Neoadjuvant versus adjuvant chemotherapy in luminal B-like breast cancer: a subset analysis of the CANTO study.
16 affiliations
- 1Department of Surgical Oncology, Institut Curie, Paris, France.
- 2Department of Medical Oncology, Institut Curie, Paris, France.
- 3Institut Curie, Institut Hospitalo-Universitaire des Cancers des Femmes (ANR-23-IAHU-0006), Paris, France.
- 4Université Paris Cité, Paris, France.
- 5Unicancer Breast Cancer Group, Unicancer, Paris, France.
- 6Department of Medical Oncology, Institut Léon Bérard, Lyon, France.
- 7Data and Partnerships Department, UNICANCER, Paris, France.
- 8Department of Methodology and Biostatistics, Centre Georges François Leclerc, Dijon, France.
- 9Department of Medical Oncology, Centre Oscar Lambret, Lille, France.
- 10Department of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
- 11Department of Medical Oncology, Centre François Baclesse, Caen, France.
- 12Department of Medical Oncology, Institut de Cancérologie de L'ouest, Nantes Saint-Herblain, France.
- 13Department of Medical Oncology, Centre Jean Perrin, Clermont-Ferrand, France.
- 14Department of Medical Oncology, Cancer Survivorship Program, INSERM U981, Gustave Roussy, Villejuif, France.
- 15Department of Surgical Oncology, Institut Godinot, Reims, France.
- 16Residual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, INSERM, U932 Immunity and Cancer, Institut Curie, Paris, France.
Abstract
Background
The benefit of neoadjuvant chemotherapy (NAC) in hormone receptor (HR)-positive/human epidermal growth factor receptor 2 (HER2)-negative breast cancer (BC) remains uncertain, given low pathologically documented complete response (pCR) rates and limited long-term comparative data. We compared overall survival (OS) between NAC and adjuvant chemotherapy (AC) in luminal B-like breast cancer treated in routine practice.Patients and methods
Patients enrolled in the prospective French CANTO cohort between January 2012 and December 2018 with unilateral, nonmetastatic, grade 3 HR-positive/HER2-negative BC (cT2-T3N0-N3M0) treated with NAC followed by surgery or with primary surgery followed by AC were included. The primary endpoint was OS; secondary endpoints were distant recurrence-free survival (DRFS) and invasive disease-free survival; exploratory endpoints were BC-specific survival, locoregional recurrence-free survival (LRFS) and breast recurrence-free survival. Inverse probability of treatment weighting (IPTW) was applied, with weighted Kaplan-Meier estimates and Cox models.Results
Among 544 patients, 165 received NAC and 379 AC; median follow-up was 72 months. Breast-conserving surgery was more frequent after NAC (64% compared with 45%, P < 0.001) and the pCR rate was 19%. After IPTW, the hazard ratio for OS with NAC was 1.36 [95% confidence interval (CI) 0.94-1.97, P = 0.10] univariably and 1.62 (95% CI 1.10-2.38, P = 0.014) after multivariable adjustment. No difference was observed for DRFS (hazard ratio 1.05, 95% CI 0.80-1.38, P = 0.70). LRFS was worse with NAC (hazard ratio 2.29, 95% CI 1.15-4.58, P = 0.018) in 19 events. In interaction tests, the association with OS was confined to cN0 (hazard ratio 2.39) and cT2 (hazard ratio 1.94) disease and absent in cN+ (hazard ratio 0.83) and cT3 (hazard ratio 0.88) tumors.Conclusions
NAC was associated with more locoregional recurrence without any difference in DRFS and the association with OS was confined to subgroups in whom a neoadjuvant indication is least established. These hypothesis-generating findings do not support the routine use of NAC in luminal B-like BC without an anticipated surgical benefit.
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BibTeX
@article{gaillard2026neoadjuvant,
title = {{Neoadjuvant versus adjuvant chemotherapy in luminal B-like breast cancer: a subset analysis of the CANTO study.}},
author = {T Gaillard and P Cottu and O Tredan and A-L Martin and C Gaudin and A Bertaut and C Cheymol and C Kaderbhai and F Cherifi and M Campone and M-A Mouret-Reynier and A Di-Meglio and F Reyal and A S Hamy-Petit and E Laas},
journal = {ESMO real world data and digital oncology},
year = {2026},
month = oct,
doi = {10.1016/j.esmorw.2026.100789},
url = {https://europepmc.org/article/MED/42903650},
note = {CC BY},
}
RIS
TY - JOUR
TI - Neoadjuvant versus adjuvant chemotherapy in luminal B-like breast cancer: a subset analysis of the CANTO study.
AU - T Gaillard
AU - P Cottu
AU - O Tredan
AU - A-L Martin
AU - C Gaudin
AU - A Bertaut
AU - C Cheymol
AU - C Kaderbhai
AU - F Cherifi
AU - M Campone
AU - M-A Mouret-Reynier
AU - A Di-Meglio
AU - F Reyal
AU - A S Hamy-Petit
AU - E Laas
PY - 2026
DA - 2026/10/12
JO - ESMO real world data and digital oncology
DO - 10.1016/j.esmorw.2026.100789
UR - https://europepmc.org/article/MED/42903650
AB - Background The benefit of neoadjuvant chemotherapy (NAC) in hormone receptor (HR)-positive/human epidermal growth factor receptor 2 (HER2)-negative breast cancer (BC) remains uncertain, given low pathologically documented complete response (pCR) rates and limited long-term comparative data. We compared overall survival (OS) between NAC and adjuvant chemotherapy (AC) in luminal B-like breast cancer treated in routine practice.Patients and methods Patients enrolled in the prospective French CANTO cohort between January 2012 and December 2018 with unilateral, nonmetastatic, grade 3 HR-positive/HER2-negative BC (cT2-T3N0-N3M0) treated with NAC followed by surgery or with primary surgery followed by AC were included. The primary endpoint was OS; secondary endpoints were distant recurrence-free survival (DRFS) and invasive disease-free survival; exploratory endpoints were BC-specific survival, locoregional recurrence-free survival (LRFS) and breast recurrence-free survival. Inverse probability of treatment weighting (IPTW) was applied, with weighted Kaplan-Meier estimates and Cox models.Results Among 544 patients, 165 received NAC and 379 AC; median follow-up was 72 months. Breast-conserving surgery was more frequent after NAC (64% compared with 45%, P < 0.001) and the pCR rate was 19%. After IPTW, the hazard ratio for OS with NAC was 1.36 [95% confidence interval (CI) 0.94-1.97, P = 0.10] univariably and 1.62 (95% CI 1.10-2.38, P = 0.014) after multivariable adjustment. No difference was observed for DRFS (hazard ratio 1.05, 95% CI 0.80-1.38, P = 0.70). LRFS was worse with NAC (hazard ratio 2.29, 95% CI 1.15-4.58, P = 0.018) in 19 events. In interaction tests, the association with OS was confined to cN0 (hazard ratio 2.39) and cT2 (hazard ratio 1.94) disease and absent in cN+ (hazard ratio 0.83) and cT3 (hazard ratio 0.88) tumors.Conclusions NAC was associated with more locoregional recurrence without any difference in DRFS and the association with OS was confined to subgroups in whom a neoadjuvant indication is least established. These hypothesis-generating findings do not support the routine use of NAC in luminal B-like BC without an anticipated surgical benefit.
SN - 2949-8201
ER -