Osteoporosis in Breast and Prostate Cancer Survivors

April 15, 2005
Ana O. Hoff, MD

,
Robert F. Gagel, MD

Oncology, ONCOLOGY Vol 19 No 5, Volume 19, Issue 5

Recent advances in treatment modalities for breast and prostate cancerhave resulted in an increasing number of patients that are cured orthat, despite residual disease, live long enough to start experiencingcomplications from cancer treatment. Osteoporosis is one such problemthat has been increasingly identified in cancer patients. Hypogonadismand glucocorticoid use are the two major causes of bone loss inthese patients. Osteoporosis is characterized by low bone mass and abnormalbone microarchitecture, which results in an increased risk offractures. Vertebral body and hip fractures commonly result in a drasticchange of quality of life as they can result in disabling chronic pain,loss of mobility, and loss of independence in performing routine dailyactivities, as well as in increased mortality. In patients with prostatecarcinoma, androgen-deprivation therapy by either treatment with agonadotropin-releasing hormone (GnRH) or bilateral orchiectomy resultsin increased bone turnover, significant bone loss, and increasedrisk of fractures. Patients with breast cancer are at increased risk forestrogen deficiency due to age-related menopause, ovarian failure fromsystemic chemotherapy, or from the use of drugs such as aromataseinhibitors and GnRH analogs. Several studies have indicated that theprevalence of fractures is higher in breast and prostate cancer patientscompared to the general population. Therefore, patients at risk for boneloss should have an assessment of their bone mineral density so thatprevention or therapeutic interventions are instituted at an early enoughstage to prevent fractures. This article will address the characteristicsof bone loss observed in breast and prostate cancer patients and potentialtreatments.

Recent advances in treatment modalities for breast and prostate cancer have resulted in an increasing number of patients that are cured or that, despite residual disease, live long enough to start experiencing complications from cancer treatment. Osteoporosis is one such problem that has been increasingly identified in cancer patients. Hypogonadism and glucocorticoid use are the two major causes of bone loss in these patients. Osteoporosis is characterized by low bone mass and abnormal bone microarchitecture, which results in an increased risk of fractures. Vertebral body and hip fractures commonly result in a drastic change of quality of life as they can result in disabling chronic pain, loss of mobility, and loss of independence in performing routine daily activities, as well as in increased mortality. In patients with prostate carcinoma, androgen-deprivation therapy by either treatment with a gonadotropin-releasing hormone (GnRH) or bilateral orchiectomy results in increased bone turnover, significant bone loss, and increased risk of fractures. Patients with breast cancer are at increased risk for estrogen deficiency due to age-related menopause, ovarian failure from systemic chemotherapy, or from the use of drugs such as aromatase inhibitors and GnRH analogs. Several studies have indicated that the prevalence of fractures is higher in breast and prostate cancer patients compared to the general population. Therefore, patients at risk for bone loss should have an assessment of their bone mineral density so that prevention or therapeutic interventions are instituted at an early enough stage to prevent fractures. This article will address the characteristics of bone loss observed in breast and prostate cancer patients and potential treatments.

Advances in the medical treatment of breast and prostate cancer have improved cure rates or disease-free survival. Increasing longevity has resulted in the emergence of medical problems associated with the malignancy or caused by the oncologic treatment. Bone loss is one such complication. In breast and prostate cancer patients, hypogonadism is the predominant cause of bone loss. In breast cancer patients, estrogen deficiency caused by premature ovarian failure, a result of systemic chemotherapy, or from drugs such as aromatase inhibitors or GnRH analogs causes bone loss.[1-5] Acute estrogen deficiency results in higher bone turnover and rapid bone loss, at a rate greater than that seen during natural menopause.[ 4] In patients with prostate cancer, hypogonadism as a result of androgen-deprivation therapy also leads to higher bone turnover, bone loss, and increased risk of fractures.[6-8] The aim of this review is to discuss the known frequency, magnitude, and mechanisms of bone loss observed in breast and prostate cancer patients, as well as to summarize the current recommendations on how to prevent bone loss or treat patients with osteoporosis. Definition and Diagnosis of Osteoporosis Osteoporosis is defined as a metabolic bone disease characterized by low bone mass and microarchitectural deterioration of bone tissue, leading to enhanced bone fragility and increased risk of fractures.[9] Vertebral body and hip fractures commonly result in a significant change in quality of life; they cause chronic pain, loss of mobility, and loss of independence in performing daily activities. Hip fracture is the most devastating complication of osteoporosis. Epidemiologic studies show clearly that survival probability is reduced dramatically, at any age over 60 years,[10] suggesting that untreated osteoporosis could have an independent effect on survival in women with breast cancer. There are similar and even more striking results for men with hip or vertebral fractures.[10] Therefore it is important to evaluate bone mass in hypogonadal patients and initiate therapy for those at risk. Bone mass can be measured by several noninvasive methods. These include dual-energy x-ray absorptiometry (DXA), quantitative computed tomography scan (QCT), and ultrasound. The method of choice is DXA, as it is easily accessible, provides low radiation exposure, and has good precision. It can be used to diagnose osteopenia or osteoporosis, to determine fracture risk, and to monitor response to therapy. The definition of normal bone mass, osteopenia, or osteoporosis is based on the World Health Organization (WHO) criteria. Risk is defined by comparing an individual patient's bone mineral density (BMD) with an age, sex, and ethnically appropriate population. Osteoporosis is defined as a BMD ≥ 2.5 standard deviations (SD) below average peak adult bone mass. This is designated as a T score of -2.5 or less (Table 1). A higher BMD, but one that is less than normal (-1 to -2.5), is defined as osteopenia. These patients do not currently have a greater risk of fractures, but nevertheless form a high-risk population for future fractures.[11]

