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Published in: Cancer and Metastasis Reviews 2-3/2014

01-09-2014

Bone-targeting agents in prostate cancer

Authors: Daniel L. Suzman, Sosipatros A. Boikos, Michael A. Carducci

Published in: Cancer and Metastasis Reviews | Issue 2-3/2014

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Abstract

Bone metastases are present in the vast majority of men with advanced prostate cancer, representing the main cause for morbidity and mortality. Recurrent or metastatic disease is managed initially with androgen deprivation but the majority of the patients eventually will progress to castration-resistant prostate cancer, with patients developing bone metastases in most of the cases. Survival and growth of the metastatic prostate cancer cells is dependent on a complex microenvironment (onco-niche) that includes the osteoblasts, the osteoclasts, the endothelium, and the stroma. This review summarizes agents that target the pathways involved in this complex interaction between prostate cancer and bone microenvironment and aim to transform lethal metastatic prostate cancer into a chronic disease.
Literature
1.
go back to reference Tannock, I. F., de Wit, R., Berry, W. R., et al. (2004). Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. The New England Journal of Medicine, 351(15), 1502–1512.PubMedCrossRef Tannock, I. F., de Wit, R., Berry, W. R., et al. (2004). Docetaxel plus prednisone or mitoxantrone plus prednisone for advanced prostate cancer. The New England Journal of Medicine, 351(15), 1502–1512.PubMedCrossRef
2.
go back to reference Kantoff, P. W., Higano, C. S., Shore, N. D., et al. (2010). Sipuleucel-T immunotherapy for castration-resistant prostate cancer. The New England Journal of Medicine, 363(5), 411–422.PubMedCrossRef Kantoff, P. W., Higano, C. S., Shore, N. D., et al. (2010). Sipuleucel-T immunotherapy for castration-resistant prostate cancer. The New England Journal of Medicine, 363(5), 411–422.PubMedCrossRef
3.
go back to reference de Bono, J. S., Oudard, S., Ozguroglu, M., et al. (2010). Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. The Lancet, 376(9747), 1147–1154.CrossRef de Bono, J. S., Oudard, S., Ozguroglu, M., et al. (2010). Prednisone plus cabazitaxel or mitoxantrone for metastatic castration-resistant prostate cancer progressing after docetaxel treatment: a randomised open-label trial. The Lancet, 376(9747), 1147–1154.CrossRef
4.
go back to reference Parker, C., Nilsson, S., Heinrich, D., et al. (2013). Alpha emitter radium-223 and survival in metastatic prostate cancer. The New England Journal of Medicine, 369(3), 213–223.PubMedCrossRef Parker, C., Nilsson, S., Heinrich, D., et al. (2013). Alpha emitter radium-223 and survival in metastatic prostate cancer. The New England Journal of Medicine, 369(3), 213–223.PubMedCrossRef
5.
go back to reference Fizazi, K., Scher, H. I., Molina, A., et al. (2012). Abiraterone acetate for treatment of metastatic castration-resistant prostate cancer: final overall survival analysis of the COU-AA-301 randomised, double-blind, placebo-controlled phase 3 study. The Lancet Oncology, 13, 983–992.PubMedCrossRef Fizazi, K., Scher, H. I., Molina, A., et al. (2012). Abiraterone acetate for treatment of metastatic castration-resistant prostate cancer: final overall survival analysis of the COU-AA-301 randomised, double-blind, placebo-controlled phase 3 study. The Lancet Oncology, 13, 983–992.PubMedCrossRef
6.
go back to reference Scher, H. I., Fizazi, K., Saad, F., et al. (2012). Effect of MDV3100, an androgen receptor signaling inhibitor (ARSI), on overall survival in patients with prostate cancer postdocetaxel: results from the phase III AFFIRM study. Journal of Clinical Oncology, 30(Suppl 5), 1. Scher, H. I., Fizazi, K., Saad, F., et al. (2012). Effect of MDV3100, an androgen receptor signaling inhibitor (ARSI), on overall survival in patients with prostate cancer postdocetaxel: results from the phase III AFFIRM study. Journal of Clinical Oncology, 30(Suppl 5), 1.
7.
go back to reference Paget, S. (1889). The distribution of secondary growths in cancer of the breast. The Lancet, 133(3421), 571–573.CrossRef Paget, S. (1889). The distribution of secondary growths in cancer of the breast. The Lancet, 133(3421), 571–573.CrossRef
8.
go back to reference Suda, T., Takahashi, N., Udagawa, N., Jimi, E., Gillespie, M. T., & Martin, T. J. (1999). Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families. Endocrine Reviews, 20(3), 345–357.PubMedCrossRef Suda, T., Takahashi, N., Udagawa, N., Jimi, E., Gillespie, M. T., & Martin, T. J. (1999). Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families. Endocrine Reviews, 20(3), 345–357.PubMedCrossRef
9.
go back to reference Wada, T., Nakashima, T., Hiroshi, N., & Penninger, J. M. (2006). RANKL–RANK signaling in osteoclastogenesis and bone disease. Trends in Molecular Medicine, 12(1), 17–25.PubMedCrossRef Wada, T., Nakashima, T., Hiroshi, N., & Penninger, J. M. (2006). RANKL–RANK signaling in osteoclastogenesis and bone disease. Trends in Molecular Medicine, 12(1), 17–25.PubMedCrossRef
10.
