Can Tyrosine Kinase inhibitors be Discontinued in Patients with Metastatic Renal Cell Carcinoma and a Complete Response to Treatment? A Multicentre, Retrospective Analysis

被引:75
作者
Johannsen, Manfred [1 ]
Floercken, Anne [2 ]
Bex, Axel [3 ]
Roigas, Jan [4 ]
Cosentino, Marco [5 ]
Ficarra, Vincenzo [5 ]
Kloeters, Christian [6 ]
Rief, Matthias [6 ]
Rogalla, Patrik [6 ]
Miller, Kurt [1 ]
Gruenwald, Viktor [7 ]
机构
[1] Charite, Dept Urol, D-10117 Berlin, Germany
[2] Charite, Dept Haematol & Oncol, D-10117 Berlin, Germany
[3] Netherlands Canc Inst, Dept Urol, Amsterdam, Netherlands
[4] Vivantes Klinikum Urban, Dept Urol, Berlin, Germany
[5] Univ Padua, Dept Urol, Padua, Italy
[6] Charite, Dept Radiol, D-10117 Berlin, Germany
[7] Hannover Med Sch, Dept Haematol Hemostaseol & Oncol, D-3000 Hannover, Germany
关键词
Tyrosine kinase inhibitors; Renal cell carcinoma; Metastasectomy; Complete response; ANTITUMOR-ACTIVITY; SUNITINIB; INTERFERON; RESECTION; SURVIVAL; THERAPY;
D O I
10.1016/j.eururo.2008.10.021
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Discontinuation of treatment with tyrosine kinase inhibitors (TKIs) and readministration in case of recurrence could improve quality of life (QoL) and reduce treatment costs for patients with metastatic renal cell carcinoma (mRCC) in which a complete remission (CR) is achieved by medical treatment alone or with additional resection of residual metastases. Objective: To evaluate whether TKIs can be discontinued in these selected patients with mRCC. Design, setting, and participants: A retrospective analysis of medical records and imaging studies was performed on all patients with mRCC treated with TKIs (n = 266) in five institutions. Patients with a CR under TKI treatment alone or with additional metastasectomy of residual disease following a partial response (PR), in which TKIs were discontinued, were included in the analysis. Outcome criteria analysed were time to recurrence of previous metastases, occurrence of new metastases, symptomatic progression, improvement of adverse events, and response to reexposure to TKIs. Interventions: Sunitinib 50 mg/day for 4 wk on and 2 wk off, sorafenib 800 mg/day. Measurements: Response according to Response Evaluation Criteria in Solid Tumours (RECIST). Results and limitations: We identified 12 cases: 5 CRs with sunitimb, 1 CR with sorafemb, and 6 surgical CRs with sunitinib followed by residual metastasectomy. Side-effects subsided in all patients off treatment. At a median follow-up of 8.5 mo (range: 4-25) from TKI discontinuation, 7 of 12 patients remained without recurrence and 5 had recurrent disease, with new metastases in 3 cases. Median time to progression was 6 mo (range: 3-8). Readministration of TKI was effective in all cases. The study is limited by small numbers and retrospective design. Conclusions: Discontinuation of TKI in patients with mRCC and CR carries the risk of progression with new metastases and potential complications. Further investigation in a larger cohort of patients is war-ranted before such an approach can be regarded as safe. (C) 2008 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1430 / 1439
页数:10
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