LOADING...

Bone Health and Breast Cancer Management 

Bone Health and Breast Cancer Management 

No Results

No Results

processing….

Attention to bone health is an important aspect of managing breast cancer in women. Many women with breast cancer are postmenopausal and, therefore, at increased risk for osteoporosis. In addition, some of the agents used for the treatment of breast cancer have adverse effects on bone. For example, aromatase inhibitors (eg, anastrozole, letrozole, exemestane), which are used to treat early-stage breast cancer in postmenopausal women, deplete bone.

Finally, bone is the most common site of metastasis in breast cancer. Metastasis to bone causes pain, pathological fractures, hypercalcemia, and spinal cord compression, as well as contributing to mortality. [1, 2]

A study by Lipton et al found that in patients with bone-only metastases, serum beta C-terminal telopeptide (B-CTx) of type I collagen was a significant predictor of shortened recurrence-free survival (RFS). B-CTx is a marker of bone resorption, and increased resorption favors the growth of cancer cells. [3]

Increasing evidence indicates that in postmenopausal women with breast cancer, adjuvant bisphosphonate treatment not only improves bone density but also decreases bone metastasis and improves overall survival. In patients with metastatic breast cancer, bisphosphonates and denosumab have been shown to decrease skeletal-related events, including fractures; hypercalcemia; and increased need for radiation, surgery, or pain medication.

For more information, see Breast Cancer, Breast Cancer Staging, Adjuvant Therapy for Breast Cancer, and Breast Cancer Treatment Protocols.

Bisphosphonates, which inhibit resorption of bone by osteoclasts, have been studied extensively in breast cancer. Bisphosphonates can delay the development of skeletal-related events in women with metastatic breast cancer and show promise in preventing bone loss induced by chemotherapy or hormonal therapy. Emerging data suggest that adjuvant therapy with bisphosphonates may prevent disease recurrence and prolong survival, specifically in postmenopausal women. [4]

The Early Breast Cancer Trialists’ Collaborative Group found that in postmenopausal women with early breast cancer, adjuvant bisphosphonate therapy produced highly significant reductions in recurrence (rate ratio [RR] 0.86, P=0.002), distant recurrence (RR 0.82, P=0.0003), bone recurrence (RR 0.72, P=0.0002), and breast cancer mortality (RR 0.82, P=0.002). In premenopausal women, however, bisphosphonate treatment had no apparent effect on any outcome. [5]

In the setting of metastatic disease, bisphosphonates have little or no effect on survival. However, intravenously administered bisphosphonates do appear to provide a continuous effect on bone for the duration of their use.

In general, adverse effects for bisphosphonates include bone, joint, or muscle pain, as well as nausea, vomiting, and diarrhea. Oral bisphosphonates pose a higher risk of heartburn and esophagitis than their intravenously administered counterparts.

In September 2011, denosumab (Prolia) was approved by the U.S. Food and Drug Administration (FDA) to increase bone mass in women at high risk for fracture who are receiving adjuvant aromatase inhibitor therapy for breast cancer. A dose of 60 mg is administered subcutaneously every 6 months.

Denosumab is a fully human monoclonal antibody that targets the receptor activator of the nuclear factor-kappa-B ligand (RANKL), which acts as the primary signal to promote bone removal. By inhibiting the development and activity of osteoclasts, denosumab decreases bone resorption and increases bone density.

Vitamin D supplementation may be indicated in women treated for breast cancer, to aid with bone mineral density. [6] A double-blind, placebo-controlled, randomized phase 2 trial by Restelli et al found that high-dose vitamin D supplements improved aromatase inhibitor–induced musculoskeletal symptoms in women on adjuvant anastrozole for breast cancer. [7] Vitamin D also appeared to have a positive effect on bone loss on these patients. Further studies are needed.

