Quantifying the impact of treatment delays on breast cancer survival outcomes: a comprehensive meta-analysis.

IF 5.3 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Zoltan Ungvari, Mónika Fekete, Annamaria Buda, Andrea Lehoczki, Gyöngyi Munkácsy, Paola Scaffidi, Tiziana Bonaldi, János Tibor Fekete, Giampaolo Bianchini, Péter Varga, Anna Ungvari, Balázs Győrffy
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引用次数: 0

Abstract

Treatment delay in breast cancer care represents a significant concern in oncology, potentially impacting patient survival outcomes. While various factors can contribute to delayed treatment initiation, the quantitative relationship between specific delay intervals and survival remains incompletely understood in breast cancer management. Our study aims to explore the impact of treatment delays on survival outcomes in breast cancer. A comprehensive literature search was conducted in PubMed, Scopus, and Web of Science databases, covering publications from 2000 to 2025. From an initial 6222 records, 18 eligible studies comprising 25 cohorts were included. Hazard ratios (HRs) for all-cause and breast cancer-specific mortality were extracted or calculated for treatment delays of 4, 8, and 12 weeks. Random-effects meta-analyses were performed, and heterogeneity and publication bias were assessed using I2 statistics, funnel plots, and Egger's test. This meta-analysis revealed progressively increasing mortality risks with longer treatment delays. For all-cause mortality, HRs increased from 1.12 (95% CI 1.08-1.15) at 4 weeks to 1.25 (95% CI 1.17-1.33) at 8 weeks, and 1.39 (95% CI 1.26-1.53) at 12 weeks. Breast cancer-specific mortality showed more pronounced effects, with HRs of 1.20 (95% CI 1.06-1.36), 1.43 (95% CI 1.11-1.84), and 1.71 (95% CI 1.18-2.49) for 4-, 8-, and 12-week delays, respectively. Analyses combining both survival outcomes demonstrated consistent risk elevation across all time intervals (4 weeks: HR = 1.12, 95% CI 1.09-1.16; 8 weeks: HR = 1.26, 95% CI 1.18-1.34; 12 weeks: HR = 1.41, 95% CI 1.29-1.55). While heterogeneity was significant (I2 = 54-92%), no substantial publication bias was detected. Delays in initiating breast cancer treatment are associated with significantly worse survival, particularly for cancer-specific mortality. Each additional 4-week delay increases the hazard of death by over 10%, underscoring the urgency of minimizing delays in diagnosis-to-treatment pathways. These findings have critical implications for healthcare systems, clinical decision-making, and public health policy.

量化治疗延迟对乳腺癌生存结果的影响:一项综合荟萃分析。
乳腺癌治疗延误是肿瘤学的一个重要问题,可能会影响患者的生存结果。虽然各种因素可能导致延迟开始治疗,但在乳腺癌管理中,特定延迟间隔与生存之间的定量关系仍不完全清楚。我们的研究旨在探讨治疗延迟对乳腺癌生存结果的影响。在PubMed, Scopus和Web of Science数据库中进行了全面的文献检索,涵盖了2000年至2025年的出版物。从最初的6222份记录中,纳入了18项符合条件的研究,包括25个队列。提取或计算治疗延迟4周、8周和12周的全因死亡率和乳腺癌特异性死亡率的风险比(hr)。进行随机效应荟萃分析,使用I2统计量、漏斗图和Egger检验评估异质性和发表偏倚。该荟萃分析显示,随着治疗延误时间的延长,死亡风险逐渐增加。对于全因死亡率,hr从4周时的1.12 (95% CI 1.08-1.15)增加到8周时的1.25 (95% CI 1.17-1.33), 12周时的1.39 (95% CI 1.26-1.53)。乳腺癌特异性死亡率表现出更明显的影响,延迟4周、8周和12周的hr分别为1.20 (95% CI 1.06-1.36)、1.43 (95% CI 1.11-1.84)和1.71 (95% CI 1.18-2.49)。结合两种生存结果的分析显示,在所有时间间隔内风险升高一致(4周:HR = 1.12, 95% CI 1.09-1.16;8周:HR = 1.26, 95% CI 1.18-1.34;12周:HR = 1.41, 95% CI 1.29-1.55)。虽然异质性显著(I2 = 54-92%),但未发现明显的发表偏倚。延迟开始乳腺癌治疗与生存率显著降低相关,特别是癌症特异性死亡率。每多延迟4周,死亡风险就会增加10%以上,这突出了尽量减少从诊断到治疗途径延误的紧迫性。这些发现对医疗保健系统、临床决策和公共卫生政策具有重要意义。
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
GeroScience
GeroScience Medicine-Complementary and Alternative Medicine
CiteScore
10.50
自引率
5.40%
发文量
182
期刊介绍: GeroScience is a bi-monthly, international, peer-reviewed journal that publishes articles related to research in the biology of aging and research on biomedical applications that impact aging. The scope of articles to be considered include evolutionary biology, biophysics, genetics, genomics, proteomics, molecular biology, cell biology, biochemistry, endocrinology, immunology, physiology, pharmacology, neuroscience, and psychology.
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