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Curr Oncol. 2010 September; 17(Suppl 2): S49–S54.
PMCID: PMC2935711

Bone health in nonmetastatic prostate cancer: what’s the big deal?

J.B. Lattouf, MD* and F. Saad, MD

Abstract

Since 2000, the medical community has become increasingly aware of bone health in men with prostate cancer on androgen deprivation therapy (adt)—mainly because of new therapies that have been shown to reduce bone loss and associated fractures in this patient population. The threat of bone complications has become even more concerning in the prostate-specific antigen era, because adt is initiated earlier (with biochemical recurrence after local treatment) and maintained longer before the appearance of metastatic disease. The present review examines the relevance of bone health in nonmetastatic prostate cancer, with a discussion of the new treatment modalities available.

Keywords: Prostate cancer, androgen deprivation therapy, bisphosphonates, skeletal-related events

1. INTRODUCTION

The place of bone protection in nonmetastatic prostate cancer (pca) is still ill-defined. Yet patients in increasing numbers are receiving hormone deprivation therapy for biochemical recurrence after definitive local treatment, which puts them at increased risk for bone loss 1.

The concept of increased susceptibility to metastasis in patients with declining bone mineral density (bmd) has been put forth by some authorities and may justify early intervention to preserve bone in this patient population 2. Furthermore, regardless of metastatic status, bone fractures from decreased bmd may be associated with decreased survival in pca patients 3. The clinical relevance of initiating bone protection early in the natural history of the disease is of sufficient importance to justify several randomized studies now underway whose results should be available soon.

Here, we sketch the rationale for bone preservation in patients with nonmetastatic pca, with a special emphasis on the physiopathologic basis of bone loss, potential prevention strategies, and guidelines. We also discuss upcoming studies aimed at answering the question of whether bone preservation is beneficial in the nonmetastatic setting.

2. DISCUSSION

2.1. Lower BMD Correlates with Increased Risk of Fracture

It is now widely accepted that androgen deprivation therapy (adt) accelerates the decline of bmd in men 4. The danger of bmd loss is real and often translates into an increased risk of bone fracture in patients experiencing such loss. In a study that sampled 50,613 patients from the Surveillance, Epidemiology and End Results database, a higher percentage of patients receiving adt than not receiving adt had osteoporosis. Additionally, at 5 years, the risk of bone fracture in patients receiving adt was almost double that in patients not undergoing hormone ablation 4.

It has been established that previous bone fractures predict for future ones, and even fractures that may be considered minor, such as vertebral compression, are clinically relevant 5. What is perhaps more compelling is that fractures correlate with decreased survival. In a case–control study analyzing a sample of 97,142 Medicare claims, Lau et al. showed that patients with vertebral compression fractures had a mortality rate twice that of matched controls 6. Furthermore, the mortality rate was greater for men than for women 6. Another study, by Oefelein and colleagues 7, demonstrated that skeletal fractures were common in men with pca and lowered mean survival by 39 months. The relative risk of death for affected patients in that study increased by a factor of almost 7.

2.2. Effect of ADT on Bone Metabolism in Men

Decreased bmd and higher rates of bone fracture have been documented not only in patients receiving adt but also in those undergoing surgical castration 4,8,9. Surprisingly, the fractures are often not related to metastasis; instead, they are related mostly to osteopenia or osteoporosis, analogous to the process that takes place in postmenopausal women. This observation becomes even more concerning with the realization that the rate of osteopenia and osteoporosis in men on adt is probably greater than what has been measured in comparable cohorts of postmenopausal women 10. Compounding this situation is the fact that, even before being placed on adt or having bone metastases, patients with a diagnosis of pca exhibit reduced bmd as compared with age-matched subjects. Hypogonadism, lower vitamin D, lower calcium intake, and heredity may account for that observation. Notably, bmd loss generally does not occur when anti-androgens are used as monotherapy 11.

In the setting of patients with pca on or off adt, these facts provide a reasonable rationale for prophylactic measures similar to those being applied in postmenopausal women.

