Gamstätter Thomas, Weinmann Arndt, Schadmand-Fischer Simin, Spies Pia R, Niederle Ina M, Schuchmann Marcus, Galle Peter R, Wörns Marcus-Alexander
I. Medizinische Klinik und Poliklinik, Universitätsmedizin Mainz, Germany.
Onkologie. 2011;34(10):538-42. doi: 10.1159/000332137. Epub 2011 Sep 16.
The multi-targeted tyrosine kinase inhibitor sorafenib was the first agent to demonstrate a significant improvement in overall survival in patients with advanced hepatocellular carcinoma (HCC). However, survival under sorafenib treatment is still lower than 1 year in most patients in clinical practice. Sorafenib rarely produces radiological tumor regression, pointing out limitations in using conventional radiological assessment of response to targeted therapy. Serial alpha-fetoprotein (AFP) measurement may be useful in monitoring treatment response in patients with advanced HCC undergoing systemic therapy; however, this approach is poorly defined for the case of sorafenib.
We herein report the case of a 48-year-old patient with advanced HCC presenting with normalization of highly elevated AFP levels after 5 months of reduced-dose sorafenib treatment, resulting in a sustained radiological and clinical response.
Complete response to sorafenib may be possible in a small subgroup of patients with advanced HCC, strongly depending on one or more of the targets inhibited by sorafenib. Serial AFP measurement may provide additional information in monitoring treatment response to sorafenib and should be evaluated in future clinical trials in advanced HCC.
多靶点酪氨酸激酶抑制剂索拉非尼是首个在晚期肝细胞癌(HCC)患者中显示出总生存期显著改善的药物。然而,在临床实践中,大多数接受索拉非尼治疗的患者生存期仍低于1年。索拉非尼很少能使肿瘤出现影像学退缩,这表明在使用传统影像学评估靶向治疗反应方面存在局限性。连续检测甲胎蛋白(AFP)可能有助于监测晚期HCC患者接受全身治疗时的治疗反应;然而,对于索拉非尼治疗的情况,这种方法的定义并不明确。
我们在此报告一例48岁晚期HCC患者的病例,该患者在接受低剂量索拉非尼治疗5个月后,高度升高的AFP水平恢复正常,从而产生了持续的影像学和临床反应。
一小部分晚期HCC患者可能对索拉非尼产生完全反应,这在很大程度上取决于索拉非尼抑制的一个或多个靶点。连续检测AFP可能为监测索拉非尼治疗反应提供额外信息,应在未来晚期HCC的临床试验中进行评估。