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Oncogeriatric Screening and Evaluation Program (PROTEGER)

2026年9月1日 更新者:Latin American Cooperative Oncology Group

PROgrama de Tamizaje y Evaluación oncoGERiátrica

This study aims to develop, train, and validate a machine learning-based prediction model (PROTEGER) to provide treatment decision recommendations for older adults diagnosed with solid tumor cancers. The study has a two-phase observational design: a retrospective cohort using anonymized data from an oncogeriatric telecommittee to train the predictive model, followed by a prospective multicenter cohort across Chile, Peru, and Brazil. Information from Comprehensive Geriatric Assessments (CGA), treatment decisions, and 3- and 6-month clinical outcomes will be collected to evaluate and validate the decision-support platform's performance in assisting oncology teams.

研究概览

地位

尚未招聘

详细说明

Cancer incidence increases significantly with age, and up to 70% of cancer mortality occurs in patients aged 65 years or older. Despite this, older patients are frequently undertreated due to the high risk of secondary toxicity, which is associated with quality of life deterioration, increased hospitalizations, and higher mortality. Comprehensive Geriatric Assessment (CGA) has proven to be an effective tool to identify vulnerability, reduce chemotherapy-related toxicity, and tailor interventions. However, the lack of geriatricians, especially in Latin American public health systems, creates significant barriers to accessing CGA-guided oncological care.

To overcome these barriers, the PROTEGER program proposes an innovative digital health solution by developing and validating a machine learning-based clinical decision support system (CDSS) for oncogeriatric care. The study is an observational, multicenter, bidirectional cohort study conducted in two phases:

Phase 1: Retrospective Training Phase This phase uses anonymized clinical data (2021-2023) from the Oncogeriatric Tele-Committee of the Chilean Ministry of Health's Digital Hospital. Data from older patients with solid tumors who underwent a CGA will be used to train and test predictive models using machine learning techniques (e.g., Gradient Boosting Trees and Random Forest) following the CRISP-DM methodology. The predictive model aims to learn the Committee's treatment recommendation patterns based on patient functionality, comorbidities, and geriatric syndromes.

Phase 2: Prospective Validation Phase A prospective, multicenter cohort will be enrolled across healthcare centers in Chile, Peru, and Brazil. Eligible patients (aged 65+ with a solid tumor diagnosis) who undergo routine CGA and oncological care will be followed for 6 months. Data regarding baseline characteristics, treatment decisions (made by local oncology teams blinded to the AI model's recommendation), dose reductions, treatment discontinuation, disease progression, quality of life (EORTC QLQ-C30 and ELD14), and survival will be collected.

Study Objectives:

The primary objective is to develop, train, and clinically validate the PROTEGER machine learning predictive model to provide an accurate treatment recommendation (e.g., standard treatment, dose-adjusted treatment, or supportive care only) capable of assisting clinical decision-making by oncology teams. A secondary objective involves the design and development of an intuitive graphical user interface capable of being used by healthcare providers and patients for data management and result interpretation.

All predictive models will be evaluated using standard metrics, such as the Area Under the ROC Curve (AUC) and the C-statistic, to determine their discriminatory capacity in a real-world clinical setting.

研究类型

观察性的

注册 (估计的)

412

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

研究联系人备份

学习地点

    • São Paulo
      • São Paulo、São Paulo、巴西、05653-000
        • HIAE - Hospital Israelita Albert Einstein
        • 首席研究员:
          • Ludmila de Oliveira Muniz Koch
      • São Paulo、São Paulo、巴西、04004-060
        • BR192 HCOR - Hospital do Coração
        • 首席研究员:
          • Luciola Pontes Leite de Barros

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

  • 年长者

接受健康志愿者

不

取样方法

非概率样本

研究人群

The study population consists of older adults (aged 65 years and older) diagnosed with solid tumor cancers who receive care in public and private health institutions in South America (Chile, Brazil, and Peru). The retrospective cohort includes anonymized historical data from patients evaluated by the Oncogeriatric Tele-Committee of the Chilean Ministry of Health. The prospective cohort comprises consecutive patients seen in routine oncological care who undergo a Comprehensive Geriatric Assessment (CGA) and are managed by local oncogeriatric teams.