A growing body of evidence suggests that bisphosphonates may have antitumor activity. In a study of a first-generation bisphosphonate, clodronate, in patients with primary operable breast cancer, Powles et al reported a significant improvement in 5-year bone relapse–free survival. [8]

A 2008 study examined the potential role of bisphosphonates in cancer treatment–induced bone loss and found that aromatase inhibitors or androgen deprivation can be risk factors for osteopenia, osteoporosis, and bone fracture and that this risk can be mitigated with appropriate bisphosphonate therapy. [9]

A study by Winters-Stone et al found that a combined program of resistance and impact exercise reduced risk factors for fracture among postmenopausal breast cancer survivors and may be of particular benefit for those taking aromatase inhibitors. [10]

The addition of zoledronate to hormonal therapy in the adjuvant breast cancer setting, however, was found to decrease disease-free survival by 36%. A larger, randomized phase III (SWOG 0307) trial is currently ongoing to further evaluate the importance of other bisphosphonates, including zoledronate, in the treatment of early-stage breast cancer.

In a study of anastrozole therapy for breast cancer, Markopoulos et al found that patients who had pretreatment osteopenia or osteoporosis received protection against bone loss if oral risedronate was added to their regimen. [11] However, patients with a normal bone mineral density before starting treatment were at very low risk for osteoporosis.

In two studies of breast cancer patients with tumor cells detected in bone marrow, zoledronate proved to be more effective than placebo in eliminating these cells. [12, 13]

A study by Coleman et al found that zoledronic acid is well tolerated in the adjuvant setting and can be safely administered along with adjuvant therapy, including chemotherapy, in women with stage II/III breast cancer. [14] A separate study by Hatoum et al found that zoledronic acid is associated with a lower risk and frequency of skeletal complications and a longer follow-up time. [15]

A study by Scarpa et al found a previously unsuspected high prevalence of defined arthritides underlying the rheumatic complaints of women taking aromatase inhibitors. Further studies are needed. [16]

The Early Breast Cancer Trialists’ Collaborative Group meta-analysis included 26 randomized trials involving 18,766 women with early breast cancer and compared 2 to 5 years of bisphosphonate therapy with no bisphosphonate therapy. [5] Overall, the reductions in recurrence, distant recurrence, and breast cancer mortality with bisphosphonate therapy were of borderline significance, although the reduction in bone recurrence was significant (RR, 0.83; P = 0.004).

However, subsequent analysis revealed that although bisphosphonates had no benefit in premenopausal women, in postmenopausal women, bisphosphonates produced significant reductions in the following [5] :

The findings were unaffected by bisphosphonate class, treatment schedule, estrogen-receptor status, nodes, tumor grade, or concomitant chemotherapy.

In March 2017, Cancer Care Ontario and the American Society of Clinical Oncology (ASCO) issued a joint clinical practice guideline that recommends considering a bisphosphonate as adjuvant therapy for all postmenopausal women with early breast cancer who are deemed to be candidates for adjuvant therapy. The recommendation applies to women who have undergone natural menopause or menopause induced by ovarian suppression or ablation. [17, 18]

The guidelines recommend the use of either zoledronic acid or clodronate; data on adjuvant denosumab, although promising, were found to be insufficient to support a recommendation. The recommended regimen for zoledronic acid is 4 mg intravenously (infused over 15 minutes or longer) every 6 months for 3 to 5 years. Clodronate is given in a dosage of 1,600 mg/d orally for 2 to 3 years. [17, 18]

In the setting of metastatic disease, bisphosphonates have little or no survival effect. However, IV bisphosphonates do appear to provide a continuous effect on bone for the duration of their use.

Controlled trials have shown that administration of a bisphosphonate is associated with a delay in the development of new skeletal-related events (SREs), thus reducing or delaying the need for palliative radiation, orthopedic surgery to address pathologic fractures, and use of narcotic analgesics. [2] For this reason, monthly administration continues for an indefinite period in breast cancer patients with bone metastasis.

