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A population-based study on trajectories of HER2 status during neoadjuvant chemotherapy for early breast cancer and metastatic progression.
Boman, Caroline; Liu, Xingrong; Eriksson Bergman, Louise; Sun, Wenwen; Tranchell, Christian; Toli, Maria Angeliki; Acs, Balazs; Bergh, Jonas; Foukakis, Theodoros; Matikas, Alexios.
Affiliation
  • Boman C; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
  • Liu X; Breast Center, Karolinska Comprehensive Cancer Center, Stockholm, Sweden.
  • Eriksson Bergman L; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
  • Sun W; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
  • Tranchell C; Department of Surgery and Oncology, Capio Sankt Göran Hospital, Stockholm, Sweden.
  • Toli MA; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
  • Acs B; Department of Clinical Pathology and Cancer Diagnostics, Karolinska University Hospital, Stockholm, Sweden.
  • Bergh J; Breast Center, Karolinska Comprehensive Cancer Center, Stockholm, Sweden.
  • Foukakis T; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
  • Matikas A; Karolinska Institutet, Oncology/Pathology Department, Stockholm, Sweden.
Br J Cancer ; 131(4): 718-728, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38942987
ABSTRACT

BACKGROUND:

This study aimed to investigate the distribution and changes of HER2 status in untreated tumours, in residual disease and in metastasis, and their long-term prognostic implications.

METHODS:

This is a population-based cohort study of patients treated with neoadjuvant chemotherapy for breast cancer during 2007-2020 in the Stockholm-Gotland region which comprises 25% of the entire Swedish population. Information was extracted from the National Breast Cancer Registry and electronic patient charts to minimize data missingness and misclassification.

RESULTS:

In total, 2494 patients received neoadjuvant chemotherapy, of which 2309 had available pretreatment HER2 status. Discordance rates were 29.9% between primary and residual disease (kappa = 0.534), 31.2% between primary tumour and metastasis (kappa = 0.512) and 33.3% between residual disease to metastasis (kappa = 0.483). Adjusted survival curves differed between primary HER2 0 and HER2-low disease (p < 0.001), with the former exhibiting an early peak in risk for death which eventually declined below the risk of HER2-low. Across all disease settings, increasing the number of biopsies increased the likelihood of detecting HER2-low status.

CONCLUSION:

HER2 status changes during neoadjuvant chemotherapy and metastatic progression, and the long-term behaviours of HER2 0 and HER2-low disease differ, underscoring the need for obtaining tissue biopsies and for extended follow-up in breast cancer studies.
Subject(s)
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Receptor, ErbB-2 / Disease Progression / Neoadjuvant Therapy Limits: Adult / Aged / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Br J Cancer Year: 2024 Document type: Article Affiliation country: Sweden Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Receptor, ErbB-2 / Disease Progression / Neoadjuvant Therapy Limits: Adult / Aged / Female / Humans / Middle aged Country/Region as subject: Europa Language: En Journal: Br J Cancer Year: 2024 Document type: Article Affiliation country: Sweden Country of publication: United kingdom