Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Cognitive Impairment in Patients Undergoing Cell- and Antibody-based Immunotherapies for Haematological Malignancies: The COGNITOX Study (COGNITOX)

22 de abril de 2026 actualizado por: Aarhus University Hospital

Cell- and antibody-based therapies, including chimeric antigen receptor T-cell (CAR-T) therapy and bispecific antibodies, represent significant advances in the treatment of hematologic malignancies. These therapies optimise the patient's immune system to target and eliminate malignant cells, achieving profound and durable responses in patients where conventional treatment approaches have failed. However, their mechanism of action-through profound immune activation-introduces a challenging toxicity profile, including cytokine release syndrome and immune effector cell-induced neurotoxicity. Emerging evidence suggests that neurotoxicity associated with these therapies may extend beyond acute symptoms to include persistent cognitive impairments. Such impairments can manifest deficits in memory, attention, executive functioning, and processing speed, potentially compromising patients' quality of life, ability to manage daily activities and return to work.

The COGNITOX project explores the occurrence, clinical manifestations, and impact on quality of life of neuro-psychologically assessed and patient-reported cognitive impairment. The project's data set is generated through standardized neuropsychological tests (recommended by the International Cognition and Cancer) and validated patient reported outcome measures, to evaluate multiple cognitive domains. The project is developed in close collaboration between the Department of Haematology, Aarhus University Hospital and the Unit for Psychooncology and Health Psychology (EPoS), Department of Psychology and Behavioural Sciences, Aarhus University.

The current literature on cognitive impairment secondary to cell- and antibody-based therapies is limited, and none of the studies reported so far were conducted within a Danish healthcare context. Understanding the prevalence, severity, and functional impact of cognitive impairments in this patient population is critical. These insights will inform clinical practice, guide patient counseling, and support the development of targeted interventions aimed at mitigating cognitive decline. By generating robust data, this project seeks to improve the knowledge within the field and lay the foundation for an intervention study addressing the needs of patients undergoing these advanced immunotherapies.

Descripción general del estudio

Tipo de estudio

De observación

Inscripción (Estimado)

225

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

      • Aarhus, Dinamarca
        • Aarhus University Hospital
        • Contacto:
          • Astrid Lindman, PhD, MScH, RN, clinical spec.
          • Número de teléfono: +45 24900046
          • Correo electrónico: astrlind@rm.dk

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

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Método de muestreo

Muestra no probabilística

Población de estudio

Patients diagnosed with a malignant haematological disease at the Department of Haematology, Aarhus University Hospital will be enrolled according to the above mentioned treatment subsets and pre-defined inclusion criteria.

Descripción

Inclusion Criteria:

  • Patients must be ≥ 18 years old
  • Able to speak and read Danish
  • Provide informed consent

Exclusion Criteria:

  • CNS-involvement by the haematological malignancy
  • Cognitive impairment due to pre-existing psychiatric or neurological conditions

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
Cancer related cognitive impairment (CRCI)
Periodo de tiempo: Day 0, month 3, month 6, month 12, month 24, month 36
The primary endpoint of the study is the occurrence, of cancer related cognitive impairment (CRCI) in patients treated with either chimeric antigen receptor T-cell therapy (CAR-T) or bispecific antibodies (BsAbs) as compared to high dose chemotherapy with autologous haematopoietic stem cell transplantation (AutoHSCT). Clinical manifestations and severity of CRCI will also be reported as descriptive co-primary endpoints.
Day 0, month 3, month 6, month 12, month 24, month 36

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall and progression-free survival
Periodo de tiempo: 3 years
Overall and progression-free survival
3 years
Health related quality of life (HM-PRO score)
Periodo de tiempo: 3 years

The HM-PRO has 24 items in Part A and 18 items in Part B. Each question has three response options:

Part A Not at all (score = 0) A little (1) A lot (2) Not applicable Part B Not at all (score = 0) Mild (1) Severe (2) The score range for Part A is 0-48 and for Part B is 0-36. The higher the total score, the greater the effect on a patient's quality of life.

The items in the HM-PRO are divided into four categories (domains):

Physical Behaviour (the first 7 items, maximum score of 14) Social Well-being (the second 3 items, maximum score of 6) Emotional Behaviour (the third 11 items, maximum score of 22) Eating and Drinking (the last 3 items, maximum score of 6)

HM-PRO Part A score is reported as a single total score HM-PRO A-total, score range 0-48

The HM-PRO Part A score is also reported as four separate scores:

HM-PRO Physical, score range 0-14 HM-PRO Social, score range 0-6 HM-PRO Emotional, score range 0-22 HM-PRO Eating/Drinking, score range 0-6 HM-PRO B-total (score range 0-36)

3 years
Return to work (RTW)
Periodo de tiempo: 3 years

Return to work/occupational status

Day 0 the following data is collected:

  1. Self-employed
  2. Employee
  3. Working full time
  4. Working part time (hours/week)
  5. Unemployed
  6. On sick leave
  7. Early retirement
  8. Pensioner
  9. Dismissed
  10. Disability or anticipatory pensioner
  11. Enrolled in education

    1. Continue studies during the treatment
    2. Pausing studies during the treatment
    3. Dropped out of study/education
  12. Other

Data collected at 6-, 12-, 24-, 36-month follow-up:

  • Still on sick leave
  • Dismissed
  • Gradually increasing hours/week. Aiming at return to full time/part time
  • Worked full time or part time at baseline, changed to:

Working part time or part time, but less hours/week than before

• Changes in job description (yes/no) if yes: New less responsible job description Other changes in job description

  • Enrolled in education Continue/pausing studies during the cancer treatment and follow-up Completed education Dropped out of study/education
  • Retired
  • Other
3 years

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 (Estimado)

31 de marzo de 2026

Finalización primaria (Estimado)

31 de marzo de 2032

Finalización del estudio (Estimado)

31 de marzo de 2034

Fechas de registro del estudio

Enviado por primera vez

10 de marzo de 2026

Primero enviado que cumplió con los criterios de control de calidad

22 de abril de 2026

Publicado por primera vez (Actual)

30 de abril de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

30 de abril de 2026

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

22 de abril de 2026

Última verificación

1 de marzo de 2026

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. .

Suscribir