Skip to main navigation Skip to search Skip to main content

Preliminary results of the combination of bevacizumab and weekly paclitaxel in advanced melanoma

  • M. González-Cao
  • , S. Viteri
  • , A. Díaz-Lagares
  • , A. González
  • , P. Redondo
  • , Y. Nieto
  • , J. Espinós
  • , A. Chopitea
  • , M. Ponz
  • , S. Martín-Algarra

Research output: Contribution to journal › Article › peer-review

Abstract

Background: Pretreated advanced melanoma is a poor prognosis scenario with few, if any, active therapeutic options. The antibody against vascular endothelial growth factor, bevacizumab, has demonstrated increased activity in combination with chemotherapy in many tumors. We intended to evaluate the activity of the combination of weekly paclitaxel and bevacizumab in previously treated metastatic melanoma. Patients and Methods: Patients with previously treated metastatic melanoma received paclitaxel 70 mg/m2 weekly and bevacizumab 10 mg/kg biweekly for 5 consecutive weeks every 6 weeks. Results: Twelve patients were treated. Two patients (16.6%) achieved a partial response and 7 patients (58.3%) stable disease. Responses were seen in soft tissue, lung and brain metastases. Median disease-free and overall survival times were 3.7 and 7.8 months, respectively. Treatment was well tolerated. Main toxicities were grade 3 asymptomatic lymphopenia in 6 patients, grade 3 leucopenia in 2 patients, and grade 3 thrombocytopenia in 1 patient. Conclusions: Our preliminary results suggest that the combination of bevacizumab and weekly paclitaxel is active and safe in patients with metastatic melanoma, warranting further investigation.

Original languageEnglish (US)
Pages (from-to)12-16
Number of pages5
JournalOncology (Switzerland)
Volume74
Issue number1-2
DOIs
StatePublished - Jun 2008

Keywords

  • Bevacizumab
  • Melanoma
  • Paclitaxel

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'Preliminary results of the combination of bevacizumab and weekly paclitaxel in advanced melanoma'. Together they form a unique fingerprint.

Cite this