Department of Transplant Medicine, Section of Nephrology Department of Pharmaceutical Biosciences, School of Pharmacy.
Department of Medicine and Multi-organ Transplant Program, University Health Network, Toronto, Ontario, Canada.
Clin Infect Dis. 2016 May 1;62(9):1154-60. doi: 10.1093/cid/ciw084. Epub 2016 Feb 16.
The VICTOR study showed comparable efficacy of treatment with intravenous ganciclovir and oral valganciclovir for cytomegalovirus (CMV) disease in solid organ transplant recipients. Oral therapy is now recommended treatment in clinical practice and guidelines. The VICTOR biobank was used in a series of post hoc analyses that yielded unique and clinically valuable insights into CMV treatment and pathogenesis. For example, the importance of tailoring therapy to initial viral load, the effect of immunosuppression on outcomes, and the need to continue therapy until undetectable viral load to prevent recurrence and emergence of resistant strains. Data were also used to validate the use of international units (IU) in quantitative measurements of CMV DNAemia, which may help future studies to define relevant cutoffs for treatment guidance. The analyses also showed the importance of inflammation on viral outcomes and identified potential targets for future studies. Here we summarize the valuable lessons learned from analysis of the VICTOR data set and sample repository.
VICTOR 研究表明,在实体器官移植受者中,静脉用更昔洛韦和口服缬更昔洛韦治疗巨细胞病毒(CMV)疾病的疗效相当。目前,口服治疗已被推荐用于临床实践和指南中。VICTOR 生物库被用于一系列事后分析,这些分析为 CMV 治疗和发病机制提供了独特且具有临床价值的见解。例如,根据初始病毒载量调整治疗、免疫抑制对结果的影响以及需要继续治疗至病毒载量不可检测以预防复发和耐药株出现的重要性。这些数据还用于验证国际单位(IU)在 CMV DNAemia 定量测量中的使用,这可能有助于未来的研究确定相关的治疗指导界限。分析还表明炎症对病毒结果的重要性,并确定了未来研究的潜在目标。在这里,我们总结了从 VICTOR 数据集和样本库分析中获得的宝贵经验。