Comparison of HER2-zero and HER2-low in terms of clinicopathological factors and survival in early-stage breast cancer: A systematic review and meta-analysis
Özet
Background: The prognostic differences between HER2-zero and HER2-low breast cancer (BC) remain unclear. Purpose of this meta-analysis is to investigate the differences between HER2-low and HER2-zero in terms of clinicopathological factors and survival outcomes in early-stage BC. Methods: We searched major databases and congress proceedings until November 1, 2022 to identify studies comparing HER2-zero and HER2-low in early-stage BC. HER2-zero immunohistochemically (IHC) was defined as score 0, while HER2-low was defined as IHC 1+ or 2+/in situ hybridization negative. Result: A total of 23 retrospective studies involving 636,535 patients were included. HER2-low rate was 67.5% in the hormone receptor (HR)-positive group, while this rate was 48.6% in the HR-negative group. In the analysis of clinicopathological factors by HR status, the proportion of premenopausal patients within the HR-positive group was greater in the HER2-zero arm (66.5% vs 61.8%), whereas grade 3 tumors (74.2% vs 71.5%), patients younger than 50 years of age (47.3% vs 39.6%), and T3-T4 tumors (7.7% vs 6.3%) within the HR-negative group was higher in the HER2-zero arm. In both the HR-positive and HR-negative groups, the HER2-low arm showed significantly improved results for disease-free survival (DFS) and overall survival (OS). The hazard ratios for DFS and OS in the HR-positive group were 0.88 (95% CI 0.83–0.94) and 0.87 (95% CI 0.78–0.96), respectively. In the HR-negative group, the hazard ratios for DFS and OS were 0.87 (95% CI 0.79–0.97) and 0.86 (95% CI 0.84–0.89), respectively. Conclusion: In early-stage BC, HER2-low is associated with better DFS and OS compared to HER2-zero, regardless of HR status. © 2023 Elsevier Ltd
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Ergun, Yakup | |
| dc.contributor.author | Ucar, Gokhan | |
| dc.contributor.author | Akagunduz, Baran | |
| dc.date.accessioned | 2026-10-18T20:27:00.424646286Z | |
| dc.date.available | 2026-10-18T20:27:00.424646286Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | Background: The prognostic differences between HER2-zero and HER2-low breast cancer (BC) remain unclear. Purpose of this meta-analysis is to investigate the differences between HER2-low and HER2-zero in terms of clinicopathological factors and survival outcomes in early-stage BC. Methods: We searched major databases and congress proceedings until November 1, 2022 to identify studies comparing HER2-zero and HER2-low in early-stage BC. HER2-zero immunohistochemically (IHC) was defined as score 0, while HER2-low was defined as IHC 1+ or 2+/in situ hybridization negative. Result: A total of 23 retrospective studies involving 636,535 patients were included. HER2-low rate was 67.5% in the hormone receptor (HR)-positive group, while this rate was 48.6% in the HR-negative group. In the analysis of clinicopathological factors by HR status, the proportion of premenopausal patients within the HR-positive group was greater in the HER2-zero arm (66.5% vs 61.8%), whereas grade 3 tumors (74.2% vs 71.5%), patients younger than 50 years of age (47.3% vs 39.6%), and T3-T4 tumors (7.7% vs 6.3%) within the HR-negative group was higher in the HER2-zero arm. In both the HR-positive and HR-negative groups, the HER2-low arm showed significantly improved results for disease-free survival (DFS) and overall survival (OS). The hazard ratios for DFS and OS in the HR-positive group were 0.88 (95% CI 0.83–0.94) and 0.87 (95% CI 0.78–0.96), respectively. In the HR-negative group, the hazard ratios for DFS and OS were 0.87 (95% CI 0.79–0.97) and 0.86 (95% CI 0.84–0.89), respectively. Conclusion: In early-stage BC, HER2-low is associated with better DFS and OS compared to HER2-zero, regardless of HR status. © 2023 Elsevier Ltd | |
| dc.identifier.doi | 10.1016/j.ctrv.2023.102538 | |
| dc.identifier.eissn | 1532-1967 | |
| dc.identifier.issn | 0305-7372 | |
| dc.identifier.pmid | 36898351 | |
| dc.identifier.scopus | 2-s2.0-85149652836 | |
| dc.identifier.startpage | 102538 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12053 | |
| dc.identifier.volume | 115 | |
| dc.identifier.wos | WOS:000954668100001 | |
| dc.language.iso | en | |
| dc.publisher | W.B. Saunders Ltd | |
| dc.relation.ispartof | Cancer Treatment Reviews | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Breast cancer | |
| dc.subject | HER2-low | |
| dc.subject | HER2-zero | |
| dc.subject | Hormone receptor | |
| dc.subject | Meta-analysis | |
| dc.subject | Prognosis | |
| dc.subject | Breast Neoplasms | |
| dc.subject | Disease-Free Survival | |
| dc.subject | Female | |
| dc.subject | Humans | |
| dc.subject | Proportional Hazards Models | |
| dc.subject | Receptor, ErbB-2 | |
| dc.subject | Retrospective Studies | |
| dc.subject | antineoplastic agent | |
| dc.subject | epidermal growth factor receptor 2 | |
| dc.subject | bibliographic database | |
| dc.subject | breast cancer molecular subtype | |
| dc.subject | cancer grading | |
| dc.subject | cancer prognosis | |
| dc.subject | cancer risk | |
| dc.subject | cancer staging | |
| dc.subject | cancer surgery | |
| dc.subject | cancer survival | |
| dc.subject | clinical feature | |
| dc.subject | clinical outcome | |
| dc.subject | confidence interval | |
| dc.subject | correlation analysis | |
| dc.subject | data extraction | |
| dc.subject | data quality assessment | |
| dc.subject | disease free survival | |
| dc.title | Comparison of HER2-zero and HER2-low in terms of clinicopathological factors and survival in early-stage breast cancer: A systematic review and meta-analysis | |
| dc.type | Review Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 67 | |
| rdl.citation.wos | 67 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