Less-frequent bisphosphonate dosing has been the subject of active research.  An ongoing trial is testing whether giving zoledronic acid every 3 months rather than once a month is just as effective (ie, non-inferior) at reducing bone pain and SREs in patients with bone metastases. In this study, SREs are defined as any skeletal event requiring radiation therapy to bone, fractures, spinal cord compression, or surgery to bone within 24 months of initiation of the study. [19]

Results of the randomized phase 3 ZOOM trial by Amadori et al, which studied the effect of decreasing the administration of zoledronic acid from every 4 weeks to every 12 weeks during the second year of treatment, suggest that the drug maintains its therapeutic effects. The ZOOM trial included 425 patients with breast cancer who had one or more bone metastases and had completed 12-15 months of monthly treatment with zoledronic acid. [20]

After follow-up of at least 1 year, the rate of skeletal-related events per patient per year in ZOOM was 0.26 (95% confidence index [CI] 0.15-0.37) in the patients who received zoledronic acid every 12 weeks, versus 0.22 (0.14-0.29) in the patients maintained on an every-4-week schedule. The upper limit of one-tailed 97.5% CI on the 0.04 difference between the groups.was 0.17, which is lower than the non-inferiority margin. [20]

Rates of the most common grade 3-4 adverse events in the 12-week group versus the 4-week group were as follows:

 However, median N-terminal telopeptide concentration changed from baseline more in the 12-week group than in the 4-week group after 12 months (12.2% vs 0.0%; P=0.011).The authors recommend further investigation of this change before changing current practice. [20]

A randomized, open-label clinical trial that included 855 patients with metastatic breast cancer found no increased risk of skeletal events over 2 years in patients who received zoledronic acid every 12 weeks compared with the standard dosing interval of every 4 weeks. Similar results were reported in study patients with metastatic prostate cancer and multiple myeloma. The authors concluded that adminstering zoledronic acid every 12 weeks may be an acceptable option. [21]

SREs occurred in 113 patients in the 4-week group versus 119 in the 12-week group, among the 820 breast cancer patients who completed the study (hazard ratio [HR], 0.90; P = 0.43). Overall, fewer patients in 4-week group underwent bone surgery (22 vs 42; HR = 0.51; P =0.01). However, the two groups showed no significant difference in pain scores, performance status scores, incidence of jaw osteonecrosis, and kidney dysfunction. Although rates of skeletal morbidity were numerically identical in both groups, patients in the 12-week group had greater bone turnover, as indicated by higher C-terminal telopeptide levels. [21]

In general, adverse effects for bisphosphonates include bone, joint, or muscle pain, as well as nausea, vomiting, and diarrhea. Oral bisphosphonates pose a higher risk of heartburn and esophagitis than their intravenously administered counterparts.

Osteonecrosis of the jaw (ONJ), a particularly difficult and unpleasant adverse effect, has an incidence of 3% in bisphosphonate-treated breast cancer patients. Patients with underlying oral pathology (eg, previous radiation to the area, need for invasive oral procedures, poor dental hygiene) are at a higher risk of developing ONJ.

In September 2011, denosumab (Prolia) gained US Food and Drug Administration (FDA) approval to increase bone mass in women at high risk for fracture who are receiving adjuvant aromatase inhibitor therapy for breast cancer. Denosumab is a fully human monoclonal antibody that targets the receptor activator of the nuclear factor-kappa-B ligand (RANKL) protein, which acts as the primary signal to promote bone removal. By inhibiting the development and activity of osteoclasts, denosumab decreases bone resorption and increases bone density. A dose of 60 mg SC is administered once every 6 months.

FDA approval was based on a 2-year, double-blind, placebo-controlled study of 252 postmenopausal women with breast cancer receiving aromatase inhibitor therapy. Bone mineral density (BMD) was higher at 1 year in the lumbar spine in those treated with denosumab (+4.8%) compared with placebo (-0.7%). The treatment difference was 5.5% (95% confidence interval [CI], 4.8-6.3%; P<0.0001). After 2 years, differences in BMD favoring denosumab were 7.6% in the lumbar spine, 4.7% in the (total) hip, and 3.6% in the femoral neck. [22]

Current American Society of Clinical Oncology (ASCO) guidelines recommend denosumab (Xgeva) at 120 mg SC every 4 weeks as an option for patients with breast cancer and evidence of bone metastases. [23]

Melville N. Risedronate for Bone Loss With Breast-Cancer Treatment. Available at http://www.medscape.com/viewarticle/812228. Accessed: October 21, 2013.

