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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Favorable radiological antitumor response at 2?weeks after starting lenvatinib for patients with advanced hepatocellular carcinoma
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Favorable radiological antitumor response at 2?weeks after starting lenvatinib for patients with advanced hepatocellular carcinoma

机译:有利的放射性抗肿瘤反应在2次出发后Lenvatinib为先进的肝细胞癌患者

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Aim We aimed to investigate the radiological antitumor response at 2?weeks after starting lenvatinib for patients with advanced hepatocellular carcinoma in real‐world practice. Methods This retrospective study enrolled 40 patients who received lenvatinib. Radiological antitumor response was evaluated according to the modified Response Evaluation Criteria in Solid Tumors. Results The objective response rate at 2?weeks and best overall response on confirmation of complete response, partial response (PR), and stable disease required (confirmed response) were 57.5% and 32.5%, respectively. Based on confirmed response, the overall survival rate was significantly longer in patients with an objective response rate than in those with stable disease or progressive disease after 12?months (73.2% and 54.2%, P ?=?0.0358). All 13 patients with an objective response rate on confirmed response were evaluated as PR at 2?weeks. The alpha‐fetoprotein ratio at 2?weeks was a significant factor associated with PR of response rate at 2?weeks. The median relative dose intensity from 2 to 6?weeks was significantly lower than that from 0 to 2?weeks (69.6% vs. 100%, P ??0.0001). Stratified by the antitumor response at 6?weeks considering the image evaluation at 2?weeks, the median relative dose intensity from 2 to 6?weeks was significantly lower in patients with progressive disease than in those with PR or stable disease (45.2% vs. 72.6%, P ?=?0.0482). Conclusions The radiological antitumor response at 2?weeks was favorable. Information on a favorable visible therapeutic response very early after lenvatinib initiation can help patients maintain their motivation for treatment, and allow physicians to continue treatment effectively and safely.
机译:目的我们旨在调查2次出发后的肝癌患者在现实世界实践中先进的肝细胞癌患者的放射抗肿瘤反应。方法这项回顾性研究注册了40名接受Lenvatinib的患者。根据固体肿瘤的修饰响应评估标准评价放射抗肿瘤反应。导致2个时间的目标反应率和对完全反应的确认,部分反应(PR)和稳定疾病所需的最佳总体反应(确认反应)分别为57.5%和32.5%。基于确认的反应,客观反应率的患者总存活率明显更长,而且在12?月份(73.2%和54.2%,P?= 0.0358)中,患者的患者的目标反应率高于疾病或渐进性疾病的患者。所有13名患有确诊反应的客观反应率的患者被评估为PR在2?周内。 α-胎儿蛋白比率在2?周中是与响应率的PR相关的重要因素在2?周内。中位相对剂量强度为2〜6?周的时间明显低于0至2〜2周(69.6%与100%,p≤≤0.0001)。将抗肿瘤响应的抗肿瘤反应分层考虑到2个?几周的图像评估,患者患者的相对剂量强度为2〜6〜6的患者显着低于PR或稳定疾病的患者(45.2%Vs. 72.6%,p?= 0.0482)。结论在2?周的情况下,放射抗肿瘤反应有利。在Lenvatinib启动后早期的有利可见治疗反应的信息可以帮助患者维持其治疗的动机,并允许医生能够有效和安全地继续治疗。

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