Seattle Cancer Care Alliance, Breast Oncology, Seattle, WA, USA.
Division of Medical Oncology, University of Washington, Seattle, WA, USA.
Breast Cancer Res Treat. 2020 Apr;180(3):747-757. doi: 10.1007/s10549-020-05572-y. Epub 2020 Feb 15.
Delays in adjuvant breast cancer (BC) therapy have been shown to worsen outcomes. However, thus far studies have only evaluated delays to initial treatment, or a particular modality, such as chemotherapy, leaving uncertainty about the role of delay to subsequent therapy and the effects of cumulative delay, on outcomes. We investigated the associations of delays across treatment modalities with survival.
We included 3368 women with incident stage I-III BC in the Women's Health Initiative (WHI) enrolled in fee-for-service Medicare who underwent definitive surgery. This prospective analysis characterized treatment delays by linking WHI study records to Medicare claims. Delays were defined as > 8 weeks to surgery, chemotherapy, and radiation from diagnosis or prior treatment. We used Cox proportional hazards models to estimate BC-specific mortality (BCSM) and all-cause mortality (ACM) in relation to treatment delays.
We found 21.8% of women experienced delay to at least one therapy modality. In adjusted analysis, delay to chemotherapy was associated with a higher risk of BCSM (HR = 1.71; 95% CI 1.07-2.75) and ACM (HR = 1.39; 95% CI 1.02-1.90); delay in radiation increased BCSM risk (HR = 1.49; 95% CI 1.00-2.21) but not ACM risk (HR = 1.19; 95% CI 0.99-1.42). Delays across multiple treatment modalities increased BCSM risk threefold (95% CI 1.51-6.12) and ACM risk 2.3-fold (95% CI 1.50-3.50).
A delay to a single treatment modality and delay to a greater extent an accumulation of delays were associated with higher BCSM and ACM after BC. Timely care throughout the continuum of breast cancer treatment is important for optimal outcomes.
已证实,乳腺癌(BC)辅助治疗的延迟会导致预后恶化。然而,到目前为止,研究仅评估了初始治疗或特定治疗模式(如化疗)的延迟,对后续治疗延迟以及累积延迟对结局的影响仍存在不确定性。我们调查了治疗模式之间的延迟与生存之间的关联。
我们纳入了参加费用分担医疗保险的妇女健康倡议(WHI)中 3368 名患有 I-III 期局部 BC 的女性,这些女性接受了确定性手术。通过将 WHI 研究记录与医疗保险索赔相链接,本前瞻性分析对治疗延迟进行了特征描述。将从诊断或先前治疗开始至手术、化疗和放疗的时间超过 8 周定义为延迟。我们使用 Cox 比例风险模型估计与治疗延迟相关的 BC 特异性死亡率(BCSM)和全因死亡率(ACM)。
我们发现,21.8%的女性至少有一种治疗方式延迟。在调整后的分析中,化疗延迟与 BCSM(风险比 [HR] = 1.71;95%置信区间 [CI] 1.07-2.75)和 ACM(HR = 1.39;95%CI 1.02-1.90)风险升高相关;放疗延迟增加了 BCSM 风险(HR = 1.49;95%CI 1.00-2.21),但未增加 ACM 风险(HR = 1.19;95%CI 0.99-1.42)。多种治疗模式的延迟使 BCSM 风险增加了三倍(95%CI 1.51-6.12),ACM 风险增加了两倍(95%CI 1.50-3.50)。
单一治疗模式的延迟以及更广泛的延迟积累与 BC 后更高的 BCSM 和 ACM 风险相关。在乳腺癌治疗连续体中及时进行治疗对于获得最佳结局至关重要。