Wong MH, Stockler MR, Pavlakis N. Bisphosphonates and other bone agents for breast cancer. Cochrane Database Syst Rev. 2012 Feb 15. CD003474. [Medline].

Lipton A, Chapman JA, Demers L, et al. Elevated bone turnover predicts for bone metastasis in postmenopausal breast cancer: results of NCIC CTG MA.14. J Clin Oncol. 2011 Sep 20. 29(27):3605-10. [Medline].

Reeder JG, Brufsky AM. The role of bisphosphonates in the adjuvant setting for breast cancer. Oncology (Williston Park). 2010 May. 24(6):462-7, 475. [Medline].

Early Breast Cancer Trialists’ Collaborative Group (EBCTCG). Adjuvant bisphosphonate treatment in early breast cancer: meta-analyses of individual patient data from randomised trials. Lancet. 2015 Jul 23. [Medline]. [Full Text].

Peppone LJ, Huston AJ, Reid ME, et al. The effect of various vitamin D supplementation regimens in breast cancer patients. Breast Cancer Res Treat. 2011 May. 127(1):171-7. [Medline]. [Full Text].

Rastelli AL, Taylor ME, Gao F, et al. Vitamin D and aromatase inhibitor-induced musculoskeletal symptoms (AIMSS): a phase II, double-blind, placebo-controlled, randomized trial. Breast Cancer Res Treat. 2011 Aug. 129(1):107-16. [Medline].

Powles T, Paterson A, McCloskey E, Schein P, Scheffler B, Tidy A, et al. Reduction in bone relapse and improved survival with oral clodronate for adjuvant treatment of operable breast cancer [ISRCTN83688026]. Breast Cancer Res. 2006. 8(2):R13. [Medline]. [Full Text].

Saad F, Adachi JD, Brown JP, Canning LA, Gelmon KA, Josse RG, et al. Cancer treatment-induced bone loss in breast and prostate cancer. J Clin Oncol. Nov 20 2008. 26(33):5465-76.

Winters-Stone KM, Dobek J, Nail L, et al. Strength training stops bone loss and builds muscle in postmenopausal breast cancer survivors: a randomized, controlled trial. Breast Cancer Res Treat. 2011 Jun. 127(2):447-56. [Medline]. [Full Text].

Markopoulos C, Tzoracoleftherakis E, Polychronis A, Venizelos B, Dafni U, Xepapadakis G, et al. Management of anastrozole-induced bone loss in breast cancer patients with oral risedronate: results from the ARBI prospective clinical trial. Breast Cancer Res. 2010. 12(2):R24. [Medline]. [Full Text].

Rack B, Jückstock J, Genss EM, Schoberth A, Schindlbeck C, Strobl B, et al. Effect of zoledronate on persisting isolated tumour cells in patients with early breast cancer. Anticancer Res. 2010 May. 30(5):1807-13. [Medline].

Aft R, Naughton M, Trinkaus K, Watson M, Ylagan L, Chavez-MacGregor M, et al. Effect of zoledronic acid on disseminated tumour cells in women with locally advanced breast cancer: an open label, randomised, phase 2 trial. Lancet Oncol. 2010 May. 11(5):421-8. [Medline].

Coleman R, Woodward E, Brown J, et al. Safety of zoledronic acid and incidence of osteonecrosis of the jaw (ONJ) during adjuvant therapy in a randomised phase III trial (AZURE: BIG 01-04) for women with stage II/III breast cancer. Breast Cancer Res Treat. 2011 Jun. 127(2):429-38. [Medline].

Hatoum HT, Lin SJ, Smith MR, Guo A, Lipton A. Treatment persistence with monthly zoledronic acid is associated with lower risk and frequency of skeletal complications in patients with breast cancer and bone metastasis. Clin Breast Cancer. 2011 Jun. 11(3):177-83. [Medline].

Scarpa R, Atteno M, Peluso R, et al. Rheumatic complaints in women taking aromatase inhibitors for treatment of hormone-dependent breast cancer. J Clin Rheumatol. 2011 Jun. 17(4):169-72. [Medline].

