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

2026년 4월 22일 업데이트: 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.

연구 개요

연구 유형

관찰

등록 (추정된)

225

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

      • Aarhus, 덴마크
        • Aarhus University Hospital
        • 연락하다:
          • Astrid Lindman, PhD, MScH, RN, clinical spec.
          • 전화번호: +45 24900046
          • 이메일: astrlind@rm.dk

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

샘플링 방법

비확률 샘플

연구 인구

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.

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Cancer related cognitive impairment (CRCI)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Overall and progression-free survival
기간: 3 years
Overall and progression-free survival
3 years
Health related quality of life (HM-PRO score)
기간: 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)
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 3월 31일

기본 완료 (추정된)

2032년 3월 31일

연구 완료 (추정된)

2034년 3월 31일

연구 등록 날짜

최초 제출

2026년 3월 10일

QC 기준을 충족하는 최초 제출

2026년 4월 22일

처음 게시됨 (실제)

2026년 4월 30일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 4월 30일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 4월 22일

마지막으로 확인됨

2026년 3월 1일

추가 정보

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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