Cusworth Samuel, Deplano Zareen, Denniston Alastair K, Burns David, Nirantharakumar Krishnarajah, Adderley Nicola, Chandan Joht Singh
NIHR, Blood and Transplant Research Unit (BTRU) in Precision Transplant and Cellular Therapeutics, University of Birmingham, Birmingham, England, UK
Department of Applied Health Sciences, University of Birmingham, Birmingham, UK.
BMJ Open. 2025 May 21;15(5):e099354. doi: 10.1136/bmjopen-2025-099354.
Haematological cancers are common in the UK, with a variety of morphologies. Stem cell transplants and chimeric antigen receptor (CAR) T-cell therapies provide significant options for hard to treat haematological cancers, although with difficult to predict outcomes. Research into the determinates of treatment efficacy, and access to treatments, is key to ensuring equal benefit across patients and patient safety. With this, there are concerns about the small representation of minority groups in related research. We aim to report on the current knowledge to guide future research.
A variety of databases will be searched for literature on UK minority ethnic populations receiving haematopoietic stem cell transplant or CAR T-cell therapy. Searches will be restricted to the year 2011 or later. Many outcomes will be analysed, covering the patient care pathway for those of the target population, although with a focus on follow-up after therapy. Plans have been made to conduct narrative synthesis, with meta-analysis where applicable.
Ethical approval is not required for this study. Outputs will be published in an appropriate journal and discussed with the wider National Institute for Health and Care Research Blood and Transplant Research Unit in Precision Transplant and Cellular Therapeutics (BTRU) group. Discussions will also be undertaken with the BTRU patient partners group.
血液系统癌症在英国很常见,有多种形态。干细胞移植和嵌合抗原受体(CAR)T细胞疗法为难治性血液系统癌症提供了重要选择,尽管其疗效难以预测。研究治疗效果的决定因素以及治疗的可及性,是确保患者平等受益和患者安全的关键。鉴于此,人们担心少数群体在相关研究中的代表性不足。我们旨在报告当前的知识,以指导未来的研究。
将在多个数据库中搜索关于接受造血干细胞移植或CAR T细胞疗法的英国少数族裔人群的文献。搜索将限于2011年或之后。将分析多种结果,涵盖目标人群的患者护理路径,不过重点是治疗后的随访。已计划进行叙述性综合分析,并在适用时进行荟萃分析。
本研究无需伦理批准。研究结果将发表在合适的期刊上,并与更广泛的国家卫生与保健研究所精准移植与细胞治疗血液与移植研究单位(BTRU)小组进行讨论。还将与BTRU患者合作伙伴小组进行讨论。