Evaluating Intestinal Microbiome and Immune Function in Lymphoma

Overview

Información sobre este estudio

The purpose of this study is to examine the microbiome and immune function in patients with active lymphoma, and in patients with a history of lymphoma who are in clinical remission.

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:

  • Patients with a histologic diagnosis of:
    • Newly diagnosed;
    • Progressive;
    • Relapsed lymphoma (any NHL HL, or CLL histology) who are initiating or changing therapy (chemotherapy, radiotherapy, or clinical trial/ investigational agent), or who have measurable disease and are being expectantly monitored. Patients whose lymphoma is in remission and who are being monitored expectantly are eligible as a separate cohort.
  • Age > 18 years.
  • May be s/p autologous or allogeneic bone marrow transplant.
  • Ability to understand and willing to sign a written informed consent document.
  • Patients with a histologic diagnosis of relapsed lymphoma or multiple myeloma who are scheduled to undergo CAR T cell therapy (up to 25 patients).
  • Newly diagnosed, untreated DLBCL patients confirmed by pathologic review. 

​​Exclusion Criteria:

  • Patients already receiving any investigational agents or chemotherapy at time of baseline sample collection.
  • Medical illnesses with potential suppressive or activating impact on immune and bowel function as judged by the investigator.                               
  • Patients with CNS disease or lymphoma related to prior chemotherapy (new DLBCL cohort only).
  • Patients with hemoglobin level of 8 or below.

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

Eligibility last updated 3/17/23. 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

Rochester, Minn.

Investigador principal de Mayo Clinic

Thomas Witzig, M.D.

Abierto para la inscripción

Contact information:

Jacqueline Pyan

(507) 284-9050

Pyan.Jacqueline@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