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索拉非尼剂量递增治疗晚期肝细胞癌的完全缓解:长期低剂量索拉非尼联合经导管动脉化疗栓塞治疗失败后的病例报告。

Complete response of advanced hepatocellular carcinoma achieved by sorafenib dose re-escalation after failure of long-term low-dose-sorafenib treatment combined with transcatheter arterial chemoembolization: a case report.

机构信息

Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, 65 Tsuruma-cho, Showa-ku, Nagoya, 466-8550, Japan.

出版信息

Clin J Gastroenterol. 2020 Jun;13(3):397-402. doi: 10.1007/s12328-019-01066-7. Epub 2019 Nov 11.

DOI:10.1007/s12328-019-01066-7
PMID:31709503
Abstract

Few reports have described dose re-escalation after long-term low-dose sorafenib leading to good outcomes. Here, we report the case of an 80-year-old woman with advanced hepatocellular carcinoma who achieved complete response from sorafenib dose re-escalation after the failure of long-term low-dose sorafenib treatment combined with transcatheter arterial chemoembolization. Sorafenib therapy was initiated at 400 mg once daily due to old age and low platelet count. 5 months later, this dose was reduced to 200 mg once daily because of adverse events. Best radiological antitumor response by sorafenib treatment alone was judged as stable disease according to the modified Response Evaluation Criteria in Solid Tumors. 1 year later, she showed progressive disease owing to the progression of intrahepatic lesions. She received combination therapy with low-dose sorafenib (200 mg every other day) and transcatheter arterial chemoembolization, which proved relatively effective for three and a half years. Antitumor response by the fourth transcatheter arterial chemoembolization and subsequent low-dose sorafenib was clearly progressive disease. At that time, sorafenib-related adverse events were well-controlled. Sorafenib dose was re-escalated to 200 mg once daily. After this re-escalation, tumor markers declined rapidly, and adverse events remained tolerable. 4 months later, complete response was achieved.

摘要

鲜有报道描述长期低剂量索拉非尼治疗后剂量升级可获得良好结局。在此,我们报告了一例高龄(80 岁)女性 HCC 患者的病例,其在长期低剂量索拉非尼联合 TACE 治疗失败后,通过索拉非尼剂量升级实现了完全缓解。因高龄和血小板计数低,索拉非尼治疗起始剂量为 400mg,每日 1 次。5 个月后,由于不良反应,剂量减少至 200mg,每日 1 次。根据实体瘤疗效评价标准(RECIST),单独使用索拉非尼治疗的最佳影像学抗肿瘤反应判定为疾病稳定。1 年后,由于肝内病变进展,她出现疾病进展。她接受了低剂量索拉非尼(200mg,隔日 1 次)联合 TACE 治疗,该方案在 3 年半的时间里对她相对有效。第 4 次 TACE 和随后的低剂量索拉非尼治疗的抗肿瘤反应明确为疾病进展。此时,索拉非尼相关不良反应得到了很好的控制。索拉非尼剂量增加至 200mg,每日 1 次。剂量升级后,肿瘤标志物迅速下降,且不良反应仍可耐受。4 个月后,达到完全缓解。

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