ZOMETA® - For Breast Cancer Is Supported By NCCN and ASCO Guidelines
ZOMETA - Zoledronic AcidZOMETA - Zoledronic Acid Novartis Oncology
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metastases and the ZOMETA
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Learn more about the ZOMETA(zoledronic acid) mechanism of action

 
ZOMETA European Summary of Product Characteristics
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About ZOMETA: Breast Cancer About ZOMETA: defend against SREs across a broad range of tumour types

Threat of SREs What are SREs? ZOMETA reduces SREs Dose ZOMETA every 3 to 4 weeks References
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NCCN and ASCO guidelines support the use of ZOMETA®

National Comprehensive Cancer Network (NCCN) guidelines17

  • ZOMETA or pamidronate should be given (with calcium and vitamin D) to patients with bone metastases with expected survival > 3 months and creatinine <3.0 mg/dL

American Society of Clinical Oncology (ASCO) guidelines18


  • Initiation of therapy

    • — In patients with evidence of bone destruction, IV ZOMETA 4 mg or
      pamidronate 90 mg is recommended
    • — Starting bisphosphonates in women without evidence of bone destruction is
      not recommended
    • — Bone pain should not be a factor

  • Duration of therapy

    • — The optimal duration of treatment is not known
    • — "...once initiated, intravenous bisphosphonates [should] be continued until evidence of substantial decline in a patient's general performance status"

ZOMETA is proven in clinical trials to delay and reduce SREs in breast cancer through 25 months7



Achieve maximum efficacy—dose with ZOMETA 4 mg every 3 to 4 weeks





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