# Real-World Evidence of Long-Term Disease Control in HER2-Positive Metastatic Breast Cancer Patients Treated with a First-Line Combination of Trastuzumab and/or Pertuzumab Plus Chemotherapy

**Authors:** Loïc Chaigneau, Eva Lapp, Taha Jai, Erion Dobi, Berenger Martin, Elsa Curtit, Virginie Nerich

PMC · DOI: 10.3390/cancers17213532 · Cancers · 2025-10-31

## TL;DR

Some HER2-positive metastatic breast cancer patients treated with trastuzumab and chemotherapy maintain long-term disease control, suggesting potential for treatment discontinuation.

## Contribution

This study provides real-world evidence of long-term disease control in HER2-positive metastatic breast cancer patients using first-line targeted therapy plus chemotherapy.

## Key findings

- 17.5% of 280 patients maintained disease control for at least three years.
- Median progression-free survival was 11.0 years, with a 90% objective response rate.
- 15% of patients discontinued treatment without immediate disease progression.

## Abstract

This study examines women with HER2-positive metastatic breast cancer who were treated with a combination of trastuzumab and/or pertuzumab plus chemotherapy as their first treatment. Out of 280 patients, 48 (17.5%) maintained control of their disease for at least three years. Most were women with an average age of 56.7 years, and around 70% had newly diagnosed metastatic cancer. Nearly 90% of patients responded to the treatment, with a median response duration of 5.8 years and a median progression-free survival of 11.0 years. These findings suggest that some patients can achieve long-term disease control, raising questions about treatment intensification and the possibility of stopping treatment. Future research is needed to identify factors that predict long-lasting responses.

Background and Method: The overexpression of the human epidermal growth factor receptor 2 (HER2) in breast cancer is correlated with accelerated tumor progression and an unfavorable clinical outcome. Since the introduction of trastuzumab in 2002, the treatment of HER2-positive breast cancer has been revolutionized, leading to significant improvements in survival. This retrospective, multicenter study aimed to describe the characteristics of patients with HER2-positive metastatic breast cancer (MBC) who maintained disease control for a minimum of three years after first-line therapy with trastuzumab and/or pertuzumab combined with chemotherapy. Results: Among 280 eligible patients, 48 (17.5%) were classified as long-term responders. The study population primarily consisted of women with a median age of 56.7 years at diagnosis; de novo metastatic presentation was observed in approximately 70% of cases. An objective response rate of nearly 90% was observed, with a median duration of response of 5.8 years. Median progression-free survival was 11.0 years [95% CI: 6.6—not reached], and median overall survival was not reached [95% CI: 10.9—not reached]. Furthermore, about 15% of patients were able to discontinue systemic therapy without immediate disease progression. Discussion and Conclusions: These findings indicate the potential of achieving prolonged disease control in a subset of patients with HER2-positive MBC, raising questions about therapeutic intensification and potential treatment discontinuation strategies. This study underscores the need for future research to identify predictive factors of durable response and assess the feasibility of adaptive treatment strategies, including planned treatment discontinuation.

## Linked entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064]
- **Diseases:** breast cancer (MONDO:0004989)

## 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:** tumor (MESH:D009369), Breast Cancer (MESH:D001943)
- **Chemicals:** Pertuzumab (MESH:C485206), Trastuzumab (MESH:D000068878)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12606757/full.md

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Source: https://tomesphere.com/paper/PMC12606757