首页 | 本学科首页   官方微博 | 高级检索  
     


Outcomes in patients with metastatic renal cell cancer treated with individualized sunitinib therapy: Correlation with dynamic microbubble ultrasound data and review of the literature
Authors:Georg A. Bjarnason  Bishoy Khalil  John M. Hudson  Ross Williams  Laurent M. Milot  Mostafa Atri  Alex Kiss  Peter N. Burns
Affiliation:1. Division of Medical Oncology, Sunnybrook Odette Cancer Centre, Toronto, Canada;2. Imaging Research, Sunnybrook Research Institute, Toronto and Dept Medical Biophysics, University of Toronto, Canada;3. Department of Medical Imaging, Sunnybrook Health Sciences Centre, Toronto, Canada;4. Joint Department of Medical Imaging, University of Toronto Health Network, Toronto, Canada;5. Department of Research Design and Biostatistics, Sunnybrook Health Sciences Centre, Toronto, Canada
Abstract:BackgroundIncreased sunitinib exposure (area under the curve) is associated with better outcome in metastatic renal cell cancer. Recommendations for dose modification do not take this into account. A treatment strategy, based on individual patient toxicity, was developed to maximize dose and minimize time without therapy for patients who could not tolerate the standard sunitinib schedule of 50 mg given for 28 days with a 14-day break (50 mg, 28/14).MethodsA single-center retrospective review was conducted on patients with metastatic renal cell cancer treated from October 2005 to March 2010. Dose/schedule modifications (DSM) were done to keep toxicity (hematological, fatigue, skin, and gastrointestinal) at≤grade 2. DSM-1 was 50 mg, 14 days on/7 days off with individualized increases in days on treatment. DSM-2 was 50 mg, 7 days on/7 days off with individualized increase in days on treatment. DSM-3 was 37.5 mg with individualized 7-day breaks. DSM-4 was 25 mg with individualized 7-day breaks. Multivariable analysis was performed for outcome as a function of patient and treatment variables.ResultsOverall, 172 patients were included in the analysis. Most patients had clear cell histology (79.1%) with sunitinib given as a first-line therapy in 59%. The DSM-1 and 2 and DSM-3 and 4 groups had a progression-free survival (PFS) (10.9–11.9 mo) and overall survival (OS) (23.4–24.5 mo) that was significantly better than the PFS (5.3 mo; P<0.001) and OS (14.4 mo; P = 0.03 and 0.003) for the standard schedule (50 mg, 28/14). DCE-US in a subset of patients showed that maximum antiangiogenic activity was achieved after 14 days on therapy.ConclusionsIndividualized sunitinib scheduling based on toxicity may improve PFS and OS. This hypothesis is supported by several other respective data that are reviewed. A confirmatory prospective trial is ongoing.
Keywords:Imaging  Pharmacokinetics  Renal cell cancer  Sunitinib  Toxicity
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号