Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2024 Jun 19;10(1):49.
doi: 10.1038/s41523-024-00652-4.

The survival benefit of adjuvant trastuzumab with or without chemotherapy in the management of small (T1mic, T1a, T1b, T1c), node negative HER2+ breast cancer

Affiliations

The survival benefit of adjuvant trastuzumab with or without chemotherapy in the management of small (T1mic, T1a, T1b, T1c), node negative HER2+ breast cancer

Kai C C Johnson et al. NPJ Breast Cancer. .

Abstract

There is limited data regarding the added benefit of adjuvant systemic therapy in the management of small, node-negative, HER2+ breast cancer. In a multi-institutional retrospective analysis using the American Society of Clinical Oncology CancerLinQ database, we compared survival outcomes among T1a-c N0 HER2+ patients diagnosed between 2010 to 2021 who received locoregional therapy alone or in combination with adjuvant trastuzumab (+/- chemotherapy). Primary outcomes were invasive disease-free survival (iDFS) and overall survival (OS). Of the 1,184 patients, 436 received locoregional therapy alone. We found a statistically significant improvement in iDFS (HR 0.73, P = 0.003) and OS (HR 0.63, P = 0.023) on univariate analysis with adjuvant trastuzumab with or without chemotherapy which remained statistically significant on multivariate analysis. Three-arm univariate analysis found that iDFS was significantly improved with trastuzumab monotherapy (P = 0.003) and combination therapy (P = 0.027) compared to observation. Subgroup data suggests that T1b/c tumors derive the greatest benefit.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Survival outcomes with or without systemic therapy for T1N0 HER2+ breast cancer.
Univariate analysis of iDFS (a) and OS (b) in our two-group comparison of adjuvant trastuzumab with or without systemic chemotherapy versus locoregional therapy alone.
Fig. 2
Fig. 2. Survival outcomes for T1N0 HER2+ breast cancer following locoregional therapy alone versus trastuzumab monotherapy versus combination therapy.
Univariate analysis of iDFS (a) and OS (b) in our three-group comparison of locoregional therapy alone versus trastuzumab monotherapy versus chemotherapy with trastuzumab.
Fig. 3
Fig. 3. Survival outcomes for T1N0 HER2+ breast cancer based on T1 subgroup following locoregional therapy alone versus trastuzumab monotherapy versus combination therapy.
Subgroup analysis of iDFS (a, b) and OS (c, d) within the 3-arm treatment comparison with an overall test of treatment effect based on T1a (a, c) and T1b/c (b, d) tumor sub-categorization.

References

    1. Slamon DJ, et al. Human breast cancer: correlation of relapse and survival with amplification of the HER-2/neu oncogene. Science. 1987;235:177–182. doi: 10.1126/science.3798106. - DOI - PubMed
    1. Moasser MM. The oncogene HER2: its signaling and transforming functions and its role in human cancer pathogenesis. Oncogene. 2007;26:6469–6487. doi: 10.1038/sj.onc.1210477. - DOI - PMC - PubMed
    1. Slamon DJ, et al. Use of chemotherapy plus a monoclonal antibody against HER2 for metastatic breast cancer that overexpresses HER2. New Engl. J. Med. 2001;344:783–792. doi: 10.1056/NEJM200103153441101. - DOI - PubMed
    1. Romond EH, et al. Trastuzumab plus adjuvant chemotherapy for operable HER2-positive breast cancer. New Engl. J. Med. 2005;353:1673–1684. doi: 10.1056/NEJMoa052122. - DOI - PubMed
    1. Piccart-Gebhart MJ, et al. Herceptin adjuvant (HERA) trial study team. trastuzumab after adjuvant chemotherapy in HER2-positive breast cancer. New Engl. J. Med. 2005;353:1659–1672. doi: 10.1056/NEJMoa052306. - DOI - PubMed