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AB0914 (2020)
BONE LOSS AND NEW FRACTURES WITH DENOSUMAB TREATMENT
C. Sanguesa1, I. Casafont-Solé1, A. Nack1, S. Holgado Pérez1, M. Martínez-Morillo1, M. Aparicio Rovira1, Á. Prior-Español1, M. Aparicio Espinar1, A. Riveros1, L. Mateo1, A. Olive1, L. Gifre1
1Germans Trias i Pujol University Hospital, Rheumatology, Badalona, Spain

Background: The incidence and factors related to an inadequate response to denosumab (Dmab) treatment remain unclear.


Objectives: To describe clinical, analytical and densitometric characteristics of patients with inadequate response (IR) to Dmab in clinical practice. IR was defined as the presence of a new fracture [fxs-IR] or a significant decrease in BMD (≥5% lumbar or ≥4% femoral) [BMD-IR].


Methods: retrospective study of patients with IR to Dmab treatment. Data of demographic variables, risk factors for osteoporosis, history of fractures, previous anti-osteoporotic treatment, densitometric and analytical parameters were collected before and after IR.


Results: 22 patients were included (19W:3M) with mean age of 75±10years. The causes of osteoporosis were: postmenopausal (50%), induced by glucocorticoids (22.7%), alcoholic (9.09%) and multifactorial (18.8%). Most patients were previously treated with bisphosphonates (59.09%, duration 5.2±2.6y) and had previous vertebral fractures (54.54% %, median 3).

During Dmab treatment, 10 patients presented a BMD-IR (with a mean bone loss up to -3.5% at femur and -5.8% at lumbar spine) and 12 had fxs-IR (vertebral [n=8], humerus [n=1], pelvis [n=1], tibia [n=1]). No significant differences were observed in duration of Dmab between both IR groups (Fxs-IR: 3,2±1,9 vs BMD-IR: 2,4 ± 1,2y). In the BMD-IR, the BMD loss was higher at lumbar spine than at total hip (-6.6%±3.7 vs -1.9%±4.8). Only 1 patient of the fxs-IR had a secondary cause of IR (mieloma multiple).

In the fxs-IR group, most patients started combined treatment with teriparatide (n=4), 1 changed to teriparatide and 7 remained with Dmab. In the BMD-IR group, most mantained Dmab treatment (n=8) and 2 switched to zoledronate.


Conclusion: Most patients who developed IR to Dmab had been previously treated with bisphosphonates and had previous fragility fractures and appears within the first 3 years of treatment. BMD loss seems to be more marked at spine than total hip. Only one patient had a secundary cause of IR.


Disclosure of Interests: None declared


Citation: Ann Rheum Dis, volume 79, supplement 1, year 2020, page 1754
Session: Osteoporosis (Abstracts Accepted for Publication)