TY - JOUR
T1 - Increased risks of third primary cancers of non-breast origin among women with bilateral breast cancer
AU - Kwast, ABG
AU - Liu, Lifang
AU - Roukema, JA
AU - Voogd, AC
AU - Jobsen, JJ
AU - Coebergh, Jan Willem
AU - Soerjomataram, Isabelle
AU - Siesling, S
PY - 2012
Y1 - 2012
N2 - BACKGROUND: This study examined the risk of third cancer of non-breast origin (TNBC) among women with bilateral breast cancer (BBC; either synchronous or metachronous), focussing on the relation with breast cancer treatment. METHODS: Risk was assessed, among 8752 Dutch women diagnosed with BBC between 1989 and 2008, using standardised incidence ratios (SIR) and Cox regression analyses to estimate the hazard ratio (HR) of TNBC for different treatment modalities. RESULTS: Significant increased SIRs were observed for all TNBCs combined, haematological malignancies, stomach, colorectal, non-melanoma skin, lung, head and neck, endometrial, and ovarian cancer. A 10-fold increased risk was found for ovarian cancer among women younger than 50 years (SIR = 10.0, 95% confidence interval (CI) = 5.3-17.4). Radiotherapy was associated with increased risks of all TNBCs combined (HR = 1.3; 95% CI = 1.1-1.6, respectively). Endocrine therapy was associated with increas CONCLUSION: Increased risk of TNBC could be influenced by genetic factors (ovarian cancer) or an effect of treatment (radiotherapy and endocrine therapy). More insight in the TNBC risk should further optimise and individualise treatment and surveillance protocols in (young) women with BBC. British Journal of Cancer (2012) 107, 549-555. doi: 10.1038/bjc.2012.270 www.bjcancer.com Published online 19 June 2012 (C) 2012 Cancer Research UK
AB - BACKGROUND: This study examined the risk of third cancer of non-breast origin (TNBC) among women with bilateral breast cancer (BBC; either synchronous or metachronous), focussing on the relation with breast cancer treatment. METHODS: Risk was assessed, among 8752 Dutch women diagnosed with BBC between 1989 and 2008, using standardised incidence ratios (SIR) and Cox regression analyses to estimate the hazard ratio (HR) of TNBC for different treatment modalities. RESULTS: Significant increased SIRs were observed for all TNBCs combined, haematological malignancies, stomach, colorectal, non-melanoma skin, lung, head and neck, endometrial, and ovarian cancer. A 10-fold increased risk was found for ovarian cancer among women younger than 50 years (SIR = 10.0, 95% confidence interval (CI) = 5.3-17.4). Radiotherapy was associated with increased risks of all TNBCs combined (HR = 1.3; 95% CI = 1.1-1.6, respectively). Endocrine therapy was associated with increas CONCLUSION: Increased risk of TNBC could be influenced by genetic factors (ovarian cancer) or an effect of treatment (radiotherapy and endocrine therapy). More insight in the TNBC risk should further optimise and individualise treatment and surveillance protocols in (young) women with BBC. British Journal of Cancer (2012) 107, 549-555. doi: 10.1038/bjc.2012.270 www.bjcancer.com Published online 19 June 2012 (C) 2012 Cancer Research UK
U2 - 10.1038/bjc.2012.270
DO - 10.1038/bjc.2012.270
M3 - Article
C2 - 22713658
SN - 0007-0920
VL - 107
SP - 549
EP - 555
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 3
ER -