4.6 Article

Multiparametric MRI for assessment of early response to neoadjuvant sunitinib in renal cell carcinoma

期刊

PLOS ONE
卷 16, 期 10, 页码 -

出版社

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0258988

关键词

-

资金

  1. Cancer Research UK (CRUK)
  2. CRUK Cambridge Centre
  3. Cambridge Trust
  4. CRUK & Engineering and Physical Sciences Research Council Cancer Imaging Centre in Cambridge and Manchester
  5. Mark Foundation for Cancer Research
  6. National Institute for Health Research (NIHR) Cambridge Biomedical Research Centre
  7. Cambridge Experimental Cancer Medicine Centre
  8. Cambridge University Hospitals National Health Service Foundation Trust
  9. Cambridge Clinical Trials Unit (CCTU)
  10. Addenbrooke's Charitable Trust

向作者/读者索取更多资源

The study aimed to detect early response to sunitinib treatment in metastatic clear cell renal cancer using multiparametric MRI. The results showed a reduction in tumor volumes and improved diffusivity after 12 days of sunitinib therapy, with correlations to treatment response and progression-free survival. Physiological imaging confirmed efficacy of the anti-angiogenic agent and demonstrated response to treatment shortly after initiation.
Purpose To detect early response to sunitinib treatment in metastatic clear cell renal cancer (mRCC) using multiparametric MRI. Method Participants with mRCC undergoing pre-surgical sunitinib therapy in the prospective NeoSun clinical trial (EudraCtNo: 2005-004502-82) were imaged before starting treatment, and after 12 days of sunitinib therapy using morphological MRI sequences, advanced diffusionweighted imaging, measurements of R-2* (related to hypoxia) and dynamic contrastenhanced imaging. Following nephrectomy, participants continued treatment and were followed-up with contrast-enhanced CT. Changes in imaging parameters before and after sunitinib were assessed with the non-parametric Wilcoxon signed-rank test and the log-rank test was used to assess effects on survival. Results 12 participants fulfilled the inclusion criteria. After 12 days, the solid and necrotic tumor volumes decreased by 28% and 17%, respectively (p = 0.04). However, tumor-volume reduction did not correlate with progression-free or overall survival (PFS/OS). Sunitinib therapy resulted in a reduction in median solid tumor diffusivity D from 1298x10(-6) to 1200x10(-6)mm(2)/ s (p = 0.03); a larger decrease was associated with a better RECIST response (p = 0.02) and longer PFS (p = 0.03) on the log-rank test. An increase in R-2* from 19 to 28s(-1) (p = 0.001) was observed, paralleled by a decrease in K-trans from 0.415 to 0.305min(-1) (p = 0.01) and a decrease in perfusion fraction from 0.34 to 0.19 (p < 0.001). Conclusions Physiological imaging confirmed efficacy of the anti-angiogenic agent 12 days after initiating therapy and demonstrated response to treatment. The change in diffusivity shortly after starting pre-surgical sunitinib correlated to PFS in mRCC undergoing nephrectomy, however, no parameter predicted OS.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据