BACKGROUND: The deprivation gap for breast cancer survival remains unexplained by stage at presentation, treatment, or comorbidities. We hypothesised that p53 mutation might contribute to the impaired outcome observed in patients from deprived communities.
METHODS: p53 mutation status was determined using the Roche Amplichip research test in 246 women with primary breast cancer attending a single cancer centre and related to deprivation, pathology, overall, and disease-free survival.
RESULTS: p53 mutation, identified in 64/246 (26%) of cancers, was most common in 10 out of 17 (58.8%) of the lowest (10th) deprivation decile. Those patients with p53 mutation in the 10th decile had a significantly worse disease-free survival of only 20% at 5 years (Kaplan-Meier logrank chi(2) = 6.050, P = 0.014) and worse overall survival of 24% at 5 years (Kaplan-Meier logrank chi(2) = 6.791, P = 0.009) than women of deciles 1-9 with p53 mutation (c.f. 56% and 72%, respectively) or patients in the 10th decile with wildtype p53 (no disease relapse or deaths).
CONCLUSION: p53 mutation in breast cancer is associated with socio-economic deprivation and may provide a molecular basis, with therapeutic implications, for the poorer outcome in women from deprived communities. British Journal of Cancer (2010) 102, 719-726. doi:10.1038/sj.bjc.6605540 www.bjcancer.com Published online 26 January 2010 (C) 2010 Cancer Research UK
|Number of pages||8|
|Journal||British Journal of Cancer|
|Publication status||Published - 16 Feb 2010|
- primary breast cancer
- socio-economic deprivation
- overall survival
- disease-free survival
- SYSTEMIC INFLAMMATORY RESPONSE
- C-REACTIVE PROTEIN
- SOCIAL DEPRIVATION