[Guideline] Dhesy-Thind S, Fletcher GG, Blanchette PS, Clemons MJ, Dillmon MS, et al. Use of Adjuvant Bisphosphonates and Other Bone-Modifying Agents in Breast Cancer: A Cancer Care Ontario and American Society of Clinical Oncology Clinical Practice Guideline. J Clin Oncol. Published online before print March 6, 2017. [Full Text].

Jenkins K. ASCO Guidelines on Adjuvant Bisphosphonates in Breast Cancer. Medscape Medical News. Available at http://www.medscape.com/viewarticle/877252. March 15, 2017; Accessed: March 17, 2017.

Zoledronic Acid in Treating Patients With Metastatic Breast Cancer, Metastatic Prostate Cancer, or Multiple Myeloma With Bone Involvement. ClinicalTrials.gov. Available at https://clinicaltrials.gov/show/NCT00869206. October 4, 2016; Accessed: April 13, 2017.

Amadori D, Aglietta M, Alessi B, Gianni L, Ibrahim T, Farina G, et al. Efficacy and safety of 12-weekly versus 4-weekly zoledronic acid for prolonged treatment of patients with bone metastases from breast cancer (ZOOM): a phase 3, open-label, randomised, non-inferiority trial. Lancet Oncol. 2013 Jun. 14 (7):663-70. [Medline].

Himelstein AL, Foster JC, Khatcheressian JL, Roberts JD, Seisler DK, Novotny PJ, et al. Effect of Longer-Interval vs Standard Dosing of Zoledronic Acid on Skeletal Events in Patients With Bone Metastases: A Randomized Clinical Trial. JAMA. 2017 Jan 3. 317 (1):48-58. [Medline].

Muir VJ, Scott LJ. Denosumab: in cancer treatment-induced bone loss. BioDrugs. 2010 Dec 1. 24(6):379-86. [Medline].

Van Poznak CH, Temin S, Yee GC, Janjan NA, Barlow WE, Biermann JS, et al. American Society of Clinical Oncology executive summary of the clinical practice guideline update on the role of bone-modifying agents in metastatic breast cancer. J Clin Oncol. 2011 Mar 20. 29(9):1221-7. [Medline]. [Full Text].

Early Breast Trialist Collaborative Group (EBCTCG). Adjuvant bisphosphonate treatment in early breast cancer: met-analyses of individual patient data from randomized trials. Lancet. Oct 3 2015. 386:1553-1361.

Winston W Tan, MD, FACP Associate Professor of Medicine, Mayo Medical School; Consultant and Person-in-Charge of Genitourinary Oncology-Medical Oncology, Division of Hematology/Oncology, Department of Internal Medicine, Mayo Clinic Jacksonville; Vice Chairman of Education, Division of Hematology/Oncology, Mayo Clinic Florida

Winston W Tan, MD, FACP is a member of the following medical societies: American College of Physicians, American Society of Clinical Oncology, American Society of Hematology, Philippine Medical Association, Texas Medical Association

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

Marie Catherine Lee, MD, FACS Associate Professor, Department of Oncologic Sciences, Department of Surgery (Joint Appointment), University of South Florida Morsani College of Medicine; Associate Member, Comprehensive Breast Program, Moffitt McKinley Outpatient Center

Marie Catherine Lee, MD, FACS is a member of the following medical societies: American College of Surgeons, American Society of Clinical Oncology, Association for Academic Surgery, Association of Women Surgeons, Florida Society of Clinical Oncology, Society of Surgical Oncology, Society of University Surgeons

Disclosure: Received research grant from: National Cancer Institute/National Institutes of Health; Department of Defense.

