TY - JOUR
T1 - Race-related subsequent breast events after ductal carcinoma in situ
T2 - A Surveillance, Epidemiology, and End Results–based analysis
AU - Koric, Alzina
AU - Jiang, Shu
AU - Liu, Ying
AU - Colditz, Graham A.
N1 - Publisher Copyright:
© 2025 American Cancer Society.
PY - 2025/11/15
Y1 - 2025/11/15
N2 - Background: The risk of subsequent ductal carcinoma in situ (DCIS) or invasive breast cancer (IBC) has been evaluated in either breast after a DCIS diagnosis; this study modeled competing risks of ipsilateral and contralateral DCIS or IBC subtypes by self-reported race. Methods: A cohort of 198,827 women diagnosed with primary unilateral DCIS between 2000 and 2022 was identified from the US Surveillance, Epidemiology, and End Results tumor registries. Competing subdistributional hazard ratio (sHR) models were used to estimate DCIS or IBC laterality-associated risks overall and for the estrogen receptor (ER+) or progesterone receptor (PR+) overexpressing (ER+/PR+) and ER−PR− expressing tumor subtypes. Cox models were used for subanalysis to estimate the overall risk of a second event (DCIS or IBC). Results: Within an average of 10 (±6.1) years of follow-up after the initial DCIS, 16,148 women had a subsequent event (25.7% DCIS; 74.3% IBC). Overall, compared with White women, Black women had an elevated risk of IBC for either tumor subtype, whereas Asian and Hispanic women had an elevated risk of ER−PR− IBC. For tumor aggressiveness by laterality, Black women had an elevated IBC risk in either breast for ER−PR− (sHR, 1.82; 95% CI, 1.53–2.17 in the ipsilateral breast; sHR, 1.512; 95% CI, 1.24–1.86 in the contralateral breast), as did Hispanic and Asian women in the ipsilateral breast only (with stronger association vs. ER+/PR+) (phet =.0001). Conclusions: These contemporary data reflect treatment patterns since 2000, which show an elevated risk of subsequent breast tumors in either breast among Black women after DCIS.
AB - Background: The risk of subsequent ductal carcinoma in situ (DCIS) or invasive breast cancer (IBC) has been evaluated in either breast after a DCIS diagnosis; this study modeled competing risks of ipsilateral and contralateral DCIS or IBC subtypes by self-reported race. Methods: A cohort of 198,827 women diagnosed with primary unilateral DCIS between 2000 and 2022 was identified from the US Surveillance, Epidemiology, and End Results tumor registries. Competing subdistributional hazard ratio (sHR) models were used to estimate DCIS or IBC laterality-associated risks overall and for the estrogen receptor (ER+) or progesterone receptor (PR+) overexpressing (ER+/PR+) and ER−PR− expressing tumor subtypes. Cox models were used for subanalysis to estimate the overall risk of a second event (DCIS or IBC). Results: Within an average of 10 (±6.1) years of follow-up after the initial DCIS, 16,148 women had a subsequent event (25.7% DCIS; 74.3% IBC). Overall, compared with White women, Black women had an elevated risk of IBC for either tumor subtype, whereas Asian and Hispanic women had an elevated risk of ER−PR− IBC. For tumor aggressiveness by laterality, Black women had an elevated IBC risk in either breast for ER−PR− (sHR, 1.82; 95% CI, 1.53–2.17 in the ipsilateral breast; sHR, 1.512; 95% CI, 1.24–1.86 in the contralateral breast), as did Hispanic and Asian women in the ipsilateral breast only (with stronger association vs. ER+/PR+) (phet =.0001). Conclusions: These contemporary data reflect treatment patterns since 2000, which show an elevated risk of subsequent breast tumors in either breast among Black women after DCIS.
KW - breast cancer
KW - contralateral
KW - ductal carcinoma in situ (DCIS)
KW - ethnicity
KW - ipsilateral
KW - race
KW - Surveillance, Epidemiology, and End Results (SEER)
UR - https://www.scopus.com/pages/publications/105021067724
U2 - 10.1002/cncr.70164
DO - 10.1002/cncr.70164
M3 - Article
C2 - 41199479
AN - SCOPUS:105021067724
SN - 0008-543X
VL - 131
JO - Cancer
JF - Cancer
IS - 22
M1 - e70164
ER -