- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07805642
Oncogeriatric Screening and Evaluation Program (PROTEGER)
PROgrama de Tamizaje y Evaluación oncoGERiátrica
연구 개요
상태
정황
상세 설명
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.
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Project Manager
- 전화번호: +55 51 3384 5334
- 이메일: lacog0325@lacog.group
연구 연락처 백업
- 이름: Head of Clinical Operations
- 전화번호: +55 (51) 3384.5334
- 이메일: laura.voelcker@lacog.group
연구 장소
-
-
São Paulo
-
São Paulo, São Paulo, 브라질, 05653-000
- HIAE - Hospital Israelita Albert Einstein
-
수석 연구원:
- Ludmila de Oliveira Muniz Koch
-
São Paulo, São Paulo, 브라질, 04004-060
- BR192 HCOR - Hospital do Coração
-
수석 연구원:
- Luciola Pontes Leite de Barros
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
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.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
|---|
|
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.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Predictive Accuracy of the PROTEGER Machine Learning Model
기간: 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.
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Incidence of High-Grade Chemotherapy-Related Adverse Events
기간: 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)
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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.
|
공동 작업자 및 조사자
협력자
수사관
- 수석 연구원: Luciola Pontes Leite de Barros, Hospital do Coração (HCOR)
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
기타 연구 ID 번호
- LACOG 0325
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .