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美国细胞治疗活动的当前趋势与成果,包括国际血液和骨髓移植研究中心登记处对患者前瞻性报告结果的数据收集。

Current Trends and Outcomes in Cellular Therapy Activity in the United States, Including Prospective Patient-Reported Outcomes Data Collection in the Center for International Blood and Marrow Transplant Research Registry.

作者信息

Cusatis Rachel, Litovich Carlos, Feng Zhongyu, Allbee-Johnson Mariam, Kapfhammer Miranda, Mattila Deborah, Akinola Idayat, Phelan Rachel, Broglie Larisa, Auletta Jeffery J, Steinert Patricia, Bolon Yung-Tsi, Akhtar Othman, Bloomquist Jenni, Chen Min, Devine Steven M, Bupp Caitrin, Hamadani Mehdi, Hengen Mary, Jaglowski Samantha, Kaur Manmeet, Kuxhausen Michelle, Lee Stephanie J, Moskop Amy, Page Kristin M, Pasquini Marcelo C, Rizzo Doug, Saber Wael, Spellman Stephen R, Stefanski Heather E, Tuschl Eileen, Yusuf Rafeek, Zhan Keming, Flynn Kathryn E, Shaw Bronwen E

机构信息

Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.

Center for International Blood and Marrow Transplant Research, Medical College of Wisconsin, Milwaukee, Wisconsin.

出版信息

Transplant Cell Ther. 2024 Sep;30(9):917.e1-917.e12. doi: 10.1016/j.jtct.2024.06.021. Epub 2024 Jun 27.

Abstract

The Center for International Blood and Marrow Transplant Research (CIBMTR) prepares an annual set of summary slides to summarize the trends in transplantation and cellular therapies. For the first time in the 2023 summary slides, the CIBMTR incorporated data for patients receiving chimeric antigen receptor T cell (CAR-T) infusions. In addition, data on patient-reported outcomes (PROs) are included. This report aims to update the annual trends in US hematopoietic cell transplantation (HCT) activity and incorporate data on the use of CAR-T therapies. A second aim is to present and describe the development, implementation, and current status of PRO data collection. In August 2020, the CIBMTR launched the Protocol for Collection of Patient-Reported Outcomes Data (CIBMTR PRO Protocol). The CIBMTR PRO Protocol operates under a centralized infrastructure to reduce the burden to centers. Specifically, PRO data are collected from a prospective convenience sample of adult HCT and CAR-T recipients who received treatment at contributing centers and consented for research. Data are merged and stored with the clinical data and used under the governance of the CIBMTR Research Database Protocol. Participants answer a series of surveys developed by the Patient Reported Outcomes Measurement Information System (PROMIS) focusing on physical, social and emotional, and other measures assessing financial well-being, occupational functioning, and social determinants of health. To complement traditionally measured clinical outcomes, the surveys are administered at the same time points at which clinical data are routinely collected. As of September 2023, PRO data have been collected from 993 patients across 25 different centers. With the goal of incorporating these important patient perspectives into standard clinical care, the CIBMTR has added the PRO data to Data Back to Centers (DBtC). Through expanding the data types represented in the registry, the CIBMTR aims to support holistic research accounting for the patients' perspective in improving patient outcomes. CIBMTR PRO data aim to provide a foundation for future large-scale, population-level evaluations to identify areas for improvement, emerging disparities in access and health outcomes (eg, by age, race, and ethnicity), and new therapies that may impact current treatment guidelines. Continuing to collect and grow the PRO data is critical for understanding these changes and identifying methods for improving patients' quality of life.

摘要

国际血液和骨髓移植研究中心(CIBMTR)每年都会准备一套总结幻灯片,以总结移植和细胞治疗的趋势。在2023年的总结幻灯片中,CIBMTR首次纳入了接受嵌合抗原受体T细胞(CAR-T)输注患者的数据。此外,还包括患者报告结局(PRO)的数据。本报告旨在更新美国造血细胞移植(HCT)活动的年度趋势,并纳入CAR-T治疗使用的数据。第二个目标是介绍和描述PRO数据收集的开发、实施和现状。2020年8月,CIBMTR启动了患者报告结局数据收集协议(CIBMTR PRO协议)。CIBMTR PRO协议在集中式基础设施下运行,以减轻各中心的负担。具体而言,PRO数据是从前瞻性便利样本中收集的,这些样本来自在参与中心接受治疗并同意参与研究的成年HCT和CAR-T接受者。数据与临床数据合并存储,并根据CIBMTR研究数据库协议进行管理。参与者回答一系列由患者报告结局测量信息系统(PROMIS)开发的调查问卷,这些问卷侧重于身体、社会和情感方面,以及其他评估财务状况、职业功能和健康社会决定因素的指标。为了补充传统测量的临床结局,这些调查问卷在常规收集临床数据的相同时间点进行发放。截至2023年9月,已从25个不同中心的993名患者中收集了PRO数据。为了将这些重要的患者观点纳入标准临床护理,CIBMTR已将PRO数据添加到数据反馈中心(DBtC)。通过扩大登记处代表的数据类型,CIBMTR旨在支持全面研究,从患者角度考虑改善患者结局。CIBMTR PRO数据旨在为未来大规模、人群水平的评估提供基础,以确定改进领域、获取和健康结局方面新出现的差异(如按年龄、种族和民族划分),以及可能影响当前治疗指南的新疗法。持续收集和增加PRO数据对于理解这些变化以及确定改善患者生活质量的方法至关重要。

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