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Response to atezolizumab plus bevacizumab specific for lung and lymph node metastases affects survival of patients with HCC

医学 阿替唑单抗 内科学 肿瘤科 胃肠病学 贝伐单抗 危险系数 淋巴结 实体瘤疗效评价标准 进行性疾病 门静脉血栓形成 免疫疗法 置信区间 癌症 无容量 血栓形成 化疗
作者
Jiwon Yang,Jonggi Choi,Won‐Mook Choi,Kang Mo Kim,Han Chu Lee,Ju Hyun Shim
出处
期刊:Liver International [Wiley]
卷期号:44 (4): 907-919
标识
DOI:10.1111/liv.15826
摘要

Abstract Background & Aims Tumour microenvironment heterogeneity among different organs can influence immunotherapy responses. Here, we evaluated the impact of differential organ‐specific responses on survival in patients with advanced‐stage hepatocellular carcinoma (HCC) treated with atezolizumab plus bevacizumab (Atezo/Bev). Methods We retrospectively analysed 366 consecutive patients with advanced‐stage HCC treated with Atezo/Bev as first‐line systemic treatment. Therapeutic response was assessed using RECIST v1.1. Patients were divided into an intention‐to‐treat (ITT) group (patients treated with ≥1 dose of Atezo/Bev) and a per‐protocol (PP) analysis group (patients with at least one measurable lesion irrespective of location treated with ≥3 doses of Atezo/Bev). Overall response and organ‐specific response at initial and best response were evaluated in the PP group. Responders were defined as patients achieving complete remission or partial response. Initial progressors were defined as patients with progressive disease after three doses of Atezo/Bev. Results The ITT and PP groups comprised 324 and 236 patients, respectively. In the PP group, the organ‐specific response rate of lung and lymph node (LN) metastases at both initial and best responses were higher than those of intrahepatic lesions and macrovascular tumour thrombosis. Lung and LN‐specific response rates were 21.1% and 23.5%, respectively, at initial response, and 24.7% and 31.4%, respectively, at best response. Both initial pulmonary and lymphatic progressors (adjusted hazard ratios [95% confidence intervals], 6.37 [2.10–19.3], and 8.36 [2.16–32.4], respectively) were independently associated with survival regardless of intrahepatic response. Conclusions The response of metastatic HCC to the Atezo/Bev regimen may be used to determine whether to continue treatment or switch to second‐line treatment at an early phase of therapy.
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