go back to reference Shiozawa, Y., Pedersen, E. A., Havens, A. M., et al. (2011). Human prostate cancer metastases target the hematopoietic stem cell niche to establish footholds in mouse bone marrow. The Journal of Clinical Investigation, 121(4), 1298.PubMedCentralPubMedCrossRef Shiozawa, Y., Pedersen, E. A., Havens, A. M., et al. (2011). Human prostate cancer metastases target the hematopoietic stem cell niche to establish footholds in mouse bone marrow. The Journal of Clinical Investigation, 121(4), 1298.PubMedCentralPubMedCrossRef
11.
go back to reference Pedersen, E. A., Shiozawa, Y., Pienta, K. J., & Taichman, R. S. (2012). The prostate cancer bone marrow niche: more than just ‘fertile soil’. Asian Journal of Andrology, 14(3), 423–427.PubMedCentralPubMedCrossRef Pedersen, E. A., Shiozawa, Y., Pienta, K. J., & Taichman, R. S. (2012). The prostate cancer bone marrow niche: more than just ‘fertile soil’. Asian Journal of Andrology, 14(3), 423–427.PubMedCentralPubMedCrossRef
12.
go back to reference Schneider, A., Kalikin, L. M., Mattos, A. C., et al. (2005). Bone turnover mediates preferential localization of prostate cancer in the skeleton. Endocrinology, 146(4), 1727–1736.PubMedCrossRef Schneider, A., Kalikin, L. M., Mattos, A. C., et al. (2005). Bone turnover mediates preferential localization of prostate cancer in the skeleton. Endocrinology, 146(4), 1727–1736.PubMedCrossRef
13.
go back to reference Shiozawa, Y., Pedersen, E. A., Patel, L. R., et al. (2010). GAS6/AXL axis regulates prostate cancer invasion, proliferation, and survival in the bone marrow niche. Neoplasia (New York, NY), 12(2), 116. Shiozawa, Y., Pedersen, E. A., Patel, L. R., et al. (2010). GAS6/AXL axis regulates prostate cancer invasion, proliferation, and survival in the bone marrow niche. Neoplasia (New York, NY), 12(2), 116.
14.
go back to reference Taichman, R. S., Patel, L. R., Bedenis, R., et al. (2013). GAS6 receptor status is associated with dormancy and bone metastatic tumor formation. PloS one, 8(4), e61873.PubMedCentralPubMedCrossRef Taichman, R. S., Patel, L. R., Bedenis, R., et al. (2013). GAS6 receptor status is associated with dormancy and bone metastatic tumor formation. PloS one, 8(4), e61873.PubMedCentralPubMedCrossRef
15.
go back to reference Loberg, R. D., Gayed, B. A., Olson, K. B., & Pienta, K. J. (2005). A paradigm for the treatment of prostate cancer bone metastases based on an understanding of tumor cell–microenvironment interactions. Journal of Cellular Biochemistry, 96(3), 439–446.PubMedCrossRef Loberg, R. D., Gayed, B. A., Olson, K. B., & Pienta, K. J. (2005). A paradigm for the treatment of prostate cancer bone metastases based on an understanding of tumor cell–microenvironment interactions. Journal of Cellular Biochemistry, 96(3), 439–446.PubMedCrossRef
16.
go back to reference Guise, T. A., Mohammad, K. S., Clines, G., et al. (2006). Basic mechanisms responsible for osteolytic and osteoblastic bone metastases. Clinical cancer research, 12(20), 6213s–6216s.PubMedCrossRef Guise, T. A., Mohammad, K. S., Clines, G., et al. (2006). Basic mechanisms responsible for osteolytic and osteoblastic bone metastases. Clinical cancer research, 12(20), 6213s–6216s.PubMedCrossRef
17.
go back to reference Small, E. J., Smith, M. R., Seaman, J. J., Petrone, S., & Kowalski, M. O. (2003). Combined analysis of two multicenter, randomized, placebo-controlled studies of pamidronate disodium for the palliation of bone pain in men with metastatic prostate cancer. Journal of Clinical Oncology, 21(23), 4277–4284.PubMedCrossRef Small, E. J., Smith, M. R., Seaman, J. J., Petrone, S., & Kowalski, M. O. (2003). Combined analysis of two multicenter, randomized, placebo-controlled studies of pamidronate disodium for the palliation of bone pain in men with metastatic prostate cancer. Journal of Clinical Oncology, 21(23), 4277–4284.PubMedCrossRef
18.
go back to reference Saad, F., Gleason, D. M., Murray, R., et al. (2004). Long-term efficacy of zoledronic acid for the prevention of skeletal complications in patients with metastatic hormone-refractory prostate cancer. Journal of the National Cancer Institute, 96(11), 879–882.PubMedCrossRef Saad, F., Gleason, D. M., Murray, R., et al. (2004). Long-term efficacy of zoledronic acid for the prevention of skeletal complications in patients with metastatic hormone-refractory prostate cancer. Journal of the National Cancer Institute, 96(11), 879–882.PubMedCrossRef
19.
go back to reference Rosen, L. S., Gordon, D., Kaminski, M., et al. (2003). Long-term efficacy and safety of zoledronic acid compared with pamidronate disodium in the treatment of skeletal complications in patients with advanced multiple myeloma or breast carcinoma. Cancer, 98(8), 1735–1744.PubMedCrossRef Rosen, L. S., Gordon, D., Kaminski, M., et al. (2003). Long-term efficacy and safety of zoledronic acid compared with pamidronate disodium in the treatment of skeletal complications in patients with advanced multiple myeloma or breast carcinoma. Cancer, 98(8), 1735–1744.PubMedCrossRef
20.
go back to reference Smith, M. R., Halabi, S., Ryan, C. J., et al. (2013). Efficacy and safety of zoledronic acid in men with castration-sensitive prostate cancer and bone metastases: results of CALGB 90202 (alliance). ASCO Meeting Abstracts, 31(6_suppl), 27. Smith, M. R., Halabi, S., Ryan, C. J., et al. (2013). Efficacy and safety of zoledronic acid in men with castration-sensitive prostate cancer and bone metastases: results of CALGB 90202 (alliance). ASCO Meeting Abstracts, 31(6_suppl), 27.
