Global Evidence & Outcomes, Research and Development, Takeda Development Center Americas, Inc., Lexington, Massachusetts, USA.
Patient-Centered Outcomes, Adelphi Values, Bollington, UK.
Transpl Infect Dis. 2023 Jun;25(3):e14064. doi: 10.1111/tid.14064. Epub 2023 May 8.
Cytomegalovirus (CMV), a common post-transplant infection, is associated with increased healthcare resource utilization. In the Phase 3 SOLSTICE trial, maribavir was superior to investigator-assigned therapy (IAT; valganciclovir/ganciclovir, foscarnet, and cidofovir) for CMV viremia clearance at Week 8 in transplant recipients with confirmed refractory CMV infection with/without resistance. This exploratory analysis evaluated hospital admissions of patients during the SOLSTICE trial.
Patients were randomized to maribavir (400 mg twice daily) or IAT for an 8-week treatment phase with a 12-week follow-up. After ≥3 weeks of treatment, patients on IAT who met pre-specified criteria could enter a maribavir rescue arm (8-week maribavir treatment, 12-week follow-up). Adjusted hospitalization rates and length of hospital stay (LOS) were estimated using negative binomial models adjusting for the time in the relevant study phase. Subgroup analysis for the maribavir rescue arm was conducted.
Overall, 352 patients were randomized (maribavir: 235; IAT: 117); 22 entered the maribavir rescue arm. After adjusting for treatment exposure, patients on maribavir had a 34.8% reduction in hospitalization rate and 53.8% reduced LOS (days/person/year) versus IAT during the treatment phase. No significant differences between treatments were observed during the follow-up phase, although in both arms, hospitalization rates were lower than in the treatment phase. In the maribavir rescue arm, hospitalizations were 60.6% lower on/after maribavir rescue versus pre-rescue treatment (p = 0.008).
In patients requiring post-transplant CMV treatment, hospitalization rate and LOS were lower for maribavir than IAT, and hospitalization rates were lower on/after maribavir rescue than pre-rescue. Reducing hospitalizations can alleviate the burden on patients and healthcare systems.
巨细胞病毒(CMV)是一种常见的移植后感染,与增加医疗资源利用有关。在 3 期 SOLSTICE 试验中,与研究者指定的治疗(IAT;缬更昔洛韦/更昔洛韦、膦甲酸钠和西多福韦)相比,马拉韦罗在移植后确认有难治性 CMV 感染(伴或不伴耐药性)的患者中,在第 8 周时更能清除 CMV 病毒血症。本探索性分析评估了 SOLSTICE 试验中患者的住院情况。
患者被随机分配至马拉韦罗(400mg,每日两次)或 IAT 治疗 8 周,随访 12 周。在治疗≥3 周后,符合预定标准的 IAT 患者可进入马拉韦罗挽救治疗组(8 周马拉韦罗治疗,12 周随访)。采用负二项回归模型,调整与研究阶段相关的时间,估计调整后的住院率和住院时间(LOS)。对马拉韦罗挽救治疗组进行了亚组分析。
共有 352 名患者被随机分配(马拉韦罗:235 名;IAT:117 名);22 名患者进入马拉韦罗挽救治疗组。调整治疗暴露后,与 IAT 相比,马拉韦罗治疗组的住院率降低了 34.8%,住院时间(人/年/天)降低了 53.8%。在随访阶段,两种治疗方法之间没有观察到显著差异,尽管在两个治疗组中,住院率均低于治疗阶段。在马拉韦罗挽救治疗组中,与挽救治疗前相比,挽救治疗后(/开始挽救治疗后)的住院率降低了 60.6%(p = 0.008)。
在需要移植后 CMV 治疗的患者中,与 IAT 相比,马拉韦罗的住院率和 LOS 较低,且挽救治疗后(/开始挽救治疗后)的住院率低于挽救治疗前。降低住院率可以减轻患者和医疗系统的负担。