Orditura Michele, De Vita Ferdinando, Muto Paolo, Vitiello Fabiana, Murino Paola, Lieto Eva, Vecchione Loredana, Romano Anna, Martinelli Erika, Renda Andrea, Ferraraccio Francesca, Del Genio Alberto, Ciardiello Fortunato, Galizia Gennaro
Division of Medical Oncology, F. Magrassi-A. Lanzara Department of Clinical and Experimental Medicine and Surgery, Second University of Naples School of Medicine, c/o II Policlinico, Via Pansini 5, Naples, Italy.
Arch Surg. 2010 Mar;145(3):233-8. doi: 10.1001/archsurg.2010.2.
Adjuvant chemoradiotherapy does not represent the standard of care in patients with resected high-risk gastric cancer; however, results from phase 2 and randomized trials suggest improvement in overall survival. We assessed the feasibility and toxic effects of chemoradiotherapy as adjuvant treatment in locally advanced gastric cancer.
Pilot study.
University hospital.
Twenty-nine patients with T4N+ or any TN23 gastric cancer previously treated with potentially curative surgery were enrolled. All of the patients received combined adjuvant chemotherapy with FOLFOX-4 (ie, a combination of folinic acid [leucovorin], fluorouracil, and oxaliplatin [Eloxatin]) for 8 cycles and concomitant radiotherapy (45 Gy in 25 daily fractions over 5 weeks). Radiotherapy was begun after the first 2 cycles of FOLFOX-4, which was reduced by 25% during the period of concomitant radiotherapy.
Treatment toxic effects according to the National Cancer Institute-Common Toxicity Criteria classification, overall and disease-free survival rates, and identification of prognostic indicators.
All of the patients completed treatment. Severe hematologic and gastrointestinal toxic effects occurred in 10% and 33%, respectively. No acute hepatic or renal toxic effects were observed; 1 patient experienced severe neurotoxicity. Disease-free and overall survival rates at 1, 2, and 3 years were 79%, 35%, and 35% and 85%, 62.6%, and 50.1%, respectively, and were shown to be substantially better than those observed in untreated patients. Long-term outcome was related to TNM stage, basal serum tumor marker level, and, particularly, lymph node ratio.
A multimodal approach with FOLFOX-4 and radiotherapy is feasible and effective for the treatment of patients with resected high-risk gastric cancer.
辅助放化疗并非已切除的高危胃癌患者的标准治疗方案;然而,2期试验和随机试验结果提示总生存期有所改善。我们评估了放化疗作为局部进展期胃癌辅助治疗的可行性和毒性作用。
前瞻性研究。
大学医院。
纳入29例曾接受根治性手术治疗的T4N+或任何TN23期胃癌患者。所有患者接受FOLFOX-4辅助化疗(即亚叶酸钙、氟尿嘧啶和奥沙利铂[乐沙定]联合)8个周期,并同步放疗(5周内每日1次,共25次,总剂量45 Gy)。放疗在FOLFOX-4的前2个周期后开始,在同步放疗期间FOLFOX-4剂量减少25%。
根据美国国立癌症研究所通用毒性标准分类的治疗毒性作用、总生存率和无病生存率,以及预后指标的确定。
所有患者均完成治疗。严重血液学和胃肠道毒性作用分别发生在10%和33%的患者中。未观察到急性肝或肾毒性作用;1例患者出现严重神经毒性。1年、2年和3年的无病生存率和总生存率分别为79%、35%、35%和85%、62.6%、50.1%,且显著优于未治疗患者。长期预后与TNM分期、基础血清肿瘤标志物水平,特别是淋巴结比率有关。
FOLFOX-4联合放疗的多模式治疗方法对于已切除的高危胃癌患者的治疗是可行且有效的。