Hattinger Claudia Maria, Michelacci Francesca, Sella Federica, Magagnoli Giovanna, Benini Stefania, Gambarotti Marco, Palmerini Emanuela, Picci Piero, Serra Massimo, Ferrari Stefano
Laboratory of Experimental Oncology, Orthopaedic Rizzoli Institute, Bologna, Italy.
Anatomy and Pathological Histology, Orthopaedic Rizzoli Institute, Bologna, Italy.
Histopathology. 2015 Sep;67(3):338-47. doi: 10.1111/his.12653. Epub 2015 Mar 5.
To evaluate the clinical impact of excision repair cross-complementation group 1 (ERCC1) expression in high-grade osteosarcoma (OS).
Immunohistochemistry was performed on biopsies from 99 OS patients enrolled in the ISG/OS-Oss training set or ISG/SSG1 validation set neoadjuvant chemotherapy protocols, based on the use of cisplatin, adriamycin, methotrexate, and ifosfamide. In the training set, ERCC1 positivity was found in eight of 31 (26%) patients, and was significantly associated with worse event-free survival (EFS) (P = 0.042) and overall survival (OVS) (P = 0.001). In the validation set, ERCC1 positivity was found in 22 of 68 (32%) patients, and its significant associations with poorer EFS (P = 0.028) and OVS (P = 0.022) were confirmed. Multivariate analyses performed on the whole patient series indicated that ERCC1 positivity was the only marker that was significantly associated with a higher risk of worse prognosis, in terms of both EFS and OVS (P = 0.013). Co-evaluation of ERCC1 and ABCB1 expression showed that patients who were positive for both markers had a significantly worse prognosis.
The ERCC1 level at diagnosis is predictive for the outcome of patients with non-metastatic, high-grade OS treated with neoadjuvant chemotherapy, and co-evaluation with ABCB1 can identify high-risk groups of OS patients who are refractory to standard regimens.
评估切除修复交叉互补基因1(ERCC1)表达在高级别骨肉瘤(OS)中的临床影响。
对99例参加ISG/OS-Oss训练集或ISG/SSG1验证集新辅助化疗方案的骨肉瘤患者的活检组织进行免疫组化分析,这些方案使用顺铂、阿霉素、甲氨蝶呤和异环磷酰胺。在训练集中,31例患者中有8例(26%)ERCC1呈阳性,且与无事件生存期(EFS)较差显著相关(P = 0.042),与总生存期(OS)较差也显著相关(P = 0.001)。在验证集中,68例患者中有22例(32%)ERCC1呈阳性,其与较差的EFS(P = 0.028)和OS(P = 0.022)的显著相关性得到证实。对整个患者系列进行的多变量分析表明,就EFS和OS而言,ERCC1阳性是唯一与预后较差风险较高显著相关的标志物(P = 0.013)。ERCC1和ABCB1表达的联合评估显示,两种标志物均为阳性的患者预后明显较差。
诊断时的ERCC1水平可预测接受新辅助化疗的非转移性高级别骨肉瘤患者的预后,与ABCB1联合评估可识别对标准方案难治的骨肉瘤高危患者群体。