Bessa Adrieli Barros, Cristelli Marina Pontello, Felipe Claudia Rosso, Foresto Renato Demarchi, Fonseca Marcelo Cunio Machado, Pestana Jose Medina, Tedesco-Silva Helio
Universidade Federal de São Paulo, Escola Paulista de Medicina, São Paulo, SP, Brazil.
Novartis, São Paulo, SP, Brazil.
J Bras Nefrol. 2025 Jan-Mar;47(1):e20240060. doi: 10.1590/2175-8239-JBN-2024-0060en.
A new induction therapy strategy of a single 3 mg/kg dose of rabbit antithymocyte globulin (r-ATG) showed a lower incidence of acute rejection.
The objective of this study was to use real-world data to determine the incremental cost-effectiveness ratio (ICER) of r-ATG induction for the prevention of acute rejection (AR) in the first year following kidney transplantation and for kidney graft survival over 1, 4, and 10 years of post-transplantation from the perspective of the national public healthcare system. A Markov state transition model was developed utilizing real-world data extracted from medical invoices from a single center. The study population consisted of adults at low immunological risk undergoing their initial transplantation and received kidneys from either living or deceased donors. The intervention of r-ATG induction was compared to no induction. The clinical outcomes considered for this analysis were acute rejection, cytomegalovirus infection/disease, death, graft loss, and retransplantation.
The cost-effectiveness analysis in the first year revealed that the r-ATG group was more cost-effective, with an ICER of US$ 399.96 per avoided AR episode, an effectiveness gain of 0.01 year in graft survival and a total incremental cost of US$ 147.50. The 4- and 10-year analyses revealed an effectiveness gain of 0.06 and 0.16 years in graft survival in the r-ATG induction group, and a total incremental cost of US$ -321.68 and US$ -2,440.62, respectively.
The single 3 mg/kg dose of r-ATG is cost-effective in preventing acute rejection episodes and dominant in the long term of transplantation, conferring survival gain.
一种新的诱导治疗策略,即单次给予3mg/kg剂量的兔抗胸腺细胞球蛋白(r-ATG),显示出较低的急性排斥反应发生率。
本研究的目的是从国家公共医疗系统的角度,利用真实世界数据确定r-ATG诱导治疗在预防肾移植后第一年急性排斥反应(AR)以及移植后1年、4年和10年肾移植存活方面的增量成本效益比(ICER)。利用从单一中心的医疗发票中提取的真实世界数据建立了一个马尔可夫状态转移模型。研究人群包括免疫风险较低的初次接受移植的成年人,他们接受了来自活体或 deceased 供体的肾脏。将r-ATG诱导治疗与不进行诱导治疗进行比较。本分析考虑的临床结局包括急性排斥反应、巨细胞病毒感染/疾病、死亡、移植肾丢失和再次移植。
第一年的成本效益分析显示,r-ATG组更具成本效益,每避免一次AR发作的ICER为399.96美元,移植肾存活的有效性增益为0.01年,总增量成本为147.50美元。4年和10年的分析显示,r-ATG诱导治疗组移植肾存活的有效性增益分别为0.06年和0.16年,总增量成本分别为-321.68美元和-2440.62美元。
单次3mg/kg剂量的r-ATG在预防急性排斥反应发作方面具有成本效益,并且在移植的长期过程中占主导地位,可带来存活增益。