PO.CL09.02 · 临床研究
组织学亚型(导管、小叶和混合导管/小叶)对雌激素受体低(ER-low)HER2阴性乳腺癌新辅助化疗(NAC)和化疗免疫治疗(NACI)后病理完全缓解(pCR)的影响
Impact of histology subtypes (ductal, lobular, and mixed ductal/lobular) on pathological complete response (pCR) following neoadjuvant chemotherapy (NAC) and chemoimmunotherapy (NACI) for estrogen receptor low (ER-low) HER2-negative breast cancer
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
背景:关于乳腺癌混合导管/小叶组织学亚型如何影响新辅助化疗(NAC)和化疗免疫治疗(NACI)后病理完全缓解(pCR)可能性的了解甚少。同样,在这一混合组织学亚组中,关于雌激素受体(ER)表达百分位如何影响NACI后pCR可能性的文献尚缺乏。
方法:我们检查了美国国家癌症数据库中2018-2022年间诊断为HER2阴性乳腺癌的数据。我们根据组织学亚型(导管、小叶和混合)和ER百分位(包括ER-low [1-10%])对患者进行分类。使用二元logistic回归检查ER-low疾病患者中pCR与组织学类型之间的关系,校正年龄、种族、族裔、肿瘤分级、肿瘤大小、淋巴结状态、孕激素受体百分位、免疫治疗使用、内分泌治疗使用和淋巴血管侵犯(LVI)。此外,在总生存期(OS)与组织学亚型之间拟合校正后Cox比例风险回归。
结果:共检查了58072例导管、1330例混合和3500例小叶病例,均具有新辅助治疗后可用的残留病灶数据。在ER-low表达者中(导管:3319,混合:35,小叶:80),分别有46.7%(n=1549)、31.4%(n=11)和12.5%(n=10)的患者实现pCR,单变量分析显示这是一个显著差异(p<0.001)。在校正分析中,混合与导管ER-low疾病患者之间pCR的差异不显著(aOR 0.69,95% CI 0.27-1.77,参照:导管)。然而,小叶患者与导管患者相比,实现pCR的比值降低79%(aOR 0.21,95% CI 0.08-0.54)。在多变量分析中,显著改善实现pCR比值的变量为组织学类型(p=0.004)、较年轻年龄(p=0.010)、较小肿瘤大小(p<0.001)、免疫治疗使用(p<0.001)和无LVI(p<0.001)。OS方面,较大肿瘤大小(p<0.001)、淋巴结阳性状态(p<0.001)和存在LVI(p<0.001)与OS恶化相关,而接受内分泌治疗(p=0.003)则显著改善OS。组织学亚型与OS差异无显著关联(p=0.238)。
结论:混合导管/小叶组织学的肿瘤在NACI反应方面表现得与导管疾病更为相似,包括ER-low亚组。其他因素,如肿瘤大小、LVI和接受免疫治疗,在预测pCR中发挥更强作用,但在决定如何为HER2阴性ER表达疾病患者最佳安排治疗顺序时,组织学亚型仍是需要考虑的重要变量。
查看英文原文 English abstract
Background: Little is known regarding mixed ductal/lobular histology subtypes of breast cancer in terms of how they influence the likelihood of pathologic complete response (pCR) following neoadjuvant chemotherapy (NAC) & chemoimmunotherapy (NACI). Similarly, there is no literature on how estrogen receptor (ER) expression percentiles influence the likelihood of pCR after NACI among this mixed histology subgroup.
Methods: We examined data within the National Cancer Database on those diagnosed with HER2-negative breast cancer between 2018-2022. We categorized patients based on histology subtype (ductal, lobular, & mixed) and ER percentiles, including ER-low (1-10%). Binary logistic regression was used to examine the relationship between pCR & histology type among patients with ER-low disease, adjusting for age, race, ethnicity, tumor grade, tumor size, nodal status, progesterone receptor percentiles, immunotherapy use, endocrine therapy use, & lymphovascular invasion (LVI). Additionally, adjusted Cox proportional hazards regression was fitted between overall survival (OS) and histology subtype.
Results: A total of 58072 ductal, 1330 mixed, & 3500 lobular cases with available residual disease data following neoadjuvant therapy were examined. Among those with ER-low expression (ductal: 3319, mixed: 35, lobular: 80), it was shown that 46.7% (n=1549), 31.4% (n=11), & 12.5% (n=10) of patients, respectively, achieved pCR, which was a significant difference on univariate analysis (p<0.001). On adjusted analysis, the difference in pCR between patients with mixed & ductal ER-low disease was non-significant (aOR 0.69, 95%CI 0.27-1.77, reference: ductal). However, lobular patients were associated with 79% lower odds of achieving pCR compared to ductal patients (aOR 0.21, 95%CI 0.08-0.54). On multivariate analysis, variables that significantly improved the odds of achieving pCR were histology type (p=0.004), younger age (p=0.010), smaller tumor size (p<0.001), use of immunotherapy (p<0.001), and absence of LVI (p<0.001). For OS, larger tumor size (p<0.001), positive nodal status (p<0.001), & presence of LVI (p<0.001) were associated with worsened OS whereas the receipt of endocrine therapy (p=0.003) significantly improved OS. Histology subtype was not significantly associated with differences in OS (p=0.238).
Conclusion: Tumors of mixed ductal/lobular histology behave more similarly to ductal disease in terms of NACI response, including ER-low subgroups. Additional factors, such as tumor size, LVI, and receipt of immunotherapy play a stronger role in predicting pCR, but the histology subtype remains an important variable to consider when deciding how best to sequence treatment for those with HER2-negative ER-expressing disease.
利益披露 Disclosure
K. C. C. Johnson, None..
B. Slover, None..
Y. Gokun, None..
D. M. Quiroga, None..
S. Sardesai, None..
S. Jhawar, None..
N. Lopetegui-Lia, None..
A. M. Roy, None..
G. Bader, None..
A. P. Davenport, None..
N. O. Williams, None..
R. Wesolowski, None..
M. E. Gatti-Mays, None..
D. G. Stover, None.