2.2.1. Vitamin D and Calcium

It is generally recommended that patients receiving adt be systematically started on oral vitamin D and calcium. Yet the efficacy of this regimen in preventing bmd loss during adt is not established 12. These agents were insufficient to slow bone decay in the placebo arms of trials assessing pamidronate and zoledronic acid in the setting of cancer treatment–induced bone loss (ctibl) 13,14. Further, the absorption of oral calcium and vitamin D may be reduced in pca patients. That being said, initiation of vitamin D and calcium remains a required, albeit suboptimal, first step in pca patients receiving adt.

2.2.2. Oral Bisphosphonates in Nonmetastatic PCa

Currently, the only oral bisphosphonate approved by the U.S. Food and Drug Administration for the treatment of non-cancer-associated osteoporosis in men is alendronate. When used in hypogonadal men, this oral agent fails to prevent non-vertebral fractures 15. Its use in men with pca on adt may therefore be insufficient—not to mention the fact that alendronate has not been specifically approved for patients with ctibl 15. Furthermore, the toxicity of alendronate may be significant: a retrospective study of alendronate-treated women showed a 60% increase in outpatient visits or hospital admissions for acid-related upper gastrointestinal disorders in treated patients 16. Other molecules, such as etidronate, have been specifically tested in men receiving adt without showing significant efficacy for bmd preservation in that patient population 17.

Table i provides an overview of the oral bisphosphonates available for men on adt.

TABLE I
Treatments for skeletal morbidity and loss of bone mineral density (bmd) in men on androgen deprivation therapy (ADT)

2.2.3. Intravenous Bisphosphonates in Nonmetastatic PCa

Pamidronate and zoledronic acid are potent nitrogen-containing intravenous bisphosphonates that have demonstrated significant advantages relative to oral agents 12,19,20. To prevent ctibl in men on adt, they may be administered every 3 months (as compared with the daily or weekly regimen for oral bisphosphonates).

In a randomized placebo-controlled study published by Smith et al., intravenous pamidronate 60 mg administered on a 3-monthly schedule reduced bmd loss (as measured in the spine and hip) over 48 weeks of treatment in men receiving leuprolide 21. In another randomized double-blind placebo-controlled study with a crossover design, Diamond et al. demonstrated that metabolic markers for bone degradation were decreased in serum for at least 6 months after a single infusion of pamidronate 90 mg in men on adt (as compared with a placebo control group) 22. However, despite preventing ctibl in men receiving adt for pca, intravenous pamidronate did not significantly increase bmd measurements above baseline values 23.

To assess protection against ctibl, zoledronic acid (4 mg by infusion every 3 months) was tested in a 12-month randomized double-blind placebo-controlled trial in men with nonmetastatic pca receiving adt (n = 106). In contrast to other bisphosphonates, zoledronic acid not only prevented ctibl, it also increased bmd compared with baseline at all measured sites 13. The bmd improvements were particularly marked in the lumbar spine (p < 0.001). During that study, zoledronic acid showed a favourable toxicity profile, with no detectable adverse effects on renal function at any time. Probably because of the short follow-up, no measurable improvement in fracture rate could be detected in the treatment arm.

Current trials are aiming to answer the question of whether bisphosphonate therapy in nonmetastatic pca patients may delay the appearance of metastases. If that hypothesis is correct, the significant amount of time between biochemical failure and appearance of metastases in the natural history of pca will require the timing of bisphosphonate therapy to be defined with respect to optimization of cost-effectiveness.

