FEDERICO PIÑERO , Margarita Anders , Carla Bermúdez , Diego Arufe , Adriana Varón , Ana Palazzo , Jorge Rodriguez , Oscar Beltrán , Daniela Simian , Leonardo Gomes da Fonseca , Ezequiel Ridruejo , Norberto Tamagnone , Hugo Cheinquer , Diana Bejarano , Juan Ignacio Marín , Federico Orozco Ganem , Josefina Pagés , Jaime Poniachik , Sebastián Marciano , Virginia Reggiardo , Manuel Mendizabal
{"title":"与代偿性肝硬化相比,一线全身治疗前肝硬化患者的O3-再代偿与相似的生存结果相关","authors":"FEDERICO PIÑERO , Margarita Anders , Carla Bermúdez , Diego Arufe , Adriana Varón , Ana Palazzo , Jorge Rodriguez , Oscar Beltrán , Daniela Simian , Leonardo Gomes da Fonseca , Ezequiel Ridruejo , Norberto Tamagnone , Hugo Cheinquer , Diana Bejarano , Juan Ignacio Marín , Federico Orozco Ganem , Josefina Pagés , Jaime Poniachik , Sebastián Marciano , Virginia Reggiardo , Manuel Mendizabal","doi":"10.1016/j.aohep.2024.101598","DOIUrl":null,"url":null,"abstract":"<div><h3>Conflict of interest</h3><div>No</div></div><div><h3>Introduction and Objectives</h3><div>The term <em>“recompensation”</em> of cirrhosis was proposed in the latest BAVENO VII, underlying dynamic events and prognosis in cirrhosis. However, there is uncertainty regarding its prognosis in patients with advanced hepatocellular carcinoma (HCC) treated with first line systemic therapies (1L). We aimed to compare post-1L survival between compensated (CC), decompensated (DC), and recompensated (RC) cirrhosis.</div></div><div><h3>Patients / Materials and Methods</h3><div>A multicenter prospective Latin-American cohort study including advanced HCC patients with cirrhosis who received any 1L was conducted from 2018 to 2024. Three groups were defined: CC (had never presented decompensation); DC (presenting any decompensated event associated with portal hypertension at time of 1L), and RC group (prior history of any decompensation event at HCC diagnosis who were compensated at time of 1L). Survival since date of 1L was compared using Cox proportional hazard analysis.</div></div><div><h3>Results and Discussion</h3><div>Overall, 306 patients received 1L, including sorafenib 60.5%, atezolizumab + bevacizumab 29.7%, lenvatinib 9.1%, and nivo/pembrolizumab 0.6%. Of these, 83.3% presented cirrhosis. Median 1L treatment duration was 5.1 months with a median overall survival since 1L of 16.0 months (range 12.9-18.3). Significant differences were observed between CC (n=167), DC (n=31) and RC (n=42) groups (Table). In the RC group, median time from decompensation to recompensation was 12.0 months (range 1.9-25.9); being ascites the most frequent event (78.6%). DC group presented decreased post-1L survival [median 8.6 months vs 17.2 months in CC [adjusted HR 1.9 (95% CI 1.05-3.5); P=0.03], while no significant survival difference was observed between RC and CC [median survival 12.5 months; aHR 1.3 (95% CI 0.81-2.1); P=0.28] (Figure). Lower access to second line therapy was observed in DC group.</div></div><div><h3>Conclusions</h3><div>Patients with cirrhosis and advanced HCC who achieve recompensation may benefit from systemic therapies. This demands an observation period of follow up before precluding 1L in decompensated cirrhosis.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"29 ","pages":"Article 101598"},"PeriodicalIF":6.2000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"O3- RECOMPENSATION IN PATIENTS WITH CIRRHOSIS PRIOR TO FIRST LINE SYSTEMIC THERAPY IS ASSOCIATED WITH SIMILAR SURVIVAL OUTCOMES COMPARED TO COMPENSATED CIRRHOSIS\",\"authors\":\"FEDERICO PIÑERO , Margarita Anders , Carla Bermúdez , Diego Arufe , Adriana Varón , Ana Palazzo , Jorge Rodriguez , Oscar Beltrán , Daniela Simian , Leonardo Gomes da Fonseca , Ezequiel Ridruejo , Norberto Tamagnone , Hugo Cheinquer , Diana Bejarano , Juan Ignacio Marín , Federico Orozco Ganem , Josefina Pagés , Jaime Poniachik , Sebastián Marciano , Virginia Reggiardo , Manuel Mendizabal\",\"doi\":\"10.1016/j.aohep.2024.101598\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Conflict of interest</h3><div>No</div></div><div><h3>Introduction and Objectives</h3><div>The term <em>“recompensation”</em> of cirrhosis was proposed in the latest BAVENO VII, underlying dynamic events and prognosis in cirrhosis. However, there is uncertainty regarding its prognosis in patients with advanced hepatocellular carcinoma (HCC) treated with first line systemic therapies (1L). We aimed to compare post-1L survival between compensated (CC), decompensated (DC), and recompensated (RC) cirrhosis.