Showing posts with label Denosumab. Show all posts
Showing posts with label Denosumab. Show all posts

Thursday, October 12, 2017

News from NAMS 2017: “Bisphosphonate drug holiday” not mandatory



A presentation at the North American Menopause Society (NAMS) Annual Meeting in Philadelphia October 11-14, will  present new evidence regarding long term safety and effectiveness of Bisphosphonates and denosumab in treating postmenopausal osteoporosis.

According to International Osteoporosis Foundation, Osteoporosis is estimated to affect 200 million women worldwide - approximately one-tenth of women aged 60, one-fifth of women aged 70, two-fifths of women aged 80 and two-thirds of women aged 90.

Bisphosphonates and denosumab are the most commonly prescribed treatments for osteoporosis. There is no cure for osteoporosis and the effects of these drugs wear-off as treatment ceases, hence prevention is the best bet.

As Bisphosphonates therapy is started, protection from osteoporosis is gained in first few months and persists as long as treatment is continued.

If Bisphosphonate treatment is continued beyond 3 years, increasing risk of unusual or “atypical” fractures of the femur (thigh bone) is observed. The risk increases gradually as patient continue to take the drug beyond 3 years: the risk is 20/100,000 patients at 5 years and 1/1,000 patients at 8-10 years.

If the drug is stopped, protection from fractures is lost gradually in 3-5 years.

This combination of increased risk of atypical fractures on continued treatment and decline in protection from fractures as treatment is stopped led to the confusing concept of a “bisphosphonate holiday.”

The American Society for Bone and Mineral Research (ASBMR) has recently provided clear recommendations about “bisphosphonate holidays.”

ASBMR recommends that, after 3-5 years of treatment with bisphosphonates, a patient risk of fracture should be evaluated. If the patient remains at ‘high risk’ for fracture because of low BMD, previous history of hip, spine, or multiple other fractures, the treatment should not be stopped.

Patient can continue the same treatment or change to some other drugs like denosumab.

Those patients who are at ‘low risk’ for fracture, the treatment can be stopped for 3-4 years, but it is not mandatory.

The concept of ‘drug holiday’ only holds good for Bisphosphonates only, and not for other drugs like raloxifene, teriparatide, and denosumab because beneficial effects of these drugs are lost as soon as they are stopped.

Dr. Michael McClung of the Oregon Osteoporosis Center in Portland, Oregon, who will be presenting his recommendations on long-term osteoporosis therapy at the NAMS Annual Meeting said, “Because protection from fractures disappears quickly if denosumab treatment is stopped, and since there are no currently known safety issues that limit the duration of denosumab therapy, there is no justification for a drug holiday with this treatment.”

“Just as we do not recommend stopping treatment for high blood pressure or diabetes, it is necessary to have a long-term treatment plan for postmenopausal women with osteoporosis if the benefits of our therapies are to be realized,” he further added.

Dr. JoAnn Pinkerton, NAMS executive director said, “Prevention of osteoporosis should be a goal for those treating menopausal women, as up to 20% of bone loss occurs within the first five years of menopause. Once diagnosed with osteoporosis, the goal becomes lowering the risk of fractures as fractures can be life changing or life limiting. This presentation will offer valuable insights about the need for long-term treatment and will change the way health care providers approach long-term osteoporosis management.”


Wednesday, September 21, 2016

Building strong bones with biologics- Romosozumab significantly decreases fracture risk in osteoporotic postmenopausal women.

Clinical Pearls:


  • Currently, no osteoanabolic treatment exists for osteoporosis, other than parathyroid hormone.
  • Romosozumab is the first humanized, osteoanabolic, anti-sclerostin monoclonal antibody which binds and inhibits sclerostin leading to increases in bone formation and decrease in bone reabsorption.
  • This regimen is a new approach in treating osteoporosis whereby patients received sequential anabolic therapy with two biologic agents-Romosozumab and Denosumab. 
  • One year of treatment with Romosozumab resulted in clinically significant lower risk of vertebral and clinical fractures in postmenopausal women and resulted in substantial gains in Bone Mineral Density (BMD) at the spine and hip. 

According to the statistics by International Osteoporosis Foundation (IOF) [1]It is estimated that osteoporosis affects 200 million women worldwide, affecting one tenth of women over the age of 60, one fifth over the age of 70, two-fifth over the age of 80 and nearly two-third over the age of 90.[2] 

Nearly 1 in 3 women over the age of 50 will suffer osteoporotic fractures during her life time. Fewer than 25% of patients suffering osteoporotic fractures receive treatment after the incidence and even among those who start the treatment, majority of the patients terminate it prematurely.

Currently, other than the parathyroid hormone analogs all treatments aimed at osteoporosis are antiresorptive. Researchers have spent resources on development of anabolic therapies, which led them to novel therapeutic approach in the treatment of osteoporosis - sclerostin inhibition. Sclerostin is secreted by osteocytes and acts by inhibiting Wnt signaling, thereby preventing osteoblast development and function.

Romosozumab is the first humanized, osteoanabolic, anti-sclerostin monoclonal antibody which binds and inhibits sclerostin leading to increases in bone formation and decrease in bone reabsorption.[3] 

The Fracture Study in Postmenopausal Women with Osteoporosis (FRAME) is an international, randomized, double-blind, placebo-controlled, parallel-group phase 3 trial. The landmark study aims to evaluate the effect of 1 year of Romosozumab (at a dose of 210 mg, administered subcutaneously monthly) on development of fractures in post-menopausal women with osteoporosis. The FRAME trial recruited 7180 postmenopausal women between 55 -90 years of age and they were randomized to receive either 210 mg of Romosozumab placebo once a month for 12 months.

