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Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer.

Publication ,  Journal Article
Armstrong, AJ; Gupta, S; Healy, P; Kemeny, G; Leith, B; Zalutsky, MR; Spritzer, C; Davies, C; Rothwell, C; Ware, K; Somarelli, JA; Wood, K ...
Published in: PLoS One
2019

BACKGROUND: Radium-223 is a targeted alpha-particle therapy that improves survival in men with metastatic castration resistant prostate cancer (mCRPC), particularly in men with elevated serum levels of bone alkaline phosphatase (B-ALP). We hypothesized that osteomimicry, a form of epithelial plasticity leading to an osteoblastic phenotype, may contribute to intralesional deposition of radium-223 and subsequent irradiation of the tumor microenvironment. METHODS: We conducted a pharmacodynamic study (NCT02204943) of radium-223 in men with bone mCRPC. Prior to and three and six months after radium-223 treatment initiation, we collected CTCs and metastatic biopsies for phenotypic characterization and CTC genomic analysis. The primary objective was to describe the impact of radium-223 on the prevalence of CTC B-ALP over time. We measured radium-223 decay products in tumor and surrounding normal bone during treatment. We validated genomic findings in a separate independent study of men with bone metastatic mCRPC (n = 45) and publicly accessible data of metastatic CRPC tissues. RESULTS: We enrolled 20 men with symptomatic bone predominant mCRPC and treated with radium-223. We observed greater radium-223 radioactivity levels in metastatic bone tumor containing biopsies compared with adjacent normal bone. We found evidence of persistent Cellsearch CTCs and B-ALP (+) CTCs in the majority of men over time during radium-223 therapy despite serum B-ALP normalization. We identified genomic gains in osteoblast mimicry genes including gains of ALPL, osteopontin, SPARC, OB-cadherin and loss of RUNX2, and validated genomic alterations or increased expression at the DNA and RNA level in an independent cohort of 45 men with bone-metastatic CRPC and in 150 metastatic biopsies from men with mCRPC. CONCLUSIONS: Osteomimicry may contribute in part to the uptake of radium-223 within bone metastases and may thereby enhance the therapeutic benefit of this bone targeting radiotherapy.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2019

Volume

14

Issue

5

Start / End Page

e0216934

Location

United States

Related Subject Headings

  • Tumor Microenvironment
  • Survival Analysis
  • Radium
  • Prostatic Neoplasms, Castration-Resistant
  • Prostate
  • Osteopontin
  • Osteonectin
  • Neoplastic Cells, Circulating
  • Molecular Targeted Therapy
  • Male
 

Citation

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Chicago
ICMJE
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Armstrong, A. J., Gupta, S., Healy, P., Kemeny, G., Leith, B., Zalutsky, M. R., … George, D. J. (2019). Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer. PLoS One, 14(5), e0216934. https://doi.org/10.1371/journal.pone.0216934
Armstrong, Andrew J., Santosh Gupta, Patrick Healy, Gabor Kemeny, Beth Leith, Michael R. Zalutsky, Charles Spritzer, et al. “Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer.PLoS One 14, no. 5 (2019): e0216934. https://doi.org/10.1371/journal.pone.0216934.
Armstrong AJ, Gupta S, Healy P, Kemeny G, Leith B, Zalutsky MR, et al. Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer. PLoS One. 2019;14(5):e0216934.
Armstrong, Andrew J., et al. “Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer.PLoS One, vol. 14, no. 5, 2019, p. e0216934. Pubmed, doi:10.1371/journal.pone.0216934.
Armstrong AJ, Gupta S, Healy P, Kemeny G, Leith B, Zalutsky MR, Spritzer C, Davies C, Rothwell C, Ware K, Somarelli JA, Wood K, Ribar T, Giannakakou P, Zhang J, Gerber D, Anand M, Foo W-C, Halabi S, Gregory SG, George DJ. Pharmacodynamic study of radium-223 in men with bone metastatic castration resistant prostate cancer. PLoS One. 2019;14(5):e0216934.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2019

Volume

14

Issue

5

Start / End Page

e0216934

Location

United States

Related Subject Headings

  • Tumor Microenvironment
  • Survival Analysis
  • Radium
  • Prostatic Neoplasms, Castration-Resistant
  • Prostate
  • Osteopontin
  • Osteonectin
  • Neoplastic Cells, Circulating
  • Molecular Targeted Therapy
  • Male