Guo Gang, Cai Wei, Li Hongzhao, Gao Jiangping, Ma Xin, Dong Jun, Fu Weijun, Zhang Xu
Department of Urologic Surgery, The People's Liberation Army General Hospital, Beijing 100853, P.R. China.
Oncol Lett. 2017 Jul;14(1):369-375. doi: 10.3892/ol.2017.6131. Epub 2017 May 5.
The present study aimed to investigate presurgical neoadjuvant targeted therapy for patients with kidney cancer and vena cava tumor embolus, in order to examine its indications, therapeutic effects and optimal timing of surgery. Between June 2009 and June 2014, 12 patients from The People's Liberation Army General Hospital (Beijing, China) were diagnosed with kidney cancer with superior vena cava tumor embolus, and received presurgical neoadjuvant targeted therapy (sorafenib 400 mg twice a day or sunitinib 50 mg/day) for a median of 13.3 weeks. Patients included 8 males and 4 females, with a median age of 49.8 years. Kidney cancer was present on the left side in 3 patients and in the right side in 9 patients. The median tumor embolus length was 9.7 cm (range, 6.5-14.0 cm). Tumor embolus levels II, III and IV, classified by the Mayo Clinic standard, were observed in 2, 6 and 4 patients, respectively. Median treatment time and average targeted therapy discontinuation time were observed to be longer in sunitinib-treated patients compared with sorafenib-treated patients. In total, 2 patients in the present study had partial remission (PR) and 8 patients had stable disease (SD); for tumor embolus, 4 patients had PR and 8 patients had SD. Tumor embolus length decreased by a median value of 18.7% (range, 0.0-42.1%) or 1.8 cm (range, 0.1-5.2 cm). Tumor diameter decreased by a median value of 8.6% (range, 0.0-38.9%) or 0.7 cm (range, 0.0-3.5 cm). The level of the tumor thrombus, classified by the Mayo Clinic standard, was observed to decrease following sunitinib treatment, including two cases downgraded from tumor thrombus level IV to II, one case from level IV to III and two cases from level III to II. Presurgical neoadjuvant targeted molecular therapy may have the potential to reduce the tumor stage of patients, as well as decreasing the surgical difficulty for radical nephrectomy.
本研究旨在探讨肾癌合并腔静脉瘤栓患者的术前新辅助靶向治疗,以明确其适应证、治疗效果及最佳手术时机。2009年6月至2014年6月,中国人民解放军总医院(北京)的12例患者被诊断为肾癌合并上腔静脉瘤栓,并接受了术前新辅助靶向治疗(索拉非尼400mg,每日2次或舒尼替尼50mg/天),中位治疗时间为13.3周。患者包括8例男性和4例女性,中位年龄为49.8岁。3例患者肾癌位于左侧,9例位于右侧。瘤栓中位长度为9.7cm(范围6.5 - 14.0cm)。按照梅奥诊所标准分类,Ⅱ级、Ⅲ级和Ⅳ级瘤栓患者分别有2例、6例和4例。观察发现,舒尼替尼治疗患者的中位治疗时间和平均靶向治疗停药时间比索拉非尼治疗患者更长。本研究中,共有2例患者部分缓解(PR),8例患者病情稳定(SD);对于瘤栓,4例患者PR,8例患者SD。瘤栓长度中位值下降了18.7%(范围0.0 - 42.1%)或1.8cm(范围0.1 - 5.2cm)。肿瘤直径中位值下降了8.6%(范围0.0 - 38.9%)或下降了0.7cm(范围0.0 - 3.5cm)。观察发现,舒尼替尼治疗后,按照梅奥诊所标准分类的肿瘤血栓水平下降,包括2例从Ⅳ级降至Ⅱ级,1例从Ⅳ级降至Ⅲ级,2例从Ⅲ级降至Ⅱ级。术前新辅助靶向分子治疗可能有降低患者肿瘤分期以及减少根治性肾切除术手术难度的潜力。