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Biomarkers of Response to Systemic Treatments in FH-deficient RCC

15 de agosto de 2022 actualizado por: RenJi Hospital

Renji Hospital, School of Medicine, Shanghai Jiao Tong University

Fumarate hydratase-deficient renal cell carcinoma (FH-deficient RCC) is a rare subtype of RCC characterized by germline/somatic mutation of the fumarate hydratase (FH) gene, and is an extremely aggressive tumor, with a propensity to disseminate early even in the setting of a small primary tumor.

Affected individuals or individuals suspected of having a germline FH will undergo periodic clinical assessment and genetic analyses for the purpose of: 1) definition and characterization of phenotype, 2) determination of the natural history of the disorder, and 3) genotype/phenotype correlation. Genetic linkage studies may be performed in situations in which the genetic basis of the disorder has not been elucidated.

Descripción general del estudio

Descripción detallada

  • Discovery and validation of biomarker predicting FH-deficient RCC systemic treatments response
  • Analysis for expression level of ctDNA using Next generation sequencing in FH-deficient RCC blood by systemic treatments response
  • Analysis for expression level of mRNA using Next generation sequencing in FH-deficient RCC tissue by systemic treatments response
  • Analysis for expression level of small molecule metabolites using mass spectrometry in FH-deficient RCC tissue and blood by systemic treatments response
  • Analysis for genetic and protein expression at a single-cell level using a novel flow cytometry and RNA-sequencing protocol in FH-deficient RCC tissue and blood.
  • Validation of genetic and protein expression using qRT-PCR or IHC in multiple independent cohort.
  • Biological biomarkers-clinical factor combined prediction model of FH-deficient RCC systemic treatments response

Tipo de estudio

De observación

Inscripción (Anticipado)

100

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

      • Shanghai, Porcelana, 200127
        • Reclutamiento
        • Yunze Xu
        • Contacto:
          • Yunze Xu
          • Número de teléfono: +8618801967501
          • Correo electrónico: rjxuyunze@163.com

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

18 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

Participants with FH-RCC who have given prior consent for their samples and data to be used, and who have adequate samples and data available.

Descripción

Inclusion Criteria:

  1. ≥18 years old;
  2. histopathological evidence of FH-deficient renal cell carcinoma, which was confirmed by Sanger or next-generation sequencing after initial screening by IHC.
  3. included patients must be diagnosed with metastatic renal cell carcinoma or have a TNM stage IV (according to 2009 TNM Classification);
  4. new FH-RCC patients who has scheduled to start 1st cycle of systemic treatment;
  5. ECOG score ≤2;
  6. life expectancy ≥ 3 months;
  7. sign informed consent, and be able to follow the visit and related procedures stipulated in the program;
  8. agree to collect tumor tissue, blood and other specimens required by this study and apply them to relevant studies;
  9. Patients must have consent in place, for the use of tissue and imaging to be used for the purposes of clinical research; Use of tissue not required for their diagnosis or treatment to be stored and used for the purposes of clinical research, which may include genetic research. Use of relevant sections of their medical records, or by relevant regulatory authorities, where my tissue is being used for research, giving permission for those individuals to have access to their medical records. Participants must also meet at least one of the following criteria to be eligible: For tissue analysis: Patient must have tumour tissue and/or normal adjacent kidney stored (either as formalinfixed paraffin-embedded tissue, or as 'fresh frozen' tissue). For imaging analysis: Patient must have had at least 1 scan (either CT or MRI) within 28 days of starting treatment with systemic treatment for their cancer.

Exclusion Criteria:

  1. patients with other malignant tumors with different primary sites or histology from the tumor evaluated in this study within 2 years of personal history, except those with basal cell carcinoma of the skin, squamous cell carcinoma of the skin or cervical carcinoma in situ under good control;
  2. major surgery or severe trauma within 4 weeks before enrollment;
  3. known or suspected active autoimmune diseases (congenital or acquired), such as interstitial pneumonia, uveitis, enteritis, hepatitis, pituitary inflammation, vasculitis, nephritis, thyroiditis, etc. Patients with type 1 diabetes with good insulin control can also be enrolled.
  4. known allogeneic organ transplantation (except corneal transplantation) or allogeneic hematopoietic stem cell transplantation;
  5. allergic to any component of monoclonal antibody;
  6. suffering from other uncontrolled serious diseases, including but not limited to: A) severe infection in the active phase or clinically poorly controlled; B) HIV infection (HIV antibody positive); C) acute or chronic active hepatitis b (HBsAg positive and HBV DNA>1*103/ml) or acute or chronic active hepatitis c (HCV antibody positive and HCV RNA>15IU/ml); D) active tuberculosis, etc.;
  7. class iii-iv congestive heart failure (New York heart association classification), poorly controlled and clinically significant arrhythmia;
  8. uncontrolled arterial hypertension (systolic blood pressure ≥160mmHg or diastolic blood pressure ≥100mmHg);
  9. pregnant or lactating women.

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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

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Metabolomics
Periodo de tiempo: 2 years
across multiple LC-MS data files. across multiple LC-MS data files. across multiple LC-MS data files. across multiple LC-MS data files. across multiple LC-MS data files
2 years
Determine genotype/phenotype correlations
Periodo de tiempo: 3 years
Collection of blood, tissue & urine to address further scientific questions related to this protocol.
3 years
Discovery of predicting bio-markers for FH-deficient RCC systemic treatments response
Periodo de tiempo: 3 years
Combination prediction model of biologic biomarkers and clinical factors for the response of systemic treatments in FH-RCC.
3 years

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

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)

25 de mayo de 2022

Finalización primaria (Anticipado)

1 de junio de 2024

Finalización del estudio (Anticipado)

1 de junio de 2024

Fechas de registro del estudio

Enviado por primera vez

20 de diciembre de 2021

Primero enviado que cumplió con los criterios de control de calidad

7 de febrero de 2022

Publicado por primera vez (Actual)

16 de febrero de 2022

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

16 de agosto de 2022

Última actualización enviada que cumplió con los criterios de control de calidad

15 de agosto de 2022

Última verificación

1 de agosto de 2022

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

INDECISO

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

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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