Effect of postsurgical adjuvant chemotherapy timing on outcomes in patients with pancreatic cancer - a systematic review and meta-analysis.

IF 1.9 4区 医学 Q3 INFECTIOUS DISEASES
Longlan Zhou,Lin Zhang
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Abstract

To assess the association between the timing of postsurgical adjuvant chemotherapy and overall survival (OS) and disease-free survival (DFS) in patients with pancreatic cancer (PC). Literature search of PubMed, EMBASE, and Scopus databases was done for randomized controlled trials (RCTs) or observational studies (cohort studies, case-control studies), reporting outcomes of adult PC patients (aged 18 and above) who underwent surgery and received adjuvant chemotherapy at different time points after the operation. Pooled effect sizes were quantified and reported as hazard ratio (HR). The primary outcomes were OS and DFS. A random effects model to was used account for potential variability across studies. Sixteen studies were included. There was no significant difference between early and delayed initiation of adjuvant chemotherapy in terms of OS (HR 1.03, 95% CI: 0.98, 1.08) and DFS (HR 1.09, 95% CI: 0.91, 1.31). Subgroup analyses based on tumour stage, sample size, and the number of chemotherapeutic agents used did not reveal significant associations. Delayed initiation was associated with reduced OS in patients with well- to moderately differentiated tumours, with the confidence intervals approaching statistical significance (HR 1.12, 95% CI: 1.00,1.25). There was no significant association between the timing of postoperative adjuvant chemotherapy initiation and OS and DFS in patients with pancreatic cancer. These findings underscore the importance of optimizing treatment strategies and suggest that clinicians need to focus on other critical aspects such as drug selection, dosage, and patient-specific factors that might substantially impact treatment efficacy.
手术后辅助化疗时机对胰腺癌患者预后的影响--系统综述和荟萃分析。
目的:评估胰腺癌(PC)患者手术后辅助化疗的时机与总生存期(OS)和无病生存期(DFS)之间的关系。我们在 PubMed、EMBASE 和 Scopus 数据库中检索了随机对照试验(RCT)或观察性研究(队列研究、病例对照研究),这些研究报告了成年 PC 患者(18 岁及以上)接受手术并在术后不同时间点接受辅助化疗的结果。汇总的效应大小被量化并以危险比(HR)的形式报告。主要结果为OS和DFS。研究采用随机效应模型,以考虑不同研究之间的潜在差异。共纳入 16 项研究。就OS(HR 1.03,95% CI:0.98, 1.08)和DFS(HR 1.09,95% CI:0.91, 1.31)而言,早期和延迟开始辅助化疗没有明显差异。基于肿瘤分期、样本大小和所用化疗药物数量的亚组分析未显示出显著的相关性。在分化良好至中度的肿瘤患者中,延迟开始化疗与OS降低有关,置信区间接近统计学意义(HR 1.12,95% CI:1.00,1.25)。胰腺癌患者术后辅助化疗的开始时间与OS和DFS之间没有明显关系。这些发现强调了优化治疗策略的重要性,并提示临床医生需要关注其他关键方面,如药物选择、剂量和可能对疗效产生重大影响的患者特异性因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Chemotherapy
Journal of Chemotherapy 医学-药学
CiteScore
3.70
自引率
0.00%
发文量
144
审稿时长
6-12 weeks
期刊介绍: The Journal of Chemotherapy is an international multidisciplinary journal committed to the rapid publication of high quality, peer-reviewed, original research on all aspects of antimicrobial and antitumor chemotherapy. The Journal publishes original experimental and clinical research articles, state-of-the-art reviews, brief communications and letters on all aspects of chemotherapy, providing coverage of the pathogenesis, diagnosis, treatment, and control of infection, as well as the use of anticancer and immunomodulating drugs. Specific areas of focus include, but are not limited to: · Antibacterial, antiviral, antifungal, antiparasitic, and antiprotozoal agents; · Anticancer classical and targeted chemotherapeutic agents, biological agents, hormonal drugs, immunomodulatory drugs, cell therapy and gene therapy; · Pharmacokinetic and pharmacodynamic properties of antimicrobial and anticancer agents; · The efficacy, safety and toxicology profiles of antimicrobial and anticancer drugs; · Drug interactions in single or combined applications; · Drug resistance to antimicrobial and anticancer drugs; · Research and development of novel antimicrobial and anticancer drugs, including preclinical, translational and clinical research; · Biomarkers of sensitivity and/or resistance for antimicrobial and anticancer drugs; · Pharmacogenetics and pharmacogenomics; · Precision medicine in infectious disease therapy and in cancer therapy; · Pharmacoeconomics of antimicrobial and anticancer therapies and the implications to patients, health services, and the pharmaceutical industry.
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