Abstract 325P
Background
The Nottingham histological grading (NHG) system has shown robust prognostic implication in breast cancer. However, the independent prognostic value of the NHG system in neoadjuvant setting has not been demonstrated yet.
Methods
505 neoadjuvant treated (NT) patients with available grades for core needle biopsy (CNB) and subsequent resection specimen (RS) were evaluated. To adjust for pre-analytical/analytical bias between CNB and RS, the grades were compared with a control cohort (CC) of 297 primary operated patients. The change of grade between CNB and RS was compared, by Wilcoxon signed rank test and quadratic weighted kappa. As expected, the group of NHG1-cases was small with low event rate so the groups of NHG1 and NHG2 were merged. Survival curves for overall survival were estimated using the Kaplan-Meier method and a 2-sided log-rank test. Univariate Cox proportional hazards models were used to report hazard ratios (HR) with 95% CIs for NHG for CNB, RS and computed delta-values between the two. Multivariate Cox proportional hazards regression was performed calculating adjusted hazard ratios for established prognostic markers.
Results
We found a significant decrease in grade from CNB to subsequent specimen (p-value < 0,001 and kappa = 0,40). Patient group with NHG high tumors (NHG3) had significantly worse overall survival compared to that of NHG low (NHG1+2) assessed on either CNB or RS (p-value < 0.001). Univariate analysis showed higher risk for death for NHG high tumors in both CNB (HR:2.05, CI:1.39-3.03, p<0.001) and RS (HR:3.20, CI:2.17-4.71, p<0.001). In multivariate analysis adjusted for age, clinical T-stage, clinical N-stage, ER-status and Her2-status the NHG for RS remained an independent prognostic marker (HR:2.07, CI:1.25-3.43, p = 0.005).
Conclusions
Neoadjuvant treatment affects NHG with a significant decrease in grade from core biopsy sample to resection specimen. In the neoadjuvant setting, grades in core biopsy sample is not associated with independent prognostic implications. The grade for the resection specimen after neoadjuvant treatment shows independent prognostic implication adjusted for established prognostic markers. Therefore, we recommend continuing to perform NHG in resection specimen after neoadjuvant therapy.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Karolinska Institutet.
Funding
Has not received any funding.
Disclosure
B. Acs: Financial Interests, Institutional, Funding: The Swedish Society for Medical Research (Svenska Sällskapet för Medicinsk Forskning). J. Hartman: Financial Interests, Personal, Speaker, Consultant, Advisor: Roche, Novartis, Pfizer, EliLilly, MSD, Gilead, Sakura; Financial Interests, Personal, Other, Co-counder and shareholder: Stratipath; Financial Interests, Institutional, Research Funding: AstraZeneca, Roche, MSD, Novartis. All other authors have declared no conflicts of interest.
Resources from the same session
311P - Optimizing breast cancer staging: Redefining tumor size classification using big data analytics
Presenter: Bin Feng
Session: Poster session 14
312P - Early detection of metastatic disease in asymptomatic early-stage breast cancer patients using imaging: A cross-sectional analytic study at a tertiary hospital
Presenter: John kelvin Lalusis
Session: Poster session 14
313P - A longitudinal follow-up study on the prognosis of patients with breast cancer with delayed diagnosis during the COVID-19 pandemic
Presenter: Jae Pak Yi
Session: Poster session 14
314P - The impact of changes in tumor mutational landscape during neoadjuvant therapy on tumor-informed ctDNA testing in breast cancer patients
Presenter: Mark Magbanua
Session: Poster session 14
315P - Long-term tamoxifen benefit in pre- and postmenopausal patients of high and low risk with luminal A and B breast cancer
Presenter: Oscar Danielsson
Session: Poster session 14
316P - Differential long-term benefit of 2-year adjuvant tamoxifen therapy for luminal-type breast cancer: Insights from a 20-year follow-up analysis of the STO trials
Presenter: Magdalena Rios Romero
Session: Poster session 14
317TiP - A randomized, multicenter, open-label phase II neoadjuvant study to evaluate the safety and efficacy of HER2-ADC disitamab vedotin in combination toripalimab or sequence chemotherapy in participants with HR-negative, HER2 low-expressing breast cancer
Presenter: Zhimin Shao
Session: Poster session 14
318TiP - Neoadjuvant trastuzumab, pertuzumab and tucatinib without chemotherapy in stage II-III HER2-positive breast cancer: The TRAIN-4 study
Presenter: Fleur Louis
Session: Poster session 14
319TiP - NeoBREASTIM: A phase II study of atezolizumab plus RP1 oncolytic immunotherapy in the neoadjuvant setting of triple-negative breast cancer (TNBC)
Presenter: Etienne Bastien
Session: Poster session 14
321P - Sentinel lymph node biopsy in clinical T3-4c breast cancer: A retrospective multicenter cohort study
Presenter: Yasuaki Sagara
Session: Poster session 14