Both DXA and QCT can measure BMD of the spine and hips (central DXA or QCT) or BMD of peripheral sites such as the forearm (pDXA or pQCT). Measurement of spine and hip BMD is the gold standard for diagnosis and monitoring of osteoporosis, while peripheral measurements are performed mainly for screening purposes. Quantitative computed tomography is a more sensitive but less precise method than DXA for diagnosing osteoporosis in men. In older men, osteophytes or facet sclerosis of the posterior elements may increase the spine BMD values.[12] Therefore, whenever possible DXA measurements of other sites or QCT of the spine should be performed in older individuals. The most common cause of osteoporosis in women, including women with breast cancer, is estrogen deficiency. In postmenopausal osteoporosis, there is an increased rate of bone remodeling and an imbalance between bone resorption and bone formation that results in a net loss of bone.[13,14] Bone loss in postmenopausal women occurs in two phases.[ 15] In the first 5 years after menopause there is a rapid phase of bone loss (about 3%/yr in the spine) followed by a phase of slower rate of bone loss (about 0.5%/yr) that occurs not only at the spine but also at other sites. The slower phase of bone loss starts at around age 55 in both men and women. Other than gonadal function, vitamin D and calcium deficiencies are common problems in older individuals.[ 15] Approximately 30% to 50% of older individuals have subnormal plasma vitamin D concentration. Other contributors to bone loss in cancer patients that are less well-defined include direct effects of chemotherapy agents on bone cells, reduced physical activity, exposure to corticosteroids, and deficient dietary calcium intake. It is important for the oncologist or internist following this group of patients to recognize that it is a series of small but additive medical and lifestyle changes that contribute to the steady decline in bone mass. The corollary is that it is not inevitable: simple preventive measures will have profound long-term effects. The increased bone remodeling in sex steroid hormone deficiency causes deregulation of cytokines, hormones, and growth factors present in the bone microenvironment. These changes result in activation of osteoclastic bone resorption and bone loss. To better understand the mechanisms of bone loss and the rationale for the use of specific pharmacologic agents to prevent and treat osteoporosis, we will discuss how bone is remodeled in normal and sex steroid-deficient states. Bone Remodeling The adult skeleton is in a dynamic state, constantly being renewed in a continuous and coordinated fashion throughout life to maintain the structure and quality of bone. Bone remodeling, also termed bone turnover, occurs simultaneously in tens of thousands of skeletal areas. Each of these areas is called a bone-remodeling unit.[16] The initiating event in remodeling at each of these bone-remodeling units is the differentiation of monocytic cells into multinucleated cells called osteoclasts. These cells bind tightly to bone, produce acid and proteolytic enzymes, and cause the resorption of mineral and bone protein, creating a resorption lacuna of uniform size and depth. The osteoclast is then replaced with scavenger cells to clean up resorbed material, followed by osteoblasts or bone-forming cells. These cells lay down multiple layers of type 1 collagen that is mineralized to form new bone. This entire process takes 3 to 4 months. Most importantly, this process makes it possible to repair microfractures that result from normal minor trauma or other "wear and tear" to the skeleton. Normal bone remodeling is a balanced event: bone resorption is equaled by bone formation. The remodeling process occurs under control of several hormones and cytokines that are active within the bone microenvironment.[13] These include estrogen, testosterone, parathyroid hormone, and growth hormone. Other important factors include vitamin D, interleukins (IL-1, IL-4, IL-6, IL-7, IL-11, IL-17), transforming growth factor-beta (TGF-beta), tumor necrosis factor-alpha (TNF-alpha), prostaglandin E2, and the receptor activator of nuclear factor kappaB ligand (RANKL).[17,18] RANKL is a critical cytokine for osteoclastogenesis. It is expressed by osteoblasts and binds to the receptor activator of nuclear factor kappaB (RANK) present on the surface of osteoclasts precursors and mature osteoclasts. The RANKL/RANK interaction is responsible for differentiation of monocytes to osteoclasts and activates bone resorption by the mature osteoclast. Osteoprotegerin (OPG) is a decoy receptor, expressed by osteoblasts, that binds RANKL thereby preventing RANKL from activating RANK.[19] The balance between RANKL and OPG is essential for normal bone remodeling. Overexpression of RANKL will result in increased bone resorption and osteoporosis; overexpression of OPG will result in inhibition of bone resorption and osteopetrosis.[18] Alteration in the RANKL/OPG ratio has been observed in several conditions associated with osteoporosis, including estrogen deficiency, corticosteroid use, hyperparathyroidism, rheumatoid arthritis, multiple myeloma, osteolytic bone metastases, and humoral hypercalcemia of malignancy.[ 18] In most of these disorders there is overexpression of RANKL and decreased production or increased degradation of OPG. Estrogen deficiency can result in an increase of the RANKL/OPG ratio. Eghbali-Fatourechi and colleagues showed that the RANKL level was higher in marrow stromal cells and lymphocytes of postmenopausal women as compared to premenopausal women; RANKL expression was inversely correlated with estrogen levels.[ 20] These findings demonstrate the important role of the OPG/ RANKL/RANK system in mediating estrogen deficiency-induced bone resorption. As estrogen deficiency is the main cause of bone loss in breast cancer patients, one could postulate that the OPG/RANKL/RANK system plays an important role in the mechanism of bone loss in these patients. In fact, the effect of a monoclonal antibody against RANKL, which functions to prevent the RANKL-RANK interaction, is under investigation as a therapeutic agent to inhibit bone loss in estrogen-deficient breast cancer patients.

