Pusic Iskra, Pavletic Steven Z
Division of Oncology, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri.
National Institutes of Health, National Cancer Institute, Center for Cancer Research, Bethesda, Maryland.
Clin Hematol Int. 2019 Mar 18;1(1):36-44. doi: 10.2991/chi.d.190314.001. eCollection 2019 Mar.
The lack of standardized criteria for measuring therapeutic response has been a major obstacle to the development of therapeutic trials in chronic graft--host disease (cGvHD). Nevertheless, recent advances have been made in understanding of the biology and pathophysiology of cGvHD, as well as establishing more precise criteria for the diagnosis and classification of disease manifestations. The momentum has shifted, and currently there is a long list of new potential treatment targets being identified for cGvHD. Consequently, new drugs are being implemented for its prophylaxis and treatment. It is crucial to continue that trend and develop better systems to test new drugs in clinical practice that would eventually translate toward seeking regulatory review and approval. We provide a historical perspective and current challenges in conducting cGvHD clinical trials.
缺乏用于衡量治疗反应的标准化标准一直是慢性移植物抗宿主病(cGvHD)治疗试验发展的主要障碍。然而,在理解cGvHD的生物学和病理生理学方面以及为疾病表现的诊断和分类建立更精确的标准方面,最近已经取得了进展。势头已经转变,目前正在为cGvHD确定一长串新的潜在治疗靶点。因此,正在实施新药用于其预防和治疗。继续这一趋势并开发更好的系统在临床实践中测试新药至关重要,这最终将朝着寻求监管审查和批准的方向发展。我们提供了进行cGvHD临床试验的历史视角和当前挑战。