医学
前列腺癌
磁共振弥散成像
生物标志物
成像生物标志物
癌症
放射科
肿瘤科
核医学
医学物理学
内科学
磁共振成像
生物化学
化学
作者
Raquel Pérez-López,Joaquı́n Mateo,Helen Mossop,Matthew Blackledge,David J. Collins,Mihaela Rata,Veronica A. Morgan,Alison Macdonald,Shahneen Sandhu,David Lorente,Pasquale Rescigno,Zafeiris Zafeiriou,Diletta Bianchini,Núria Porta,Emma Hall,Martin O. Leach,Johann S. de Bono,Dow‐Mu Koh,Nina Tunariu
出处
期刊:Radiology
[Radiological Society of North America]
日期:2016-11-22
卷期号:283 (1): 168-177
被引量:90
标识
DOI:10.1148/radiol.2016160646
摘要
Purpose To determine the usefulness of whole-body diffusion-weighted imaging (DWI) to assess the response of bone metastases to treatment in patients with metastatic castration-resistant prostate cancer (mCRPC). Materials and Methods A phase II prospective clinical trial of the poly-(adenosine diphosphate–ribose) polymerase inhibitor olaparib in mCRPC included a prospective magnetic resonance (MR) imaging substudy; the study was approved by the institutional research board, and written informed consent was obtained. Whole-body DWI was performed at baseline and after 12 weeks of olaparib administration by using 1.5-T MR imaging. Areas of abnormal signal intensity on DWI images in keeping with bone metastases were delineated to derive total diffusion volume (tDV); five target lesions were also evaluated. Associations of changes in volume of bone metastases and median apparent diffusion coefficient (ADC) with response to treatment were assessed by using the Mann-Whitney test and logistic regression; correlation with prostate-specific antigen level and circulating tumor cell count were assessed by using Spearman correlation (r). Results Twenty-one patients were included. All six responders to olaparib showed a decrease in tDV, while no decrease was observed in all nonresponders; this difference between responders and nonresponders was significant (P = .001). Increases in median ADC were associated with increased odds of response (odds ratio, 1.08; 95% confidence interval [CI]: 1.00, 1.15; P = .04). A positive association was detected between changes in tDV and best percentage change in prostate-specific antigen level and circulating tumor cell count (r = 0.63 [95% CI: 0.27, 0.83] and r = 0.77 [95% CI: 0.51, 0.90], respectively). When assessing five target lesions, decreases in volume were associated with response (odds ratio for volume increase, 0.89; 95% CI: 0.80, 0.99; P = .037). Conclusion This pilot study showed that decreases in volume and increases in median ADC of bone metastases assessed with whole-body DWI can potentially be used as indicators of response to olaparib in mCRPC. Online supplemental material is available for this article.
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