Comparison of valganciclovir versus foscarnet for the treatment of cytomegalovirus viremia in adult acute leukemia patients after allogeneic hematopoietic cell transplantation.
Jinjin ZhuMimi XuYuhua RuHuanle GongYiyang DingZiling ZhuYang XuYi FanXiang ZhangYuqing TuAining SunHuiying QiuZhengming JinXiaowen TangYue HanChengcheng FuSuning ChenXiao MaFeng ChenTiemei SongDepei WuJia ChenPublished in: Leukemia & lymphoma (2024)
Cytomegalovirus (CMV) reactivation increases treatment-related mortality (TRM) after allogeneic hematopoietic cell transplantation (allo-HCT). We analyzed 141 adult acute leukemia (AL) patients suffered allo-HCT between 2017 and 2021, who developed CMV viremia post-HCT and treated with valganciclovir or foscarnet, to evaluate effectiveness and safety of both drugs. Viremia clearance rates (14 and 21 d post treatment) and toxicities were similar in two groups. However, valganciclovir was associated with a lower cumulative incidence of CMV recurrence within 180 days (16.7% vs. 35.7%, p =0.029) post CMV clearance. Finally, 2-year TRM was lower in valganciclovir group (9.7% ± 0.2% vs. 26.2% ± 0.3%, p = 0.026), result a superior 2-year overall survival (OS; 88.1% ± 5.2% vs. 64.4% ± 5.5%, p = 0.005) and leukemia-free survival (LFS; 82.0% ± 5.9% vs. 58.9% ± 5.6%, p = 0.009). Valganciclovir might decrease CMV viremia recurrence and led to better long-term outcome than foscarnet in adult AL patients developed CMV viremia post-HCT. Considering the inherent biases of retrospective study, well-designed trials are warranted to validate our conclusion.
Keyphrases
- end stage renal disease
- free survival
- newly diagnosed
- ejection fraction
- chronic kidney disease
- prognostic factors
- peritoneal dialysis
- bone marrow
- risk factors
- cardiovascular disease
- low dose
- coronary artery disease
- acute myeloid leukemia
- epstein barr virus
- cell death
- signaling pathway
- combination therapy
- replacement therapy
- patient reported
- drug induced