21.
go back to reference Wirth, M., Tammela, T., Huland, H., et al. (2008). Zoledronic acid for the prevention of bone metastases in high risk prostate cancer patients. A randomised, open label, multicentre study of the European Association of Urology (EAU) in cooperation with the Scandinavian Prostate Cancer Group (SPCG) and the Arbeitsgemeinschaft Urologische Onkologie (AUO). European Urology Supplements, 7(3), 232.CrossRef Wirth, M., Tammela, T., Huland, H., et al. (2008). Zoledronic acid for the prevention of bone metastases in high risk prostate cancer patients. A randomised, open label, multicentre study of the European Association of Urology (EAU) in cooperation with the Scandinavian Prostate Cancer Group (SPCG) and the Arbeitsgemeinschaft Urologische Onkologie (AUO). European Urology Supplements, 7(3), 232.CrossRef
22.
go back to reference Smith, M. R., Egerdie, B., Toriz, N. H., et al. (2009). Denosumab in men receiving androgen-deprivation therapy for prostate cancer. The New England Journal of Medicine, 361(8), 745–755.PubMedCentralPubMedCrossRef Smith, M. R., Egerdie, B., Toriz, N. H., et al. (2009). Denosumab in men receiving androgen-deprivation therapy for prostate cancer. The New England Journal of Medicine, 361(8), 745–755.PubMedCentralPubMedCrossRef
23.
go back to reference Fizazi, K., Lipton, A., Mariette, X., et al. (2009). Randomized phase II trial of denosumab in patients with bone metastases from prostate cancer, breast cancer, or other neoplasms after intravenous bisphosphonates. Journal of Clinical Oncology, 27(10), 1564–1571.PubMedCrossRef Fizazi, K., Lipton, A., Mariette, X., et al. (2009). Randomized phase II trial of denosumab in patients with bone metastases from prostate cancer, breast cancer, or other neoplasms after intravenous bisphosphonates. Journal of Clinical Oncology, 27(10), 1564–1571.PubMedCrossRef
24.
go back to reference Fizazi, K., Carducci, M., Smith, M., et al. (2011). Denosumab versus zoledronic acid for treatment of bone metastases in men with castration-resistant prostate cancer: a randomised, double-blind study. The Lancet, 377(9768), 813–822.CrossRef Fizazi, K., Carducci, M., Smith, M., et al. (2011). Denosumab versus zoledronic acid for treatment of bone metastases in men with castration-resistant prostate cancer: a randomised, double-blind study. The Lancet, 377(9768), 813–822.CrossRef
25.
go back to reference Smith, M. R., Saad, F., Coleman, R., et al. (2012). Denosumab and bone-metastasis-free survival in men with castration-resistant prostate cancer: results of a phase 3, randomised, placebo-controlled trial. The Lancet, 379(9810), 39–46.CrossRef Smith, M. R., Saad, F., Coleman, R., et al. (2012). Denosumab and bone-metastasis-free survival in men with castration-resistant prostate cancer: results of a phase 3, randomised, placebo-controlled trial. The Lancet, 379(9810), 39–46.CrossRef
26.
go back to reference Summary minutes of the Oncologic Drugs Advisory Committee meeting. 2012. Summary minutes of the Oncologic Drugs Advisory Committee meeting. 2012.
27.
go back to reference Silberstein, E. B. (1996). Dosage and response in radiopharmaceutical therapy of painful osseous metastases. Journal of Nuclear Medicine, 37(2), 249–252.PubMed Silberstein, E. B. (1996). Dosage and response in radiopharmaceutical therapy of painful osseous metastases. Journal of Nuclear Medicine, 37(2), 249–252.PubMed
28.
go back to reference Tu, S., Millikan, R. E., Mengistu, B., et al. (2001). Bone-targeted therapy for advanced androgen-independent carcinoma of the prostate: a randomised phase II trial. The Lancet, 357(9253), 336–341.CrossRef Tu, S., Millikan, R. E., Mengistu, B., et al. (2001). Bone-targeted therapy for advanced androgen-independent carcinoma of the prostate: a randomised phase II trial. The Lancet, 357(9253), 336–341.CrossRef
29.
go back to reference Sartor, O., Reid, R. H., Bushnell, D. L., Quick, D. P., & Ell, P. J. (2007). Safety and efficacy of repeat administration of samarium Sm–153 lexidronam to patients with metastatic bone pain. Cancer, 109(3), 637–643.PubMedCrossRef Sartor, O., Reid, R. H., Bushnell, D. L., Quick, D. P., & Ell, P. J. (2007). Safety and efficacy of repeat administration of samarium Sm–153 lexidronam to patients with metastatic bone pain. Cancer, 109(3), 637–643.PubMedCrossRef
30.