Zoledronic acid is the first bisphosphonate to show a protective effect against skeletal-related events in patients with metastatic castration-resistant pca. Zoledronic acid was shown to have a potency approximately 850 times that of pamidronate 24. Pamidronate was tested in a randomized placebo-controlled study in 643 patients with metastatic pca having progressed under adt, and skeletal complications were observed to be reduced by 22% 25. Zoledronic acid (4 mg monthly) reduced by 48% the mean annual incidence of skeletal-related complications (0.77 events/year vs. 1.47 events/year for placebo, p = 0.005) and prolonged the median time to first skeletal-related event by more than 5 months (488 days vs. 321 days for placebo, p = 0.009). The ongoing risk of skeletal complications was also reduced by 36% in both the 15- and 24-month data sets 14,25, which may imply that the benefits of therapy were sustained during the 24-month span of the study. Throughout the study, zoledronic acid 4 mg, as compared with placebo, consistently reduced bone pain, with significant differences at the 3-, 9-, 21-, and 24-month time points (each p ≤ 0.05) 25. Such outcomes compare favourably with studies in metastatic breast cancer patients receiving intravenous bisphosphonates 13.

Besides measurable outcomes related to therapy, bisphosphonates also provide an emotional rampart for patients that otherwise have few therapeutic options, thus giving them and their treating physicians a sense of empowerment that may translate into an improved quality of life 2628.

One concern that has received increased attention in the bisphosphonate literature is osteonecrosis of the jaw (onj), which has been reported as a complication mainly of intravenous therapy 29. This disorder presents in the maxillofacial region as exposed bone that does not show signs of improvement after 8 weeks of therapy. Despite its relative gravity, onj is probably a very rare adverse event (1/10,000 to <1/100,000 patient–treatment years) when bisphosphonates are used at therapeutic or prophylactic doses for osteoporosis. In more recent studies using bone-preserving agents with different mechanisms of action, onj has been observed at least as frequently as it has been with bisphosphonate therapy 30. That finding implies that the disorder is probably related to osteoclast inhibition and does not represent a class effect of bisphosphonates per se. The specific cause of onj is not yet well defined. Risk factors such as pre-existing dental pathology, maxillofacial surgery, and the use of dental prostheses have been identified. Prevention aims at avoiding those risk factors and having regular dental checkups during therapy 3133.

2.3. The Role and Relevance of Receptor Activator of Nuclear Factor κB and Its Ligand in Bone Metabolism

Bone mass is not static; it is the result of a dynamic equilibrium between osteoblasts (the cells that create bone matrix) and osteoclasts (the cells that degrade the matrix). Osteoblasts secrete receptor activator of nuclear factor κB ligand (rankl), which binds its receptor (rank) on osteoclasts, thus triggering maturation, activation, and prolonged survival of the latter cells. By its effect on osteoclasts, rankl therefore promotes bone resorption 34. To regulate the activity of rankl, the endogenous decoy receptor osteoprotegerin binds rankl and prevents its interaction with rank, thus cutting short activation of the osteoclasts.

2.3.1. Denosumab

Denosumab is a fully human monoclonal antibody that specifically targets rankl. Administered by subcutaneous injection twice annually, it prevents bone loss 35. Denosumab has been shown to have activity in postmenopausal osteoporotic women. In this patient population, denosumab lowered the incidence of bone fractures 36,37. It also protected against bmd loss in osteopenic postmenopausal women taking adjuvant aromatase inhibitors for breast cancer 38.

In a phase iii randomized placebo-controlled clinical trial assessing subcutaneous denosumab (60 mg every 6 months) in 1468 men with nonmetastatic pca receiving adt, the drug significantly improved bmd in the lumbar spine (primary endpoint) by 6.7% (p < 0.001), total hip by 4.8% (p < 0.001), femoral neck by 3.9% (p < 0.001), and distal radius by 5.5% (p < 0.001) at 24 months. By the end of the trial, the risk of new vertebral fractures was significantly reduced by 62% (p = 0.006). Patients recruited into this study had a more favourable bmd than is usually observed in an average pca population on adt. It is therefore reasonable to assume that in the latter scenario, risk reduction may be more substantial. It is noteworthy that denosumab, used prophylactically in a twice-yearly regimen, had a favourable toxicity profile 39.

