PO.CL04.02 · 临床研究
南佛罗里达亚族裔西班牙裔人群中独特的HER2-乳腺癌特征
Distinct HER2- breast cancer traits among subethnic Hispanics of South Florida
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
引言:针对南佛罗里达(SHFL)占主导地位的加勒比和南美亚族裔西班牙裔人群、且样本数量具有代表性的研究十分有限。本研究探讨了SHFL人群中可能与乳腺癌易感风险相关的特征,该人群占Sylvester癌症中心乳腺癌患者的45%。
方法:从我们的病历数据库中提取了971例在2019年1月1日至2024年12月1日期间有乳腺癌记录的SHFL女性队列。数据包括年龄、族裔、绝经状态、癌症分期、初潮年龄、BRCA变异、激素受体(HR)和HER2状态。对人表皮生长因子受体-2阴性(HER2-)肿瘤(n=802)进行重新评估,依据以下标准重新分类为HER2-Low:HER2免疫组化(IHC)=1+,或2+且荧光原位杂交(FISH)阴性。采用logistic回归评估风险因素与三阴性乳腺癌(TNBC)相对于非TNBC(定义为HR和/或HER2阳性)的关联。单变量分析中的多重性以Q值(经错误发现率校正的p值)报告。
结果:确诊时,队列中47%为绝经前,其中25%年龄≤45岁,13%年龄≤40岁。在诊断为4期的患者中,24%同样年龄≤45岁。71%的HR+/HER2-肿瘤被重新分类为HER2-Low,全部TNBC中亦有50%被重新分类。单变量logistic分析显示,较年轻的年龄(≤45岁 vs >45岁:OR=1.69,95%CI:1.11-2.56;q=0.042)和更高的BRCA负荷(每增加1个单位OR=2.70,95%CI:1.38-5.28;q=0.017)与TNBC显著相关。纳入年龄、HER2-、HER2-Low、BRCA及交互项的多变量分析揭示了BRCA与TNBC之间存在显著的正向交互作用(交互p=0.018),该交互作用在HER2-Low肿瘤中减弱。与0/1期相比,较晚的癌症分期与较少的雌激素暴露年数相关(2/3期p=0.008,4期p=0.038)。早初潮(年龄<10岁)的患病率为7%,而晚初潮(年龄>14岁)为14%。
结论:我们的发现揭示了SHFL乳腺癌患者中BRCA负荷、HER2-Low模式、雌激素暴露以及诊断和初潮年龄的独特模式和新型关联。例如,与乳腺癌通常与老年女性相关的情况相反,我们队列中近半数为绝经前,四分之一年龄在45岁或以下。这令人担忧,因为较年轻的患者可能尚未达到从预防性乳腺X线摄影中获益的年龄,且更可能患有TNBC(治疗选择最少的最具侵袭性肿瘤)。将大多数HER2-肿瘤重新分类为HER2-Low可能扩大其治疗选择,纳入首个针对HER2-Low的基于trastuzumab的疗法。BRCA与TNBC在HER2-Low中减弱的交互作用提示其遗传基础与HER2- IHC=0肿瘤不同。最后,与普通人群相比,早初潮和晚初潮的患病率均升高。
查看英文原文 English abstract
Introduction: Studies with representative numbers of the predominant Caribbean and South American subethnic Hispanics of South Florida (SHFL) are limited. This study explored traits potentially linked to breast cancer susceptibility risk among SHFL, which comprise 45% of Sylvester Cancer Center's breast cancer patients.
Methods: A cohort of 971 SHFL females with breast cancer records between 1/1/2019 and 12/1/2024 was extracted from our medical record database. Data included age, ethnicity, menopausal state, cancer stage, menarche age, BRCA variants, hormone receptors (HR) and HER2 status. Human Epidermal growth factor Receptor-2 negative (HER2-) tumors (n=802) were re-evaluated for reclassification to HER2-Low using criteria: HER2 immunohistochemistry (IHC) = 1+ or 2+ with fluorescence in-situ hybridization (FISH) negative. Association of risk factors with Triple-Negative Breast Cancer (TNBC) vs non-TNBC (defined as positivity for HR and/or HER2) was assessed using logistic regression. Multiplicity in univariable analysis was reported by Q-values (p-values adjusted for false discovery rate).
Results: At diagnosis, 47% of the cohort was pre-menopausal, with 25% aged ≤45 and 13% aged ≤40. Among those diagnosed with stage 4, 24% were also aged ≤45. 71% of HR+/HER2- tumors were reclassified to HER2-Low, along with 50% of all TNBC. Univariable logistic analysis showed that younger ages (≤45 vs >45: OR=1.69, 95%CI: 1.11-2.56; q=0.042) and greater BRCA burden (1-unit increase OR=2.70, 95%CI: 1.38-5.28; q=0.017) were significantly associated with TNBC. Multivariable analysis including age, HER2-, HER2-Low, BRCA and interaction terms revealed significant positive interaction between BRCA and TNBC (p interaction =0.018) which was weakened in HER2-Low tumors. Later cancer stages were associated with less years of estrogen exposure when compared to stages 0/1 (p=0.008 for stages 2/3 and p=0.038 for stage 4). Prevalence of early menarche (age <10) was 7% whereas late menarche (age >14) was 14%.
Conclusions: Our findings reveal distinct patterns and novel associations of BRCA burden, HER2-Low patterns, estrogen exposure and ages at diagnosis and menarche in SHFL with breast cancer. For instance, in contrast to the usual association of breast cancer with older women, nearly half of our cohort was pre-menopausal, with one quarter aged 45 or younger. This is concerning as younger patients may not be old enough to benefit from preventive mammograms and are more likely to have TNBC (the most aggressive tumors with the least treatment options). Reclassification of most HER2- tumors into HER2-Low potentially expands their therapy options to include the first trastuzumab-based therapy for HER2-Low. A weakened interaction of BRCA with TNBC in HER2-Low suggests distinct genetic basis compared to HER2- IHC=0 tumors. Lastly, prevalence of both early and late menarches was elevated compared to the general population.
利益披露 Disclosure
J. Darkwah, None..
M. G. Spillane, None..
T. Omlor, None..
S. Han, None..
F. Ye, None..
H. Ng-Chen, None..
G. Fonte, None..
S. D. C. Bianco, None.