- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT04492969
Prospective Observation of Failure Patterns in NSCLC Treated With ICIs
Prospective Observational Study of Failure Patterns in Non-small Cell Lung Cancer Patients Treated With Immune Checkpoint Inhibitors
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Xiao Chu, PhD
- Número de teléfono: +86-15821383376
- Correo electrónico: crazychu0044@163.com
Ubicaciones de estudio
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Shanghai
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Shanghai, Shanghai, Porcelana, 200031
- Fudan University Shanghai Cancer Center
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Contacto:
- Xiao Chu
- Número de teléfono: 15821383376
- Correo electrónico: crazychu0044@163.com
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria (Part I):
- Age between 18 and 75 years.
- ECOG PS 0-1.
- Pathologically confirmed stage IV NSCLC.
- Negative for driver genes including EGFR, ALK, and ROS-1.
- Patients achieved PR or CR after ICI treatment, as defined by RECIST 1.1.
- Patients with complete radiological information of baseline lesions.
- Life expectancy of more than 3 months.
- Ability to understand and willingness to provide the informed consent.
Exclusion Criteria (Part I):
- Severe autoimmune disease or other contradictions to ICI treatment.
- Mixed small cell with non-small cell lung cancer histology.
- Driver gene positive, including EGFR, ALK, and ROS-1.
- Pregnant or lactating women.
- History of any other malignancy.
- Active infection, congestive heart failure, myocardial infarction within the 6 months prior to enrollment, unstable angina pectoris or cardiac arrhythmia.
- Patients receiving immunosuppressive agents,or other investigational treatment. Long-term corticosteroid users are also excluded.
- Mental disorders, drug abuse, and social condition that may negatively impact compliance in the opinion of the investigator.
Inclusion Criteria (Part II, patients with OPD):
- Patients with oligo-progression disease (1-3 progression lesions in 1-2 organs) when developing acquired resistance to ICI.
- Radiotherapy to at least one of the OPD lesions is indicated in the opinion of the investigator. At least one of the irradiated lesion(s) should be evaluable according to RECIST 1.1.
- ECOG PS 0-2.
- Life expectancy of more than 3 months.
- Complete radiological information of all lesions during the follow-up.
- Patients with a prior history of surgery are eligible if they have recovered adequately from the toxicity and/or complications of surgery.
- Adequate bone marrow function within 1 week prior to the enrollment: hemoglobin ≥80g/L, white blood cell (WBC) count ≥ 4.0 * 10 ^ 9/L or neutrophil count ≥ 1.5 * 10 ^ 9/L, and platelet count ≥ 100 * 10 ^ 9/L;
- Ability to understand and willingness to provide the informed consent.
Exclusion Criteria (Part II):
- Secondary malignancy.
- Histology transformation to non-NSCLC.
- Ineligible for radiotherapy in the opinion of the investigator. Or none of the OPD are evaluable by RECIST 1.1.
- ECOG PS 3 or worse.
- Short life expectancy (less than 3 months).
- Unable to provide complete radiological information of lesions.
- Inadequate bone marrow function.
- Cannot understand or unwilling to provide the informed consent.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Oligo-progression disease rate in NSCLC patients developing acquired resistance to ICI treatment.
Periodo de tiempo: at least 2 months after ICI treatment.
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Acquired resistance (AR) was defined as disease progression after partial or complete response (PR or CR) to ICI treatment. (by RECIST standard v1.1) When observing disease progression in ICI treatment, the number and distribution of progression lesions were recorded. Oligo-progression disease (OPD) was defined as 1-3 progression lesions in 1-2 organs. The OPD rate in all AR cases will be calculated. |
at least 2 months after ICI treatment.
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Porcentaje de participantes con eventos adversos
Periodo de tiempo: Dos años
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Los eventos adversos relacionados con el tratamiento se evaluaron y calificaron de acuerdo con CTCAE v. 5.0.
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Dos años
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Overall objective response rate to radiotherapy.
Periodo de tiempo: at least 4 weeks after radiotherapy.
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When radiotherapy to at least one of the OPD lesions is indicated in the opinion of the investigator.
Overall objective response rate (ORR) to radiotherapy will be recorded.
ORR was defined as the proportion of participants with partial response (PR) or complete response (CR) to treatment as defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1.
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at least 4 weeks after radiotherapy.
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Objective response rate in non-irradiated lesion
Periodo de tiempo: at least 4 weeks after radiotherapy.
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Objective response rate (ORR) in Non-irradiated Lesion was defined as the proportion of patients with at least 30% reduction from baseline in the longest diameter of any of non-irradiated target lesions defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 at any time-point from the date of treatment initiation to the date of last follow-up.
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at least 4 weeks after radiotherapy.
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Overall Survival since AR development.
Periodo de tiempo: Two years
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OS was defined as the time from the date of enrollment until death by any cause.
Participants still alive at the time of data analysis were censored at the date of last follow-up.
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Two years
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Anticipado)
Finalización primaria (Anticipado)
Finalización del estudio (Anticipado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 2019-CSCOBMS
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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