go back to reference Fizazi, K., Beuzeboc, P., Lumbroso, J., et al. (2009). Phase II trial of consolidation docetaxel and samarium-153 in patients with bone metastases from castration-resistant prostate cancer. Journal of Clinical Oncology, 27(15), 2429–2435.PubMedCrossRef Fizazi, K., Beuzeboc, P., Lumbroso, J., et al. (2009). Phase II trial of consolidation docetaxel and samarium-153 in patients with bone metastases from castration-resistant prostate cancer. Journal of Clinical Oncology, 27(15), 2429–2435.PubMedCrossRef
31.
go back to reference James, N. D., Pirrie, S., Barton, D., et al. (2013). Clinical outcomes in patients with castrate-refractory prostate cancer (CRPC) metastatic to bone randomized in the factorial TRAPEZE trial to docetaxel (D) with strontium-89 (Sr89), zoledronic acid (ZA), neither, or both (ISRCTN 12808747). ASCO Meeting Abstracts, 31(18_suppl), LBA5000. James, N. D., Pirrie, S., Barton, D., et al. (2013). Clinical outcomes in patients with castrate-refractory prostate cancer (CRPC) metastatic to bone randomized in the factorial TRAPEZE trial to docetaxel (D) with strontium-89 (Sr89), zoledronic acid (ZA), neither, or both (ISRCTN 12808747). ASCO Meeting Abstracts, 31(18_suppl), LBA5000.
32.
go back to reference Nilsson, S., Franzén, L., Parker, C., et al. (2007). Bone-targeted radium-223 in symptomatic, hormone-refractory prostate cancer: a randomised, multicentre, placebo-controlled phase II study. The Lancet Oncology, 8(7), 587–594.PubMedCrossRef Nilsson, S., Franzén, L., Parker, C., et al. (2007). Bone-targeted radium-223 in symptomatic, hormone-refractory prostate cancer: a randomised, multicentre, placebo-controlled phase II study. The Lancet Oncology, 8(7), 587–594.PubMedCrossRef
33.
go back to reference Nilsson, S., Strang, P., Aksnes, A. K., et al. (2012). A randomized, dose–response, multicenter phase II study of radium-223 chloride for the palliation of painful bone metastases in patients with castration-resistant prostate cancer. European Journal of Cancer, 48(5), 678–686.PubMedCrossRef Nilsson, S., Strang, P., Aksnes, A. K., et al. (2012). A randomized, dose–response, multicenter phase II study of radium-223 chloride for the palliation of painful bone metastases in patients with castration-resistant prostate cancer. European Journal of Cancer, 48(5), 678–686.PubMedCrossRef
34.
go back to reference Morris, M. J., Hammers, H. J., Sweeney, C., et al. (2013). Safety of radium-223 dichloride (ra-223) with docetaxel (D) in patients with bone metastases from castration-resistant prostate cancer (CRPC): a phase I prostate cancer clinical trials consortium study. ASCO Meeting Abstracts, 31(15_suppl), 5021. Morris, M. J., Hammers, H. J., Sweeney, C., et al. (2013). Safety of radium-223 dichloride (ra-223) with docetaxel (D) in patients with bone metastases from castration-resistant prostate cancer (CRPC): a phase I prostate cancer clinical trials consortium study. ASCO Meeting Abstracts, 31(15_suppl), 5021.
35.
go back to reference Carducci, M. A., Padley, R. J., Breul, J., et al. (2003). Effect of endothelin-A receptor blockade with atrasentan on tumor progression in men with hormone-refractory prostate cancer: a randomized, phase II, placebo-controlled trial. Journal of Clinical Oncology, 21(4), 679–689.PubMedCrossRef Carducci, M. A., Padley, R. J., Breul, J., et al. (2003). Effect of endothelin-A receptor blockade with atrasentan on tumor progression in men with hormone-refractory prostate cancer: a randomized, phase II, placebo-controlled trial. Journal of Clinical Oncology, 21(4), 679–689.PubMedCrossRef
36.
go back to reference Schelman, W. R., Liu, G., Wilding, G., Morris, T., Phung, D., & Dreicer, R. (2011). A phase I study of zibotentan (ZD4054) in patients with metastatic, castrate-resistant prostate cancer. Investigational New Drugs, 29(1), 118–125.PubMedCentralPubMedCrossRef Schelman, W. R., Liu, G., Wilding, G., Morris, T., Phung, D., & Dreicer, R. (2011). A phase I study of zibotentan (ZD4054) in patients with metastatic, castrate-resistant prostate cancer. Investigational New Drugs, 29(1), 118–125.PubMedCentralPubMedCrossRef
37.
go back to reference James, N. D., Caty, A., Payne, H., et al. (2010). Final safety and efficacy analysis of the specific endothelin A receptor antagonist zibotentan (ZD4054) in patients with metastatic castration–resistant prostate cancer and bone metastases who were pain–free or mildly symptomatic for pain: a double–blind, placebo–controlled, randomized phase II trial. BJU International, 106(7), 966–973.PubMedCrossRef James, N. D., Caty, A., Payne, H., et al. (2010). Final safety and efficacy analysis of the specific endothelin A receptor antagonist zibotentan (ZD4054) in patients with metastatic castration–resistant prostate cancer and bone metastases who were pain–free or mildly symptomatic for pain: a double–blind, placebo–controlled, randomized phase II trial. BJU International, 106(7), 966–973.PubMedCrossRef
38.
go back to reference Nelson, J. B., Love, W., Chin, J. L., et al. (2008). Phase 3, randomized, controlled trial of atrasentan in patients with nonmetastatic, hormone–refractory prostate cancer. Cancer, 113(9), 2478–2487.PubMedCentralPubMedCrossRef Nelson, J. B., Love, W., Chin, J. L., et al. (2008). Phase 3, randomized, controlled trial of atrasentan in patients with nonmetastatic, hormone–refractory prostate cancer. Cancer, 113(9), 2478–2487.PubMedCentralPubMedCrossRef
39.
