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撤回:不可切除的晚期胰腺癌的化疗和放疗。

WITHDRAWN: Chemotherapy and radiotherapy for inoperable advanced pancreatic cancer.

作者信息

Yip Desmond, Karapetis Christos, Strickland Andrew, Steer Christopher B, Goldstein David

机构信息

Medical Oncology Unit, The Canberra Hospital, Yamba Drive, Garran, ACT, Australia, 2605.

出版信息

Cochrane Database Syst Rev. 2009 Oct 7;2009(4):CD002093. doi: 10.1002/14651858.CD002093.pub3.

Abstract

BACKGROUND

Pancreatic cancer has a poor prognosis. The benefit of chemotherapy, radiotherapy or both as a palliative treatment of advanced or relapsed disease is uncertain.

OBJECTIVES

To assess the effects of chemotherapy and/or radiotherapy in the management of pancreatic adenocarcinoma in people with inoperable advanced disease.

SEARCH STRATEGY

We searched the Cochrane Central Register of Controlled Trials (CENTRAL), which includes the Cochrane Upper Gastrointestinal and Pancreatic Diseases (UGPD) Group Trials Register (The Cochrane Library 2005, Issue 1); CANCERLIT (1975-2002); MEDLINE (1966 to January 2005); and EMBASE (1980 to January 2005). We handsearched reference lists from trials revealed by electronic searches to identify further relevant trials. We searched published abstracts from relevant conference proceedings. We contacted colleagues and experts in the field, and asked them to provide details of outstanding clinical trials and any relevant unpublished materials.

SELECTION CRITERIA

Randomised controlled trials (single- or double-blind) in patients with advanced inoperable pancreatic cancer, in which one of the intervention types (chemotherapy or radiotherapy) was contrasted with either placebo or another type of intervention. Studies comparing non-chemotherapy agents such as biological agents, hormones, immunostimulants, vaccines and cytokines were excluded.

DATA COLLECTION AND ANALYSIS

Studies were assessed for eligibility and quality. Data were extracted by groups of two independent reviewers, with conflicts resolved by a third reviewer. Study authors were contacted for more information.

MAIN RESULTS

Fifty trials (7043 participants) were included. Chemotherapy significantly reduced the one-year mortality (odds ratio (OR) 0.37, 95% confidence interval (CI) 0.25 to 0.57, P value < 0.00001) when compared to best supportive care. Also, chemoradiation improved one year survival (0% versus 58%, P value 0.001) when compared to best supportive care. There was no significant difference in one-year mortality for 5FU alone versus 5FU combinations (OR 0.90, 95% CI 0.62 to 1.30); single-agent chemotherapy versus gemcitabine (OR 1.34, 95% CI 0.88 to 2.02, P value 0.17); or gemcitabine alone versus gemcitabine combinations (OR 0.88, 95% CI 0.74 to 1.05). However, subgroup analysis showed that platinum-gemcitabine combinations reduced six-month mortality compared to gemcitabine alone (OR 0.59, 95% CI 0.43 to 0.81, P value 0.001). A qualitative overview suggested that chemoradiation produced better survivals than either best supportive care or radiotherapy. Chemoradiation treatment was associated with more toxicity.

AUTHORS' CONCLUSIONS: Chemotherapy appears to prolong survival in people with advanced pancreatic cancer and can confer clinical benefits and improve quality of life. Combination chemotherapy did not improve overall survival compared to single-agent chemotherapy. Gemcitabine is an acceptable control arm for future trials investigating scheduling and combinations with novel agents. There is insufficient evidence to recommend chemoradiation in patients with locally advanced inoperable pancreatic cancer as a superior alternative to chemotherapy alone.

摘要

背景

胰腺癌预后较差。化疗、放疗或两者联合作为晚期或复发性疾病的姑息治疗的益处尚不确定。

目的

评估化疗和/或放疗对无法手术的晚期胰腺癌患者的治疗效果。

检索策略

我们检索了Cochrane对照试验中心注册库(CENTRAL),其中包括Cochrane上消化道和胰腺疾病(UGPD)小组试验注册库(《Cochrane图书馆》2005年第1期);癌症文献数据库(CANCERLIT,1975 - 2002年);医学文献数据库(MEDLINE,1966年至2005年1月);以及荷兰医学文摘数据库(EMBASE,1980年至2005年1月)。我们手工检索了电子检索所发现试验的参考文献列表,以识别更多相关试验。我们检索了相关会议论文集的已发表摘要。我们联系了该领域的同事和专家,要求他们提供未发表的临床试验详情及任何相关未发表材料。

选择标准

针对无法手术的晚期胰腺癌患者的随机对照试验(单盲或双盲),其中一种干预类型(化疗或放疗)与安慰剂或另一种干预类型进行对比。排除比较非化疗药物(如生物制剂、激素、免疫刺激剂、疫苗和细胞因子)的研究。

数据收集与分析

评估研究的合格性和质量。由两组独立的审阅者提取数据,如有冲突则由第三位审阅者解决。与研究作者联系以获取更多信息。

主要结果

纳入了50项试验(7043名参与者)。与最佳支持治疗相比,化疗显著降低了一年死亡率(比值比(OR)0.37,95%置信区间(CI)0.25至0.57,P值<0.00001)。此外,与最佳支持治疗相比,放化疗提高了一年生存率(0%对58%,P值0.001)。单独使用5-氟尿嘧啶(5FU)与5FU联合用药的一年死亡率无显著差异(OR 0.90,95% CI 0.62至1.30);单药化疗与吉西他滨相比(OR 1.34,95% CI 0.88至2.02,P值0.17);或单独使用吉西他滨与吉西他滨联合用药相比(OR 0.88,95% CI 0.74至1.05)。然而,亚组分析显示,与单独使用吉西他滨相比,铂类-吉西他滨联合用药降低了六个月死亡率(OR 0.59,95% CI 0.43至0.81,P值0.001)。定性综述表明,放化疗比最佳支持治疗或单纯放疗产生了更好的生存率。放化疗治疗伴随更多毒性。

作者结论

化疗似乎可延长晚期胰腺癌患者的生存期,并能带来临床益处及改善生活质量。与单药化疗相比,联合化疗并未改善总生存期。吉西他滨是未来研究给药方案及与新型药物联合使用的试验中可接受的对照组。没有足够证据推荐对局部晚期无法手术的胰腺癌患者进行放化疗作为单纯化疗的更佳替代方案。

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