-CHOP) induction, with or without maintenance rituximab.
Immunohistochemical staining of 197 paraffin-embedded biopsy specimens was scored by an independent panel of experts.
The cyclin-dependent kinase inhibitor, p21, was expressed in 55% of cases examined. In a multivariable analysis adjusting for International Prognostic Index score and BCL2 status, p21 expression was a significant, independent, favorable predictive factor for failure-free survival (relative risk, 0.3; P = 0.001) and overall survival (relative risk, 0.3; P = 0.003) for patients treated with R-CHOP. Expression of p21 was not predictive of outcome for CHOP-treated patients. Only p21-positive cases benefited from the addition of rituximab to CHOP. Among p21-positive patients, treatment with R-CHOP was associated with a higher failure-free survival rate at 5 years compared with CHOP (61% versus 24%; P = 0.01). In contrast, no significant differences were detected in failure-free survival according to treatment arm for p21-negative patients. Expression of p53, alone or in combination with p21, did not predict for outcome in univariable or multivariable analyses.
In this study, p21 protein expression emerged as an important independent predictor of a favorable clinical outcome when rituximab was added to CHOP therapy. These data suggest that rituximab-related effects on lymphoma survival pathways may be functionally linked to p21 activity.
在美国一项多中心试验的背景下,前瞻性研究p21和p53表达在弥漫性大B细胞淋巴瘤中的预后意义。该试验比较了传统的环磷酰胺、阿霉素、长春新碱和泼尼松(CHOP)化疗与利妥昔单抗-CHOP(R-CHOP)诱导化疗,以及是否联合维持性利妥昔单抗治疗。
由一个独立的专家小组对197份石蜡包埋活检标本进行免疫组织化学染色评分。
在检测的病例中,55%表达细胞周期蛋白依赖性激酶抑制剂p21。在一项针对国际预后指数评分和BCL2状态进行校正的多变量分析中,p21表达是接受R-CHOP治疗患者无进展生存期(相对风险,0.3;P = 0.001)和总生存期(相对风险,0.3;P = 0.003)的显著、独立、有利预测因素。p21表达对接受CHOP治疗的患者的预后无预测价值。只有p21阳性的病例从CHOP方案中添加利妥昔单抗中获益。在p21阳性患者中,与CHOP相比,R-CHOP治疗的5年无进展生存率更高(61%对24%;P = 0.01)。相比之下,p21阴性患者根据治疗组的无进展生存期未检测到显著差异。在单变量或多变量分析中,p53单独或与p21联合表达均不能预测预后。
在本研究中,当利妥昔单抗加入CHOP治疗时,p21蛋白表达成为有利临床结果的重要独立预测因素。这些数据表明,利妥昔单抗对淋巴瘤生存途径的相关作用可能在功能上与p21活性相关。