FEDERICO PIÑERO , Margarita Anders , Carla Bermúdez , Ezequiel Demirdjian , Adriana Varón , Daniela Perez , Jorge Rodriguez , Oscar Beltrán , Javier Delgado García , Leonardo Gomes da Fonseca , Ezequiel Ridruejo , Pablo Caballini , Alexandre Araujo , Juan Diego Torres Florez , Juan Ignacio Marín , Marina Villa , Federico Orozco Ganem , Jaime Poniachik , Sebastián Marciano , Fernando Bessone , Manuel Mendizabal
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The aim of this study was describe the incidence rate of irAEs and its impact on survival.</div></div><div><h3>Patients / Materials and Methods</h3><div>A multicenter prospective Latin-American cohort study was conducted including HCC patients who received A+B since its regional approval, either as first or sub-sequent systemic lines, to March 15, 2024. Overall survival since A+B, and survival since date of irAE was compared between patients developing and not developing irAEs (date since A+B), through Cox proportional hazard analysis (Harrell's c-index).</div></div><div><h3>Results and Discussion</h3><div>Overall, 99 patients treated with A+B were included (n=8 received it as second line post sorafenib), 82.3% presented cirrhosis. The median treatment duration was 6 months [number of cycles 5 (range 3-11.5)], with a median overall survival of 17.0 months (range 12.6-19.8). Over a median follow-up of 7.7 months (range 4.5-17.2), the irAE incidence rate was 2.1 cases per 100 persons-months [cumulative incidence 18.1% (95% CI 11.1-27.2%); n=18]. Median time to irAE was 2.3 months (range 1.4-4.8), most frequently hepatitis (n=6), thyroiditis (n=5), and 8/18 required steroids (Table). Follow-up and treatment duration times were similar regardless irAEs occurrence. On multivariable Cox regression model, AFP values before A+B >400ng/ml [HR 2.9 (95% CI 1.1-7.6)], adjusted for HCC diffuse intrahepatic pattern was associated with irAE development (c-statistic 0.66). Patients developing irAEs presented decreased overall and post-irAE survival [median 2.9 months vs 18.5 months; HR 6.2 (95% CI 2.7-14.2); P<.0001] (Figure).</div></div><div><h3>Conclusions</h3><div>Cautions management in patients with irAEs is of relevant importance in our region, highlighting the role of onco-hepatologists in the clinical-decision making process of these patients.</div></div>","PeriodicalId":7979,"journal":{"name":"Annals of hepatology","volume":"29 ","pages":"Article 101667"},"PeriodicalIF":4.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"P-53 IMMUNE-MEDIATED ADVERSE EVENTS FOLLOWING ATEZOLIZUMAB PLUS BEVACIZUMAB IS ASSOCIATED WITH DECREASED SURVIVAL IN PATIENTS WITH CIRRHOSIS\",\"authors\":\"FEDERICO PIÑERO , Margarita Anders , Carla Bermúdez , Ezequiel Demirdjian , Adriana Varón , Daniela Perez , Jorge Rodriguez , Oscar Beltrán , Javier Delgado García , Leonardo Gomes da Fonseca , Ezequiel Ridruejo , Pablo Caballini , Alexandre Araujo , Juan Diego Torres Florez , Juan Ignacio Marín , Marina Villa , Federico Orozco Ganem , Jaime Poniachik , Sebastián Marciano , Fernando Bessone , Manuel Mendizabal\",\"doi\":\"10.1016/j.aohep.2024.101667\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Conflict of interest</h3><div>No</div></div><div><h3>Introduction and Objectives</h3><div>Clinical trials evaluating the efficacy of first line systemic immune therapies for patients with advanced hepatocellular carcinoma (HCC) have recruited a lower proportion of patients with cirrhosis. In this group of patients, immune related adverse events (irAEs) may lead to decreased prognostic outcomes. The aim of this study was describe the incidence rate of irAEs and its impact on survival.</div></div><div><h3>Patients / Materials and Methods</h3><div>A multicenter prospective Latin-American cohort study was conducted including HCC patients who received A+B since its regional approval, either as first or sub-sequent systemic lines, to March 15, 2024. Overall survival since A+B, and survival since date of irAE was compared between patients developing and not developing irAEs (date since A+B), through Cox proportional hazard analysis (Harrell's c-index).