In clinical practice, bone resorption and formation are easily quantified. Table 2 shows several readily available markers of formation and resorption. The formation markers include bone proteins incorporated into the matrix (osteocalcin or collagen) or enzymes involved in mineralization (alkaline phosphatase). All bone resorption markers are fragments of bone-specific collagen released by the osteoclast.[21] Bone Loss in Breast Cancer Patients Breast cancer is the most common malignancy in women, with an estimated 40,410 new cases in the United States predicted for 2005.[22] Early detection and improved treatment modalities have resulted in a significant improvement of disease-free and overall survival. More than 90% of patients with early-stage breast cancer are alive 10 years after diagnosis,[23] a survival improvement that is mainly due to advances in adjuvant chemotherapy and radiation therapy. Unfortunately, adjuvant systemic chemotherapy can induce ovarian failure in premenopausal patients with early breast cancer and exacerbate the expected bone loss in postmenopausal patients. Premature menopause occurs in 50% to 85% of patients treated with adjuvant chemotherapy regimens that include cyclophosphamide, metho trexate, fluorouracil, and doxorubicin.[ 1] The effect of chemotherapy (cyclophosphamide-based) on ovarian function is dose- and age-dependent. The frequency of ovarian failure rises as patients approach the natural age of menopause, reaching nearly 100% by the age of 50 years.[1] A few studies have investigated the magnitude and frequency of bone loss in patients undergoing adjuvant chemotherapy (Table 3). All highlight the tight correlation between development of ovarian failure and bone loss. Shapiro and colleagues investigated the BMD and markers of bone turnover (osteocalcin, bone alkaline phosphatase) at baseline, 6 months, and 12 months in 49 patients receiving adjuvant systemic chemotherapy. Patients who developed ovarian failure lost 4% BMD in the lumbar spine at 6 months and an additional 3.7% bone loss at 12 months. The bone loss was accompanied by a significant increase of serum osteocalcin and bonespecific alkaline phosphatase. In contrast, no significant bone loss was observed in patients who had maintained normal ovarian function.[4] This has been corroborated in other studies. Headley and colleagues evaluated 27 patients with breast cancer treated with adjuvant chemotherapy who were premenopausal at the time of diagnosis.[2] The BMD was assessed 2 years after treatment with adjuvant chemotherapy. Patients who became amenorrheic (16) had a BMD 14% lower than patients with intact ovarian function. Another study by Vehmanen and colleagues evaluated the long-term impact of chemotherapy-induced ovarian failure on bone mineral density.[ 3] This study involved 75 patients who received adjuvant chemotherapy for breast cancer. Patients who developed ovarian failure suffered a 12% reduction of lumbar spine BMD 5 years later, while patients who maintained gonadal function lost 3%.[3] Most of the other studies are retrospective and involved fewer numbers of patients. Collectively, these studies have included a small number of patients followed for short periods; accordingly there is no substantial information on fracture prevalence in this group of patients. One study by Kanis and colleagues[ 24] investigated the incidence of osteoporotic fractures in patients with breast cancer as a subprotocol of two trials designed to assess the effect of clodronate on the incidence of skeletal metastases. The authors followed three groups of patients for 3 years: newly diagnosed breast cancer patients (356), healthy controls (776), and patients presenting with soft-tissue recurrence (82). They performed x-rays of the spine at baseline and every 6 months. The annual incidence of vertebral fracture was higher in any of the breast cancer groups compared to healthy controls: 19% in patients with recurrent disease, 2.7% in patients presenting with newly diagnosed disease, and 0.5% in controls.