# Screening and exploration of neoadjuvant “de-escalation” therapy for early breast cancer

**Authors:** Nana Zhang, Ming Shan, Zhenfeng Huang, Fei Gao, Bingqi Xu, Wenli Kang, Jian Zhang, Li Song, Jun Liu, Jiawei Zhang, Mingyang Liu, Haitao Jiang, Xinhang Liu, Zibo Shen, Peng Zhang, Abiyasi Nanding, Guoqiang Zhang

PMC · DOI: 10.3389/fphar.2025.1574665 · Frontiers in Pharmacology · 2025-03-25

## TL;DR

This study explores whether patients with early breast cancer who achieve a complete response after initial chemotherapy can safely avoid further treatment.

## Contribution

The study identifies that achieving pCR after a short neoadjuvant therapy may allow for de-escalation of treatment without compromising survival.

## Key findings

- Patients achieving pCR after short neoadjuvant therapy had high 4-year DFS and OS rates.
- Postoperative adjuvant chemotherapy significantly improved DFS compared to no adjuvant therapy.
- Targeted therapy or platinum drugs did not improve outcomes for HER2+ or TNBC patients with pCR.

## Abstract

Neoadjuvant therapy for breast cancer improves the prognosis of high-risk patients. However, whether pathological completed response (pCR) can be used as a surrogate endpoint for de-escalation therapy in patients who are relatively sensitive to treatment remains to be elucidated.

We retrospectively reviewed 143 breast cancer patients, with clinical stage (cStage) II–IIIA who received neoadjuvant chemotherapy and achieved pCR in a short time (within 16 weeks) from 2012 to 2022. The prognosis of patients was analysed using the Kaplan-Meier method, Cox proportional hazards regression models to identify independent clinicopathologic factors affecting prognosis.

The median follow-up period was 47 months, the overall 4-year disease-free survival (DFS) and overall survival (OS) were 95.3% and 96.9%, respectively, in 143 patients with pCR after neoadjuvant chemotherapy. The 4-year DFS between the postoperative adjuvant chemotherapy and no adjuvant chemotherapy groups was 76.4% and 95.2%, with a significant statistical difference between both groups (P < 0.05). For HER2-positive (HER2+) and Triple negative breast cancer (TNBC), the addition of targeted therapy or platinum-based drugs had no impact on prognosis. Univariate and multivariate analyses of prognosis showed that only postoperative adjuvant chemotherapy significantly affected prognosis.

Patients with operable cStage II–IIIA breast cancer who achieved pCR after a short period of neoadjuvant chemotherapy have a satisfactory prognosis and may be suitable for chemotherapy “de-escalation.” This approach is also a dominant application of neoadjuvant “tailoring therapy.”

## Linked entities

- **Diseases:** breast cancer (MONDO:0004989), Triple negative breast cancer (MONDO:0005494)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}
- **Diseases:** TNBC (MESH:D064726), breast cancer (MESH:D001943)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11975863/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC11975863/full.md

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Source: https://tomesphere.com/paper/PMC11975863