go back to reference Nelson, J. B., Fizazi, K., Miller, K., et al. (2012). Phase 3, randomized, placebo–controlled study of zibotentan (ZD4054) in patients with castration–resistant prostate cancer metastatic to bone. Cancer, 118(22), 5709–5718.PubMedCrossRef Nelson, J. B., Fizazi, K., Miller, K., et al. (2012). Phase 3, randomized, placebo–controlled study of zibotentan (ZD4054) in patients with castration–resistant prostate cancer metastatic to bone. Cancer, 118(22), 5709–5718.PubMedCrossRef
40.
go back to reference Miller, K., Moul, J., Gleave, M., et al. (2013). Phase III, randomized, placebo-controlled study of once-daily oral zibotentan (ZD4054) in patients with non-metastatic castration-resistant prostate cancer. Prostate cancer and prostatic diseases, 16(2), 187–192.PubMedCrossRef Miller, K., Moul, J., Gleave, M., et al. (2013). Phase III, randomized, placebo-controlled study of once-daily oral zibotentan (ZD4054) in patients with non-metastatic castration-resistant prostate cancer. Prostate cancer and prostatic diseases, 16(2), 187–192.PubMedCrossRef
41.
go back to reference Akhavan, A., McHugh, K. H., Guruli, G., et al. (2006). Endothelin receptor A blockade enhances taxane effects in prostate cancer. Neoplasia, 8(9), 725–732.PubMedCentralPubMedCrossRef Akhavan, A., McHugh, K. H., Guruli, G., et al. (2006). Endothelin receptor A blockade enhances taxane effects in prostate cancer. Neoplasia, 8(9), 725–732.PubMedCentralPubMedCrossRef
42.
go back to reference Kim, L. C., Song, L., & Haura, E. B. (2009). Src kinases as therapeutic targets for cancer. Nature Reviews Clinical Oncology, 6(10), 587–595.PubMedCrossRef Kim, L. C., Song, L., & Haura, E. B. (2009). Src kinases as therapeutic targets for cancer. Nature Reviews Clinical Oncology, 6(10), 587–595.PubMedCrossRef
43.
go back to reference Summy, J. M., & Gallick, G. E. (2003). Src family kinases in tumor progression and metastasis. Cancer and Metastasis Reviews, 22(4), 337–358.PubMedCrossRef Summy, J. M., & Gallick, G. E. (2003). Src family kinases in tumor progression and metastasis. Cancer and Metastasis Reviews, 22(4), 337–358.PubMedCrossRef
44.
go back to reference Edwards, J. (2010). Src kinase inhibitors: an emerging therapeutic treatment option for prostate cancer. Expert Opinion on Investigational Drugs, 19(5), 605–614.PubMedCrossRef Edwards, J. (2010). Src kinase inhibitors: an emerging therapeutic treatment option for prostate cancer. Expert Opinion on Investigational Drugs, 19(5), 605–614.PubMedCrossRef
45.
go back to reference Tatarov, O., Mitchell, T. J., Seywright, M., Leung, H. Y., Brunton, V. G., & Edwards, J. (2009). SRC family kinase activity is up-regulated in hormone-refractory prostate cancer. Clinical Cancer Research, 15(10), 3540–3549.PubMedCrossRef Tatarov, O., Mitchell, T. J., Seywright, M., Leung, H. Y., Brunton, V. G., & Edwards, J. (2009). SRC family kinase activity is up-regulated in hormone-refractory prostate cancer. Clinical Cancer Research, 15(10), 3540–3549.PubMedCrossRef
46.
go back to reference Nam, S., Kim, D., Cheng, J. Q., et al. (2005). Action of the src family kinase inhibitor, dasatinib (BMS-354825), on human prostate cancer cells. Cancer Research, 65(20), 9185–9189.PubMedCrossRef Nam, S., Kim, D., Cheng, J. Q., et al. (2005). Action of the src family kinase inhibitor, dasatinib (BMS-354825), on human prostate cancer cells. Cancer Research, 65(20), 9185–9189.PubMedCrossRef
47.
go back to reference Brownlow, N., Mol, C., Hayford, C., Ghaem-Maghami, S., & Dibb, N. (2008). Dasatinib is a potent inhibitor of tumour-associated macrophages, osteoclasts and the FMS receptor. Leukemia, 23(3), 590–594.PubMedCrossRef Brownlow, N., Mol, C., Hayford, C., Ghaem-Maghami, S., & Dibb, N. (2008). Dasatinib is a potent inhibitor of tumour-associated macrophages, osteoclasts and the FMS receptor. Leukemia, 23(3), 590–594.PubMedCrossRef
48.
go back to reference Lee, Y., Huang, C., Murshed, M., Chu, K., Araujo, J. C., & Ye, X. (2010). Src family kinase/abl inhibitor dasatinib suppresses proliferation and enhances differentiation of osteoblasts. Oncogene, 29(22), 3196–3207.PubMedCentralPubMedCrossRef Lee, Y., Huang, C., Murshed, M., Chu, K., Araujo, J. C., & Ye, X. (2010). Src family kinase/abl inhibitor dasatinib suppresses proliferation and enhances differentiation of osteoblasts. Oncogene, 29(22), 3196–3207.PubMedCentralPubMedCrossRef
49.
go back to reference Araujo, J. C., Trudel, G. C., Saad, F., Armstrong, A. J., Yu, E. Y., Bellmunt, J., et al. (2013). Docetaxel and dasatinib or placebo in men with metastatic castration-resistant prostate cancer (READY): a randomised, double-blind phase 3 trial. Lancet Oncol, 14(13), 1307–1316. Araujo, J. C., Trudel, G. C., Saad, F., Armstrong, A. J., Yu, E. Y., Bellmunt, J., et al. (2013). Docetaxel and dasatinib or placebo in men with metastatic castration-resistant prostate cancer (READY): a randomised, double-blind phase 3 trial. Lancet Oncol, 14(13), 1307–1316.