</div></div><div><h3>Patients / Materials and Methods</h3><div>A multicenter prospective Latin-American cohort study including advanced HCC patients with cirrhosis who received any 1L was conducted from 2018 to 2024. Three groups were defined: CC (had never presented decompensation); DC (presenting any decompensated event associated with portal hypertension at time of 1L), and RC group (prior history of any decompensation event at HCC diagnosis who were compensated at time of 1L). Survival since date of 1L was compared using Cox proportional hazard analysis.</div></div><div><h3>Results and Discussion</h3><div>Overall, 306 patients received 1L, including sorafenib 60.5%, atezolizumab + bevacizumab 29.7%, lenvatinib 9.1%, and nivo/pembrolizumab 0.6%. Of these, 83.3% presented cirrhosis. Median 1L treatment duration was 5.1 months with a median overall survival since 1L of 16.0 months (range 12.9-18.3). Significant differences were observed between CC (n=167), DC (n=31) and RC (n=42) groups (Table). In the RC group, median time from decompensation to recompensation was 12.0 months (range 1.9-25.9); being ascites the most frequent event (78.6%). DC group presented decreased post-1L survival [median 8.6 months vs 17.2 months in CC [adjusted HR 1.9 (95% CI 1.05-3.5); P=0.03], while no significant survival difference was observed between RC and CC [median survival 12.5 months; aHR 1.3 (95% CI 0.81-2.1); P=0.28] (Figure). Lower access to second line therapy was observed in DC group.</div></div><div><h3>Conclusions</h3><div>Patients with cirrhosis and advanced HCC who achieve recompensation may benefit from systemic therapies. 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引用次数: 0
摘要
利益冲突介绍和目的最新的BAVENO VII中提出了肝硬化的“再补偿”一词,它是肝硬化的潜在动态事件和预后。然而,在接受一线全身治疗(1L)的晚期肝细胞癌(HCC)患者中,其预后尚不确定。我们的目的是比较代偿(CC)、失代偿(DC)和再代偿(RC)肝硬化的1l后生存率。患者/材料和方法一项多中心前瞻性拉丁美洲队列研究,包括2018年至2024年接受任何1L治疗的晚期HCC合并肝硬化患者。定义了三组:CC(从未出现失代偿);DC组(在1L时出现与门脉高压相关的失代偿事件)和RC组(在HCC诊断时有任何失代偿事件的病史,在1L时进行了补偿)。采用Cox比例风险分析比较1L后的生存率。结果和讨论总体而言,306例患者接受1L治疗,其中索拉非尼60.5%,阿特唑单抗 + 贝伐单抗29.7%,lenvatinib 9.1%, nivo/pembrolizumab 0.6%。其中,83.3%为肝硬化。1L治疗的中位持续时间为5.1个月,1L后的中位总生存期为16.0个月(12.9-18.3)。CC组(n=167)、DC组(n=31)和RC组(n=42)之间存在显著差异(表)。在RC组,从失代偿到再代偿的中位时间为12.0个月(范围1.9-25.9);最常见的是腹水(78.6%)。DC组1l后生存期降低[中位8.6个月vs中位17.2个月][调整后危险度1.9 (95% CI 1.05-3.5);P=0.03],而RC和CC的生存期无显著差异[中位生存期12.5个月;aHR为1.3 (95% CI 0.81-2.1);P = 0.28](图)。DC组二线治疗的可及性较低。结论肝硬化和晚期HCC患者获得再代偿可能受益于全身治疗。这需要在排除失代偿期肝硬化的1L之前进行一段观察期的随访。
O3- RECOMPENSATION IN PATIENTS WITH CIRRHOSIS PRIOR TO FIRST LINE SYSTEMIC THERAPY IS ASSOCIATED WITH SIMILAR SURVIVAL OUTCOMES COMPARED TO COMPENSATED CIRRHOSIS
Conflict of interest
No
Introduction and Objectives
The term “recompensation” of cirrhosis was proposed in the latest BAVENO VII, underlying dynamic events and prognosis in cirrhosis. However, there is uncertainty regarding its prognosis in patients with advanced hepatocellular carcinoma (HCC) treated with first line systemic therapies (1L). We aimed to compare post-1L survival between compensated (CC), decompensated (DC), and recompensated (RC) cirrhosis.
Patients / Materials and Methods
A multicenter prospective Latin-American cohort study including advanced HCC patients with cirrhosis who received any 1L was conducted from 2018 to 2024. Three groups were defined: CC (had never presented decompensation); DC (presenting any decompensated event associated with portal hypertension at time of 1L), and RC group (prior history of any decompensation event at HCC diagnosis who were compensated at time of 1L). Survival since date of 1L was compared using Cox proportional hazard analysis.
Results and Discussion
Overall, 306 patients received 1L, including sorafenib 60.5%, atezolizumab + bevacizumab 29.7%, lenvatinib 9.1%, and nivo/pembrolizumab 0.6%. Of these, 83.3% presented cirrhosis. Median 1L treatment duration was 5.1 months with a median overall survival since 1L of 16.0 months (range 12.9-18.3). Significant differences were observed between CC (n=167), DC (n=31) and RC (n=42) groups (Table). In the RC group, median time from decompensation to recompensation was 12.0 months (range 1.9-25.9); being ascites the most frequent event (78.6%). DC group presented decreased post-1L survival [median 8.6 months vs 17.2 months in CC [adjusted HR 1.9 (95% CI 1.05-3.5); P=0.03], while no significant survival difference was observed between RC and CC [median survival 12.5 months; aHR 1.3 (95% CI 0.81-2.1); P=0.28] (Figure). Lower access to second line therapy was observed in DC group.
Conclusions
Patients with cirrhosis and advanced HCC who achieve recompensation may benefit from systemic therapies. This demands an observation period of follow up before precluding 1L in decompensated cirrhosis.
期刊介绍:
Annals of Hepatology publishes original research on the biology and diseases of the liver in both humans and experimental models. Contributions may be submitted as regular articles. The journal also publishes concise reviews of both basic and clinical topics.