[24] Adjuvant hormonal treatment has resulted in significant improvement in disease-free and overall survival for women with hormone receptor- positive breast cancer.[25] For several years tamoxifen was the standard hormonal treatment in postmenopausal women. Recently, several multicenter, randomized, phase III adjuvant trials have compared the new generation of aromatase inhibitors to tamoxifen or placebo following tamoxifen therapy (5 or fewer years). These trials include the ATAC trial, comparing initial therapy with anastrozole (Arimidex) to tamoxifen[26]; the MA- 17 trial, which evaluated the effects of letrozole (Femara) vs placebo[27] after 5 years of tamoxifen; and the Intergroup Exemestane Study, which included women treated with tamoxifen for 2 to 3 years, randomized to complete 5 years of tamoxifen or 2 to 3 years of exemestane (Aromasin).[ 28] In all of these trials, treatment with an aromatase inhibitor was superior to tamoxifen, providing a lower risk of tumor recurrence and better disease-free survival. Treatment with aromatase inhibitors rather than tamoxifen has become the preferred primary form of therapy for women with hormone receptor- positive breast cancer. As the aromatase inhibitors cause a marked reduction in the circulating levels of estrogen, it is expected that they will exacerbate bone loss in postmenopausal patients. This is of concern as many of these patients have already suffered accelerated bone loss from premature menopause, and rather than being treated with tamoxifen-a drug that maintains bone mass in postmenopausal women-are placed on aromatase inhibitors that result in further bone loss. Information regarding the effects of aromatase inhibitors on bone mass is still limited. The best information available to date can be obtained from a substudy of the ATAC trial.[5] In this study 308 patients underwent a BMD study at baseline and after 1 and 2 years of treatment. Patients who received anastrozole lost 4% of bone mass at the lumbar spine at 2 years while no bone loss was observed in other groups. In addition, the number of fractures was higher in patients who received anastrozole.[5] Therefore, in contrast to tamoxifen, which has beneficial effects to the bone mass of postmenopausal women,[29-31] anastrozole has been shown to result in bone loss and to increase the risk of fractures.[5] Prostate Cancer and Bone Loss Prostate cancer is one of the most common malignancies in men. It has been estimated that in 2005 there will be 232,000 new cases of prostate cancer causing approximately 30,000 deaths.[22] Androgen-deprivation therapy (ADT) is the primary treatment for patients with metastatic disease; this therapy results in reduced morbidity and improved survival when combined with radiation therapy. Despite the fact that it can ameliorate survival, ADT is a palliative rather than curative treatment. More recently androgen-deprivation therapy has been used in patients presenting with locally advanced or locally recurrent disease. As these patients survive longer than patients with widespread metastatic disease, they are exposed longer to ADT and are at a higher risk to manifest the complications of chronic androgen deprivation. Androgen-deprivation therapy includes all treatments that will result in a reduction of testosterone level or blockade of testosterone action. These include bilateral orchiectomy, gonadotropin- releasing hormone (GnRH) agonists, antiandrogen therapy (androgen receptor blockers), and combined androgen blockade (GnRH agonist with antiandrogens). Androgen- deprivation therapy can result in loss of libido, erectile dysfunction, gynecomastia, loss of muscle, and loss of bone mass. In bone, testosterone deficiency results in increased bone turnover; osteoclast resorption exceeds bone formation resulting in a net loss of bone.

