Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Oncogeriatric Screening and Evaluation Program (PROTEGER)

1 de setembro de 2026 atualizado por: 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.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

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.

Tipo de estudo

Observacional

Inscrição (Estimado)

412

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Método de amostragem

Amostra Não Probabilística

População do estudo

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.

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

Coortes e Intervenções

Grupo / Coorte
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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Predictive Accuracy of the PROTEGER Machine Learning Model
Prazo: 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.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Incidence of High-Grade Chemotherapy-Related Adverse Events
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Colaboradores

Investigadores

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

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

1 de setembro de 2026

Conclusão Primária (Estimado)

1 de janeiro de 2027

Conclusão do estudo (Estimado)

1 de julho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

24 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

1 de setembro de 2026

Primeira postagem (Real)

4 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

4 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

1 de setembro de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • LACOG 0325

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Se inscrever