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Update on novel therapeutic agents for cervical cancer. | LitMetric

AI Article Synopsis

  • Effective treatment options for advanced cervical cancer are limited, with cisplatin-based chemotherapy showing low success rates and poor survival outcomes.
  • Increased interest in targeted therapies has emerged due to a deeper understanding of tumor cell molecular changes, leading to new treatment possibilities.
  • Promising targets for therapy include EGFR and VEGF, with monoclonal antibodies and receptor tyrosine kinase inhibitors under clinical evaluation for their effectiveness in treating cervical cancer.

Article Abstract

Effective cytotoxic treatment options for advanced cervical cancer are exceedingly limited. Cisplatin-based combination chemotherapy, the most commonly used cytotoxic therapy, has produced response rates ranging from 20% to 30% and overall survival of less than 10 months. Because of the minimal degree of success with cytotoxic therapies and the poor prognosis of patients with this disease, interest has increased in targeted therapeutics for the treatment of cervical cancer. In recent years, significant improvements in our understanding of the altered molecular events in tumor cells have led to the discovery of new targets and agents for clinical testing. Two of these promising targets are epidermal growth factor receptor (EGFR) and the vascular endothelial growth factor (VEGF) signaling pathway, which play critical roles in tumor growth and angiogenesis. Two monoclonal antibodies, cetuximab, which targets EGFR, and bevacizumab, which target the VEGF signaling pathway, are being evaluated as monotherapy and in combination with other agents and/or radiotherapy for the treatment of cervical cancer. In addition, VEGF receptor tyrosine kinase inhibitors, such as sorafenib and pazopanib, are being studied in phase I/II clinical trials. In this review, we discuss potential molecular targets and novel therapeutic strategies that are being investigated for the treatment of cervical cancer.

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Source
http://dx.doi.org/10.1016/j.ygyno.2008.04.016DOI Listing

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