Robert C Shepard, MD, FACP Associate Professor of Medicine in Hematology and Oncology at University of North Carolina at Chapel Hill; Vice President of Scientific Affairs, Therapeutic Expertise, Oncology, at PRA International

Robert C Shepard, MD, FACP is a member of the following medical societies: American Association for Cancer Research, American Association for Physician Leadership, European Society for Medical Oncology, Association of Clinical Research Professionals, American Federation for Clinical Research, Eastern Cooperative Oncology Group, Society for Immunotherapy of Cancer, American Medical Informatics Association, American College of Physicians, American Federation for Medical Research, American Medical Association, American Society of Hematology, Massachusetts Medical Society

Disclosure: Nothing to disclose.

Alison T Stopeck, MD Professor of Medicine, Arizona Cancer Center, University of Arizona Health Sciences Center; Director of Clinical Breast Cancer Program, Arizona Cancer Center; Medical Director of Coagulation Laboratory, University Medical Center; Director of Arizona Hemophilia and Thrombosis Center

Alison T Stopeck, MD is a member of the following medical societies: American Association for Cancer Research, American College of Physicians, American Society of Hematology, SWOG, American Society of Clinical Oncology, Hemophilia and Thrombosis Research Society

Disclosure: Received honoraria from Genentech for speaking and teaching; Received honoraria from AstraZeneca for speaking and teaching; Received grant/research funds from AstraZeneca for other.

Rachel Swart, MD, PhD Assistant Professor of Medicine, Department of Hematology and Oncology, Arizona Cancer Center, University of Arizona

Rachel Swart, MD, PhD is a member of the following medical societies: American Association for Cancer Research, Arizona Medical Association, SWOG, American Society of Clinical Oncology

Disclosure: Received grant/research funds from Roche for other.

Leona Downey, MD Assistant Professor of Internal Medicine, Section of Oncology and Hematology, University of Arizona, Arizona Cancer Center

Leona Downey, MD is a member of the following medical societies: American Geriatrics Society, SWOG, American Society of Clinical Oncology

Disclosure: Nothing to disclose.

Robert B Livingston, MD Professor of Clinical Medicine and Director, Clinical Research Shared Services, Arizona Cancer Center

Robert B Livingston, MD is a member of the following medical societies: American Association for Cancer Research, American Society of Clinical Oncology, American Federation for Clinical Research

Disclosure: Nothing to disclose.

Patricia A Thompson, PhD Assistant Professor, Department of Pathology, University of Arizona College of Medicine

Disclosure: Nothing to disclose.

Julie Lang, MD Associate Professor of Surgery, Norris Comprehensive Cancer Center, Keck School of Medicine of the University of Southern California

Julie Lang, MD is a member of the following medical societies: American College of Surgeons, American Society of Breast Surgeons, American Society of Clinical Oncology, Association for Academic Surgery, and Society of Surgical Oncology

Disclosure: Genomic Health, Grant/research funds, Speaking and teaching; Agendia, Grant/research funds, Speaking and teaching; Surgical Tools, Grant/research funds, Research; Sysmex, Grant/research funds, Research

Bone Health and Breast Cancer Management 

Research & References of Bone Health and Breast Cancer Management |A&C Accounting And Tax Services
Source

41 Replies to “Bone Health and Breast Cancer Management ”

  1. Pingback: viagra by mail
  2. Pingback: cialis coupons
  3. Pingback: new ed pills
  4. Pingback: impotence pills
  5. Pingback: ed pills
  6. Pingback: pharmacy online
  7. Pingback: levitra canada
  8. Pingback: levitra vardenafil
  9. Pingback: parx casino online
  10. Pingback: slot games
  11. Pingback: tadalafil 5mg
  12. Pingback: cash advance
  13. Pingback: pay day loans
  14. Pingback: cash loans
  15. Pingback: viagra pills
  16. Pingback: cialis buy
  17. Pingback: Casinos 2020
  18. Pingback: generic cialis
  19. Pingback: cialis 20
  20. Pingback: 5 mg cialis
  21. Pingback: 5 mg cialis
  22. Pingback: online casino
  23. Pingback: w
  24. Pingback: casino games
  25. Pingback: viagra samples
  26. Pingback: generic viagra
  27. Pingback: buy viagra canada
  28. Pingback: viagra samples
  29. Pingback: online viagra
  30. Pingback: casino slot games
  31. Pingback: gambling casino

Leave a Reply