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Published on: October 27, 2014
BODY MASS INDEX AS A PROGNOSTIC FACTOR FOR DISEASE PROGRESSION IN PATIENTS WITH METASTATIC COLORECTAL CANCER TREATED
C Hopirtean1, T Ciuleanu1,2, C Cainap1,2
1"Ion Chiricuţă" Oncology Institute, Cluj-Napoca, Romania.
Obesity, indicated by a body mass index (BMI) of 27 kg/sqm or higher, negatively impacts progression-free survival for metastatic colorectal cancer (mCRC) patients treated with bevacizumab. This finding highlights BMI as a significant prognostic factor in mCRC.
Area of Science:
- Oncology
- Clinical Research
- Cancer Prognostics
Background:
- Obesity is linked to increased colorectal cancer risk and poorer prognosis.
- Bevacizumab, an anti-VEGF therapy, is crucial for metastatic colorectal cancer (mCRC).
- Obesity may drive resistance to anti-VEGF therapies due to elevated vascular endothelial growth factor (VEGF).
Purpose of the Study:
- To assess the efficacy of bevacizumab systemic therapy in mCRC patients.
- To evaluate the impact of body mass index (BMI) on treatment outcomes.
Main Methods:
- Retrospective, single-center cohort study.
- Analysis of 112 mCRC patients treated with bevacizumab-based therapy from 2007-2012.
- Comparison of progression-free survival (PFS) and overall survival (OS) based on BMI cut-off of 27 kg/sqm.
Main Results:
- Patients with BMI < 27 kg/sqm had significantly longer PFS (24 months) than those with BMI ≥ 27 kg/sqm (17.9 months; p=0.04).
- In patients with liver metastases, lower BMI (< 27 kg/sqm) correlated with longer PFS (24.5 months) compared to higher BMI (≥ 27 kg/sqm; 17.5 months; p=0.02).
- Five-year OS was not significantly influenced by BMI in either the overall cohort or in patients with liver metastases.
Conclusions:
- Elevated BMI (≥ 27 kg/sqm) negatively affects PFS in mCRC patients treated with bevacizumab, both overall and in those with liver metastases.
- A BMI cut-off of 27 kg/sqm emerged as a clinically relevant prognostic factor.
- BMI should be considered a significant prognostic indicator for mCRC patients undergoing anti-VEGF therapy.
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