Division of Urology, Department of Surgery, University of California San Diego, School of Medicine San Diego, CA, USA.
BJU Int. 2010 Nov;106(9):1270-6. doi: 10.1111/j.1464-410X.2010.09357.x.
To investigate efficacy of neoadjuvant tyrosine kinase-inhibitor therapy (TKI) before imperative nephron-sparing surgery (NSS), as NSS in patients with large locally advanced or centrally located tumours can be challenging, and TKI therapy might result in a reduction of primary tumour burden and increase the feasibility of NSS.
This was a multicentre retrospective review and prospective pilot study of patients undergoing neoadjuvant sunitinib before planned NSS from February 2006 to February 2009. All patients underwent confirmatory biopsy for clear cell renal cell carcinoma. Patients received two 28-day cycles of sunitinib before NSS. Demographics/tumour characteristics, tumour response (by the Response Evaluation Criteria In Solid Tumors), outcomes and complications were analysed.
Twelve patients (seven men and five women; mean age 60.1 years, tumours on 14 renal units) were given TKI before NSS for imperative indications. The mean pretreatment tumour diameter was 7.1 cm; all patients had a decrease in size of the primary tumour after TKI, with a mean reduction in maximum diameter of 1.5 cm (21.1%). Four of 14 and 10 of 14 primary tumours had a partial response and stable disease after TKI. NSS was achievable in all 14 kidneys. Four patients had a concurrent metastasectomy. The mean warm ischaemia time was 22.5 min; postoperative dialysis was not required in any patients. Final pathology revealed negative tumour margins in all 14 tumours. The mean creatinine and estimated glomerular filtration rate (before/after NSS) were 1.34/1.40 mg/dL (P = 0.431) and 57.7/53.4 mL/min/1.73 m(2) (P = 0.475), respectively. At a mean follow-up of 23.9 months, 10 of the 12 patients were alive, one died from metastatic RCC and none required dialysis. Three of the 14 renal units developed delayed urinary leaks, all in patients who also received postoperative sunitinib. All leaks resolved with conservative measures.
Neoadjuvant TKI followed by NSS is safe and feasible, with all patients achieving a reduction in maximum tumour diameter, and with NSS being achievable with negative margins and with no requirement for postoperative dialysis. Further investigation is required.
探讨新辅助酪氨酸激酶抑制剂(TKI)治疗在前瞻性保肾手术(NSS)前的疗效,因为对于大的局部进展或中央部位的肿瘤,NSS 可能具有挑战性,而 TKI 治疗可能会导致原发性肿瘤负荷降低,并增加 NSS 的可行性。
这是一项多中心回顾性研究和前瞻性试点研究,纳入了 2006 年 2 月至 2009 年 2 月期间接受新辅助舒尼替尼治疗后计划行 NSS 的患者。所有患者均接受了肾细胞癌的确认性活检。患者在 NSS 前接受了两个 28 天周期的舒尼替尼治疗。分析了人口统计学/肿瘤特征、肿瘤反应(根据实体瘤反应评价标准)、结果和并发症。
12 名患者(7 名男性,5 名女性;平均年龄 60.1 岁,14 个肾脏中有 14 个肿瘤)因迫切的适应证接受了 NSS 前的 TKI 治疗。术前肿瘤直径平均为 7.1cm;所有患者在 TKI 治疗后肿瘤大小均有缩小,最大直径平均缩小 1.5cm(21.1%)。TKI 治疗后,14 个原发性肿瘤中有 4 个部分缓解,10 个稳定。14 个肾脏均可行 NSS。4 名患者同时进行了转移灶切除术。平均热缺血时间为 22.5 分钟;术后没有患者需要透析。最终病理显示 14 个肿瘤均切缘阴性。14 个肿瘤的平均血肌酐和估算肾小球滤过率(NSS 前后)分别为 1.34/1.40mg/dL(P=0.431)和 57.7/53.4mL/min/1.73m²(P=0.475)。在平均 23.9 个月的随访中,12 名患者中有 10 名存活,1 名死于转移性肾细胞癌,无患者需要透析。14 个肾脏中有 3 个发生了延迟性尿漏,均发生在接受术后舒尼替尼治疗的患者中。所有漏尿均通过保守治疗解决。
新辅助 TKI 联合 NSS 是安全可行的,所有患者的最大肿瘤直径均有缩小,NSS 可实现切缘阴性,且无需术后透析。需要进一步研究。