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Diagnostic Prediction Model for De Novo Metastatic Breast Cancer

2026年8月10日 更新者:Oliver Laszlo Stari、Markusovszky University Teaching Hospital os County Vas

Development of a Diagnostic Prediction Model for de Novo Metastatic Breast Cancer Using Routinely Available Baseline Parameters

The goal of this observational study is to create a tool to estimate the risk of macroscopic distant tumor spread in women with newly diagnosed breast cancer. The main question it aims to answer is:

• Can a model, which combines routine medical information collected at diagnosis, accurately predict if a patient has metastasis large enough to be found during systemic imaging? Researchers will review the past medical records of participants who were treated at a university hospital. Because this study looks at past data, participants will not be asked to do any new tasks, take new tests, or change their medical care.

研究概览

地位

招聘中

详细说明

BACKGROUND AND RATIONALE

Baseline risk assessment traditionally relies on anatomical extent, while intrinsic tumour aggressiveness is established as a key determinant of distant spread. In addition, the systemic inflammatory response is increasingly recognized as a driver of tumour progression. The evaluation of these diverse and often conflicting factors complicates early clinical decision-making.

OBJECTIVE

The objective of this study is to develop and internally validate a multivariable diagnostic prediction model using routinely available baseline parameters to estimate the individualised probability of macroscopic distant metastasis among patients with newly diagnosed invasive breast cancer.

STUDY DESIGN AND SETTING

This is an investigator-initiated, single-centre, retrospective cohort study adhering to the TRIPOD+AI statement. The study is conducted at a university teaching hospital, where comprehensive baseline systemic staging is the institutional standard for all newly diagnosed breast cancer patients.

PREDICTORS

The model integrates routinely available baseline parameters: clinical tumor size, clinical lymphnode status, the Ki-67 proliferation marker, and a composite systemic inflammatory marker (Pan-immune-inflammation value).

DATA COLLECTION AND QUALITY ASSURANCE

Data extraction is performed independently by two multidisciplinary teams. Any discrepancies are resolved through a formal adjudication process by an expert panel not involved in data collection (senior oncologist, radiologist, pathologist, and surgeon).

SAMPLE SIZE AND MISSING DATA Based on the criteria proposed by Riley et al., the study requires a minimum of 925 participants and 93 events to accommodate maximum model complexity. Missing data will be handled using complete-case analysis if the rate is <5%, or multiple imputation if >5%.

STATISTICAL ANALYSIS AND MODEL DEVELOPMENT

For the multivariable logistic regression model, all pre-specified predictors are entered simultaneously. Continuous variables are retained in their continuous form. Non-linear relationships modeled using restricted cubic splines. Model performance is evaluated via discrimination and calibration metrics, while clinical utility is assessed through decision curve analysis. Internal validation is conducted using bootstrapping. To correct for model optimism, a global shrinkage factor based on the bootstrap calibration slope is applied. Instability plots are used to illustrate the stability of predictions, calibration, and net benefit.

PATIENT AND PUBLIC INVOLVEMENT (PPI)

To initiate Patient and Public Involvement, an inaugural patient engagement event will be held to discuss the clinical acceptability of a diagnostic prediction model and its potential role in shared decision-making. This event will serve as the foundation to establish a voluntary Patient Advisory Group (PAG). In subsequent project stages, the newly formed PAG will collaborate to co-produce a Plain Language Summary and explore potential pathways for the tool's future clinical application.

研究类型

观察性的

注册 (估计的)

925

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Vas County
      • Szombathely、Vas County、匈牙利、9700
        • 招聘中
        • Markusovszky University Teaching Hospital
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

A consecutive cohort of adult female patients with newly diagnosed invasive breast cancer.

描述

Inclusion Criteria:

  • Female sex, aged 18 years or older.
  • Newly diagnosed invasive breast cancer.
  • Case reviewed by the Multidisciplinary Tumour Board at the study site during the inclusion period (between October 1, 2018, and July 31, 2025).
  • No history of prior or synchronous invasive malignancies, except for synchronous bilateral breast cancer.
  • Intent for primary treatment and clinical management at the study site.
  • Availability of longitudinal clinical records throughout the 12-month follow-up period or until death.

Exclusion Criteria:

-Absence of baseline systemic staging.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

队列和干预

团体/队列
Primary study cohort

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
De novo metastatic breast cancer
大体时间:From the initial diagnostic mammogram up to 12 months of follow-up.
A newly diagnosed breast cancer with distant spread identified at baseline systemic staging. Distant lesions are categorized as de novo metastasis if confirmed via biopsy, secondary imaging, follow-up imaging, or Multidisciplinary Tumor Board consensus based on definitive clinical evidence. Equivocal cases are adjudicated through a review of the 12 month clinical follow-up.
From the initial diagnostic mammogram up to 12 months of follow-up.

次要结果测量

结果测量
措施说明
大体时间
Incidence of rapid metastatic recurrence
大体时间:Up to 12 months from the initial diagnostic mammogram.
Patients developing systemic spread within the 12-month follow-up period, subsequent to an initially negative baseline systemic staging. Patients with rapid metastatic recurrence are excluded from the multivariable analysis and reported descriptively.
Up to 12 months from the initial diagnostic mammogram.
Systemic staging interval
大体时间:Up to 12 months from the initial diagnostic mammogram.
The time elapsed from the initial diagnostic mammogram to the completion of baseline systemic staging.
Up to 12 months from the initial diagnostic mammogram.
Diagnostic interval
大体时间:Up to 12 months from the initial diagnostic mammogram.
The time elapsed from the initial diagnostic mammogram to the confirmation of macroscopic distant metastasis.
Up to 12 months from the initial diagnostic mammogram.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年8月10日

初级完成 (估计的)

2026年10月31日

研究完成 (估计的)

2027年2月28日

研究注册日期

首次提交

2026年8月3日

首先提交符合 QC 标准的

2026年8月3日

首次发布 (实际的)

2026年8月7日

研究记录更新

最后更新发布 (实际的)

2026年8月12日

上次提交的符合 QC 标准的更新

2026年8月10日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • VAS-RKEB/BNJ-6/2026

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

A complete, cleaned, and de-identified copy of the final dataset will be shared. Sensitive data types, including digital images, specific event dates, and demographic details other than categorical age groups, will be redacted.

IPD 共享时间框架

Data will become available upon the publication of the study results and will remain accessible in a restricted-access repository for a period of 5 years.

IPD 共享访问标准

Access will be granted to qualified researchers who submit a methodologically sound proposal for multicenter collaboration, external validation, further research, or independent verification of the results. Data access requests must be submitted through the repository's access management portal, and researchers will be required to sign a Data Use Agreement.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 分析代码

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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