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Objective tumor response to denosumab in patients with giant cell tumor of bone: a multicenter phase II trial.
Ueda, T; Morioka, H; Nishida, Y; Kakunaga, S; Tsuchiya, H; Matsumoto, Y; Asami, Y; Inoue, T; Yoneda, T.
Afiliação
  • Ueda T; Department of Orthopaedic Surgery, Osaka National Hospital, Osaka uedat@onh.go.jp.
  • Morioka H; Department of Orthopaedic Surgery, School of Medicine, Keio University, Tokyo.
  • Nishida Y; Department of Orthopaedic Surgery, Nagoya University Graduate School of Medicine, Nagoya.
  • Kakunaga S; Department of Orthopaedic Surgery, Osaka National Hospital, Osaka.
  • Tsuchiya H; Department of Orthopaedic Surgery, Graduate School of Medical Science, Kanazawa University, Kanazawa.
  • Matsumoto Y; Department of Orthopaedic Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka.
  • Asami Y; Daiichi Sankyo Co., Ltd, Tokyo, Japan.
  • Inoue T; Daiichi Sankyo Co., Ltd, Tokyo, Japan.
  • Yoneda T; Division of Hematology/Oncology, Indiana University School of Medicine, Indianapolis, USA.
Ann Oncol ; 26(10): 2149-54, 2015 Oct.
Article em En | MEDLINE | ID: mdl-26205395
ABSTRACT

BACKGROUND:

Giant cell tumor of bone (GCTB) is a rare primary bone tumor, characterized by osteoclast-like giant cells that express receptor activator of nuclear factor-kappa B (RANK), and stromal cells that express RANK ligand (RANKL), a key mediator of osteoclast activation. A RANKL-specific inhibitor, denosumab, was predicted to reduce osteolysis and control disease progression in patients with GCTB. PATIENTS AND

METHODS:

Seventeen patients with GCTB were enrolled. Patients were treated with denosumab at 120 mg every 4 weeks, with a loading dose of 120 mg on days 8 and 15. To evaluate efficacy, objective tumor response was evaluated prospectively by an independent imaging facility on the basis of prespecified criteria.

RESULTS:

The proportion of patients with an objective tumor response was 88% based on best response using any tumor response criteria. The proportion of patients with an objective tumor response using individual response criteria was 35% based on the modified Response Evaluation Criteria in Solid Tumors (RECIST) criteria, 82% based on the modified European Organization for Research and Treatment of Cancer (EORTC) criteria, and 71% based on inverse Choi criteria. The median time of study treatment was 13.1 months.

CONCLUSION:

The findings demonstrate that denosumab has robust clinical efficacy in the treatment of GCTB.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Tumor de Células Gigantes do Osso / Conservadores da Densidade Óssea / Denosumab / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ósseas / Tumor de Células Gigantes do Osso / Conservadores da Densidade Óssea / Denosumab / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Assunto da revista: NEOPLASIAS Ano de publicação: 2015 Tipo de documento: Article