Impact of HER2 Status Assessed by Immunohistochemistry on Treatment Response in Patients with Metastatic Breast Cancer Receiving Trastuzumab Emtansine

<i>Background and Objectives</i>: HER2-positive breast cancer accounts for approximately 20-30% of all breast cancer cases and is associated with aggressive tumor behavior. Trastuzumab emtansine (T-DM1), an antibody-drug conjugate targeting HER2, is a standard second-line therapy for patients with metastatic disease. However, the impact of HER2 immunohistochemistry (IHC) expression levels on T-DM1 efficacy remains unclear. <i>Materials and Methods</i>: This retrospective study examined 87 patients with HER2-positive metastatic breast cancer who received T-DM1 following trastuzumab-based therapy. Patients were divided into IHC 2+ and IHC 3+ groups. Progression-free survival (PFS) and overall survival (OS) were evaluated via Kaplan-Meier analysis, and group comparisons were conducted using the log-rank test. <i>Results</i>: The median progression-free survival (PFS) for the entire cohort was 7.3 months (95% CI: 5.277-9.323), with a numerically longer PFS in the IHC 3+ group (8.4 months, 95% CI: 5.915-10.952) compared to the IHC 2+ group (6.3 months, 95% CI: 4.178-8.422). However, this difference was insignificant (HR: 0.91, 95% CI: 0.61-1.35; <i>p</i> = 0.778). Similarly, the median overall survival (OS) was 23.3 months (95% CI: 18.039-28.495), with the IHC 3+ group exhibiting a slightly longer OS (24.5 months, 95% CI: 18.600-30.400) compared to the IHC 2+ group (23.2 months, 95% CI: 12.387-34.147). Again, this difference did not reach statistical significance (HR: 0.93, 95% CI: 0.63-1.42; <i>p</i> = 0.369). <i>Conclusions</i>: Although the association between HER2 IHC 3+ expression and longer PFS and OS is promising, the lack of statistical significance suggests that IHC-based HER2 stratification alone may not be sufficient to predict the response to T-DM1. The potential of conducting prospective studies with larger cohorts and comprehensive molecular profiling to refine predictive biomarkers for optimizing therapeutic outcomes in HER2-positive metastatic breast cancer is a beacon of hope and should be pursued with optimism.

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Journal
Medicina
Published
2025-04-29
DOI
https://doi.org/10.3390/medicina61050819
Citations
1
Primary Topic
HER2/EGFR in Cancer Research
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article
Field-Weighted Citation Impact
1.05
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article

Impact of HER2 Status Assessed by Immunohistochemistry on Treatment Response in Patients with Metastatic Breast Cancer Receiving Trastuzumab Emtansine

Sıla Öksüz, Heves Sürmeli, Oğuzcan Kınıkoğlu, Nedim Turan et al.
1 citations
Medicina
HER2/EGFR in Cancer Research
1.05
article

Impact of HER2 Status Assessed by Immunohistochemistry on Treatment Response in Patients with Metastatic Breast Cancer Receiving Trastuzumab Emtansine

Sıla Öksüz, Heves Sürmeli, Oğuzcan Kınıkoğlu, Nedim Turan, Uğur Özkerim, Hatice Odabaş, Deniz Işık, Seval Ay, Yunus Emre Altıntaş, Tuğba Başoğlu
article en
1 citations

Abstract

<i>Background and Objectives</i>: HER2-positive breast cancer accounts for approximately 20-30% of all breast cancer cases and is associated with aggressive tumor behavior. Trastuzumab emtansine (T-DM1), an antibody-drug conjugate targeting HER2, is a standard second-line therapy for patients with metastatic disease. However, the impact of HER2 immunohistochemistry (IHC) expression levels on T-DM1 efficacy remains unclear. <i>Materials and Methods</i>: This retrospective study examined 87 patients with HER2-positive metastatic breast cancer who received T-DM1 following trastuzumab-based therapy. Patients were divided into IHC 2+ and IHC 3+ groups. Progression-free survival (PFS) and overall survival (OS) were evaluated via Kaplan-Meier analysis, and group comparisons were conducted using the log-rank test. <i>Results</i>: The median progression-free survival (PFS) for the entire cohort was 7.3 months (95% CI: 5.277-9.323), with a numerically longer PFS in the IHC 3+ group (8.4 months, 95% CI: 5.915-10.952) compared to the IHC 2+ group (6.3 months, 95% CI: 4.178-8.422). However, this difference was insignificant (HR: 0.91, 95% CI: 0.61-1.35; <i>p</i> = 0.778). Similarly, the median overall survival (OS) was 23.3 months (95% CI: 18.039-28.495), with the IHC 3+ group exhibiting a slightly longer OS (24.5 months, 95% CI: 18.600-30.400) compared to the IHC 2+ group (23.2 months, 95% CI: 12.387-34.147). Again, this difference did not reach statistical significance (HR: 0.93, 95% CI: 0.63-1.42; <i>p</i> = 0.369). <i>Conclusions</i>: Although the association between HER2 IHC 3+ expression and longer PFS and OS is promising, the lack of statistical significance suggests that IHC-based HER2 stratification alone may not be sufficient to predict the response to T-DM1. The potential of conducting prospective studies with larger cohorts and comprehensive molecular profiling to refine predictive biomarkers for optimizing therapeutic outcomes in HER2-positive metastatic breast cancer is a beacon of hope and should be pursued with optimism.

MedicinaVol. 61(5)
Dr Lütfi Kırdar Kartal Eğitim ve Araştırma Hastanesi (TR), Sağlık Bilimleri Üniversitesi (TR)
Good health and well-being
Openalex Percentile: Top 22%
HER2/EGFR in Cancer Research
1.05
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