Several prospective studies have investigated the effects of ADT on bone mass (Table 4). Despite the small number of patients enrolled in these studies, they clearly demonstrate sub- stantial bone loss.[7,8,32-34] Maillefert and colleagues evaluated BMD in six patients undergoing ADT; within 18 months they observed a 7.1% and 6.6% reduction in bone mass of the lumbar spine and femoral neck, respectively.[33] Mittan and colleagues evaluated BMD at baseline and at 6 and 12 months after initiating ADT (15 patients), and compared the results to 13 sex-matched controls without prostate cancer.[34] While no bone loss was observed in the control group, patients receiving ADT lost a significant amount of bone in the hips and distal radius. Another study by Daniell showed a 10% decrease in BMD 2 years following orchiectomy (10 patients) and a 6.5% reduction in bone mass in 16 men receiving GnRH agonist alone or in combination with antiandrogens.[8]

In summary, the observed rates of bone loss during ADT are higher than those associated with menopause. The rates observed vary by study population and by the type of ADT, but ranged from 2% to 8% in the lumbar spine and from 1.8% to 6.5% in the femoral neck after 12 months of continuous ADT.[32,35] The fracture risk in these patients has been retrospectively reviewed (Table 5). Fractures start to occur within 2 years of treatment and increase in frequency with longer durations of ADT.[35] Melton and colleagues reported a fracture prevalence of 40% in a group of patients on ADT (bilateral orchiectomy) for a mean of 15 years.[6] In a recent study, Shahinian and colleagues evaluated the records of 50,613 men with prostate cancer who were listed in the linked database of the Surveillance, Epidemiology, and End Results (SEER) program and Medicare from 1992 and 1997 and found that ADT was associated with an increase in risk of fracture; the risk was proportional to the number of doses of GnRH agonist administered in the first year after diagnosis.[36] How to Prevent or Treat Bone Loss in Cancer Patients Early screening and identification of patients at increased risk for bone loss is a key element of management of bone health in breast and prostate cancer patients. The American Society of Clinical Oncology has published guidelines for the identification and management of bone loss in breast cancer patients.[37] These guidelines recommend that any patient at risk for osteoporosis undergo a DXA scan to evaluate the bone mineral density followed by appropriate treatment. High-risk patients include women older than 65 years of age, postmenopausal women receiving aromatase inhibitors, women who develop premature menopause as a result of the breast cancer treatment, and patients with other known risk factors for osteoporosis (Table 6). All patients with breast cancer, including the ones not at risk for osteoporosis, should be counseled on lifestyle changes and appropriate calcium and vitamin D supplementation.[37] All patients with natural or drug-induced estrogen deficiency should have periodic evaluation of their bone mass in addition to calcium/vitamin D supplementation and exercise; patients with osteoporosis or significant bone loss over time should be started on therapy.[37] The American Society of Clinical Oncology has not yet provided guidelines for maintenance of bone health in prostate cancer patients. However, several authors have published recommendations for this group of patients. In a recent publication, Diamond and colleagues recommended that patients with risk factors for fractures (on ADT, previous fracture) undergo assessment of their bone mass by using DXA or QCT.[35] Patients with osteoporosis should be started on treatment, patients with osteopenia should have a repeat BMD evaluation in 6 to 12 months, and patients with normal BMD should be reassessed in 2 years. Patients with osteoporotic fractures confirmed by imaging studies should also be started on therapy.[35] While these guidelines are an important first step, there are compelling reasons for being more proactive. Current guidelines from several bone (www.nof.org/professionals/ clinical.htm), endocrine,[38] and rheumatologic[ 39] societies recommend prevention of bone loss rather than the more passive approach of waiting until it happens suggested by oncologic guidelines. Current therapies for osteoporosis make it difficult to increase bone mass by more than 10%, arguing persuasively for a strategy focused on prevention. Oncologists should be mindful of these guidelines. There are several drugs approved or under investigation for treatment of osteoporosis.[40-44] The two classes of drugs available include bone resorption inhibitors and anabolic agents. The bone resorption inhibitors include estrogen, selective estrogen receptor modulators (SERMS), nasal calcitonin (Miacalcin), bisphosphonates, and the RANKL monoclonal antibody.