Cognitive Impairment in Patients Undergoing Cell- and Antibody-based Immunotherapies for Haematological Malignancies: The COGNITOX Study (COGNITOX)
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.
調査の概要
状態
研究の種類
入学 (推定)
連絡先と場所
研究場所
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Aarhus、デンマーク
- Aarhus University Hospital
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コンタクト:
- Astrid Lindman, PhD, MScH, RN, clinical spec.
- 電話番号:+45 24900046
- メール:astrlind@rm.dk
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Cancer related cognitive impairment (CRCI)
時間枠:Day 0, month 3, month 6, month 12, month 24, month 36
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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.
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Day 0, month 3, month 6, month 12, month 24, month 36
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Overall and progression-free survival
時間枠:3 years
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Overall and progression-free survival
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3 years
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Health related quality of life (HM-PRO score)
時間枠:3 years
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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
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Return to work (RTW)
時間枠:3 years
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Return to work/occupational status Day 0 the following data is collected:
Data collected at 6-, 12-, 24-, 36-month follow-up:
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
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3 years
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協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 血管疾患
- 心血管疾患
- 新生物
- 免疫系疾患
- 組織型別の新生物
- 血液疾患
- リンパ疾患
- リンパ増殖性疾患
- 免疫増殖性疾患
- リンパ腫、非ホジキン
- リンパ腫、B細胞
- 新生物、形質細胞
- 止血障害
- パラタンパク血症
- 血液タンパク質障害
- 出血性疾患
- ヘミックおよびリンパ疾患
- リンパ腫
- 多発性骨髄腫
- リンパ腫、B細胞、辺縁帯
- 保健サービス管理
- ヘルスケアの質、アクセス、評価
- 調査手法
- 疫学的方法
- データ収集
- ヘルスケア評価メカニズム
- ヘルスケアの質
- 公衆衛生
- 環境と公衆衛生
- 行動の分野と活動
- ヘルスケアの経済学と組織
- 結果の評価、ヘルスケア
- 結果とプロセス評価、ヘルスケア
- 心理的検査
- 調査とアンケート
- 健康計画
- ヘルスケア調査
- 医療サービスの研究
- 患者の転帰評価
- 神経心理学的検査
- 患者はアウトカム測定を報告しました
その他の研究ID番号
- File nr. 1-10-72-128-25
- Ethics (その他の識別子:Komisja Bioetyczna przy Dolnoslaskiej Izbie Lekarskiej)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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