50.
go back to reference Araujo, J. C., Mathew, P., Armstrong, A. J., et al. (2012). Dasatinib combined with docetaxel for castration–resistant prostate cancer. Cancer, 118(1), 63–71.PubMedCentralPubMedCrossRef Araujo, J. C., Mathew, P., Armstrong, A. J., et al. (2012). Dasatinib combined with docetaxel for castration–resistant prostate cancer. Cancer, 118(1), 63–71.PubMedCentralPubMedCrossRef
51.
go back to reference Anderson, G., Gries, M., Kurihara, N., et al. (2006). Thalidomide derivative CC-4047 inhibits osteoclast formation by down-regulation of PU.1. Blood, 107(8), 3098–3105.PubMedCrossRef Anderson, G., Gries, M., Kurihara, N., et al. (2006). Thalidomide derivative CC-4047 inhibits osteoclast formation by down-regulation of PU.1. Blood, 107(8), 3098–3105.PubMedCrossRef
52.
go back to reference Efstathiou, E., Troncoso, P., Wen, S., et al. (2007). Initial modulation of the tumor microenvironment accounts for thalidomide activity in prostate cancer. Clinical Cancer Research, 13(4), 1224–1231.PubMedCrossRef Efstathiou, E., Troncoso, P., Wen, S., et al. (2007). Initial modulation of the tumor microenvironment accounts for thalidomide activity in prostate cancer. Clinical Cancer Research, 13(4), 1224–1231.PubMedCrossRef
53.
go back to reference Vallet, S., Palumbo, A., Raje, N., et al. (2008). Thalidomide and lenalidomide: mechanism-based potential drug combinations. Leuk Lymphoma, 49(7), 1238–1245.PubMedCrossRef Vallet, S., Palumbo, A., Raje, N., et al. (2008). Thalidomide and lenalidomide: mechanism-based potential drug combinations. Leuk Lymphoma, 49(7), 1238–1245.PubMedCrossRef
54.
go back to reference Dahut, W. L., Gulley, J. L., Arlen, P. M., et al. (2004). Randomized phase II trial of docetaxel plus thalidomide in androgen-independent prostate cancer. Journal of Clinical Oncology, 22(13), 2532–2539.PubMedCrossRef Dahut, W. L., Gulley, J. L., Arlen, P. M., et al. (2004). Randomized phase II trial of docetaxel plus thalidomide in androgen-independent prostate cancer. Journal of Clinical Oncology, 22(13), 2532–2539.PubMedCrossRef
55.
go back to reference Petrylak D, Fizazi K, Sternberg C, Budnik N, Wit Rd WP. A phase 3 study to evaluate the efficacy and safety of docetaxel and prednisone (DP) with or without lenalidomide in patients with castrate-resistant prostate cancer (CRPC): the MAINSAIL trial. 2012. Petrylak D, Fizazi K, Sternberg C, Budnik N, Wit Rd WP. A phase 3 study to evaluate the efficacy and safety of docetaxel and prednisone (DP) with or without lenalidomide in patients with castrate-resistant prostate cancer (CRPC): the MAINSAIL trial. 2012.
56.
go back to reference Chott, A., Sun, Z., Morganstern, D., et al. (1999). Tyrosine kinases expressed in vivo by human prostate cancer bone marrow metastases and loss of the type 1 insulin-like growth factor receptor. The American Journal of Pathology, 155(4), 1271–1279.PubMedCentralPubMedCrossRef Chott, A., Sun, Z., Morganstern, D., et al. (1999). Tyrosine kinases expressed in vivo by human prostate cancer bone marrow metastases and loss of the type 1 insulin-like growth factor receptor. The American Journal of Pathology, 155(4), 1271–1279.PubMedCentralPubMedCrossRef
57.
go back to reference Sulpice, E., Ding, S., Muscatelli-Groux, B., et al. (2009). Cross-talk between the VEGF-A and HGF signalling pathways in endothelial cells. Biology of the Cell, 101(9), 525–539.PubMedCrossRef Sulpice, E., Ding, S., Muscatelli-Groux, B., et al. (2009). Cross-talk between the VEGF-A and HGF signalling pathways in endothelial cells. Biology of the Cell, 101(9), 525–539.PubMedCrossRef
58.
go back to reference Tsai, S., Huang, Y., Yang, W., & Tang, C. (2012). Hepatocyte growth factor-induced BMP-2 expression is mediated by c-met receptor, FAK, JNK, Runx2, and p300 pathways in human osteoblasts. International Immunopharmacology, 13(2), 156–162.PubMedCrossRef Tsai, S., Huang, Y., Yang, W., & Tang, C. (2012). Hepatocyte growth factor-induced BMP-2 expression is mediated by c-met receptor, FAK, JNK, Runx2, and p300 pathways in human osteoblasts. International Immunopharmacology, 13(2), 156–162.PubMedCrossRef
59.