描述

Inclusion Criteria:

  • Age 65 years or older.
  • Diagnosis of solid tumor cancer.
  • Must have been evaluated and followed up by a local oncology team.
  • Signed Informed Consent Form (ICF) applied in accordance with the local ethics committee.
  • Must have undergone a Comprehensive Geriatric Assessment (CGA).

Exclusion Criteria:

- Patients who are unable or unwilling to consent to providing information will be excluded.

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
Retrospective Training Cohort (Chile)
Anonymized data from cases submitted to the Oncogeriatrics Telecommittee from 2021 to the end of 2023, obtained from the Chilean Ministry of Health's Digital Hospital database, along with patient survival data, will be used to train and validate the predictive model using machine learning techniques.
Prospective Validation Cohort (Chile, Brasil, Peru)
Older adults with cancer receive a comprehensive geriatric assessment at their respective centers and are introduced to an oncogeriatric team. They will share their baseline characteristics, the results of their CGA, clinical data related to cancer treatment, and 3- and 6-month follow-up for the development and validation of a predictive model using machine learning techniques.

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
Predictive Accuracy of the PROTEGER Machine Learning Model
大体时间:Up to 6 months post-enrollment.
Discrimination performance of the machine learning predictive model in recommending oncogeriatric treatment decisions (standard treatment, dose-adjusted treatment, or supportive care/no treatment) based on Comprehensive Geriatric Assessment (CGA) data, measured by the Area Under the Receiver Operating Characteristic Curve (AUC-ROC), with scores ranging from 0.5 (no discrimination/chance) to 1.0 (perfect discrimination).
Up to 6 months post-enrollment.

次要结果测量

结果测量
措施说明
大体时间
Incidence of High-Grade Chemotherapy-Related Adverse Events
大体时间:At 3 and 6 months post-enrollment.
Percentage of participants experiencing Grade 3 or higher toxicities/adverse reactions evaluated using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
At 3 and 6 months post-enrollment.
General Quality of Life Score (EORTC QLQ-C30)
大体时间:Baseline, 3 months, and 6 months post-enrollment.
Global health status and quality of life assessed using the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ-C30). Scores range from 0 to 100, where higher scores represent a better overall quality of life and higher functioning.
Baseline, 3 months, and 6 months post-enrollment.
Elderly-Specific Quality of Life Score (EORTC QLQ-ELD14)
大体时间:Baseline, 3 months, and 6 months post-enrollment.
Elderly-specific quality of life issues assessed using the EORTC QLQ-ELD14 module. Scores range from 0 to 100. For symptom scales, higher scores represent worse outcomes (higher level of symptoms/problems); for functional scales, higher scores represent better outcomes.
Baseline, 3 months, and 6 months post-enrollment.
Incidence of Hospitalizations
大体时间:At 3 and 6 months post-enrollment.
Number of patients requiring unplanned hospital admissions during the treatment course
At 3 and 6 months post-enrollment.
Treatment Discontinuation and Dose Reduction Rates
大体时间:At 3 and 6 months post-enrollment.
Percentage of patients undergoing chemotherapy dose reductions (planned vs. received dose) or early treatment discontinuation.
At 3 and 6 months post-enrollment.
Patient Survival and Disease Progression
大体时间:At 3 and 6 months post-enrollment.
Overall survival status and disease progression rate assessed according to RECIST 1.0 criteria.
At 3 and 6 months post-enrollment.

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。

合作者

调查人员

  • 首席研究员:Luciola Pontes Leite de Barros、Hospital do Coração (HCOR)

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 (估计的)

2026年9月1日

初级完成 (估计的)

2027年1月1日

研究完成 (估计的)

2027年7月1日

研究注册日期

首次提交

2026年8月24日

首先提交符合 QC 标准的

2026年9月1日

首次发布 (实际的)

2026年9月4日

研究记录更新

最后更新发布 (实际的)

2026年9月4日

上次提交的符合 QC 标准的更新

2026年9月1日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • LACOG 0325

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

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