TY - JOUR
T1 - Contralateral breast cancer risk in irradiated breast cancer patients with a germline-BRCA1/2 pathogenic variant
AU - van Barele, Mark
AU - Akdeniz, Delal
AU - Heemskerk-Gerritsen, Bernadette A M
AU - Andrieu, Nadine
AU - Noguès, Catherine
AU - van Asperen, Christi J
AU - Wevers, Marijke
AU - Ausems, Margreet G E M
AU - de Bock, Geertruida H
AU - Dommering, Charlotte J
AU - Gómez-García, Encarnacion B
AU - van Leeuwen, Flora E
AU - Mooij, Thea M
AU - Easton, Douglas F
AU - Antoniou, Antonis C
AU - Evans, D Gareth
AU - Izatt, Louise
AU - Tischkowitz, Marc
AU - Frost, Debra
AU - Brewer, Carole
AU - Olah, Edit
AU - Simard, Jacques
AU - Singer, Christian F
AU - Thomassen, Mads
AU - Kast, Karin
AU - Rhiem, Kerstin
AU - Engel, Christoph
AU - de la Hoya, Miguel
AU - Foretová, Lenka
AU - Jakubowska, Anna
AU - Jager, Agnes
AU - Sattler, Margriet G A
AU - Schmidt, Marjanka K
AU - Hooning, Maartje J
AU - GENEPSO
AU - HEBON
AU - EMBRACE
AU - ONC
AU - IBCCS
PY - 2023/11
Y1 - 2023/11
N2 - BACKGROUND: Radiation-induced secondary breast cancer may be a concern after radiotherapy for primary breast cancer (PBC), especially in young germline (g)BRCA-associated breast cancer patients with already high contralateral breast cancer (CBC) risk and potentially increased genetic susceptibility to radiation. AIM: To investigate whether adjuvant radiotherapy for PBC increases the risk of CBC in gBRCA1/2-associated BC patients. METHODS: gBRCA1/2 pathogenic variant carriers diagnosed with PBC were selected from the prospective International BRCA1/2 Carrier Cohort Study. We used multivariable Cox proportional hazards models to investigate the association between radiotherapy (yes versus no) and CBC risk. We further stratified for BRCA status and PBC age (<40 and >40?years). Statistical significance tests were two-sided. RESULTS: Of 3,602 eligible patients, 2,297 (64%) received adjuvant radiotherapy. Median follow-up was 9.6?years. The radiotherapy group had more stage III PBC patients compared to the non-radiotherapy group (15% versus 3%, p?<?0.001), received more often chemotherapy (81% vs. 70%, p?<?0.001) and endocrine therapy (50% vs. 35%, p?<?0.001). The radiotherapy group had an increased CBC risk compared to the non-radiotherapy group (adjusted HR: 1.44, 95% CI: 1.12-1.86). Statistical significance was observed in gBRCA2 (HR: 1.77, 95% CI: 1.13-2.77), but not in gBRCA1 pathogenic variant carriers (HR: 1.29, 95% CI: 0.93-1.77; p-value for interaction, 0.39). In the combined gBRCA1/2 group, patients irradiated below and above age 40 at PBC diagnosis showed similar risks (HR: 1.38, 95% CI: 0.93-2.04 and HR: 1.56, 95% CI: 1.11-2.19, respectively). DISCUSSION/CONCLUSION: Radiotherapy regimens minimizing contralateral breast dose should be considered in gBRCA1/2 pathogenic variant carriers.
AB - BACKGROUND: Radiation-induced secondary breast cancer may be a concern after radiotherapy for primary breast cancer (PBC), especially in young germline (g)BRCA-associated breast cancer patients with already high contralateral breast cancer (CBC) risk and potentially increased genetic susceptibility to radiation. AIM: To investigate whether adjuvant radiotherapy for PBC increases the risk of CBC in gBRCA1/2-associated BC patients. METHODS: gBRCA1/2 pathogenic variant carriers diagnosed with PBC were selected from the prospective International BRCA1/2 Carrier Cohort Study. We used multivariable Cox proportional hazards models to investigate the association between radiotherapy (yes versus no) and CBC risk. We further stratified for BRCA status and PBC age (<40 and >40?years). Statistical significance tests were two-sided. RESULTS: Of 3,602 eligible patients, 2,297 (64%) received adjuvant radiotherapy. Median follow-up was 9.6?years. The radiotherapy group had more stage III PBC patients compared to the non-radiotherapy group (15% versus 3%, p?<?0.001), received more often chemotherapy (81% vs. 70%, p?<?0.001) and endocrine therapy (50% vs. 35%, p?<?0.001). The radiotherapy group had an increased CBC risk compared to the non-radiotherapy group (adjusted HR: 1.44, 95% CI: 1.12-1.86). Statistical significance was observed in gBRCA2 (HR: 1.77, 95% CI: 1.13-2.77), but not in gBRCA1 pathogenic variant carriers (HR: 1.29, 95% CI: 0.93-1.77; p-value for interaction, 0.39). In the combined gBRCA1/2 group, patients irradiated below and above age 40 at PBC diagnosis showed similar risks (HR: 1.38, 95% CI: 0.93-2.04 and HR: 1.56, 95% CI: 1.11-2.19, respectively). DISCUSSION/CONCLUSION: Radiotherapy regimens minimizing contralateral breast dose should be considered in gBRCA1/2 pathogenic variant carriers.
U2 - 10.1093/jnci/djad116
DO - 10.1093/jnci/djad116
M3 - Article
SN - 0027-8874
VL - 115
SP - 1318
EP - 1328
JO - Journal of the National Cancer Institute
JF - Journal of the National Cancer Institute
IS - 11
ER -