The study findings were presented at the at the American Society for Bone and Mineral Research (ASBMR) 2016 Annual Meeting.[4] The results were also published simultaneously in The New England Journal of Medicine.[5]

After I year of therapy with the monoclonal antibody treatment, patient received 2 doses of denosumab 60 mg subcutaneously at an interval of 6months. This regimen is a new approach in treating osteoporosis whereby patients received sequential anabolic therapy with two biologic agents.

The results were statistically significant since the relative risk of new vertebral fractures was reduced by 75% and the relative risk of a clinical fracture by 36% through 12 months compared to those receiving placebo.

The study met the coprimary end points of reducing the cumulative incidence of new vertebral fractures at the end of 1 year and 24 months. By reducing the incidence of clinical fractures (vertebral and non-vertebral) at the end of 12 months’ secondary end point werealso met, however when only incidence of non-vertebral fractures was analyzed, the study was short of meeting the goal.

In the study Romosozumab did reduce non-vertebral fractures but the data was not statistically significant. This was explained due to the geographical location of the study population. Majority of the study subjects were from Latin America were the incidence of non-vertebral fracture is extremely low. When the analysis was conducted after excluding the Latin American cohort, Romosozumab led to a significant 42% reduction in the risk of nonvertebral fractures over 1 year compared with placebo patients.

The clinical benefits seen in trials were also supported by lab results of increase in bone-formation marker P1NP and decrease in bone-resorption marker β-CTX during the 12 months’ period of therapy.

Adverse events were reported in control as well as placebo groups equally. Hypersensitivity reactions were more common in the Romosozumab group along with single incidence of jaw bone necrosis and atypical femoral fracture.

In an accompanying editorial, Dr Rosen and Dr Ingelfinger quote "The long-term treatment of osteoporosis remains challenging, and Romosozumab may be one answer. More trials are needed before we can embrace a new approach."

The study received funding from Amgen and UCB Pharma as well as Dr Cosman received personal fees from Amgen and other pharma company. The editorial authors are employee of NEJM.  





[1] https://www.iofbonehealth.org/facts-statistics
[2] Kanis JA (2007) WHO Technical Report, University of Sheffield, UK: 66.
[3] http://www.ncbi.nlm.nih.gov/pubmed/24842796
[4] http://www.asbmr.org/meetings/annualmeeting.aspx
[5] http://www.nejm.org/doi/full/10.1056/NEJMoa1607948#t=article

Wednesday, June 22, 2016

Osteoporosis drug can prevent the development of breast cancer in women who are BRCA1 mutation carriers.

Individuals who carry a mutation in breast cancer susceptibility gene(BRCA1) are highly prone to develop breast cancer.  As compared to general population who have 8% chance of developing breast cancer, women who harbor this germline mutation have a 55-65% chance of developing breast cancer by the age 70.[1]

These women frequently undergo prophylactic risk reducing surgeries ( (bilateral prophylactic mastectomy and bilateral prophylactic salpingo-oophorectomy) to minimize the chances of developing breast cancer.[2]

Scientist around the world are long looking for chemoprevention to reduce the risk of cancer in BRCA1 mutation carriers. Currently Tamoxifen is in use for chemoprevention.  

 A recent paper published in Nature[3] offers a breakthrough for millions of next generation women with BRCA1 mutation carrier. Researchers are already considering it as ‘holy grail’ of breast cancer prevention.

Denosumab is a human monoclonal antibody for the treatment of osteoporosis. It is also a RANKL signaling inhibitor, RANKand RANK−  are two subsets of luminal progenitors present in the histological normal breast tissue of BRCA1 mutation carriers. RANK+ cells are highly proliferative, have grossly aberrant DNA repair and bear a molecular signature similar to that of basal-like breast cancer. Denosumab inhibited the RANKsignaling and stopped the progesterone induced proliferation of pre-neoplastic cells and also tissues from breast biopsies of BRCA1 mutation carriers. The same effect was also seen in mouse model of mammary tumorigenesis. Denosumab is already in use for treatment of osteoporosis and for patients with bone metastasis of breast cancer. 

Geoff Lindeman, a clinician-scientist at the Walter and Eliza Hall Institute and a co-author of the study said "Over the last few years, it has become increasingly clear from the work of several groups that RANK ligand, which switches on RANK, is an important regulator of cell growth in the breast. We have now been able to pinpoint the precise culprit cells and were very excited to see that they express the RANK protein."

As a part of pilot study three women were also treated with Denosumab and the results are encouraging days Dr. Lindeman.

Dr. Francisco Esteva (researcher at NYU Langone Medical Center and a part of the pilot study) and his colleagues are looking forward to conducting large scale clinical trials. "The new study does not change any management or clinical use of any drugs at this point, but it provides data that can be tested in a clinical trial," he said. "The data are compelling."

He also added that we are looking at least 10 years down the lane, but it offers hope for future generations of women.



[1]http://ww5.komen.org/BreastCancer/InheritedGeneticMutations.html
[2] http://www.cancer.gov/about-cancer/causes-prevention/genetics/brca-fact-sheet