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Possible survival benefits from zoledronic acid treatment in patients with bone metastases from solid tumours and poor prognostic features-An exploratory analysis of placebo-controlled trials.
Coleman, Robert E; Lipton, Allan; Costa, Luis; Cook, Richard J; Lee, Ker-Ai; Saad, Fred; Brown, Janet E; Terpos, Evangelos; Major, Pierre P; Kohno, Norio; Smith, Matthew; Body, Jean-Jacques.
Afiliación
  • Coleman RE; Department of Oncology, Cancer Clinical Trials Centre, University of Sheffield, Weston Park Hospital, Cancer Research Centre, Sheffield, UK.
  • Lipton A; College of Medicine, Penn State Milton S. Hershey Medical Center, Hershey, PA, USA.
  • Costa L; Clinical and Translational Oncology Research Unit, Instituto de Medicina Molecular, Lisbon, Portugal.
  • Cook RJ; Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada.
  • Lee KA; Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada.
  • Saad F; Division of Urology, Centre Hospitalier de l'Université de Montréal, Hôpital Notre-Dame, Montréal, QC, Canada.
  • Brown JE; Department of Oncology, Cancer Clinical Trials Centre, University of Sheffield, Weston Park Hospital, Cancer Research Centre, Sheffield, UK; Department of Oncology and Clinical Research, Cancer Research UK Centre, St James's Hospital, Leeds, UK.
  • Terpos E; Department of Clinical Therapeutics, University of Athens School of Medicine, Athens, Greece.
  • Major PP; Department of Oncology, Division of Medical Oncology, McMaster University, Juravinski Cancer Centre, Hamilton, ON, Canada.
  • Kohno N; Division of Breast Oncology, Tokyo Medical University, Tokyo, Japan.
  • Smith M; Genitourinary Malignancies Program, Massachusetts General Hospital Cancer Center, Boston, MA, USA.
  • Body JJ; Department of Medicine, University Hospital Brugmann, ULB, Brussels, Belgium.
J Bone Oncol ; 2(2): 70-6, 2013 Jun.
Article en En | MEDLINE | ID: mdl-26909273
ABSTRACT

BACKGROUND:

Zoledronic acid (ZOL) is an important component of therapy for patients with metastatic bone disease (MBD) to reduce the risk of skeletal-related events (SREs). We evaluated overall survival (OS) in patients with MBD secondary to solid tumours included in placebocontrolled ZOL trials. PATIENTS AND

METHODS:

Exploratory analyses were performed using databases from three randomised trials of ZOL versus placebo. 1126 patients (ZOL, n=731; placebo, n=395) with complete baseline data for 18 predefined parameters were evaluated for OS. Relative risks (RRs) with 95% confidence intervals were assessed using stratified and adjusted Cox regression models. Baseline covariates defining patient populations with significantly different effects of ZOL treatment on OS (identified by stepwise backward elimination) were included in multivariate models.

RESULTS:

Although OS was similar between the overall treatment groups, ZOL significantly improved OS in the subset of patients (n=423; 38%) with elevated baseline NTX (≥100 nmol/mmol creatinine; RR, 0.692; P=.0028). Notably, this effect was independent of SRE prevention. Additional covariates associated with OS benefits with ZOL (e.g., low albumin, SRE history, elevated lactate dehydrogenase, shorter cancer duration) were characteristic of advanced disease.

CONCLUSION:

These exploratory analyses suggest a beneficial effect of ZOL on OS in patients with highly aggressive or advanced MBD.
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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Bone Oncol Año: 2013 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Clinical_trials / Prognostic_studies Idioma: En Revista: J Bone Oncol Año: 2013 Tipo del documento: Article País de afiliación: Reino Unido