Immune Response to Antigens

Overview

Información sobre este estudio

The purpose of this study is to sequence patient germline and tumor samples, and nominate top neoantigen candidates using an in-house developed bioinformatics pipeline, and to validate the neoantigen candidates by laboratory assays using patient peripheral blood immune cells or serum.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Age > 18 years
  • For cancer patients:
    • 100 samples from different cancer types, solid or blood tumors. We expect we’ll have the largest number of breast cancer patients as mentioned above.
    • Stages II, III, or IV disease.
  • Provide written informed consent.
  • Willingness to provide blood samples for neoantigen validation and T-cell activity assays.

 

Exclusion Criteria:

  • Immunocompromised patients including patients known to be HIV positive.
  • Patients receiving systemic steroid therapy or any other immunosuppressive therapy ≤ 30 days prior to registration. NOTE: Inhaled steroids, low-dose corticosteroids (e.g. equivalent to or less than oral prednisone 10 mg daily), and steroid use for primary prevention of nausea per institutional guidelines are allowed.
  • Patients who received radiation therapy to the planned biopsy site within 6 months.
  • Recent chemotherapy is not an exclusion criterion.
  • Patients will also be excluded based on tissue/RNA/DNA quality and quantity
    • If any of the following quality and quantity thresholds are not met, the patient will be excluded:
      • Tumor tissue cellularity equal to or greater than 30%;
      • There are ≥ 2 cores with passing cellularity;
      • ≥ 30% of tumor RNA with fragment sizes are ≥ 200 base pairs;  
      • < 10% of DNA fragments are smaller than 1 kb; and
      • Sufficient amount of both DNA (blood and tumor) and RNA (tumor) for exome sequencing and standard RNAseq according to the Mayo sequencing core (note: kits and technologies change overtime, so these are not fixed numbers). Note that since long-read RNAseq is optional, poor long-read RNAseq data (if generated) quality is not an exclusion criterion.
  • Pregnant women will not be allowed to enroll on this study.
  • Patients will either have the archived frozen tissue or consented to give fresh tissue biopsy and blood samples to the study.  Alternatively, if tumor sequence data is already available from 14-004094, that data can be used in the place of a newly collected or archived frozen sample.  However, fresh blood must still be collected.

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 11/15/22. Questions regarding updates should be directed to the study team contact

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Jacksonville, Fla.

Investigador principal de Mayo Clinic

Yan Asmann, Ph.D.

Abierto para la inscripción

Contact information:

Yan Asmann Ph.D.

(904) 953-6717

asmann.Yan@mayo.edu

More information

Publicaciones

Publications are currently not available

Información adicional de contacto

Formulario de contacto para ensayos sobre cáncer

Teléfono: 855-776-0015 (toll-free)

Preguntas de estudios clínicos para pacientes internacionales