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1

&NA;. "Denosumab." Reactions Weekly &NA;, no. 1358 (July 2011): 15. http://dx.doi.org/10.2165/00128415-201113580-00056.

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Tolman, Cae. "Denosumab." Australian Prescriber 34 (June 1, 2011): 63–66. http://dx.doi.org/10.18773/austprescr.2011.037.

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&NA;. "Denosumab." Reactions Weekly &NA;, no. 1415 (August 2012): 19. http://dx.doi.org/10.2165/00128415-201214150-00067.

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&NA;. "Denosumab." Reactions Weekly &NA;, no. 1416 (August 2012): 20. http://dx.doi.org/10.2165/00128415-201214160-00064.

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TIKOO, DEEPIKA, and GUPTA MEENAKSHI. "DENOSUMAB:." Professional Medical Journal 19, no. 02 (February 22, 2012): 141–44. http://dx.doi.org/10.29309/tpmj/2012.19.02.2027.

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Osteoporosis is the most common metabolic bone disease in developed countries. One of its major problems is the long termmorbidity and poor quality of life of patients. Receptor activator of nuclear factor-kB, its ligand and osteoprotegrin pathway plays an importantrole in bone remodeling. Receptor activator of nuclear factor-kB interacts with receptor activator of nuclear factor-kB ligand leading to activationof osteoclasts. Denosumab, a fully monoclonal antibody to receptor activator of nuclear factor-kB ligand prevents its binding to receptoractivator of nuclear factor-kB and can effectively suppress the bone loss in osteoporosis. Various clinical studies have shown that Denosumabhas good efficacy in decreasing bone resorption and has a favourable safety profile also.
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6

Moen, Marit D., and Susan J. Keam. "Denosumab." Drugs & Aging 28, no. 1 (January 2011): 63–82. http://dx.doi.org/10.2165/11203300-000000000-00000.

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7

Muir, Victoria J., and Lesley J. Scott. "Denosumab." BioDrugs 24, no. 6 (December 2010): 379–86. http://dx.doi.org/10.2165/11203310-000000000-00000.

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8

Scott, Lesley J., and Victoria J. Muir. "Denosumab." Drugs 71, no. 8 (May 2011): 1059–69. http://dx.doi.org/10.2165/11207370-000000000-00000.

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Dubois, Eline A., Robert Rissmann, and Adam F. Cohen. "Denosumab." British Journal of Clinical Pharmacology 71, no. 6 (May 12, 2011): 804–6. http://dx.doi.org/10.1111/j.1365-2125.2011.03969.x.

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&NA;. "Denosumab." Reactions Weekly &NA;, no. 1306 (June 2010): 19. http://dx.doi.org/10.2165/00128415-201013060-00062.

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Cada, Dennis J., Terri L. Levien, and Danial E. Baker. "Denosumab." Hospital Pharmacy 45, no. 10 (October 2010): 785–96. http://dx.doi.org/10.1310/hpj4510-785.

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12

Rizzoli, René, Uma Yasothan, and Peter Kirkpatrick. "Denosumab." Nature Reviews Drug Discovery 9, no. 8 (August 2010): 591–92. http://dx.doi.org/10.1038/nrd3244.

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13

Grimer, R. J. "Denosumab." Bone & Joint 360 2, no. 5 (October 2013): 43–44. http://dx.doi.org/10.1302/2048-0105.25.360183.

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14

Lipton, Allan, and Ira Jacobs. "Denosumab." Current Opinion in Supportive and Palliative Care 5, no. 3 (September 2011): 258–64. http://dx.doi.org/10.1097/spc.0b013e328349731c.

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15

Pfeiffer, Naomi. "Denosumab." Oncology Times 3, no. 1 (January 2006): 18. http://dx.doi.org/10.1097/01434893-200601000-00015.

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16

Wilcock, Andrew, Sarah Charlesworth, Claire Stark Toller, Rahul Girish, Mary Mihalyo, and Paul Howard. "Denosumab." Journal of Pain and Symptom Management 56, no. 2 (August 2018): 295–301. http://dx.doi.org/10.1016/j.jpainsymman.2018.05.021.

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17

Rogol, Elizaveta V., Scott Jun, Cory J. Broehm, and Jessica Belmonte. "Aggressive Central Giant Cell Granuloma of the Jaw and Adjuvant Denosumab Therapy: Decreased Morbidity and Preserved Function in a 3 Patient Case Series." FACE, September 7, 2022, 273250162211213. http://dx.doi.org/10.1177/27325016221121356.

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We show the benefits of denosumab as adjuvant treatment of gnathic central giant cell granulomas (CGCGs) in 3 female patients, ages 18 to 65. This case series contributes to the growing experience in the medical therapy of these aggressive lesions, and demonstrates denosumab’s potential to decrease surgical morbidity. Central giant cell lesions of the jaw can be locally aggressive and thereby result in severe tissue destruction. Several medications have been evaluated as adjuvant therapy for CGCGs, with investigation of denosumab being the most recent. Our goal was to definitively treat patients with large CGCGs while minimizing unnecessary tissue and function loss. All 3 patients were offered adjuvant therapy with denosumab, since surgical resection alone would have resulted in large segmental defects requiring jaw reconstruction with free tissue transfer. Treatment instead consisted of lesion curettage and adjuvant denosumab therapy. The denosumab treatment protocol we used was based on what is currently recommended for unresectable giant cell tumors of bone (GCTB). Patients have been monitored for 40 months with clinical and radiographic exams, and 2 of them have also had histological evaluation following initiation of denosumab treatment. The 3 patients improved subjectively after the first few denosumab injections and had objective clinical and radiographic improvement after less than 6 months of therapy. Medication treatment length ranged from 10 to 15 months. Radiographic exams showed cortical thickening, resolution of cortical perforations, and calcification within a previously radiolucent region. Our findings are consistent with previous reports, and further support for the use of denosumab in locally aggressive central giant cell lesions. Our patients have thus far avoided large segmental resections, temporomandibular joint disarticulation, and sensory loss which would have resulted from surgical treatment alone. These 3 cases show that denosumab can be effective as adjuvant therapy in the treatment of aggressive gnathic CGCGs.
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18

"Denosumab." Reactions Weekly 1838, no. 1 (January 2021): 178. http://dx.doi.org/10.1007/s40278-021-89497-y.

