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Oncogeriatric Screening and Evaluation Program (PROTEGER)

1 september 2026 uppdaterad av: 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.

Studieöversikt

Status

Har inte rekryterat ännu

Betingelser

Detaljerad beskrivning

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.

Studietyp

Observationell

Inskrivning (Beräknad)

412

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Studieorter

    • São Paulo
      • São Paulo, São Paulo, Brasilien, 05653-000
        • HIAE - Hospital Israelita Albert Einstein
        • Huvudutredare:
          • Ludmila de Oliveira Muniz Koch
      • São Paulo, São Paulo, Brasilien, 04004-060
        • BR192 HCOR - Hospital do Coração
        • Huvudutredare:
          • Luciola Pontes Leite de Barros

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Äldre vuxen

Tar emot friska volontärer

Nej

Testmetod

Icke-sannolikhetsprov

Studera befolkning

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.

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Predictive Accuracy of the PROTEGER Machine Learning Model
Tidsram: 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.

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of High-Grade Chemotherapy-Related Adverse Events
Tidsram: 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)
Tidsram: 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)
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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.

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Utredare

  • Huvudutredare: Luciola Pontes Leite de Barros, Hospital do Coração (HCOR)

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 september 2026

Primärt slutförande (Beräknad)

1 januari 2027

Avslutad studie (Beräknad)

1 juli 2027

Studieregistreringsdatum

Först inskickad

24 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

1 september 2026

Första postat (Faktisk)

4 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

4 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

1 september 2026

Senast verifierad

1 augusti 2026

Mer information

Termer relaterade till denna studie

Nyckelord

Andra studie-ID-nummer

  • LACOG 0325

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