Division of Oncology, Stanford University School of Medicine, Stanford, CA 94305, USA.
Urol Oncol. 2013 Apr;31(3):379-85. doi: 10.1016/j.urolonc.2011.01.005. Epub 2011 Feb 25.
Tyrosine kinase inhibitors (TKI) have dramatically changed the management paradigm of advanced renal cell carcinoma (RCC) and are increasingly being used preoperatively to achieve cytoreduction.
To review our case series of post-TKI surgical procedures to add to the current perioperative efficacy and complication profile.
Between October 2006 and February 2010, 14 cytoreductive nephrectomies, radical nephrectomies, and metastectomies were performed after neoadjuvant sunitinib or sorafenib for advanced RCC. During the same time frame, a control group of 73 consecutive patients underwent radical nephrectomy, cytoreductive nephrectomy, or metastectomy in the absence of prior systemic therapy. We compared the incidence of perioperative complications and outcomes after surgical procedures between the two cohorts.
Median preoperative renal mass size was 11 cm (6.7-24.2 cm). Primary tumor shrinkage was seen in 57%; median shrinkage was 18% (8%-25%). The median treatment period was 17 weeks, and the median time from TKI discontinuation was 2 weeks. Compared with a control group and after adjusting for confounding covariates, presurgical TKI use was not associated with a significant increase in perioperative complications (50% vs. 40%, P = 0.25) or perioperative bleeding (36% vs. 34%, P = 0.97) but was associated with increased incidence and grade of intraoperative adhesions (86% vs. 58%, P = 0.001; grade 3 vs. 1, P = 0.002).
Compared with the published reports, we observed less hemorrhagic and wound healing issues but a significant increase in incidence and severity of intraoperative adhesions, which can present a formidable technical challenge. Potential reasons for our lower complication rate could be increased time from TKI discontinuation to surgery, longer time to postoperative TKI re-initiation, increased use of preoperative angioembolization, and the lack of preoperative bevacizumab administration. Presurgical TKI therapy can permit effective surgical cytoreduction with a safety and complication profile equivalent to that of non-TKI-nephrectomy; however safety data continue to evolve, and preoperative TKI use requires further prospective investigation.
酪氨酸激酶抑制剂(TKI)极大地改变了晚期肾细胞癌(RCC)的治疗模式,并且越来越多地被用于术前实现细胞减灭术。
回顾我们的 TKI 术后手术病例系列,以增加当前围手术期疗效和并发症概况。
在 2006 年 10 月至 2010 年 2 月期间,在新辅助舒尼替尼或索拉非尼治疗晚期 RCC 后,进行了 14 例细胞减灭性肾切除术、根治性肾切除术和转移切除术。在同一时间段内,73 例连续患者在没有先前系统治疗的情况下接受了根治性肾切除术、细胞减灭性肾切除术或转移切除术。我们比较了两组患者术后围手术期并发症和结果的发生率。
中位术前肾肿块大小为 11cm(6.7-24.2cm)。57%的患者可见原发性肿瘤缩小,中位缩小率为 18%(8%-25%)。中位治疗期为 17 周,TKI 停药后中位时间为 2 周。与对照组相比,并且在校正混杂协变量后,术前 TKI 使用与围手术期并发症(50%比 40%,P=0.25)或围手术期出血(36%比 34%,P=0.97)无显著增加,但与术中粘连的发生率和严重程度增加相关(86%比 58%,P=0.001;3 级比 1 级,P=0.002)。
与已发表的报告相比,我们观察到更少的出血和伤口愈合问题,但术中粘连的发生率和严重程度显著增加,这可能是一个艰巨的技术挑战。我们并发症发生率较低的潜在原因可能是 TKI 停药至手术的时间增加,术后 TKI 重新开始的时间延长,术前血管栓塞术的使用增加,以及缺乏术前贝伐单抗治疗。术前 TKI 治疗可实现有效的手术细胞减灭术,安全性和并发症概况与非 TKI 肾切除术相当;然而,安全性数据仍在不断发展,术前 TKI 使用需要进一步进行前瞻性研究。