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首页> 外文期刊>Journal of chemotherapy >Postoperative chemotherapy in resected gastric cancer: results of a single center experience.
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Postoperative chemotherapy in resected gastric cancer: results of a single center experience.

机译:切除性胃癌的术后化疗:单中心经验的结果。

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Gastric cancer remains a major health problem despite its decline in incidence in Western countries. Although radical surgery represents the primary curative option for gastric cancer patients, most of them relapse and die due to their disease despite an R0 resection. At present the routine use of postoperative adjuvant therapy to reduce disease recurrence is still considered an investigational approach. Out of a total of 275 patients (stage IB through IV M0 AJCC/UICC) who underwent surgery for gastric cancer at our Surgery Unit between 1993 and 2001, 156 were eligible for adjuvant chemotherapy, of whom only 52 accepted to undergo this treatment. This group of patients was retrospectively compared with a control group (1:2) and overall survival was assessed using hazard ratio and Kaplan-Meier estimates. Five-year survival was 40% in the chemotherapy group and 37.8% in the group which underwent surgery alone. Indeed, chemotherapy did not reduce the risk of death (HR 0.87, 95% CI = 0.57-1.34, p=0.54). Serosal involvement and the invasion of more than 6 lymph nodes were the main independent prognostic factors identified by multivariate analysis. The current study did not show a clear advantage of chemotherapy over surgery alone. However, our results can help to define strategies for future clinical trials with the use of new regimens based on more effective and less toxic drugs.
机译:尽管在西方国家胃癌的发病率下降,但它仍然是一个主要的健康问题。尽管根治性手术是胃癌患者的主要治疗选择,但尽管进行了R0切除,但大多数患者仍会复发并死于疾病。目前,常规的术后辅助治疗以减少疾病复发仍被认为是一种研究方法。在1993年至2001年之间,在我们的手术室接受胃癌手术的275例患者(IB期至IV M0 AJCC / UICC期)中,有156例符合辅助化疗的条件,其中只有52例接受了这种化疗。将这组患者与对照组(1:2)进行回顾性比较,并使用危险比和Kaplan-Meier估计评估总生存期。化疗组的五年生存率为40%,仅接受手术的组为37.8%。确实,化学疗法并未降低死亡风险(HR 0.87,95%CI = 0.57-1.34,p = 0.54)。浆膜受累和侵犯6个以上淋巴结是多因素分析确定的主要独立预后因素。目前的研究并未显示化学疗法比单纯手术有明显优势。但是,我们的结果可以通过使用基于更有效和毒性较小的药物的新方案来帮助确定未来临床试验的策略。

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