go back to reference Ryan, C. J., Rosenthal, M., Ng, S., et al. (2013). Targeted MET inhibition in castration-resistant prostate cancer: a randomized phase II study and biomarker analysis with rilotumumab plus mitoxantrone and prednisone. Clinical Cancer Research, 19(1), 215–224.PubMedCrossRef Ryan, C. J., Rosenthal, M., Ng, S., et al. (2013). Targeted MET inhibition in castration-resistant prostate cancer: a randomized phase II study and biomarker analysis with rilotumumab plus mitoxantrone and prednisone. Clinical Cancer Research, 19(1), 215–224.PubMedCrossRef
60.
go back to reference Kelly, W. K., Halabi, S., Carducci, M., et al. (2012). Randomized, double-blind, placebo-controlled phase III trial comparing docetaxel and prednisone with or without bevacizumab in men with metastatic castration-resistant prostate cancer: CALGB 90401. Journal of Clinical Oncology, 30(13), 1534–1540.PubMedCentralPubMedCrossRef Kelly, W. K., Halabi, S., Carducci, M., et al. (2012). Randomized, double-blind, placebo-controlled phase III trial comparing docetaxel and prednisone with or without bevacizumab in men with metastatic castration-resistant prostate cancer: CALGB 90401. Journal of Clinical Oncology, 30(13), 1534–1540.PubMedCentralPubMedCrossRef
61.
go back to reference Smith, D. C., Smith, M. R., Sweeney, C., et al. (2013). Cabozantinib in patients with advanced prostate cancer: results of a phase II randomized discontinuation trial. Journal of Clinical Oncology, 31(4), 412–419.PubMedCrossRef Smith, D. C., Smith, M. R., Sweeney, C., et al. (2013). Cabozantinib in patients with advanced prostate cancer: results of a phase II randomized discontinuation trial. Journal of Clinical Oncology, 31(4), 412–419.PubMedCrossRef
62.
go back to reference Isaacs, J. T., Pili, R., Qian, D. Z., et al. (2006). Identification of ABR–215050 as lead second generation quinoline–3–carboxamide anti–angiogenic agent for the treatment of prostate cancer. Prostate, 66(16), 1768–1778.PubMedCrossRef Isaacs, J. T., Pili, R., Qian, D. Z., et al. (2006). Identification of ABR–215050 as lead second generation quinoline–3–carboxamide anti–angiogenic agent for the treatment of prostate cancer. Prostate, 66(16), 1768–1778.PubMedCrossRef
63.
go back to reference Isaacs, J. T. (2010). The long and winding road for the development of tasquinimod as an oral second-generation quinoline-3-carboxamide antiangiogenic drug for the treatment of prostate cancer. Expert Opinion on Investigational Drugs, 19(10), 1235–1243.PubMedCrossRef Isaacs, J. T. (2010). The long and winding road for the development of tasquinimod as an oral second-generation quinoline-3-carboxamide antiangiogenic drug for the treatment of prostate cancer. Expert Opinion on Investigational Drugs, 19(10), 1235–1243.PubMedCrossRef
64.
go back to reference Olsson, A., Björk, A., Vallon-Christersson, J., Isaacs, J. T., & Leanderson, T. (2010). Tasquinimod (ABR-215050), a quinoline-3-carboxamide anti-angiogenic agent, modulates the expression of thrombospondin-1 in human prostate tumors. Molecular Cancer, 9(1), 107.PubMedCentralPubMedCrossRef Olsson, A., Björk, A., Vallon-Christersson, J., Isaacs, J. T., & Leanderson, T. (2010). Tasquinimod (ABR-215050), a quinoline-3-carboxamide anti-angiogenic agent, modulates the expression of thrombospondin-1 in human prostate tumors. Molecular Cancer, 9(1), 107.PubMedCentralPubMedCrossRef
65.
go back to reference Isaacs, J. T., Antony, L., Dalrymple, S. L., et al. (2013). Tasquinimod is an allosteric modulator of HDAC4 survival signaling within the compromised cancer microenvironment. Cancer Research, 73(4), 1386–1399.PubMedCentralPubMedCrossRef Isaacs, J. T., Antony, L., Dalrymple, S. L., et al. (2013). Tasquinimod is an allosteric modulator of HDAC4 survival signaling within the compromised cancer microenvironment. Cancer Research, 73(4), 1386–1399.PubMedCentralPubMedCrossRef
66.
go back to reference Jennbacken, K., Welén, K., Olsson, A., et al. (2012). Inhibition of metastasis in a castration resistant prostate cancer model by the quinoline–3–carboxamide tasquinimod (ABR–215050). Prostate, 72(8), 913–924.PubMedCrossRef Jennbacken, K., Welén, K., Olsson, A., et al. (2012). Inhibition of metastasis in a castration resistant prostate cancer model by the quinoline–3–carboxamide tasquinimod (ABR–215050). Prostate, 72(8), 913–924.PubMedCrossRef
67.
go back to reference Bratt, O., Häggman, M., Ahlgren, G., Nordle, Ö., Björk, A., & Damber, J. (2009). Open-label, clinical phase I studies of tasquinimod in patients with castration-resistant prostate cancer. British Journal of Cancer, 101(8), 1233–1240.PubMedCentralPubMedCrossRef Bratt, O., Häggman, M., Ahlgren, G., Nordle, Ö., Björk, A., & Damber, J. (2009). Open-label, clinical phase I studies of tasquinimod in patients with castration-resistant prostate cancer. British Journal of Cancer, 101(8), 1233–1240.PubMedCentralPubMedCrossRef
68.
