Arizumi Tadaaki, Ueshima Kazuomi, Chishina Hirokazu, Kono Masashi, Takita Masahiro, Kitai Satoshi, Inoue Tatsuo, Yada Norihisa, Hagiwara Satoru, Minami Yasunori, Sakurai Toshiharu, Nishida Naoshi, Kudo Masatoshi
Department of Gastroenterology and Hepatology, Kinki University Faculty of Medicine, Osaka-Sayama, Japan.
Dig Dis. 2014;32(6):733-9. doi: 10.1159/000368013. Epub 2014 Oct 29.
Sorafenib is a multikinase inhibitor targeting Raf and protein tyrosine kinases, which are involved in cell growth and tumor angiogenesis. Sorafenib administration induces temporary inhibition of tumor growth and a decrease in arterial blood flow in a considerable number of hepatocellular carcinoma (HCC) patients. We retrospectively evaluated the association between decreased blood flow and the overall survival (OS) of HCC patients after the initiation of sorafenib therapy.
Therapeutic responses of 158 advanced HCC patients with hypervascular tumors who had received sorafenib for more than 1 month were analyzed. To assess their therapeutic response, patients underwent radiological evaluation before and every 4-6 weeks after the initiation of sorafenib treatment. After the classification of patients into three groups based on the change in arterial enhancement during treatment (no change, decrease and disappearance), the OS of each group was compared using the Kaplan-Meier method.
Statistically significant differences in OS were observed among the three groups (p < 0.001). A decrease or disappearance of arterial enhancement was significantly associated with improved OS compared to patients with no change in arterial enhancement; the median OS was 19.9 months (95% confidence interval, CI, 16.4-24.5 months) and 6.0 months (95% CI, 4.0-8.8 months), respectively (p < 0.001). However, there was no difference in OS between the decrease and disappearance groups (p = 0.88).
We conclude that decreased arterial enhancement during sorafenib treatment was associated with the longest OS and could therefore reflect an effective response.
索拉非尼是一种靶向Raf和蛋白酪氨酸激酶的多激酶抑制剂,这些激酶参与细胞生长和肿瘤血管生成。在相当数量的肝细胞癌(HCC)患者中,给予索拉非尼可诱导肿瘤生长的暂时抑制和动脉血流减少。我们回顾性评估了索拉非尼治疗开始后血流减少与HCC患者总生存期(OS)之间的关联。
分析了158例接受索拉非尼治疗超过1个月的高血供肿瘤晚期HCC患者的治疗反应。为评估其治疗反应,患者在索拉非尼治疗开始前及开始后每4 - 6周接受一次影像学评估。根据治疗期间动脉强化的变化将患者分为三组(无变化、减少和消失),采用Kaplan - Meier法比较每组的OS。
三组之间观察到OS有统计学显著差异(p < 0.001)。与动脉强化无变化的患者相比,动脉强化减少或消失与OS改善显著相关;中位OS分别为19.9个月(95%置信区间,CI,16.4 - 24.5个月)和6.0个月(95%CI,4.0 - 8.8个月)(p < 0.001)。然而,减少组和消失组之间的OS无差异(p = 0.88)。
我们得出结论,索拉非尼治疗期间动脉强化减少与最长的OS相关,因此可以反映有效反应。