2.4. Guidelines on Surveillance of Bone Density in Men on ADT

An authoritative international panel of experts has put forward basic guidelines for screening and investigating patients receiving adt 40. As a first step, risk stratification according to readily obtainable clinical data such as age, smoking history, and body weight should be applied (see Table ii). After this categorization, patients will be assigned to one of two risk groups: low or high risk. Then, dual-energy X-ray absorptiometry or a quantitative computed tomography scan is obtained to help assess bmd. Using these basic clinical data, follow-up proceeds according to the flow chart depicted in Figure 1.

Figure 1
Flow chart for bone follow-up in patients on androgen deprivation therapy (adapted from Higano 200442).
TABLE II
Risk stratification for bone lossa

An unanswered question involves the timing of therapy with respect to initiation and duration. Most authorities agree that starting early is probably the optimal strategy.

2.5. General Recommendations on Preventive Measures for BMD Loss in Men Taking ADT

As first-line prophylaxis, basic recommendations include smoking cessation and reduction of alcohol intake. Increasing physical activity, particularly through a regular training program and resistance exercise, should be encouraged 40,4345.

Supplementation with vitamin D (400 IU daily at a minimum) and calcium (500 mg daily at a minimum) represents an interesting first-line prophylactic measure in patients on adt. Unfortunately, these agents are not potent enough to preserve bmd during adt 12. However, their use remains a required minimum in this patient population.

Finally, available options for preventing bone loss and fractures in patients receiving adt now include denosumab as well as bisphosphonates, which should be considered at least in patients categorized as high risk or having low bmd 39.

3. SUMMARY

Bone health should be of concern for every physician caring for patients with nonmetastatic pca on adt. The consequences of bone-related events on quality of life and overall survival are of sufficient magnitude to justify early prophylaxis against bone loss. Results of ongoing trials using bisphosphonates or denosumab in the nonmetastatic setting are eagerly anticipated and will help shed light on the efficacy of these agents in preventing or delaying the appearance of bone metastases.

4. ACKNOWLEDGMENTS

The authors acknowledge the support of the Urologues Associés du Centre hospitalier de l’Université de Montréal.

Footnotes

5. CONFLICT OF INTEREST DISCLOSURES

Jean-Baptiste Lattouf is a member of advisory boards for Amgen and Novartis. Fred Saad has conducted research with, and is a member of, the advisory boards of Novartis, Amgen, and Sanofi–Aventis.

