Neoadjuvant Chemotherapy and Nodal Response Rates in Luminal Breast Cancer: Effects of Age and Tumor Ki67
- PMID: 35569077
- PMCID: PMC9466990
- DOI: 10.1245/s10434-022-11871-z
Neoadjuvant Chemotherapy and Nodal Response Rates in Luminal Breast Cancer: Effects of Age and Tumor Ki67
Abstract
Background: Neoadjuvant chemotherapy (NAC) is standard for most triple-negative and human epidermal growth factor receptor 2 (HER2)+ breast cancers, and frequently downstages node-positive (cN+) disease, permitting omission of axillary dissection. In estrogen receptor (ER)+/HER2- disease, response rates are lower. Whether Ki67 is associated with axillary downstaging in ER+/HER2- disease is unknown.
Methods: With institutional review board approval, we queried our institutional database to identify all patients with primary ER+/HER2- biopsy-proven cN+ breast cancer treated with NAC followed by surgery from January 2012 to December 2021. Nodal pathologic complete response (pCR) rates were evaluated by pretreatment Ki67 and patient age.
Results: 315 patients (median age 50 years) were included. Nodal pCR rate was 24.8% (78/315) and was higher in patients aged < 50 years than ≥ 50 years (31.8% versus 17.7%, p = 0.004). Ki67 was available on 236 patients (74.9%). Median Ki67 was 29.0% (range 1-98%) and did not differ by age category (p = 0.23). Patients with nodal pCR had higher Ki67 (median 40.3% versus 25.0%, p < 0.001). Nodal pCR rates were 28.4% (Ki67 ≥ 20%) versus 8.1% (Ki67 < 20%) (p < 0.001). On multivariable analysis, Ki67 and age category were predictive of nodal pCR. Combining these two parameters together, nodal pCR rates in age < 50 years were 35.8% when Ki67 ≥ 20% versus 14.3% with Ki67 < 20% (p = 0.02). In contrast, for age ≥ 50 years, nodal pCR was 21.0% for Ki67 ≥ 20% versus 2.6% with Ki67 < 20% (p = 0.008).
Conclusions: In ER+/HER2- breast cancer, nodal downstaging with NAC is associated with age (< 50 years) and Ki67 (≥ 20%). Age and Ki67 should be considered for NAC decision-making and can identify patients with high rates of nodal downstaging (36%) who would benefit from NAC to enable axillary preservation.
© 2022. Society of Surgical Oncology.
Figures




Similar articles
-
Neoadjuvant Chemotherapy and Pathologic Complete Response in HR+/HER2- Breast Cancer: Impact of Tumor Ki67 and ER Status.Chemotherapy. 2024;69(3):141-149. doi: 10.1159/000537874. Epub 2024 Feb 16. Chemotherapy. 2024. PMID: 38368871
-
Nodal pCR and overall survival following neoadjuvant chemotherapy for node positive ER+/Her2- breast cancer.Breast Cancer Res Treat. 2024 Feb;203(3):419-428. doi: 10.1007/s10549-023-07152-2. Epub 2023 Oct 25. Breast Cancer Res Treat. 2024. PMID: 37878154 Free PMC article. Review.
-
Standard Pathologic Features Can Be Used to Identify a Subset of Estrogen Receptor-Positive, HER2 Negative Patients Likely to Benefit from Neoadjuvant Chemotherapy.Ann Surg Oncol. 2017 Sep;24(9):2556-2562. doi: 10.1245/s10434-017-5898-z. Epub 2017 May 30. Ann Surg Oncol. 2017. PMID: 28560596 Free PMC article.
-
How Often Does Neoadjuvant Chemotherapy Avoid Axillary Dissection in Patients With Histologically Confirmed Nodal Metastases? Results of a Prospective Study.Ann Surg Oncol. 2016 Oct;23(11):3467-3474. doi: 10.1245/s10434-016-5246-8. Epub 2016 May 9. Ann Surg Oncol. 2016. PMID: 27160528 Free PMC article.
-
Tolerance and Outcomes of Neoadjuvant Chemotherapy in Geriatric Breast Cancer Patients.J Surg Res. 2023 Mar;283:329-335. doi: 10.1016/j.jss.2022.10.092. Epub 2022 Nov 22. J Surg Res. 2023. PMID: 36427442 Review.
Cited by
-
Contrast-Enhanced Mammography (CEM) Capability to Distinguish Molecular Breast Cancer Subtypes.Biomedicines. 2022 Sep 24;10(10):2384. doi: 10.3390/biomedicines10102384. Biomedicines. 2022. PMID: 36289645 Free PMC article.
-
Study on pathological factors affecting the sensitivity of neoadjuvant therapy in hypopharyngeal cancer.Cancer Immunol Immunother. 2025 Feb 25;74(4):118. doi: 10.1007/s00262-025-03957-w. Cancer Immunol Immunother. 2025. PMID: 39998637 Free PMC article.
-
Retrieval of the Clipped Axillary Lymph Node and Its Impact on Treatment Decisions.Cancers (Basel). 2024 Aug 29;16(17):3001. doi: 10.3390/cancers16173001. Cancers (Basel). 2024. PMID: 39272859 Free PMC article.
-
Comparing survival outcomes between neoadjuvant and adjuvant chemotherapy within T2N1M0 stage hormone receptor-positive, HER2-negative breast cancer: a retrospective cohort study based on SEER database.Breast Cancer. 2024 Jul;31(4):684-694. doi: 10.1007/s12282-024-01583-5. Epub 2024 Apr 21. Breast Cancer. 2024. PMID: 38643430 Free PMC article.
-
Factors Affecting Pathological Complete Response in Locally Advanced Breast Cancer Cases Receiving Neoadjuvant Therapy: A Comprehensive Literature Review.Eur J Breast Health. 2023 Dec 27;20(1):8-14. doi: 10.4274/ejbh.galenos.2023.2023-11-2. eCollection 2024 Jan. Eur J Breast Health. 2023. PMID: 38187111 Free PMC article. Review.
References
-
- Murphy BL, Day CN, Hoskin TL, Habermann EB, Boughey JC. Neoadjuvant chemotherapy use in breast cancer is greatest in excellent responders: triple-negative and HER2+ subtypes. Ann Surg Oncol. 2018;25(8):2241–8. - PubMed
-
- Cortazar P, Zhang L, Untch M, et al. Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis. Lancet. 2014;384(9938):164–72. - PubMed
-
- Boughey JC, McCall LM, Ballman KV, et al. Tumor biology correlates with rates of breast-conserving surgery and pathologic complete response after neoadjuvant chemotherapy for breast cancer: findings from the ACOSOG Z1071 (Alliance) prospective multicenter clinical trial. Ann Surg. 2014;260(4):608–14 (discussion 614-6). - PMC - PubMed
-
- Harbeck N, Rastogi P, Martin M, et al. Adjuvant abemaciclib combined with endocrine therapy for high-risk early breast cancer: updated efficacy and Ki-67 analysis from the MonarchE study. Ann Oncol. 2021;32(12):1571–81. - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous