Leslie Macall, Pathak Rashmi, Dooley William C, Squires Ronald A, Rui Hallgeir, Chervoneva Inna, Tanaka Takemi
University of Oklahoma Health Sciences Center, Stephenson Cancer Center, 975 NE, 10th, Oklahoma City, OK 73104, USA.
University of Oklahoma Health Sciences Center, School of Medicine, Dept. of Surgery, 800 Stanton L. Young Blvd., Oklahoma City, OK 73104, USA.
Res Sq. 2024 Apr 8:rs.3.rs-4171651. doi: 10.21203/rs.3.rs-4171651/v1.
Substantial evidence supports that delay of surgery after breast cancer diagnosis is associated with increased mortality risk, leading to the introduction of a new Commission on Cancer quality measure for receipt of surgery within 60 days of diagnosis for non-neoadjuvant patients. Breast cancer subtype is a critical prognostic factor and determines treatment options; however, it remains unknown whether surgical delay-associated breast cancer-specific mortality (BCSM) risk differs by subtype. This retrospective cohort study aimed to assess whether the impact of delayed surgery on survival varies by subtype (hormone [HR]+/HER2-, HR-/HER2-, and HER2+) in patients with loco-regional breast cancer who received surgery as their first treatment between 2010-2017 using the SEER-Medicare. Continuous time to surgery from diagnostic biopsy (TTS; days) in reference to TTS = 30 days. BCSM were evaluated as flexibly dependent on continuous time (days) to surgery from diagnosis (TTS) using Cox proportional hazards and Fine and Gray competing-risk regression models, respectively, by HR status. Inverse propensity score-weighting was used to adjust for demographic, clinical, and treatment variables impacting TTS. Adjusted BCSM risk grew with increasing TTS across all subtypes, however, the pattern and extent of the association varied. HR+/HER2- patients exhibited the most pronounced increase in BCSM risk associated with TTS, with approximately exponential growth after 42 days, with adjusted subdistribution hazard ratios (sHR) of 1.21 (95% CI: 1.06-1.37) at TTS = 60 days, 1.79 (95% CI: 1.40-2.29) at TTS = 90 days, and 2.83 (95% CI: 1.76-4.55) at TTS = 120 days. In contrast, both HER2 + and HR-/HER2- patients showed slower, approximately linear growth in sHR, although non-significant in HR-HER2-.
大量证据表明,乳腺癌确诊后手术延迟与死亡风险增加相关,这促使癌症委员会引入了一项新的质量指标,即非新辅助治疗患者在确诊后60天内接受手术。乳腺癌亚型是一个关键的预后因素,决定着治疗方案;然而,手术延迟相关的乳腺癌特异性死亡率(BCSM)风险是否因亚型而异仍不清楚。这项回顾性队列研究旨在评估2010年至2017年间接受手术作为首次治疗的局部区域性乳腺癌患者中,延迟手术对生存的影响是否因亚型(激素[HR]+/HER2-、HR-/HER2-和HER2+)而异,研究使用了监测、流行病学和最终结果(SEER)医疗保险数据库。从诊断性活检到手术的连续时间(TTS;天),以TTS = 30天为参照。分别采用Cox比例风险模型和Fine和Gray竞争风险回归模型,根据HR状态,将BCSM评估为灵活依赖于从诊断到手术的连续时间(天)(TTS)。采用逆倾向评分加权法对影响TTS的人口统计学、临床和治疗变量进行调整。在所有亚型中,调整后的BCSM风险均随着TTS的增加而增加,然而,关联的模式和程度各不相同。HR+/HER2-患者的BCSM风险与TTS相关的增加最为明显,42天后呈近似指数增长,TTS = 60天时调整后的亚分布风险比(sHR)为1.21(95%置信区间:1.06 - 1.37),TTS = 90天时为1.79(95%置信区间:1.40 - 2.29),TTS = 120天时为2.83(95%置信区间:1.76 - 4.55)。相比之下,HER2+和HR-/HER2-患者的sHR增长较慢,近似呈线性,尽管HR-HER2-患者的增长不显著。