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首页> 外文期刊>British Journal of Cancer >Adjuvant chemotherapy for oesophagogastric cancer with epirubicin, cisplatin and infusional 5-fluorouracil (ECF): a Royal Marsden pilot study
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Adjuvant chemotherapy for oesophagogastric cancer with epirubicin, cisplatin and infusional 5-fluorouracil (ECF): a Royal Marsden pilot study

机译:联合表柔比星,顺铂和输注5-氟尿嘧啶(ECF)的食管胃癌辅助化疗:Royal Marsden试点研究

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Previous trials of adjuvant chemotherapy for oesophagogastric cancer have shown only modest or no improvement in survival. However, the regimens used in these studies produce low response rates in patients with advanced disease. ECF is a new regimen which results in higher response rates and may therefore be more effective in the adjuvant setting. Twenty-nine patients who had undergone a potentially curative resection for oesphagogastric carcinoma were treated with ECF [epirubicin 50 mg m-2 and cisplatin 60 mg m-2 for 18 weeks]. The median age was 52.5 years. Three patients had oesophageal tumours, 14 had tumours of the oesophagogastric junction (OGJ) and 12 had gastric tumours. All were adenocarcinomas apart from one undifferentiated carcinoma. One patient had stage I disease, nine stage II, 17 stage II and two stage IV. The mean number of chemotherapy cycles per patient was 5.2 (range 2-8). The median follow-up was 8.4 months (1.5-36.3 months). Eleven patients relapsed during follow-up (38%). One patient had an anastomotic recurrence and ten patients distant metastases. Overall 3 year survival was 61.5% (95% confidence interval 42-79); 3 year survival in stage II was 50% (21.2-86.3) and in stage III 65.6% (40-86). Chemotherapy was well tolerated, with grade 3/4 toxicity as follows: leucopenia 13.5%, nausea and vomiting 10%, diarrhoea 3.5%, infection 3.5% and thrombocytopenia 3.5%. There were no treatment-related deaths. We conclude that ECF can be administered safely as adjuvant treatment to patients with surgically resected gastro-oesophageal carcinoma. The results, especially in patients with stage III disease, are encouraging and support the investigation of this regimen within a prospective randomised trial.
机译:食管胃癌辅助化疗的先前试验表明,生存率仅改善或无改善。但是,这些研究中使用的方案对晚期疾病患者的应答率较低。 ECF是一种新方案,可导致更高的应答率,因此在佐剂治疗中可能更有效。二十九例接受食管胃癌根治性切除术的患者接受了ECF治疗[阿霉素50 mg m-2和顺铂60 mg m-2 18周]。中位年龄是52.5岁。 3例患有食道肿瘤,14例患有食管胃交界处(OGJ)肿瘤,12例患有胃肿瘤。除一种未分化癌外,其余均为腺癌。一名患者患有I期疾病,九名处于II期,17处于II期和两个IV期。每位患者的平均化疗周期数为5.2(范围2-8)。中位随访时间为8.4个月(1.5-36.3个月)。随访期间11例患者复发(38%)。 1例患者发生吻合口复发,10例患者发生远处转移。 3年总生存率为61.5%(95%置信区间42-79); II期的3年生存率为50%(21.2-86.3),III期的65.6%(40-86)。化学疗法耐受良好,其毒性为3/4级,如下:白细胞减少症13.5%,恶心和呕吐10%,腹泻3.5%,感染3.5%和血小板减少症3.5%。没有与治疗有关的死亡。我们得出结论,ECF可以安全地作为手术切除的胃食管癌患者的辅助治疗药物。该结果,特别是在III期疾病患者中,令人鼓舞,并支持在前瞻性随机试验中对该方案的研究。

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