Department of Hematology and Oncology, Taussig Cancer Institute, Cleveland Clinic, Cleveland, Ohio.
Division of Stem Cell Transplantation and Cellular Therapy, Dana Farber Cancer Institute, Boston, Massachusetts.
Transplant Cell Ther. 2022 Aug;28(8):419-425. doi: 10.1016/j.jtct.2022.05.002. Epub 2022 May 9.
The need for prospective randomized clinical trials investigating novel graft-versus-host disease (GVHD) prevention strategies that include other clinical outcomes impacted by GVHD has been highlighted as a priority for the field of hematopoietic cell transplantation. A recently completed study through the Blood and Marrow Transplant Clinical Trials Network (BMT CTN 1301) comparing CD34 selection and post-transplantation cyclophosphamide with tacrolimus/methotrexate (Tac/MTX) for GVHD prevention demonstrated no significant differences in the primary endpoint of chronic GVHD relapse-free survival among the 3 approaches. The trial did not demonstrate a superior approach compared with Tac/MTX; however, it did highlight several challenges in determining the best and most relevant approaches to clinical trial design, particularly in the context of current and ongoing changes in real-world practices. Here we review the results of BMT CTN 1301 and their implications for clinical practice and future clinical trial design.
需要前瞻性随机临床试验来研究新的移植物抗宿主病(GVHD)预防策略,这些策略包括受 GVHD 影响的其他临床结果,这已成为造血细胞移植领域的优先事项。通过血液和骨髓移植临床试验网络(BMT CTN 1301)最近完成的一项研究比较了 CD34 选择和移植后环磷酰胺与他克莫司/甲氨蝶呤(Tac/MTX)在 GVHD 预防方面的效果,结果显示在 3 种方法中,慢性 GVHD 无复发存活率的主要终点没有显著差异。该试验与 Tac/MTX 相比并没有显示出优越的方法;然而,它确实强调了在确定最佳和最相关的临床试验设计方法方面存在的一些挑战,特别是在当前和正在进行的现实实践变化的背景下。在这里,我们回顾了 BMT CTN 1301 的结果及其对临床实践和未来临床试验设计的意义。