- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04323579
Validation of Multiparametric Models and Circulating and Imaging Biomarkers to Improve Lung Cancer EARLY Detection. (CLEARLY)
25 de marzo de 2020 actualizado por: Istituto Clinico Humanitas
CLEARLY will focus on validation of a multifactorial "bio-radiomic" protocol for early diagnosis of lung cancer that combines circulating biomarkers and radiomic analysis.
It will (a) assess the role of molecular and cellular biomarkers (exosomes, protein signatures, circulating tumor cells - CTCs, microRNA) and radiomic signature, as complementary to assist early detection of lung cancer by low dose computed tomography-LDCT, using bioinformatics techniques; (b) assess the prognostic role of CTCs including the role of cells epithelial mesenchymal transition (EMT) and (c) standardize a method for genomic analysis of CTCs for early detection of treatment resistance.
Descripción general del estudio
Estado
Desconocido
Condiciones
Tipo de estudio
De observación
Inscripción (Anticipado)
2000
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
-
Milano
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Rozzano, Milano, Italia, 20089
- Reclutamiento
- Istituto Clinico Humanitas
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-
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
55 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Método de muestreo
Muestra no probabilística
Población de estudio
The study population should have the following inclusion criteria: Inclusion Criteria: - Age ≥ 55 years old and exposure to smoking more than 30 packsyear; which corresponds to 6-year risk of lung cancer, calculated according to the plco score (≥ 2%).
- Smoker or former smoker Former smokers must have ceased smoking within the 15 years prior to enrollment in the study.
- Absence of symptoms of lung cancer such as worsening of cough, hoarseness, hemoptysis and weight loss.
Descripción
Inclusion Criteria:
- Age ≥ 55 years old and exposure to smoking more than 30 packs-year; which corresponds to 6-year risk of lung cancer, calculated according to the plco score (≥ 2%).
- Smoker or former smoker Former smokers must have ceased smoking within the 15 years prior to enrollment in the study.
- Absence of symptoms of lung cancer such as worsening of cough, hoarseness, hemoptysis and weight loss.
Exclusion Criteria:
- Previous diagnosis of lung cancer.
- Positive extrapulmonary cancer history in the last 5 years (excluding in situ tumors or skin epidermoid tumor).
- Performing a chest CT scan in the last 18 months.
- Severe lung or extrapulmonary diseases that may preclude or invalidate appropriate therapy in case of diagnosis of malignant pulmonary neoplasia.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: Control de caso
- Perspectivas temporales: Futuro
Cohortes e Intervenciones
Grupo / Cohorte |
|---|
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prospective cohort of stage I-II lung cancer patients
A prospective cohort of stage I-II lung cancer patients (N=80) candidates to surgery at Humanitas, and 40 controls with benign nodules.
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retrospective screening cohort of 50 patients
A retrospective screening cohort of 50 patients with screened lung cancer at MUG.
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prospective screening cohort of 30 patients
A prospective screening cohort of 30 patients with screened lung cancer and 100 matched negative controls enrolled at Humanitas cohort of 1000 participants (expected annual rate 1.5%).
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retrospective screening cohort from the NELSON study
A retrospective screening cohort from the NELSON study.
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Prospective cohort of stage IV lung cancer patients
A Prospective cohort of stage IV lung cancer patients (N=30) candidate to systemic therapy.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Validation of the role of a bio-radiomic protocol as complementary tool to assist early detection of lung cancer by LDCT
Periodo de tiempo: 01 July 2018 - 01 July 2021
|
CTC analysis will be performed using fresh plasma samples.
Blood collection will be obtained for each lung cancer patient before and after surgery and once for controls.
45- and 16-miRNA signatures will be analyzed on plasma samples of the retrospective cohort (150 lung cancer patients and 120 matched controls).
We will perform the exosome antigens analysis in the retrospective cohort.
We will validate the 8-protein signature in the retrospective cohort.
We will validate the radiomic signature on CT images, and further validation will be performed on CT images of the prospective cohorts collected and 70 screened individuals of the retrospective cohort.
We will integrate results of biomarkers and radiomic data and will build a multiparametric risk model to improve early detection of lung cancer.
The final predictive model will be then applied to the cohorts analysed and integrated with LDCT results to evaluate the improvement in diagnostic accuracy.
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01 July 2018 - 01 July 2021
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Correlation of CTC spread to angiogenesis.
Periodo de tiempo: 01 July 2018 - 01 July 2021
|
Number of CTC isolated with ISET technique in the prospective cohort of lung cancer patients and controls will be correlated to angiogenesis aspects of the primary tumor at CT scan, using dynamic perfusion data and quantitative and qualitative assessment of angiogenesis (surface fractal dimension and microvessel density) on hysthological examination.
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01 July 2018 - 01 July 2021
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Assessment of epithelial mesenchymal transition (EMT) in CTC as a hallmark of poor prognosis.
Periodo de tiempo: 01 July 2018 - 01 July 2021
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The presence of CTC passed through EMT will be identified using immunoistochimical specific exams.
The correlation between the presence of CTCs in EMT and prognostic factors of primary tumor (disease stage, volume doubling time, etc) will show the possible prognostic role of CTC immunoistochemical analysis.
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01 July 2018 - 01 July 2021
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Standardise a method for genomic analysis from isolated CTCs for the early detection of resistance to treatments
Periodo de tiempo: 01 July 2018 - 01 July 2021
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A population of patients with advanced stage disease (stage III and IV) will be first analyzed to enrich for CTCs in the collected blood samples.
This would help the initial refinement of the experimental protocol to detect CTC and analyse their mutational profile by single-cell NGS analysis.
In addition, since most of these patients will undergo systemic treatment, we will setup a longitudinal study where the mutational profile of CTC will be investigated and correlated to chemotherapy response, to early identify theranostic mutations.
The same refined protocol will be next validated on the prospective cohort of LDCT screened patients to further prove its validity to early detect cancer driver mutations.
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01 July 2018 - 01 July 2021
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de julio de 2018
Finalización primaria (Anticipado)
1 de julio de 2021
Finalización del estudio (Anticipado)
1 de julio de 2021
Fechas de registro del estudio
Enviado por primera vez
10 de enero de 2019
Primero enviado que cumplió con los criterios de control de calidad
25 de marzo de 2020
Publicado por primera vez (Actual)
26 de marzo de 2020
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
26 de marzo de 2020
Última actualización enviada que cumplió con los criterios de control de calidad
25 de marzo de 2020
Última verificación
1 de marzo de 2020
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2122
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
producto fabricado y exportado desde los EE. UU.
No
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