6. REFERENCES

1. Saad F, Clarke N, Colombel M. Natural history and treatment of bone complications in prostate cancer. Eur Urol. 2006;49:429–40. [PubMed]
2. Higano CS. Bone loss and the evolving role of bisphosphonate therapy in prostate cancer. Urol Oncol. 2003;21:392–8. [PubMed]
3. Oefelein MG, Ricchiuti VS, Conrad PW, et al. Clinical predictors of androgen-independent prostate cancer and survival in the prostate-specific antigen era. Urology. 2002;60:120–4. [PubMed]
4. Shahinian VB, Kuo YF, Freeman JL, Goodwin JS. Risk of fracture after androgen deprivation for prostate cancer. N Engl J Med. 2005;352:154–6. [PubMed]
5. Melton LJ, 3rd, Atkinson EJ, Cooper C, O’Fallon WM, Riggs BL. Vertebral fractures predict subsequent fractures. Osteoporos Int. 1999;10:214–21. [PubMed]
6. Lau E, Ong K, Kurtz S, Schmier J, Edidin A. Mortality following the diagnosis of a vertebral compression fracture in the Medicare population. J Bone Joint Surg Am. 2008;90:1479–86. [PubMed]
7. Oefelein MG, Ricchiuti V, Conrad W, Resnick MI. Skeletal fractures negatively correlate with overall survival in men with prostate cancer. J Urol. 2002;168:1005–7. [PubMed]
8. Hatano T, Oishi Y, Furuta A, Iwamuro S, Tashiro K. Incidence of bone fracture in patients receiving luteinizing hormone releasing hormone agonists for prostate cancer. BJU Int. 2000;86:449–52. [PubMed]
9. Galvao DA, Spry NA, Taaffe Dr, et al. Changes in muscle, fat and bone mass after 36 weeks of maximal androgen blockade for prostate cancer. BJU Int. 2008;102:44–7. [PubMed]
10. Smith MR. Osteoporosis during androgen deprivation therapy for prostate cancer. Urology. 2002;60(suppl 1):79–85. [PubMed]
11. Smith MR, Fallon MA, Goode MJ. Cross-sectional study of bone turnover during bicalutamide monotherapy for prostate cancer. Urology. 2003;61:127–31. [PubMed]
12. Smith MR, McGovern FJ, Zietman AL, et al. Pamidronate to prevent bone loss during androgen-deprivation therapy for prostate cancer. N Engl J Med. 2001;345:948–55. [PubMed]
13. Smith MR, Eastham J, Gleason DM, Shasha D, Tchekmedyian S, Zinner N. Randomized controlled trial of zoledronic acid to prevent bone loss in men receiving androgen deprivation therapy for nonmetastatic prostate cancer. J Urol. 2003;169:2008–12. [PubMed]
14. Saad F, Gleason DM, Murray R, et al. A randomized, placebo-controlled trial of zoledronic acid in patients with hormonerefractory metastatic prostate carcinoma. J Natl Cancer Inst. 2002;94:1458–68. [PubMed]
15. Orwoll E, Ettinger M, Weiss S, et al. Alendronate for the treatment of osteoporosis in men. N Eng J Med. 2000;343:604–10. [PubMed]
16. Ettinger B, Pressman A, Schein J. Clinic visits and hospital admissions for care of acid-related upper gastrointestinal disorders in women using alendronate for osteoporosis. Am J Manag Care. 1998;4:1377–82. [PubMed]
17. Diamond T, Campbell J, Bryant C, Lynch W. The effect of combined androgen blockade on bone turnover and bone mineral densities in men treated for prostate carcinoma: longitudinal evaluation and response to intermittent cyclic etidronate therapy. Cancer. 1998;83:1561–6. [PubMed]
18. Saad F. Treatment of bone complications in advanced prostate cancer: rationale for bisphosphonate use and results of a phase iii trial with zoledronic acid. Semin Oncol. 2002;29(suppl 21):19–27. [PubMed]
19. Small EJ, Smith MR, Seaman JJ, Petrone S, Kowalski MO. Combined analysis of two multicenter, randomized, placebo-controlled studies of pamidronate disodium for the palliation of bone pain in men with metastatic prostate cancer. J Clin Oncol. 2003;21:4277–84. [PubMed]
20. Reid IR, Brown JP, Burckhardt P, et al. Intravenous zoledronic acid in postmenopausal women with low bone mineral density. N Eng J Med. 2002;346:653–61. [PubMed]
21. Smith MR, McGovern FJ, Zietman AL, et al. Pamidronate to prevent bone loss during androgen-deprivation therapy for prostate cancer. N Eng J Med. 2001;345:948–55. [PubMed]
22. Diamond TH, Winters J, Smith A, et al. The antiosteoporotic efficacy of intravenous pamidronate in men with prostate carcinoma receiving combined androgen blockade: a double blind, randomized, placebo-controlled crossover study. Cancer. 2001;92:1444–50. [PubMed]
