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Evaluation of trophoblast cell surface antigen-2 (TROP2) protein expression in chemotherapy-resistant and metastatic
Mieke R Van Bockstal1, Marie-Caroline Depelsemaeker2, Lina Daoud2
1Department of Pathology, Cliniques universitaires Saint-Luc, Avenue Hippocrate 10, Brussels 1200, Belgium; Pôle de Morphologie (MORF), Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Avenue Hippocrate 10, Brussels 1200, Belgium.
Abstract:
Trophoblast cell-surface antigen 2 (TROP2), a transmembrane receptor expressed in many carcinomas, is a target for novel antibody-drug conjugates such as sacituzumab govitecan. TROP2-targeted therapy is used for unresectable locally advanced or metastatic triple-negative and hormone receptor-positive, HER2-negative breast cancers. The role of TROP2 as a predictive marker is yet unclear. Standardized interpretation criteria for TROP2 immunohistochemistry (IHC) are lacking. Here, we compared three antibody clones and two methods for semi-quantitative assessment, aiming to establish reproducible evaluation criteria. First, TROP2 IHC was performed on normal tissues and nine breast cancers, using the BSB-148, EPR20043 and SP293 clones. EPR20043 was selected for subsequent evaluation in 69 breast cancers without pathological complete response to neoadjuvant chemotherapy (NAC). Four pathologists applied the ASCO/CAP guidelines for HER2 IHC testing (designated as the 'membrane score') and the H-score. All H-scores were categorized as low (0-100), intermediate (101-200) and high (201-300). Although the membrane scores strongly correlated with the categorized H-scores, the latter showed higher interobserver variability. Next, TROP2 IHC was performed on 94 breast cancer metastases and evaluated by six pathologists, confirming the strong correlation between the membrane scores and H-scores. In metastases, the interobserver variability was similar for both methods. Our observations support the application of the HER2 ASCO/CAP guidelines for semi-quantitative evaluation of membranous TROP2 protein expression, as this method strongly correlates with the H-score and is less prone to interobserver variability in post-NAC breast resections. Future studies should investigate the association between the TROP2 membrane score and response to TROP2-targeted therapy.
Insights
Standardized Trophoblast cell-surface antigen 2 (TROP2) immunohistochemistry (IHC) interpretation is needed for targeted therapies. This study suggests using ASCO/CAP HER2 guidelines for TROP2 IHC evaluation, showing strong correlation and reduced variability.
Area of Science:
- Oncology
- Immunohistochemistry
- Biomarker Analysis
Background:
- Trophoblast cell-surface antigen 2 (TROP2) is a key target for antibody-drug conjugates in breast cancer treatment.
- Standardized interpretation criteria for TROP2 immunohistochemistry (IHC) are currently lacking.
- Reproducible evaluation methods are crucial for TROP2's role as a predictive marker.
Purpose of the Study:
- To compare antibody clones and semi-quantitative assessment methods for TROP2 IHC.
- To establish reproducible evaluation criteria for TROP2 protein expression.
- To assess the utility of ASCO/CAP HER2 guidelines for TROP2 IHC scoring.
Main Methods:
- Compared three TROP2 antibody clones (BSB-148, EPR20043, SP293) on normal tissues and breast cancers.
- Evaluated TROP2 IHC using ASCO/CAP HER2 guidelines ('membrane score') and H-score in 69 breast cancers post-neoadjuvant chemotherapy (NAC).
- Assessed TROP2 IHC in 94 breast cancer metastases with multiple pathologists, comparing membrane scores and H-scores.
Main Results:
- The EPR20043 clone was selected for further evaluation.
- Membrane scores strongly correlated with categorized H-scores in both primary tumors and metastases.
- The ASCO/CAP HER2 guideline-based membrane score method showed lower interobserver variability, especially in post-NAC breast resections.
Conclusions:
- The ASCO/CAP HER2 guidelines provide a reproducible method for semi-quantitative TROP2 IHC evaluation.
- This method correlates well with the H-score and minimizes interobserver variability.
- Future research should link TROP2 membrane scores to treatment response in TROP2-targeted therapies.
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