Department of Urology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita City, Osaka, 565-0871, Japan.
Med Oncol. 2012 Dec;29(5):3298-305. doi: 10.1007/s12032-012-0236-6. Epub 2012 Apr 29.
Sunitinib is a multikinase inhibitor used as first- and second-line treatment of metastatic renal cell carcinoma. However, there are few reports on the necessary doses of sunitinib to get better clinical outcome in general practice with Japanese patients. We examined the relationship between the efficacy and the necessary doses of sunitinib therapy in a multi-institutional retrospective study. A study population of 94 metastatic renal cell carcinoma patients was eligible for this investigation. The most frequent grade 3/4 laboratory adverse events were decreased platelet (31.9 %) and white blood cell (21.3 %) counts. Treatment was discontinued in 18 patients (31.0 %) initially receiving a 50-mg/day dose within only one course, and median 1-month relative dose intensity was 74.3 %. Median progression-free survival time was 2.3 months in patients treated for only one course and 10.8 months in patients treated for more than one course (P < 0.001). Multivariate analysis showed that only one course of treatment and 60 % and less of 1-month relative dose intensity were significantly associated with inferior progression-free survival (P < 0.001 and P = 0.027, respectively). Moreover, modified Memorial Sloan-Kettering Cancer Center poor risk was significantly associated with progression-free survival time. It is difficult for Japanese patients to continue an initial dose of sunitinib therapy without drug withdrawal. Continuing therapy for more than one course and maintaining more than 60 % of 1-month relative dose intensity were very important in the prolongation of progression-free survival time regardless of the initial treatment doses.
舒尼替尼是一种多激酶抑制剂,用于转移性肾细胞癌的一线和二线治疗。然而,在日本患者的常规实践中,关于舒尼替尼的必要剂量以获得更好的临床结果的报道很少。我们在一项多机构回顾性研究中检查了疗效与舒尼替尼治疗的必要剂量之间的关系。这项研究的患者群体包括 94 名转移性肾细胞癌患者。最常见的 3/4 级实验室不良事件是血小板计数(31.9%)和白细胞计数(21.3%)减少。在仅一个疗程内,最初接受 50mg/天剂量的 18 名患者(31.0%)停止了治疗,中位 1 个月相对剂量强度为 74.3%。仅接受一个疗程治疗的患者中位无进展生存期为 2.3 个月,而接受多个疗程治疗的患者为 10.8 个月(P<0.001)。多变量分析显示,仅接受一个疗程和 1 个月相对剂量强度低于 60%与无进展生存期较差显著相关(P<0.001 和 P=0.027)。此外,改良的 Memorial Sloan-Kettering 癌症中心不良风险与无进展生存期显著相关。日本患者很难在不停药的情况下继续初始剂量的舒尼替尼治疗。无论初始治疗剂量如何,继续治疗超过一个疗程并保持 1 个月相对剂量强度超过 60%对于延长无进展生存期非常重要。