TY - JOUR
T1 - International Expert Consensus Recommendations for HER2 Reporting in Breast Cancer
T2 - Focus on HER2-Low and Ultralow Categories
AU - UK National Coordinating Committee of Breast Pathology, the Association of Breast Pathology, the European Working Group for Breast Screening Pathology and the International Society of Breast Pathology
AU - Rakha, Emad A.
AU - Tan, Puay Hoon
AU - Van Bockstal, Mieke R.
AU - Allison, Kimberly H.
AU - Brogi, Edi
AU - Callagy, Grace
AU - Cserni, Gábor
AU - Jaffer, Shabnam
AU - Foschini, Maria Pia
AU - Gobbi, Helenice
AU - Kulka, Janina
AU - Li, Xiaoxian
AU - Provenzano, Elena
AU - Shaaban, Abeer M.
AU - Tse, Gary M.
AU - Varga, Zsuzsanna
AU - Vincent-Salomon, Anne
AU - Yamaguchi, Rin
AU - Yang, Wentao
AU - ElSheikh, Soha
AU - Bhargava, Rohit
AU - De Brot, Marina
AU - Canas-Marques, Rita
AU - Marchiò, Caterina
AU - Warren, Madhuri V.
AU - van Deurzen, Carolien H.M.
AU - Mir, Yasmeen
AU - Deb, Rahul
AU - Wen, Hannah
AU - Ellis, Ian O.
AU - Schnitt, Stuart J.
AU - Pinder, Sarah E.
AU - Raymond, Wendy
AU - Quinn, Cecily
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2026/1
Y1 - 2026/1
N2 - The concept of “HER2-negative” breast cancer is evolving, with the recognition of HER2-low and HER2-ultralow subsets. These subsets are clinically relevant regarding treatment with the antibody-drug conjugate trastuzumab deruxtecan (T-DXd), which has shown survival benefit in patients with metastatic carcinoma with minimal HER2 protein expression that lack HER2 gene amplification by in situ hybridization. In clinical trials using T-DXd, HER2-low was defined as an immunohistochemistry (IHC) score 1+ or an IHC score 2+ without HER2 gene amplification. HER2-ultralow was defined as faint or barely perceptible, incomplete membrane staining in >0% to ≤10% of tumor cells (IHC score 0+/with membrane staining) and HER2-null as the complete absence of staining (IHC score 0/absent membrane staining). These results now necessitate more detailed evaluation and reporting of traditional “HER2-negative” results to identify patients with metastatic breast cancer who may benefit from T-DXd therapy. Both the US Food and Drug Administration and the European Medicines Agency have extended the regulatory approval of T-DXd to patients with metastatic breast cancer showing HER2-low or HER2-ultralow expressions. Updated clinical management guidelines now, therefore, incorporate the spectrum of HER2 results into treatment selection algorithms in the metastatic setting. To align histopathologic practice with these developments, the College of American Pathologists has issued a new biomarker-reporting template that recommends explicit distinction between IHC 0/absent membrane staining and IHC 0+/with membrane staining. Key concerns among pathologists include assay variability, scoring reproducibility, and quality assurance standards for accurately detecting such low levels of HER2 expression. This manuscript provides expert consensus, evidence-based practical recommendations for identifying and reporting tumors with HER2-low and HER2-ultralow expression. We emphasize standardized testing protocols, validated assays, robust internal and external controls, and focused training for pathologists. A universal structured pathology report is proposed to highlight the accurate distinction between IHC 0 (null), IHC 0+ (ultralow), and HER2-low expressions.
AB - The concept of “HER2-negative” breast cancer is evolving, with the recognition of HER2-low and HER2-ultralow subsets. These subsets are clinically relevant regarding treatment with the antibody-drug conjugate trastuzumab deruxtecan (T-DXd), which has shown survival benefit in patients with metastatic carcinoma with minimal HER2 protein expression that lack HER2 gene amplification by in situ hybridization. In clinical trials using T-DXd, HER2-low was defined as an immunohistochemistry (IHC) score 1+ or an IHC score 2+ without HER2 gene amplification. HER2-ultralow was defined as faint or barely perceptible, incomplete membrane staining in >0% to ≤10% of tumor cells (IHC score 0+/with membrane staining) and HER2-null as the complete absence of staining (IHC score 0/absent membrane staining). These results now necessitate more detailed evaluation and reporting of traditional “HER2-negative” results to identify patients with metastatic breast cancer who may benefit from T-DXd therapy. Both the US Food and Drug Administration and the European Medicines Agency have extended the regulatory approval of T-DXd to patients with metastatic breast cancer showing HER2-low or HER2-ultralow expressions. Updated clinical management guidelines now, therefore, incorporate the spectrum of HER2 results into treatment selection algorithms in the metastatic setting. To align histopathologic practice with these developments, the College of American Pathologists has issued a new biomarker-reporting template that recommends explicit distinction between IHC 0/absent membrane staining and IHC 0+/with membrane staining. Key concerns among pathologists include assay variability, scoring reproducibility, and quality assurance standards for accurately detecting such low levels of HER2 expression. This manuscript provides expert consensus, evidence-based practical recommendations for identifying and reporting tumors with HER2-low and HER2-ultralow expression. We emphasize standardized testing protocols, validated assays, robust internal and external controls, and focused training for pathologists. A universal structured pathology report is proposed to highlight the accurate distinction between IHC 0 (null), IHC 0+ (ultralow), and HER2-low expressions.
KW - HER2 classification
KW - breast cancer
KW - low
KW - reporting guidelines
KW - ultralow
UR - https://www.scopus.com/pages/publications/105022625191
U2 - 10.1016/j.modpat.2025.100925
DO - 10.1016/j.modpat.2025.100925
M3 - Review article
C2 - 41167529
AN - SCOPUS:105022625191
SN - 0893-3952
VL - 39
JO - Modern Pathology
JF - Modern Pathology
IS - 1
M1 - 100925
ER -