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造血细胞移植:2023年的实践预测

Hematopoietic Cell Transplantation: Practice Predictions for the Year 2023.

作者信息

Farhadfar Nosha, Burns Linda J, Mupfudze Tatenda, Shaw Bronwen E, Bollard Catherine M, Devine Steven M, Horowitz Mary M, Jones Richard J, Murthy Hemant S, Wingard John R, Lee Stephanie J

机构信息

Division of Hematology and Oncology, University of Florida College of Medicine, Gainesville, Florida.

National Marrow Donor Program/Be The Match and Center for International Blood and Marrow Transplant Research, Minneapolis, MN.

出版信息

Transplant Cell Ther. 2021 Feb;27(2):183.e1-183.e7. doi: 10.1016/j.bbmt.2020.10.006. Epub 2020 Oct 9.

DOI:10.1016/j.bbmt.2020.10.006
PMID:33045387
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7546661/
Abstract

Research priorities are best determined by the most pressing scientific questions, in the context of current knowledge. However, definitive research studies take time, while real-world experience accumulates. Adoption of new practices before adequate comparison with current treatments threatens successful study conduct and may expose patients to what ultimately turns out to be inferior treatment. We conducted a survey to understand the hematopoietic cell transplantation (HCT) community's predictions about future practice trends in the HCT field and results of ongoing Blood and Marrow Transplant Clinical Trials Network (BMT CTN) trials to gauge how the HCT community views the treatments being studied. The survey was distributed between February and March 2019 to an electronic mailing list of HCT clinicians practicing in the United States maintained by the Center for International Blood and Marrow Transplant Research (CIBMTR). Of 986 clinicians surveyed, 315 responded (32%). They predicted an increase in the number of HCTs performed for malignant hematologic diseases and benign diseases such as sickle cell, autoimmune, and genetic disorders. The majority (63%) predicted that matched related donors will remain the preferred donor source for adult HCT recipients in 2023, but 21% predicted haploidentical (haplo) donors and 17% predicted matched unrelated donors would be the preferred source. Most respondents (65%) predicted a decrease in the use of umbilical cord blood (UCB) as a graft source for HCT. Most respondents also predicted that calcineurin-based graft-versus-host disease (GVHD) prophylaxis would be replaced by post-transplantation cyclophosphamide (PTCy) (55%), biomarker use would become standard practice to guide GVHD therapy (73%), and steroids would be combined with other agents as first-line therapy for newly diagnosed acute (53%) and chronic GVHD (54%). In ongoing BMT CTN trials in which outcomes are not yet known, 60% to 92% of respondents had an opinion about which arm they thought would be superior. However, not all respondents predicted the same outcome, with 44% to 88% choosing the same arm. There was no clear relationship between the proportion predicting the same arm would win and accrual to the trial. Survey respondents were optimistic about an increasing volume of transplantation procedures, and they also expected significant changes in HCT practice over the next few years, including wider adoption of PTCy GVHD prophylaxis, increased use of biomarkers to guide GVHD therapy, and decreased use of UCB HCT. The degree of equipoise in the community about the relative efficacy of therapies being studied did not seem to affect accrual to current BMT CTN trials, but this is an area that needs further investigation.

摘要

研究重点最好在当前知识背景下,由最紧迫的科学问题来确定。然而,确定性的研究需要时间,而现实世界的经验却在不断积累。在与现有治疗方法进行充分比较之前就采用新的治疗方法,会威胁到研究的顺利开展,并且可能使患者接受最终被证明是较差的治疗。我们开展了一项调查,以了解造血细胞移植(HCT)领域的专业人士对HCT领域未来实践趋势的预测,以及正在进行的血液和骨髓移植临床试验网络(BMT CTN)试验的结果,以此来评估HCT领域专业人士对正在研究的治疗方法的看法。该调查于2019年2月至3月期间,分发给国际血液和骨髓移植研究中心(CIBMTR)维护的在美国执业的HCT临床医生的电子邮件列表。在986名接受调查的临床医生中,315人回复(32%)。他们预测,针对恶性血液病以及镰状细胞病、自身免疫性疾病和遗传性疾病等良性疾病进行的HCT数量将会增加。大多数人(63%)预测,在2023年,匹配的相关供体仍将是成人HCT受者的首选供体来源,但21%的人预测单倍体(haplo)供体,17%的人预测匹配的无关供体将成为首选来源。大多数受访者(65%)预测,作为HCT移植物来源的脐带血(UCB)的使用将会减少。大多数受访者还预测,基于钙调神经磷酸酶的移植物抗宿主病(GVHD)预防措施将被移植后环磷酰胺(PTCy)取代(55%),使用生物标志物将成为指导GVHD治疗的标准做法(73%),并且类固醇将与其他药物联合作为新诊断的急性(53%)和慢性GVHD(54%)的一线治疗药物。在结果未知的正在进行的BMT CTN试验中,60%至92%的受访者对他们认为哪一组会更优有看法。然而,并非所有受访者都预测了相同的结果,44%至88%的人选择了同一组。预测同一组会胜出的比例与试验入组人数之间没有明显关系。参与调查的受访者对移植手术数量的增加持乐观态度,他们还预计在未来几年HCT实践会发生重大变化,包括更广泛地采用PTCy预防GVHD、更多地使用生物标志物来指导GVHD治疗以及减少UCB HCT的使用。该领域对于正在研究的治疗方法的相对疗效的平衡程度,似乎并未影响当前BMT CTN试验的入组情况,但这是一个需要进一步研究的领域。

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