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Набор по приглашению NCT07372261

Validation of a Prognostic Method for Assessing the Risk of Distant Metastasis in Early-stage Breast Cancer

Наблюдательное Breast Cancer Early Stage Breast Cancer (Stage 1-3)

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Validation of Prognostic tool.
Кому может быть актуально
Состояния в реестре: Breast Cancer Early Stage Breast Cancer (Stage 1-3). Базовые параметры: от 18 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Италия
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Dissecting the Role of miR-3916 and miR3613-5p in Breast Cancer and Developing a Metastases Predictor PORTENT Algorithm

Обзор

This is a multicenter, observational validation study designed to evaluate the prognostic performance of the PORTENT algorithm in patients with early-stage breast cancer. The model integrates clinicopathological variables and the expression levels of two small non-coding RNAs (miR-3916 and miR-3613-5p) to estimate individual risk of developing distant metastases. The primary objective is to assess the discriminatory ability of the PORTENT algorithm for predicting distant metastasis at predefined time points after diagnosis.

Подробное описание

This multicenter retrospective observational study aims to clinically validate the PORTENT prognostic algorithm for predicting the risk of distant metastases in women with early-stage breast cancer. Female patients with Stage I-III disease from three independent cohorts with available residual tumor tissue and follow-up data will be included.

The primary endpoint of the study is the discriminatory performance of the PORTENT algorithm, assessed by the area under the receiver operating characteristic curve (AUC) for the prediction of distant metastases at 5 and 10 years from diagnosis.

The algorithm integrates established clinicopathological prognostic factors (tumor stage, histological grade, and Ki67-MIB1) with the expression levels of miR-3916 and miR-3613-5p. MicroRNA expression and target protein expression will be evaluated using RT-qPCR and immunohistochemistry.

Secondary and exploratory analyses will include model calibration assessed using calibration curves and the Integrated Calibration Index (ICI), as well as survival analyses (overall survival, progression-free survival, and metastasis-free survival) performed using Cox proportional hazards models.

Вмешательства

  • Диагностический тест Validation of Prognostic tool
    Collection of Clinical History: Clinical data, including medical history, clinicopathological features (e.g., age, histology, receptor and nodal status), and follow-up information (presence or absence of metastasis, patient vital status), will be collected and entered into a dedicated platform by. Follow-up updates are scheduled by Month 48 of the project (December 31, 2025) to ensure timely and accurate patient outcome data. Laboratory Analysis: Residual tumor sections prepared by the Patholog

Первичные конечные точки

  • Discriminatory Performance of the Prognostic Algorithm (AUC) for Prediction of Distant Metastasis Within 5 Years From Diagnosis [Срок оценки: 5 years from diagnosis; interim analysis at March 2027.]
  • Discriminatory Performance of the Prognostic Algorithm (AUC) for Prediction of Distant Metastasis Within 10 Years From Diagnosis [Срок оценки: 10 years from diagnosis; final analysis after completion of 10-year follow-up for all participants (expected by 2029).]
Вторичные конечные точки (8)
  • Calibration of the Prognostic Model at 5 Years (Integrated Calibration Index) [Срок оценки: 5 years from diagnosis; interim analysis at March 2027.]
  • Calibration of the Prognostic Model at 10 Years (Integrated Calibration Index) [Срок оценки: 10 years from diagnosis; final analysis after completion of 10-year follow-up (expected by 2029).]
  • Difference in Discriminatory Performance Between Prognostic Models (ΔAUC) at 5 Years [Срок оценки: 5 years from diagnosis; interim analysis at March 2027.]
  • Difference in Discriminatory Performance Between Prognostic Models (ΔAUC) at 10 Years [Срок оценки: 10 years from diagnosis; final analysis after completion of 10-year follow-up (expected by 2029).]
  • Classification Performance of the Prognostic Algorithm at 10 Years (Sensitivity, Specificity, PPV, NPV) [Срок оценки: 10 years from diagnosis; final analysis after completion of 10-year follow-up (expected by 2029).]
  • Association Between miR-3916 and miR-3613-5p Expression and Overall Survival [Срок оценки: Up to 10 years from diagnosis; final analysis after completion of follow-up (expected by 2029).]
  • Prognostic Algorithm Performance Within PAM50 Molecular Subgroups [Срок оценки: 5 and 10 years from diagnosis; final analysis after completion of follow-up (expected by 2029).]
  • Analytical Validity of miRNA Expression Assessment [Срок оценки: Data collection and analysis completed by March 2027.]

Критерии участия

Критерии включения

  • Stage I-III breast cancer
  • Residual tumor tissue available
  • Written informed consent

Критерии исключения

  • Age <18
  • Stage IV at diagnosis
  • Refusal or inability to provide informed consent

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

Италия · 1 центр
  • Fondazione Casa Sollievo della Sofferenza IRCCS — San Giovanni Rotondo

Публикации

  • Fontana A, Barbano R, Pasculli B, Mazza T, Palumbo O, Binda E, Trivieri N, Mencarelli G, Laurenzana I, Lamorte D, De Luca L, Caivano A, Biagini T, Rendina M, Lo Mele A, Prencipe G, Bravaccini S, Murgo R, Ciuffreda L, Morritti M, Valori VM, Di Lisa FS, Vici P, Castelvetere M, Carella M, Graziano P, Maiello E, Copetti M, Esteller M, Parrella P. Development of a microRNA-based prognostic model for ac PMID 41024243

Идентификаторы

NCT: NCT07372261 · PORTENT

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