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"Denosumab." Reactions Weekly 1838, no. 1 (January 2021): 180. http://dx.doi.org/10.1007/s40278-021-89499-y.

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"Denosumab." Reactions Weekly 1840, no. 1 (January 2021): 147. http://dx.doi.org/10.1007/s40278-021-90290-z.

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"Denosumab." Reactions Weekly 1837, no. 1 (January 2021): 206. http://dx.doi.org/10.1007/s40278-021-88805-2.

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"Denosumab." Reactions Weekly 1837, no. 1 (January 2021): 205. http://dx.doi.org/10.1007/s40278-021-88804-2.

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"Denosumab." Reactions Weekly 1850, no. 1 (April 2021): 114. http://dx.doi.org/10.1007/s40278-021-93919-x.

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"Denosumab." Reactions Weekly 1851, no. 1 (April 2021): 130. http://dx.doi.org/10.1007/s40278-021-94220-7.

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"Denosumab." Reactions Weekly 1851, no. 1 (April 2021): 131. http://dx.doi.org/10.1007/s40278-021-94221-7.

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"Denosumab." Reactions Weekly 1856, no. 1 (May 2021): 170. http://dx.doi.org/10.1007/s40278-021-96163-z.

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"Denosumab." Reactions Weekly 1857, no. 1 (May 2021): 130. http://dx.doi.org/10.1007/s40278-021-96515-9.

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"Denosumab." Reactions Weekly 1848, no. 1 (March 2021): 154. http://dx.doi.org/10.1007/s40278-021-93156-9.

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"Denosumab." Reactions Weekly 1846, no. 1 (March 2021): 101. http://dx.doi.org/10.1007/s40278-021-92349-9.

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"Denosumab." Reactions Weekly 1852, no. 1 (April 2021): 162. http://dx.doi.org/10.1007/s40278-021-94615-0.

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"Denosumab." Reactions Weekly 1852, no. 1 (April 2021): 163. http://dx.doi.org/10.1007/s40278-021-94616-0.

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32

"Denosumab." Reactions Weekly 1913, no. 1 (July 2022): 175. http://dx.doi.org/10.1007/s40278-022-18325-7.

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"Denosumab." Reactions Weekly 1913, no. 1 (July 2022): 176. http://dx.doi.org/10.1007/s40278-022-18326-7.

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"Denosumab." Reactions Weekly 1915, no. 1 (July 2022): 163. http://dx.doi.org/10.1007/s40278-022-19192-1.

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"Denosumab." Reactions Weekly 1919, no. 1 (August 13, 2022): 221. http://dx.doi.org/10.1007/s40278-022-21163-y.

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"Denosumab." Reactions Weekly 1919, no. 1 (August 13, 2022): 222. http://dx.doi.org/10.1007/s40278-022-21164-y.

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"Denosumab." Reactions Weekly 1916, no. 1 (July 2022): 173. http://dx.doi.org/10.1007/s40278-022-19632-x.

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"Denosumab." Reactions Weekly 1916, no. 1 (July 2022): 172. http://dx.doi.org/10.1007/s40278-022-19631-x.

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"Denosumab." Reactions Weekly 1916, no. 1 (July 2022): 174. http://dx.doi.org/10.1007/s40278-022-19633-x.

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"Denosumab." Reactions Weekly 1917, no. 1 (July 2022): 217. http://dx.doi.org/10.1007/s40278-022-20088-1.

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"Denosumab." Reactions Weekly 1921, no. 1 (August 27, 2022): 112. http://dx.doi.org/10.1007/s40278-022-22106-1.

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42

"Denosumab." Reactions Weekly 1925, no. 1 (September 24, 2022): 206. http://dx.doi.org/10.1007/s40278-022-23983-0.

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"Denosumab." Reactions Weekly 1907, no. 1 (May 2022): 169. http://dx.doi.org/10.1007/s40278-022-15428-1.

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"Denosumab." Reactions Weekly 1927, no. 1 (October 8, 2022): 214. http://dx.doi.org/10.1007/s40278-022-24950-0.

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"Denosumab." Reactions Weekly 1924, no. 1 (September 17, 2022): 181. http://dx.doi.org/10.1007/s40278-022-23534-0.

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"Denosumab." Reactions Weekly 1924, no. 1 (September 17, 2022): 184. http://dx.doi.org/10.1007/s40278-022-23537-0.

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"Denosumab." Reactions Weekly 1924, no. 1 (September 17, 2022): 182. http://dx.doi.org/10.1007/s40278-022-23535-0.

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"Denosumab." Reactions Weekly 1924, no. 1 (September 17, 2022): 183. http://dx.doi.org/10.1007/s40278-022-23536-0.

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"Denosumab." Reactions Weekly 1923, no. 1 (September 10, 2022): 178. http://dx.doi.org/10.1007/s40278-022-23041-9.

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"Denosumab." Reactions Weekly 1923, no. 1 (September 10, 2022): 179. http://dx.doi.org/10.1007/s40278-022-23042-9.

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