[40,41,43,44] The only anabolic agent currently approved for use in osteoporosis is teriparatide (Forteo)-recombinant human parathyroid hormone (hPTH 1-34)-a potent enhancer of bone formation that results in significant improvement of bone mineral density in women with postmenopausal osteoporosis and in men with osteoporosis.[ 42] Teriparatide has not yet been investigated in breast or prostate cancer patients; therefore the risks and benefits of this agent should be carefully considered before using it in this group of patients. There is a fully humanized monoclonal antibody against RANKL (AMG 162) that has been under investigation and is a promising bone resorption inhibitor. AMG 162 has been investigated in postmenopausal osteoporosis in phase I and II studies. A single subcutaneous dose of AMG 162 (1 mg/kg or 60 mg) resulted in suppression of bone resorption for more than 6 months and increase in bone mineral density.[44] Studies with AMG 162 in breast cancer patients for control of bone loss as well as for bone metastatic disease are currently under way. Bisphosphonates are potent inhibitors of osteoclast differentiation and activity. This class of drugs is widely used for treatment of postmenopausal, steroid-induced, and male osteoporosis. In breast cancer patients, several studies have addressed the role of bisphosphonates in preventing bone loss after chemotherapy-induced premature menopause. Clodronate and risedronate (Actonel), both oral bisphosphonates, have been investigated and were shown to be effective in reducing the rate of bone loss.[45,46] The use of intravenous bisphosphonates in these patients is still under investigation, but preliminary data from a study that has evaluated the effect of zoledronic acid (Zometa) in patients receiving tamoxifen or anastrozole have indicated that zoledronic acid is able to counteract the bone loss induced by anastrozole in these patients.[47] In prostate cancer patients, intravenous bisphosphonates have proven to reduce bone loss in at least two studies. Smith and colleagues have investigated the effects of both intravenous pamidronate (Aredia) and zoledronic acid on bone mass in patients receiving androgen therapy and compared their bone mineral densities to individuals who received androgen-deprivation therapy alone.[48,49] In the pamidronate study, 47 patients who were being treated with androgen-deprivation therapy were randomized to receive pamidronate at 60 mg or placebo every 3 months. Pamidronate treatment protected patients from developing the bone loss associated with ADT.[48] Another study investigated the use of zoledronic acid vs placebo in patients undergoing androgen deprivation therapy. Zoledronic acid was given at a dose of 4 mg every 3 months for 12 months. Patients who received zoledronic acid were not only protected against bone loss, but gained a significant amount of bone mass.[49] Diamond and colleagues investigated the effect of an oral bisphosphonate (etidronate [Didronel]) in patients undergoing ADT. Despite the small number of patients included in the study, they were able to show a gain of bone mass at the lumbar spine in patients treated with etidronate.[50] As estrogen plays an important role in male bone metabolism and can be used in patients with prostate cancer, it has been studied as a potential treatment for ADT-induced bone loss. Taxel and colleagues investigated the effects of micronized estradiol on bone turnover in prostate cancer patients on ADT; they observed a significant reduction in bone turnover markers.[ 51] Subsequently, two studies have addressed the question of whether estrogen or a SERM is a potential treatment for prevention or treatment of osteoporosis associated with ADT. Smith and colleagues have studied the effects of raloxifene (Evista), a SERM, in patients with nonmetastatic prostate cancer being treated with ADT.[52] A total of 48 patients were randomized to receive raloxifene or placebo. At 12 months, patients on raloxifene maintained their bone mass at the spine and hips while patients receiving placebo suffered a reduction in BMD.[52] Ockrim et al investigated transdermal estradiol in patients with prostate cancer and also noted a significant improvement in bone mass with this agent.[53] Conclusion In conclusion, gonadal insufficiency caused by cancer treatment can cause rapid bone loss in women with breast cancer or men with prostate cancer. Therefore, high-risk patients should be assessed by bone mineral density testing. Patients with severe osteopenia or osteoporosis should undergo early treatment to prevent fractures, pain, and deformities associated with osteoporosis.

Disclosures:

Dr. Hoff has received grants and research support from Novartis Pharmaceuticals.

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