go back to reference Pili, R., Häggman, M., Stadler, W. M., et al. (2011). Phase II randomized, double-blind, placebo-controlled study of tasquinimod in men with minimally symptomatic metastatic castrate-resistant prostate cancer. Journal of Clinical Oncology, 29(30), 4022–4028.PubMedCrossRef Pili, R., Häggman, M., Stadler, W. M., et al. (2011). Phase II randomized, double-blind, placebo-controlled study of tasquinimod in men with minimally symptomatic metastatic castrate-resistant prostate cancer. Journal of Clinical Oncology, 29(30), 4022–4028.PubMedCrossRef
69.
go back to reference Armstrong, A. J., Haggman, M., Stadler, W. M., et al. (2012). Tasquinimod and survival in men with metastatic castration-resistant prostate cancer: results of long-term follow-up of a randomized phase II placebo-controlled trial. Journal of Clinical Oncology, 30(15 Suppl), 4550. Armstrong, A. J., Haggman, M., Stadler, W. M., et al. (2012). Tasquinimod and survival in men with metastatic castration-resistant prostate cancer: results of long-term follow-up of a randomized phase II placebo-controlled trial. Journal of Clinical Oncology, 30(15 Suppl), 4550.
70.
go back to reference Scher, H. I., Fizazi, K., Saad, F., et al. (2012). Increased survival with enzalutamide in prostate cancer after chemotherapy. The New England Journal of Medicine, 367(13), 1187–1197.PubMedCrossRef Scher, H. I., Fizazi, K., Saad, F., et al. (2012). Increased survival with enzalutamide in prostate cancer after chemotherapy. The New England Journal of Medicine, 367(13), 1187–1197.PubMedCrossRef
71.
go back to reference Ryan, C. J., Smith, M. R., de Bono, J. S., et al. (2013). Abiraterone in metastatic prostate cancer without previous chemotherapy. The New England Journal of Medicine, 368(2), 138–148.PubMedCentralPubMedCrossRef Ryan, C. J., Smith, M. R., de Bono, J. S., et al. (2013). Abiraterone in metastatic prostate cancer without previous chemotherapy. The New England Journal of Medicine, 368(2), 138–148.PubMedCentralPubMedCrossRef
72.
go back to reference Logothetis, C. J., Basch, E., Molina, A., et al. (2012). Effect of abiraterone acetate and prednisone compared with placebo and prednisone on pain control and skeletal-related events in patients with metastatic castration-resistant prostate cancer: exploratory analysis of data from the COU-AA-301 randomised trial. The lancet oncology., 13, 1210–7.PubMedCrossRef Logothetis, C. J., Basch, E., Molina, A., et al. (2012). Effect of abiraterone acetate and prednisone compared with placebo and prednisone on pain control and skeletal-related events in patients with metastatic castration-resistant prostate cancer: exploratory analysis of data from the COU-AA-301 randomised trial. The lancet oncology., 13, 1210–7.PubMedCrossRef
73.
go back to reference Tran, C., Ouk, S., Clegg, N. J., et al. (2009). Development of a second-generation antiandrogen for treatment of advanced prostate cancer. Science, 324(5928), 787–790.PubMedCentralPubMedCrossRef Tran, C., Ouk, S., Clegg, N. J., et al. (2009). Development of a second-generation antiandrogen for treatment of advanced prostate cancer. Science, 324(5928), 787–790.PubMedCentralPubMedCrossRef
74.
go back to reference Fizazi, K., Scher, H., Saad, F., et al. (2012). Impact of enzalutamide, an androgen receptor signaling inhibitor, on time to first skeletal related event (SRE) and pain in the phase 3 AFFIRM study. Annals of Oncology, 23, 295–296.CrossRef Fizazi, K., Scher, H., Saad, F., et al. (2012). Impact of enzalutamide, an androgen receptor signaling inhibitor, on time to first skeletal related event (SRE) and pain in the phase 3 AFFIRM study. Annals of Oncology, 23, 295–296.CrossRef
75.
go back to reference Jensen, A. B., Wynne, C., Ramirez, G., et al. (2010). The cathepsin K inhibitor odanacatib suppresses bone resorption in women with breast cancer and established bone metastases: results of a 4-week, double-blind, randomized, controlled trial. Clinical Breast Cancer, 10(6), 452–458.PubMedCrossRef Jensen, A. B., Wynne, C., Ramirez, G., et al. (2010). The cathepsin K inhibitor odanacatib suppresses bone resorption in women with breast cancer and established bone metastases: results of a 4-week, double-blind, randomized, controlled trial. Clinical Breast Cancer, 10(6), 452–458.PubMedCrossRef
76.
go back to reference Taichman, R. S. (2005). Blood and bone: two tissues whose fates are intertwined to create the hematopoietic stem-cell niche. Blood, 105(7), 2631–2639.PubMedCrossRef Taichman, R. S. (2005). Blood and bone: two tissues whose fates are intertwined to create the hematopoietic stem-cell niche. Blood, 105(7), 2631–2639.PubMedCrossRef
Metadata
Title
Bone-targeting agents in prostate cancer
Authors
Daniel L. Suzman
Sosipatros A. Boikos
Michael A. Carducci
Publication date
01-09-2014
Publisher
Springer US
Published in
Cancer and Metastasis Reviews / Issue 2-3/2014
Print ISSN: 0167-7659
Electronic ISSN: 1573-7233
DOI
https://doi.org/10.1007/s10555-013-9480-2

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