Department of Hematology-Oncology, Ajou University School of Medicine, Suwon, 443-721, Republic of Korea.
Dig Dis Sci. 2011 Jan;56(1):131-8. doi: 10.1007/s10620-010-1280-8. Epub 2010 May 26.
Platinum and 5-fluorouracil (5-FU)-based regimens have been used the most frequently in palliative chemotherapy for gastric cancer. The present study evaluated the prognostic significance of Bax, excision repair cross-complementation group 1 (ERCC1), and thymidylate synthase (TS) in advanced gastric cancer patients treated with 5-FU, leucovorin, and oxaliplatin (FOLFOX) palliative chemotherapy.
Seventy-two patients with metastatic or recurrent gastric cancer were treated with FOLFOX regimen. Pretreatment tumor biopsy specimens were analyzed for Bax, ERCC1, and TS expression by immunohistochemistry.
High expression of Bax, ERCC1, and TS was observed in 31 (43%), 33 (46%), and 35 (49%) patients, respectively. The median overall survival (OS) of patients was 12 months. Low expression of Bax was associated with poor OS (median, 9 months vs. 18 months; 2-year, 10% vs. 48%; p=0.0005) in univariate analysis, while expression of ERCC1 and TS was not correlated with patient outcome. In multivariate analysis, low expression of Bax was a significant independent predictor of poor OS (p=0.028). Low expression of Bax was significantly associated with poor survival of patients with metastatic or recurrent gastric cancer treated with FOLFOX chemotherapy.
Immunohistochemical staining for Bax with pretreatment biopsy specimen may be useful in selecting FOLFOX regimen as a treatment option for advanced gastric cancer patients.
铂类和 5-氟尿嘧啶(5-FU)为基础的方案已被广泛应用于胃癌的姑息化疗。本研究评估了 Bax、切除修复交叉互补基因 1(ERCC1)和胸苷酸合成酶(TS)在接受氟尿嘧啶、亚叶酸钙和奥沙利铂(FOLFOX)姑息化疗的晚期胃癌患者中的预后意义。
72 例转移性或复发性胃癌患者接受 FOLFOX 方案治疗。采用免疫组织化学法检测预处理肿瘤活检标本中 Bax、ERCC1 和 TS 的表达。
31(43%)、33(46%)和 35(49%)例患者 Bax、ERCC1 和 TS 的高表达率分别为 31、33 和 35。患者的中位总生存期(OS)为 12 个月。单因素分析显示,Bax 低表达与较差的 OS 相关(中位 OS:9 个月 vs. 18 个月;2 年生存率:10% vs. 48%;p=0.0005),而 ERCC1 和 TS 的表达与患者预后无关。多因素分析显示,Bax 低表达是 OS 不良的独立预测因素(p=0.028)。Bax 低表达与转移性或复发性胃癌患者接受 FOLFOX 化疗后的不良生存显著相关。
采用预处理活检标本进行 Bax 的免疫组织化学染色可能有助于选择 FOLFOX 方案作为晚期胃癌患者的治疗选择。