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可切除胸段食管癌的术前化疗。

Preoperative chemotherapy for resectable thoracic esophageal cancer.

作者信息

Malthaner R, Fenlon D

机构信息

Department of Surgery, University of Western Ontario, London Health Sciences Centre, 375 South Street, Suite N345, London, Ontario, Canada, N6A 4G5.

出版信息

Cochrane Database Syst Rev. 2003(4):CD001556. doi: 10.1002/14651858.CD001556.

Abstract

BACKGROUND

Surgery has been the treatment of choice for localized esophageal cancer. A number of studies have investigated whether preoperative chemotherapy followed by surgery leads to an improvement in cure rates, but the individual reports have been conflicting. An explicit systematic update of the role of preoperative chemotherapy in the treatment of resectable thoracic esophageal cancer is therefore warranted.

OBJECTIVES

The objective of this review is to determine the role of preoperative chemotherapy on patients with resectable thoracic esophageal carcinomas.

SEARCH STRATEGY

Trials were identified by searching the Cochrane Controlled Trials Register, MEDLINE (1966 - 2003), EMBASE (1988 - 2003) and CancerLit (1993 - 2003). There were no language restrictions.

SELECTION CRITERIA

Types of studies. Studies that randomised patients with potentially resectable carcinomas of the esophagus (of any histologic type) to chemotherapy or no chemotherapy before surgeries were included in this review. Types of participants. The participants consisted of patients with localized potentially resectable thoracic esophageal carcinomas. Trials involving patients with carcinomas of the cervical esophagus were excluded. Types of interventions. Trials that compared chemotherapy before surgery (esophagectomy) with surgical resections alone (esophagectomy) were included. Types of outcome measures. The primary outcome was overall survival at yearly intervals after randomisation. Secondary outcomes of interest included rates of resections, response to chemotherapy, rates of local and distant recurrences, quality-of-life, and treatment morbidity and mortality.

DATA COLLECTION AND ANALYSIS

All analyses were carried out on intention-to-treat. Survival at 1, 2, 3, 4 and five years were used as endpoints of clinical relevance along with the median survival. The risk ratio (relative risk; RR) was the primary measure of effect for survival, rates of resections, and tumour recurrences. The risk difference (RD) was used to describe differences in response to chemotherapy, treatment morbidity and mortality.

MAIN RESULTS

There were 11 randomised trials involving 2051 patients. At 1- year and 2-year the risk ratios showed no difference in survival between preoperative chemotherapy and surgery alone. The 3-year risk ratios found a 21% increase in survival (RR = 1.21; 95% CI 0.88 to 1.68; p = 0.25) and a 24% increase in survival with preoperative chemotherapy at 4 years (RR = 1.24; 95% CI 0.92 to 1.68; p = 0.15) but they did not reach statistical significance. Only at 5 years did the results become significant (RR = 1.44; 95% CI 1.05 to 1.97; p = 0.02). The overall rate of resections and the rate of complete resections (R0) did not differ between the preoperative chemotherapy arm and surgery alone. The pooled clinical response to chemotherapy was about 36% (RD = 0.36; 95% CI 0.26 to 0.47) but the complete pathologic response was a disappointing 3% (RD = 0.03; 95% CI 0.01 to 0.04). No single agent or combination of chemotherapeutic agents was found to be superior to the others. There was a 19% reduction in local recurrence with preoperative chemotherapy, but this was not significant (RR = 0.81; 95% CI 0.54 to 1.22; p = 0.3). Preoperative chemotherapy was somewhat more harmful to patients than surgery alone.

REVIEWER'S CONCLUSIONS: In summary, preoperative chemotherapy plus surgery appears to offer a survival advantage at 3, 4, and 5 years, which reached significance only at 5 years compared to surgery alone for resectable thoracic esophageal cancer of any histologic type. The number needed to treat for one extra survivor at five years is eleven patients. The results are tempered by the increased toxicity and mortality associated with chemotherapy. The most beneficial chemotherapy combination appears to be cisplatin and 5-flurouracil based, however, the dosing is unclear.

摘要

背景

手术一直是局限性食管癌的首选治疗方法。多项研究探讨了术前化疗后再行手术是否能提高治愈率,但各研究报告的结果相互矛盾。因此,有必要对术前化疗在可切除胸段食管癌治疗中的作用进行明确的系统更新。

目的

本综述的目的是确定术前化疗对可切除胸段食管癌患者的作用。

检索策略

通过检索Cochrane对照试验注册库、MEDLINE(1966 - 2003年)、EMBASE(1988 - 2003年)和CancerLit(1993 - 2003年)来识别试验。无语言限制。

入选标准

研究类型。将潜在可切除食管癌(任何组织学类型)患者随机分为术前化疗组或未化疗组的研究纳入本综述。参与者类型。参与者包括局限性潜在可切除胸段食管癌患者。涉及颈段食管癌患者的试验被排除。干预类型。纳入比较术前化疗(食管切除术)与单纯手术切除(食管切除术)的试验。结局指标类型。主要结局是随机分组后每年的总生存率。感兴趣的次要结局包括切除率、对化疗的反应、局部和远处复发率、生活质量以及治疗的发病率和死亡率。

数据收集与分析

所有分析均基于意向性治疗。将1年、2年、3年、4年和5年的生存率作为具有临床相关性的终点,同时包括中位生存期。风险比(相对风险;RR)是生存、切除率和肿瘤复发的主要效应指标。风险差(RD)用于描述化疗反应、治疗发病率和死亡率的差异。

主要结果

有11项随机试验,涉及2051例患者。1年和2年时,风险比显示术前化疗与单纯手术在生存率上无差异。3年风险比显示生存率提高21%(RR = 1.21;95%CI 0.88至1.68;p = 0.25),4年时术前化疗生存率提高24%(RR = 1.24;95%CI 0.92至1.68;p = 0.15),但均未达到统计学显著性。仅在5年时结果具有显著性(RR = 1.44;95%CI 1.05至1.97;p = 0.02)。术前化疗组与单纯手术组的总切除率和完全切除率(R0)无差异。化疗的总体临床反应约为36%(RD = 0.36;95%CI 0.26至0.47),但完全病理反应令人失望,仅为3%(RD = 0.03;95%CI 0.01至0.04)。未发现单一化疗药物或联合化疗方案优于其他方案。术前化疗使局部复发率降低19%,但无显著性(RR = 0.81;95%CI 0.54至1.22;p = 0.3)。术前化疗对患者的危害略大于单纯手术。

综述作者结论

总之,术前化疗加手术似乎在3年、4年和5年时具有生存优势,与单纯手术相比,仅在5年时具有显著性,适用于任何组织学类型的可切除胸段食管癌。5年时多获得1例生存者所需治疗的患者数为11例。结果因化疗相关的毒性和死亡率增加而受到影响。最有益的化疗联合方案似乎是以顺铂和5-氟尿嘧啶为基础,但给药方案尚不清楚。

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