Radium-223 in metastatic castration-resistant prostate cancer: whole-body diffusion-weighted magnetic resonance imaging scanning to assess response

Author:

Parker Chris12ORCID,Tunariu Nina12,Tovey Holly2,Alonzi Roberto3,Blackledge Matthew D2,Cook Gary J R4,Chua Sue1,Du Yong1,Hafeez Shaista12,Murray Iain1,Padhani Anwar R5,Staffurth John6,Tree Alison12,Stidwill Helen1,Finch Jessica3,Curcean Andra12,Chatfield Peter2,Perry Sophie2,Koh Dow-Mu12,Hall Emma2

Affiliation:

1. The Royal Marsden NHS Foundation Trust , London, UK

2. The Institute of Cancer Research , London, UK

3. Mount Vernon Cancer Centre , Northwood, UK

4. Cancer Imaging Department and King’s College London and Guy’s and St Thomas’ PET Centre, King’s College London , London, UK

5. Paul Strickland Scanner Centre, Mount Vernon Cancer Centre , Northwood, UK

6. Velindre Cancer Centre , Cardiff, UK

Abstract

Abstract Background Radium-223 is a bone-seeking, ɑ-emitting radionuclide used to treat men with bone metastases from castration-resistant prostate cancer. Sclerotic bone lesions cannot be evaluated using Response Evaluation Criteria in Solid Tumors. Therefore, imaging response biomarkers are needed. Methods We conducted a phase 2 randomized trial to assess disease response to radium-223. Men with metastatic castration-resistant prostate cancer and bone metastases were randomly allocated to 55 or 88 kBq/kg radium-223 every 4 weeks for 6 cycles. Whole-body diffusion-weighted magnetic resonance imaging (DWI) was performed at baseline, at cycles 2 and 4, and after treatment. The primary endpoint was defined as a 30% increase in global median apparent diffusion coefficient. Results Disease response on DWI was seen in 14 of 36 evaluable patients (39%; 95% confidence interval = 23% to 56%), with marked interpatient and intrapatient heterogeneity of response. There was an association between prostate-specific antigen response and MRI response (odds ratio = 18.5, 95% confidence interval = 1.32 to 258, P = .013). Mean administered activity of radium-223 per cycle was not associated with global MRI response (P = .216) but was associated with DWI response using a 5-target-lesion evaluation (P = .007). In 26 of 36 (72%) patients, new bone metastases, not present at baseline, were seen on DWI scans during radium-223 treatment. Conclusions DWI is useful for assessment of disease response in bone. Response to radium-223 is heterogeneous, both between patients and between different metastases in the same patient. New bone metastases appear during radium-223 treatment. The REASURE trial is registered under ISRCTN17805587.

Funder

Bayer

Cancer Research UK

National Institute for Health Research

National Cancer Research Network

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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