Division of Hematology-Oncology, Department of Internal Medicine, Busan Paik Hospital, Inje University College of Medicine, Busan, South Korea.
Division of Hematology-Oncology, Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, South Korea.
Eur J Cancer. 2014 Mar;50(4):746-52. doi: 10.1016/j.ejca.2013.11.029. Epub 2013 Dec 11.
Patients with metastatic renal cell carcinoma (mRCC) with renal insufficiency are generally excluded from clinical trials, despite their increasing numbers. Thus, we evaluated the efficacy and toxicity of sunitinib in such patients.
Korean patients with mRCC with renal insufficiency who had received sunitinib as first-line treatment between January 2008 and May 2012 were included. Patient characteristics, clinical outcomes and toxicities were evaluated. Overall survival (OS) and progression-free survival (PFS) were determined according to the degree of renal impairment.
The median age of the 34 patients evaluated was 66 years, 90% had an Eastern Cooperative Oncology Group performance status of 0 or 1 and the median glomerular filtration rate was 46.5 mL min(-1) · 1.73 m(-2) (range, 21.1-59.5). The starting sunitinib dose was 37.5 and 50mg for 12 and 22 patients, respectively. A 4-weeks-on-2-weeks-off regimen was followed for 31 patients; a 2-weeks-on-2-weeks-off regimen, for one patient; and a daily regimen, for two patients. The best response was partial response in eight patients and stable disease in 12. Median OS and PFS times were 26.3 months (95% confidence interval [CI]: 17.1-35.3) and 12.2 months (95% CI: 10.2-13.2), respectively. Common non-haematologic adverse events (AEs) were stomatitis, rash, general oedema and fatigue. The most common AEs of ⩾ grade 3 severity were fatigue, neutropenia and thrombocytopenia.
In patients with mRCC with renal insufficiency, sunitinib was efficacious and did not cause increased toxicity. Thus, clinicians should not hesitate to treat patients with mRCC with renal insufficiency with sunitinib.
患有肾功能不全的转移性肾细胞癌(mRCC)患者通常被排除在临床试验之外,尽管这类患者的数量在不断增加。因此,我们评估了舒尼替尼在这类患者中的疗效和毒性。
纳入了 2008 年 1 月至 2012 年 5 月期间接受舒尼替尼作为一线治疗的肾功能不全的 mRCC 韩国患者。评估了患者特征、临床结局和毒性。根据肾功能损害程度确定总生存期(OS)和无进展生存期(PFS)。
34 例患者的中位年龄为 66 岁,90%的患者东部肿瘤协作组(ECOG)体能状态为 0 或 1,中位肾小球滤过率为 46.5mL min(-1) · 1.73 m(-2)(范围,21.1-59.5)。起始舒尼替尼剂量分别为 37.5mg 和 50mg,分别用于 12 例和 22 例患者。31 例患者采用 4 周/2 周方案,1 例患者采用 2 周/2 周方案,2 例患者采用每日方案。最佳反应为 8 例部分缓解和 12 例稳定疾病。中位 OS 和 PFS 时间分别为 26.3 个月(95%置信区间[CI]:17.1-35.3)和 12.2 个月(95%CI:10.2-13.2)。常见的非血液学不良事件(AE)为口腔炎、皮疹、全身性水肿和疲劳。 ⩾3 级最常见的 AE 为疲劳、中性粒细胞减少和血小板减少。
在肾功能不全的 mRCC 患者中,舒尼替尼是有效的,不会增加毒性。因此,临床医生不应犹豫用舒尼替尼治疗肾功能不全的 mRCC 患者。