23. Lipton A, Small E, Saad F, et al. The new bisphosphonate, Zometa (zoledronic acid), decreases skeletal complications in both osteolytic and osteoblastic lesions: a comparison to pamidronate. Cancer Invest. 2002;20(suppl 2):45–54. [PubMed]
24. Green JR, Müller K, Jaeggi KA. Preclinical pharmacology of CGP 42′446, a new, potent, heterocyclic bisphosphonate compound. J Bone Miner Res. 1994;9:745–51. [PubMed]
25. Saad F, Gleason DM, Murray R, et al. Long-term efficacy of zoledronic acid for the prevention of skeletal complications in patients with metastatic hormone-refractory prostate cancer. J Natl Cancer Inst. 2004;96:879–82. [PubMed]
26. Ross RW, Small EJ. Osteoporosis in men treated with androgen deprivation therapy for prostate cancer. J Urol. 2002;167:1952–6. [PubMed]
27. Saad F, Schulman CC. Role of bisphosphonates in prostate cancer. Eur Urol. 2004;45:26–34. [PubMed]
28. Wong R, Wiffen PJ. Bisphosphonates for the relief of pain secondary to bone metastases. Cochrane Database Syst Rev. 2002:CD002068. [PubMed]
29. Khosla S, Burr D, Cauley J, et al. Bisphosphonate-associated osteonecrosis of the jaw: report of a task force of the American Society for Bone and Mineral Research. J Bone Miner Res. 2007;22:1479–91. [PubMed]
30. Kyrgidis A, Toulis KA. Denosumab-related osteonecrosis of the jaws. Osteoporos Int. 2010. [Epub ahead of print] [PubMed]
31. Conte P, Guarneri V. Safety of intravenous and oral bisphosphonates and compliance with dosing regimens. Oncologist. 2004;9(suppl 4):28–37. [PubMed]
32. Aapro M, Abrahamsson PA, Body JJ, et al. Guidance on the use of bisphosphonates in solid tumours: recommendations of an international expert panel. Ann Oncol. 2008;19:420–32. [PubMed]
33. Polascik TJ. Bone health in prostate cancer patients receiving androgen-deprivation therapy: the role of bisphosphonates. Prostate Cancer Prostatic Dis. 2008;11:13–19. [PubMed]
34. Boyle WJ, Simone WS, Lacey DL. Osteoclast differentiation and activation. Nature. 2003;423:337–42. [PubMed]
35. Schwarz EM, Ritchlin CT. Clinical development of anti-rankl therapy. Arthritis Res Ther. 2007;9(suppl 1):S7. [PMC free article] [PubMed]
36. McClung MR, Lewiecki EM, Cohen SB, et al. Denosumab in postmenopausal women with low bone mineral density. N Engl J Med. 2006;354:821–31. [PubMed]
37. Cummings SR, San Martin J, McClung MR, et al. Denosumab for prevention of fractures in postmenopausal women with osteoporosis. N Engl J Med. 2009;361:756–65. [PubMed]
38. Ellis GK, Bone HG, Chlebowski R, et al. Randomized trial of denosumab in patients receiving adjuvant aromatase inhibitors for nonmetastatic breast cancer. J Clin Oncol. 2008;26:4875–82. [PubMed]
39. Smith MR, Egerdie B, Hernàndez Toriz N, et al. Denosumab in men receiving androgen-deprivation therapy for prostate cancer. N Engl J Med. 2009;361:745–55. [PMC free article] [PubMed]
40. Saad F, Higano CS, Sartor O, et al. The role of bisphosphonates in the treatment of prostate cancer: recommendations from an expert panel. Clinical Genitourin Cancer. 2006;4:257–62. [PubMed]
41. Saad F, Adashi JD, Brown JP, et al. Cancer treatment induced bone loss in breast and prostate cancer. J Clin Oncol. 2008;26:5465–76. [PubMed]
42. Higano CS. Understanding treatment for bone loss and bone metastases in patients with prostate cancer: a practical review and guide for the clinician. Urol Clin North Am. 2004;31:331–52. [PubMed]
43. Oncken C, Prestwood K, Kleppinger A, Wang Y, Cooney J, Raisz L. Impact of smoking cessation on bone mineral density in postmenopausal women. J Womens Health (Larchmt) 2006;15:1141–50. [PubMed]
44. Tucker KL, Morita K, Qiao N, Hannan MT, Cupples LA, Kiel DP. Colas, but not other carbonated beverages, are associated with low bone mineral density in older women: the Framingham Osteoporosis Study. Am J Clin Nutr. 2006;84:936–42. [PubMed]
45. Prentice A. Diet, nutrition, and the prevention of osteoporosis. Public Health Nutr. 2004;7:227–43. [PubMed]

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