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晚期肾细胞癌患者原发性肿瘤对新辅助舒尼替尼的反应。

Response of the primary tumor to neoadjuvant sunitinib in patients with advanced renal cell carcinoma.

作者信息

Thomas Anil A, Rini Brian I, Lane Brian R, Garcia Jorge, Dreicer Robert, Klein Eric A, Novick Andrew C, Campbell Steven C

机构信息

Glickman Urological and Kidney Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

J Urol. 2009 Feb;181(2):518-23; discussion 523. doi: 10.1016/j.juro.2008.10.001. Epub 2008 Dec 18.

Abstract

PURPOSE

We assessed the activity of neoadjuvant sunitinib on primary renal tumors in patients with advanced renal cell carcinoma as well as the feasibility and safety of subsequent surgical resection.

METHODS

A total of 19 patients with advanced renal cell carcinoma deemed unsuitable for initial nephrectomy due to locally advanced disease or extensive metastatic burden were treated with 50 mg sunitinib daily for 4 weeks on followed by 2 weeks off. Tumor response was assessed by Response Evaluation Criteria in Solid Tumors every 2 cycles and the rate of conversion to resectable status was estimated.

RESULTS

Median patient age was 64 years and initial median radiographic renal tumor size was 10.5 cm. Clinical stage was N+ (10) and M+ (15). No patients experienced a complete response. Partial responses of the primary tumor were noted in 3 patients (16%), 7 (37%) had stable disease and 9 (47%) had disease progression in the primary tumor. Overall tumor response included 2 patients (11%) with partial response, 7 (37%) with stable disease and 10 (53%) with disease progression. At a median followup of 6 months (range 1 to 15) 4 patients (21%) had undergone nephrectomy and 5 died of disease progression. No unexpected surgical morbidity was encountered. Viable tumor was present in all 4 specimens. Sunitinib was associated with grade 3-4 toxicity in 7 patients (37%) and treatment was discontinued in 1 due to toxicity.

CONCLUSIONS

Administration of sunitinib in patients with advanced renal cell carcinoma with the primary tumor in place is feasible and can lead to a reduction in tumor burden that can facilitate subsequent surgical resection.

摘要

目的

我们评估了新辅助舒尼替尼对晚期肾细胞癌患者原发性肾肿瘤的活性,以及后续手术切除的可行性和安全性。

方法

共有19例因局部晚期疾病或广泛转移负担而被认为不适合初始肾切除术的晚期肾细胞癌患者,接受每日50 mg舒尼替尼治疗,持续4周,随后停药2周。每2个周期根据实体瘤疗效评价标准评估肿瘤反应,并估计转化为可切除状态的比例。

结果

患者中位年龄为64岁,初始肾肿瘤影像学中位大小为10.5 cm。临床分期为N+(10例)和M+(15例)。没有患者出现完全缓解。3例患者(16%)原发性肿瘤出现部分缓解,7例(37%)病情稳定,9例(47%)原发性肿瘤病情进展。总体肿瘤反应包括2例(11%)部分缓解、7例(37%)病情稳定和10例(53%)病情进展。中位随访6个月(范围1至15个月)时,4例患者(21%)接受了肾切除术,5例死于疾病进展。未遇到意外的手术并发症。所有4个标本中均存在存活肿瘤。7例患者(37%)出现3-4级毒性,1例因毒性而停药。

结论

对原发性肿瘤仍存在的晚期肾细胞癌患者给予舒尼替尼是可行的,并且可以减轻肿瘤负担,便于后续手术切除。

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