Does body mass index affect progression-free or overall survival in patients with ovarian cancer? Results from SCOTROC I trial

Ann Oncol. 2008 May;19(5):898-902. doi: 10.1093/annonc/mdm606. Epub 2008 Feb 13.

Abstract

Background: Previous studies have indicated an association between obesity and poor survival in several tumour types, including ovarian cancer. We sought to test the hypothesis that obesity reduces survival in a large, well-characterised and relatively homogeneous cohort of ovarian cancer patients.

Patients and methods: The relationship between body mass index (BMI) and overall survival (OS) and progression-free survival (PFS) in 1067 patients participating in the Scottish Randomised Trial in Ovarian Cancer I trial was assessed. All patients received first-line carboplatin/taxane chemotherapy. The dose of carboplatin was determined by a measured glomerular filtration rate (GFR), ensuring accurate dosing in all categories of BMI and the dose of taxane was not capped. Patients were assigned to one of four categories: underweight (BMI < 18.5), ideal weight (BMI 18.5-24.9), overweight (BMI 25-29.9) or obese (BMI >or= 30).

Results: There were neither statistically significant differences in PFS or OS between these four groups nor were there any differences in taxane or carboplatin dose intensity. Furthermore, there was no association between BMI and tumour stage or grade at presentation, or completeness of debulking surgery.

Conclusions: Obese patients with epithelial ovarian cancer do not have a poorer prognosis, provided that they receive optimal doses of chemotherapy based on measured GFR and actual body weight.

Publication types

  • Clinical Trial, Phase III
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Body Mass Index*
  • Carboplatin / administration & dosage
  • Carcinoma / complications
  • Carcinoma / drug therapy
  • Carcinoma / mortality*
  • Carcinoma / pathology
  • Combined Modality Therapy
  • Disease Progression
  • Disease-Free Survival
  • Docetaxel
  • Dose-Response Relationship, Drug
  • Female
  • Glomerular Filtration Rate
  • Humans
  • Middle Aged
  • Obesity / complications
  • Ovarian Neoplasms / complications
  • Ovarian Neoplasms / drug therapy
  • Ovarian Neoplasms / mortality*
  • Ovarian Neoplasms / pathology
  • Ovarian Neoplasms / surgery
  • Overweight / complications
  • Paclitaxel / administration & dosage
  • Survival Analysis
  • Taxoids / administration & dosage
  • Thinness / complications

Substances

  • Taxoids
  • Docetaxel
  • Carboplatin
  • Paclitaxel