Oncogeriatric Screening and Evaluation Program (PROTEGER)
PROgrama de Tamizaje y Evaluación oncoGERiátrica
調査の概要
状態
条件
詳細な説明
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.
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Project Manager
- 電話番号:+55 51 3384 5334
- メール:lacog0325@lacog.group
研究連絡先のバックアップ
- 名前:Head of Clinical Operations
- 電話番号:+55 (51) 3384.5334
- メール:laura.voelcker@lacog.group
研究場所
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São Paulo
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São Paulo、São Paulo、ブラジル、05653-000
- HIAE - Hospital Israelita Albert Einstein
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主任研究者:
- Ludmila de Oliveira Muniz Koch
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São Paulo、São Paulo、ブラジル、04004-060
- BR192 HCOR - Hospital do Coração
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主任研究者:
- Luciola Pontes Leite de Barros
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参加基準
適格基準
就学可能な年齢
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
コホートと介入
グループ/コホート |
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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.
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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.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Predictive Accuracy of the PROTEGER Machine Learning Model
時間枠:Up to 6 months post-enrollment.
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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).
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Up to 6 months post-enrollment.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Incidence of High-Grade Chemotherapy-Related Adverse Events
時間枠:At 3 and 6 months post-enrollment.
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Percentage of participants experiencing Grade 3 or higher toxicities/adverse reactions evaluated using the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
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At 3 and 6 months post-enrollment.
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General Quality of Life Score (EORTC QLQ-C30)
時間枠:Baseline, 3 months, and 6 months post-enrollment.
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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.
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Baseline, 3 months, and 6 months post-enrollment.
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Elderly-Specific Quality of Life Score (EORTC QLQ-ELD14)
時間枠:Baseline, 3 months, and 6 months post-enrollment.
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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.
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Baseline, 3 months, and 6 months post-enrollment.
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Incidence of Hospitalizations
時間枠:At 3 and 6 months post-enrollment.
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Number of patients requiring unplanned hospital admissions during the treatment course
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At 3 and 6 months post-enrollment.
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Treatment Discontinuation and Dose Reduction Rates
時間枠:At 3 and 6 months post-enrollment.
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Percentage of patients undergoing chemotherapy dose reductions (planned vs. received dose) or early treatment discontinuation.
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At 3 and 6 months post-enrollment.
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Patient Survival and Disease Progression
時間枠:At 3 and 6 months post-enrollment.
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Overall survival status and disease progression rate assessed according to RECIST 1.0 criteria.
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At 3 and 6 months post-enrollment.
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協力者と研究者
協力者
捜査官
- 主任研究者:Luciola Pontes Leite de Barros、Hospital do Coração (HCOR)
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- LACOG 0325
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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