Department of Clinical Therapeutics, University of Athens School of Medicine, Athens, Greece.
Cancer Chemother Pharmacol. 2010 May;65(6):1009-21. doi: 10.1007/s00280-010-1256-6. Epub 2010 Feb 4.
The optimal adjuvant treatment for gastric cancer remains controversial. We compared the efficacy of a docetaxel and platinum adjuvant chemotherapy regimen, in patients with high-risk gastric cancer, with that of the same chemotherapy plus radiation therapy (RT). In addition, we evaluated the prognostic and/or predictive value of a panel of molecular markers. Patients with histologically proven, radically resected gastric cancer, stage > or =T3 and/or N+ were randomized to 6 cycles of docetaxel with cisplatin, both at 75 mg/m2 every 3 weeks (arm A) or the same treatment with RT (arm B; 45 Gy). Due to excessive nausea and vomiting, cisplatin was substituted by carboplatin at AUC (area under the curve) of 5 after the first 45 patients (22 group A, 23 group B). The prognostic value of EGFR, ERCC1, HER2, MET/HGFR, MAP-Tau, and PTEN expression was also studied in a subset of 67 patients using immunohistochemistry on tissue microarrays (TMAs). A total of 147 patients were randomized. After a median follow-up of 53.7 months, no differences in overall (OS) and disease-free survival (DFS) were found between the two arms. The most common grade 3/4 toxicities for arms A and B (excluding alopecia) were non-febrile neutropenia (11 and 17%, respectively), febrile neutropenia (9 and 7%) and diarrhea (7 and 4%, respectively). Patients with ERCC1 positive tumors had significantly longer median DFS (33.1 vs. 11.8 months, Wald P = 0.016) and OS (63.2 vs. 18.8 months, Wald P = 0.046). Our results indicate that the addition of RT to platinum/docetaxel adjuvant chemotherapy does not appear to improve survival in high-risk, radically resected gastric cancer. However, the possibility that a benefit by the addition of RT was not detected due to decreased power of the study should not be excluded.
胃癌的最佳辅助治疗仍存在争议。我们比较了高风险胃癌患者接受多西紫杉醇和铂类辅助化疗方案与相同化疗加放疗(RT)的疗效。此外,我们还评估了一组分子标志物的预后和/或预测价值。患者为组织学证实的、根治性切除的胃癌,分期>或=T3 和/或 N+,随机分为 6 个周期的多西紫杉醇联合顺铂,均为 75mg/m2,每 3 周一次(A 组)或相同治疗加 RT(B 组;45Gy)。由于恶心和呕吐过多,在前 45 例患者(A 组 22 例,B 组 23 例)后,顺铂被卡铂替代,曲线下面积(AUC)为 5。使用组织微阵列(TMA)上的免疫组织化学对 67 例患者的一组进行了 EGFR、ERCC1、HER2、MET/HGFR、MAP-Tau 和 PTEN 表达的预后价值研究。共随机分配了 147 例患者。中位随访 53.7 个月后,两组患者的总生存期(OS)和无病生存期(DFS)无差异。A 组和 B 组最常见的 3/4 级毒性(不包括脱发)为非发热性中性粒细胞减少症(分别为 11%和 17%)、发热性中性粒细胞减少症(分别为 9%和 7%)和腹泻(分别为 7%和 4%)。ERCC1 阳性肿瘤患者的中位 DFS(33.1 个月 vs. 11.8 个月,Wald P = 0.016)和 OS(63.2 个月 vs. 18.8 个月,Wald P = 0.046)显著延长。我们的结果表明,在高风险、根治性切除的胃癌中,RT 联合铂类/多西紫杉醇辅助化疗似乎并不能提高生存率。然而,由于研究效能降低,不能排除 RT 增加可能没有检测到获益的可能性。