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Eur J Cancer ; 76: 118-124, 2017 05.
Article in English | MEDLINE | ID: mdl-28324746

ABSTRACT

BACKGROUND: Giant-cell tumours of bone (GCTB) are RANK/RANK-ligand (RANKL) positive, aggressive and progressive osteolytic tumours. Denosumab, a RANKL inhibitor, was FDA-approved for adults and skeletally mature adolescents with unresectable GCTB or when surgical resection is likely to result in severe morbidity. Data on long-term toxicity and activity of denosumab monthly 'GCTB-schedule' (120 mg per 12/year, 1440 mg total dose/year) are lacking. METHODS: Patients with GCTB receiving denosumab, 120 mg on days 1, 8, 15, 29 and every 4 weeks thereafter, from 2006 to 2015 treated in two centres were included. Long-term toxicity was evaluated. RESULTS: Ninety-seven patients were identified. 43 patients underwent resection of the tumour with a median time on denosumab treatment of 12 months (range 6-45 months). Fifty-four patients had unresectable GCTB's (male/female 23/31, median age 35 years [range: 13-76 years], 26% presented with lung metastases, 31% had primary tumor located to the spine, 63% were relapsed after previous surgery) with a median time on denosumab of 54 months (9-115 months). In the unresectable GCTB group, tumour control and clinical benefits were observed in all patients undergoing denosumab, whereas 40% of patients discontinuing denosumab had tumour progression after a median of 8 months (range 7-15 months). ADVERSE EVENTS: Overall, six (6%) patients developed osteonecrosis of jaw (ONJ): 1/43 (2%) in the resectable group, 5/54 (9%) in the unresectable group, with a 5-year ONJ-free survival of 92% (95% CI 84-100). Only patients with prolonged treatment experienced mild peripheral neuropathy (6/54, 11%), skin rash (5/54, 9%), hypophosphataemia (2/54, 4%) and atypical femoral fracture (2/54, 4%). CONCLUSIONS: Prolonged treatment with denosumab has sustained activity in GCTB, with a mild toxicity profile. The dose-dependent toxicity observed recommends a careful and strict monitoring of patients who need prolonged treatment. Decreased dose-intensity schedules should be further explored in unresectable GCTB.


Subject(s)
Bone Density Conservation Agents/administration & dosage , Bone Neoplasms/drug therapy , Denosumab/administration & dosage , Giant Cell Tumor of Bone/drug therapy , Lung Neoplasms/drug therapy , Adolescent , Adult , Aged , Bisphosphonate-Associated Osteonecrosis of the Jaw/epidemiology , Bisphosphonate-Associated Osteonecrosis of the Jaw/etiology , Bone Neoplasms/diagnostic imaging , Bone Neoplasms/pathology , Cohort Studies , Disease Progression , Dose-Response Relationship, Drug , Female , Femoral Neoplasms/drug therapy , Femoral Neoplasms/pathology , Giant Cell Tumor of Bone/diagnostic imaging , Giant Cell Tumor of Bone/secondary , Humans , Ischium , Lung Neoplasms/diagnostic imaging , Lung Neoplasms/secondary , Male , Middle Aged , Radius/diagnostic imaging , Retrospective Studies , Sacrum , Skull Neoplasms/drug therapy , Skull Neoplasms/pathology , Spinal Neoplasms/drug therapy , Spinal Neoplasms/pathology , Tibia , Time Factors , Young Adult
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