Genitourinary Oncology Service, Institute of Oncology, Meir Medical Center and the Sackler School of Medicine, Tel Aviv University, Kfar-Saba, Israel; Department of Oncology, Rambam Medical Center, Haifa, Israel; Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, Maryland, USA; Roswell Park Cancer Institute, Buffalo, New York, USA; Department of Oncology, Wolfson Medical Center, Holon, Israel; Department of Oncology, Asaf Harofe Medical Center, Zerifin, Israel; Department of Oncology, Sheba Medical Center, Tel Hashomer, Israel; Department of Oncology, Soroka University Medical Center, Beer-sheva, Israel.
Oncologist. 2014 Jan;19(1):51-60. doi: 10.1634/theoncologist.2012-0335. Epub 2013 Dec 5.
Obesity, smoking, hypertension, and diabetes are risk factors for renal cell carcinoma development. Their presence has been associated with a worse outcome in various cancers. We sought to determine their association with outcome of sunitinib treatment in metastatic renal cell carcinoma (mRCC).
An international multicenter retrospective study of sunitinib-treated mRCC patients was performed. Multivariate analyses were performed to determine the association between outcome and the pretreatment status of smoking, body mass index, hypertension, diabetes, and other known prognostic factors.
Between 2004 and 2013, 278 mRCC patients were treated with sunitinib: 59 were active smokers, 67 were obese, 73 were diabetic, and 165 had pretreatment hypertension. Median progression-free survival (PFS) was 9 months, and overall survival (OS) was 22 months. Factors associated with PFS were smoking status (past and active smokers: hazard ratio [HR]: 1.17, p = .39; never smokers: HR: 2.94, p < .0001), non-clear cell histology (HR: 1.62, p = .011), pretreatment neutrophil-to-lymphocyte ratio >3 (HR: 3.51, p < .0001), use of angiotensin system inhibitors (HR: 0.63, p = .01), sunitinib dose reduction or treatment interruption (HR: 0.72, p = .045), and Heng risk (good and intermediate risk: HR: 1.07, p = .77; poor risk: HR: 1.87, p = .046). Factors associated with OS were smoking status (past and active smokers: HR: 1.25, p = .29; never smokers: HR: 2.7, p < .0001), pretreatment neutrophil-to-lymphocyte ratio >3 (HR: 2.95, p < .0001), and sunitinib-induced hypertension (HR: 0.57, p = .002).
Active smoking may negatively affect the PFS and OS of sunitinib-treated mRCC. Clinicians should consider advising patients to quit smoking at initiation of sunitinib treatment for mRCC.
肥胖、吸烟、高血压和糖尿病是肾癌发生的危险因素。它们的存在与各种癌症的不良预后有关。我们试图确定它们与舒尼替尼治疗转移性肾细胞癌(mRCC)的结果之间的关系。
对接受舒尼替尼治疗的 mRCC 患者进行了一项国际多中心回顾性研究。进行了多变量分析,以确定治疗前吸烟状况、体重指数、高血压、糖尿病和其他已知预后因素与结局之间的关系。
2004 年至 2013 年间,278 例 mRCC 患者接受舒尼替尼治疗:59 例为现吸烟者,67 例为肥胖者,73 例为糖尿病患者,165 例为治疗前高血压患者。中位无进展生存期(PFS)为 9 个月,总生存期(OS)为 22 个月。与 PFS 相关的因素包括吸烟状态(既往和现吸烟者:HR:1.17,p =.39;从不吸烟者:HR:2.94,p <.0001)、非透明细胞组织学(HR:1.62,p =.011)、治疗前中性粒细胞与淋巴细胞比值>3(HR:3.51,p <.0001)、血管紧张素系统抑制剂的使用(HR:0.63,p =.01)、舒尼替尼剂量减少或治疗中断(HR:0.72,p =.045)和 Heng 风险(良好和中等风险:HR:1.07,p =.77;不良风险:HR:1.87,p =.046)。与 OS 相关的因素包括吸烟状态(既往和现吸烟者:HR:1.25,p =.29;从不吸烟者:HR:2.7,p <.0001)、治疗前中性粒细胞与淋巴细胞比值>3(HR:2.95,p <.0001)和舒尼替尼诱导的高血压(HR:0.57,p =.002)。
现吸烟可能会对接受舒尼替尼治疗的 mRCC 患者的 PFS 和 OS 产生负面影响。临床医生在开始 mRCC 舒尼替尼治疗时应考虑建议患者戒烟。