Risk factors for the exacerbation of esophageal varices in patients receiving atezolizumab plus bevacizumab therapy for unresectable hepatocellular carcinoma.

IF 1.8 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2025-09-29 DOI:10.1159/000548667
Hitomi Takada, Leona Osawa, Yasuyuki Komiyama, Masaru Muraoka, Yuichiro Suzuki, Mitsuaki Sato, Shoji Kobayashi, Takashi Yoshida, Shinichi Takano, Shinya Maekawa, Atsunori Tsuchiya, Nobuyuki Enomoto
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引用次数: 0

Abstract

Introduction: Atezolizumab plus bevacizumab (AB) therapy is an effective systemic therapy for unresectable hepatocellular carcinoma (u-HCC). However, exacerbations of esophageal varices (EV) often occur, and EV management should be clarified to attain a better prognosis in patients with u-HCC. Our research aimed to explore the actual situation of EV exacerbation and its risk factors in patients receiving AB therapy.

Methods: We recruited 82 patients receiving AB therapy for u-HCC. All patients underwent esophagogastroduodenoscopy (EGD) within 3 months before AB induction to assess EV presence. The emergence of EV findings requiring urgent or planned endoscopic treatment defined EV exacerbation. The frequency and risk factors for EV exacerbation after AB introduction were analyzed.

Results: Of the participants, 49% had EV findings on preinduction EGD. Within the observation period, 17% had EV exacerbation, and 7.2% experienced rupture. Among those with EV exacerbation, 7 had positive red color signs, and 1 had formal deterioration to F3. In EV rupture, 4 had eruptive hemorrhage, 1 had gushing hemorrhage, and 1 had a white plug. Independent factors requiring therapeutic intervention for EV exacerbation were EV treatment history, drug-resistant ascites effusion, esophageal intramural vessel (EIV) diameter >3.3 mm, and left gastric vein (LGV) diameter >4.9 mm on computed tomography (CT) scan.

Conclusion: Patients with EV treatment history, drug-resistant ascites effusion, and EIV and LGV diameters >3.3 and 4.9 mm via CT, respectively, may require careful monitoring for possible EV exacerbation, enabling better EV management, adequate AB therapy, and finally, prolonged patient survival.

不可切除的肝癌患者接受阿特唑单抗加贝伐单抗治疗时食管静脉曲张恶化的危险因素
简介:Atezolizumab联合贝伐单抗(AB)治疗是一种有效的全身治疗不可切除的肝细胞癌(u-HCC)。然而,食管静脉曲张(EV)的恶化经常发生,为了在u-HCC患者中获得更好的预后,应该明确食管静脉曲张的管理。我们的研究旨在探讨AB治疗患者EV加重的实际情况及其危险因素。方法:我们招募了82例接受AB治疗的u-HCC患者。所有患者在AB诱导前3个月内接受食管胃十二指肠镜检查(EGD)以评估EV的存在。出现需要紧急或有计划的内窥镜治疗的EV发现定义了EV恶化。分析AB引入后EV加重的频率及危险因素。结果:49%的参与者在诱发前EGD中有EV发现。观察期内,有17%的患者发生房间隔加重,7.2%的患者发生房间隔破裂。在EV加重患者中,7例有红色阳性征象,1例有正式恶化至F3。在静脉破裂中,4例为爆发性出血,1例为涌出性出血,1例为白色塞。EV加重需要治疗干预的独立因素为EV治疗史、耐药腹水积液、食管壁内血管(EIV)直径>3.3 mm、胃左静脉(LGV)直径>4.9 mm。结论:有EV治疗史、耐药腹水积液、经CT显示EIV和LGV直径分别为>3.3和4.9 mm的患者,可能需要仔细监测可能的EV加重,从而实现更好的EV管理和充分的AB治疗,最终延长患者的生存期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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