乳腺癌治疗的分散性:大于各部分的总和。

IF 3 3区 医学 Q2 ONCOLOGY Breast Cancer Research and Treatment Pub Date : 2024-12-01 Epub Date: 2024-08-03 DOI:10.1007/s10549-024-07442-3
Hadley D Freeman, Linnea C Burke, Ja'Neil G Humphrey, Ashley J Wilbers, Halley Vora, Rhami Khorfan, Naveenraj L Solomon, Jukes P Namm, Liang Ji, Sharon S Lum
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引用次数: 0

摘要

简介:医疗分散(FC,在一家以上的医疗机构接受治疗)已被证明会对癌症治疗效果产生负面影响。鉴于乳腺癌治疗的多模式性质,我们试图找出与FC相关的因素及其对乳腺癌患者生存的影响:我们对 2004-2020 年国家癌症数据库中接受过手术治疗的 I-III 期乳腺癌患者(不包括接受新辅助治疗的患者)进行了回顾性分析。患者被分为两组:FC 或非 FC 治疗组。治疗延迟的定义是确诊后大于 60 天的明确手术。通过多变量逻辑回归确定了预测 FC 的因素,并使用 Kaplan-Meier 和多变量 Cox 比例危险度法比较了生存率:在已确认的 531,644 例患者中,340,297 例(64.0%)接受了 FC 治疗。经调整后,FC(OR 1.27,95% CI 1.25-1.29)与治疗延迟有独立关联。预测 FC 的因素包括西班牙裔(OR 1.04,95% CI:1.01-1.07)、在综合社区癌症项目(OR 1.06,95% CI:1.03-1.08)和综合网络癌症项目(OR 1.55,95% CI:1.51-1.59)、AJCC II 期(OR 1.06,95% CI 1.05-1.07)和 III 期肿瘤(OR 1.06,95% CI:1.02-1.10)以及 HR + /HER2 + 肿瘤(OR 1.05,95% CI:1.02-1.07)。治疗延迟与死亡风险增加(HR 1.23,95% CI 1.20-1.26)独立相关,而FC(HR 0.87,95% CI 0.86-0.88)则显示出生存获益:尽管治疗延迟会对乳腺癌患者的生存产生负面影响,但我们的研究结果表明,FC可以作为多专科护理的标志,从而减轻其中的一些影响。
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Fragmentation of care in breast cancer: greater than the sum of its parts.

Introduction: Fragmentation of care (FC, the receipt of care at > 1 institution) has been shown to negatively impact cancer outcomes. Given the multimodal nature of breast cancer treatment, we sought to identify factors associated with FC and its effects on survival of breast cancer patients.

Methods: A retrospective analysis was performed of surgically treated, stage I-III breast cancer patients in the 2004-2020 National Cancer Database, excluding neoadjuvant therapy recipients. Patients were stratified into two groups: FC or non-FC care. Treatment delay was defined as definitive surgery > 60 days after diagnosis. Multivariable logistic regression was performed to identify factors predictive of FC, and survival was compared using Kaplan-Meier and multivariable Cox proportional hazards methods.

Results: Of the 531,644 patients identified, 340,297 (64.0%) received FC. After adjustment, FC (OR 1.27, 95% CI 1.25-1.29) was independently associated with treatment delay. Factors predictive of FC included Hispanic ethnicity (OR 1.04, 95% CI: 1.01-1.07), treatment at comprehensive community cancer programs (OR 1.06, 95% CI: 1.03-1.08) and integrated network cancer programs (OR 1.55, 95% CI: 1.51-1.59), AJCC stage II (OR 1.06, 95% CI 1.05-1.07) and stage III tumors (OR 1.06, 95% CI: 1.02-1.10), and HR + /HER2 + tumors (OR 1.05, 95% CI: 1.02-1.07). Treatment delay was independently associated with increased risk of mortality (HR 1.23, 95% CI 1.20-1.26), whereas FC (HR 0.87, 95% CI 0.86-0.88) showed survival benefit.

Conclusions: While treatment delay negatively impacts survival in breast cancer patients, our findings suggest FC could be a marker for multispecialty care that may mitigate some of these effects.

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来源期刊
CiteScore
6.80
自引率
2.60%
发文量
342
审稿时长
1 months
期刊介绍: Breast Cancer Research and Treatment provides the surgeon, radiotherapist, medical oncologist, endocrinologist, epidemiologist, immunologist or cell biologist investigating problems in breast cancer a single forum for communication. The journal creates a "market place" for breast cancer topics which cuts across all the usual lines of disciplines, providing a site for presenting pertinent investigations, and for discussing critical questions relevant to the entire field. It seeks to develop a new focus and new perspectives for all those concerned with breast cancer.
期刊最新文献
Correction: FBLN2 is associated with basal cell markers Krt14 and ITGB1 in mouse mammary epithelial cells and has a preferential expression in molecular subtypes of human breast cancer. A randomised trial comparing 6-monthly adjuvant zoledronate with a single one-time dose in patients with early breast cancer. Alterations in the expression of homologous recombination repair (HRR) genes in breast cancer tissues considering germline BRCA1/2 mutation status. Efficacy of antiobesity medications among breast cancer survivors taking aromatase inhibitors. Cost containment analysis of superparamagnetic iron oxide (SPIO) injection in patients with ductal carcinoma in situ.
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