</div></div><div><h3>Results and Discussion</h3><div>Overall, 99 patients treated with A+B were included (n=8 received it as second line post sorafenib), 82.3% presented cirrhosis. The median treatment duration was 6 months [number of cycles 5 (range 3-11.5)], with a median overall survival of 17.0 months (range 12.6-19.8). Over a median follow-up of 7.7 months (range 4.5-17.2), the irAE incidence rate was 2.1 cases per 100 persons-months [cumulative incidence 18.1% (95% CI 11.1-27.2%); n=18]. Median time to irAE was 2.3 months (range 1.4-4.8), most frequently hepatitis (n=6), thyroiditis (n=5), and 8/18 required steroids (Table). Follow-up and treatment duration times were similar regardless irAEs occurrence. On multivariable Cox regression model, AFP values before A+B >400ng/ml [HR 2.9 (95% CI 1.1-7.6)], adjusted for HCC diffuse intrahepatic pattern was associated with irAE development (c-statistic 0.66). Patients developing irAEs presented decreased overall and post-irAE survival [median 2.9 months vs 18.5 months; HR 6.2 (95% CI 2.7-14.2); P<.0001] (Figure).</div></div><div><h3>Conclusions</h3><div>Cautions management in patients with irAEs is of relevant importance in our region, highlighting the role of onco-hepatologists in the clinical-decision making process of these patients.</div></div>\",\"PeriodicalId\":7979,\"journal\":{\"name\":\"Annals of hepatology\",\"volume\":\"29 \",\"pages\":\"Article 101667\"},\"PeriodicalIF\":4.4000,\"publicationDate\":\"2024-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of hepatology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1665268124004502\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/12/6 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of hepatology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1665268124004502","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/6 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
利益冲突前言和目的评价一线全身免疫疗法治疗晚期肝细胞癌(HCC)疗效的临床试验招募了较低比例的肝硬化患者。在这组患者中,免疫相关不良事件(irAEs)可能导致预后下降。本研究的目的是描述irAEs的发病率及其对生存的影响。患者/材料和方法进行了一项多中心前瞻性拉丁美洲队列研究,包括自A+B在该地区获得批准以来接受A+B治疗的HCC患者,无论是作为首个或后续系统线,截止到2024年3月15日。通过Cox比例风险分析(Harrell’s c-index),比较发生和未发生irAE患者(自A+B起)的总生存率和irAE发生之日起的生存率。结果和讨论总体而言,纳入99例A+B治疗的患者(n=8例作为索拉非尼后的二线治疗),82.3%出现肝硬化。中位治疗持续时间为6个月[周期数5(范围3-11.5)],中位总生存期为17.0个月(范围12.6-19.8)。在中位随访7.7个月(范围4.5-17.2)期间,irAE发病率为每100人月2.1例[累积发病率18.1% (95% CI 11.1-27.2%);n = 18)。到irAE的中位时间为2.3个月(1.4-4.8个月),最常见的是肝炎(n=6),甲状腺炎(n=5), 8/18需要类固醇(表)。不论是否发生irAEs,随访时间和治疗时间相似。在多变量Cox回归模型中,经HCC弥漫性肝内模式调整后,A+B前AFP值400ng/ml [HR 2.9 (95% CI 1.1-7.6)]与irAE发生相关(c统计量0.66)。发生irae的患者总体生存期和irae后生存期均下降[中位2.9个月vs 18.5个月;Hr 6.2 (95% ci 2.7-14.2);术;。0001](图)。结论:对irAEs患者的谨慎管理在本地区具有重要意义,强调了肿瘤肝病学家在这些患者的临床决策过程中的作用。
P-53 IMMUNE-MEDIATED ADVERSE EVENTS FOLLOWING ATEZOLIZUMAB PLUS BEVACIZUMAB IS ASSOCIATED WITH DECREASED SURVIVAL IN PATIENTS WITH CIRRHOSIS
Conflict of interest
No
Introduction and Objectives
Clinical trials evaluating the efficacy of first line systemic immune therapies for patients with advanced hepatocellular carcinoma (HCC) have recruited a lower proportion of patients with cirrhosis. In this group of patients, immune related adverse events (irAEs) may lead to decreased prognostic outcomes. The aim of this study was describe the incidence rate of irAEs and its impact on survival.
Patients / Materials and Methods
A multicenter prospective Latin-American cohort study was conducted including HCC patients who received A+B since its regional approval, either as first or sub-sequent systemic lines, to March 15, 2024. Overall survival since A+B, and survival since date of irAE was compared between patients developing and not developing irAEs (date since A+B), through Cox proportional hazard analysis (Harrell's c-index).
Results and Discussion
Overall, 99 patients treated with A+B were included (n=8 received it as second line post sorafenib), 82.3% presented cirrhosis. The median treatment duration was 6 months [number of cycles 5 (range 3-11.5)], with a median overall survival of 17.0 months (range 12.6-19.8). Over a median follow-up of 7.7 months (range 4.5-17.2), the irAE incidence rate was 2.1 cases per 100 persons-months [cumulative incidence 18.1% (95% CI 11.1-27.2%); n=18]. Median time to irAE was 2.3 months (range 1.4-4.8), most frequently hepatitis (n=6), thyroiditis (n=5), and 8/18 required steroids (Table). Follow-up and treatment duration times were similar regardless irAEs occurrence. On multivariable Cox regression model, AFP values before A+B >400ng/ml [HR 2.9 (95% CI 1.1-7.6)], adjusted for HCC diffuse intrahepatic pattern was associated with irAE development (c-statistic 0.66). Patients developing irAEs presented decreased overall and post-irAE survival [median 2.9 months vs 18.5 months; HR 6.2 (95% CI 2.7-14.2); P<.0001] (Figure).
Conclusions
Cautions management in patients with irAEs is of relevant importance in our region, highlighting the role of onco-hepatologists in the clinical-decision making process of these patients.
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.