Title Comparing Biomarkers for Predicting Pathological Responses to Neoadjuvant Therapy in HER2-Positive Breast Cancer: A Systematic Review and Meta-Analysis
Authors Zhao, Fuxing
Huo, Xingfa
Wang, Miaozhou
Liu, Zhen
Zhao, Yi
Ren, Dengfeng
Xie, Qiqi
Liu, Zhilin
Li, Zitao
Du, Feng
Shen, Guoshuang
Zhao, Jiuda
Affiliation Qinghai Univ, Affiliated Hosp, Breast Dis Diag & Treatment Ctr, Xining, Peoples R China
Qinghai Univ, Affiliated Canc Hosp, Xining, Peoples R China
Peking Univ, Med Dept, VIPII Gastrointestinal Canc Div, Minist Educ,Key Lab Carcinogenesis & Translat Res, Beijing, Peoples R China
Keywords TUMOR-INFILTRATING LYMPHOCYTES
PHASE-II
OPEN-LABEL
PLUS TRASTUZUMAB
PIK3CA MUTATIONS
FREE SURVIVAL
HER2-TARGETED THERAPY
CHEMOTHERAPY PLUS
ANTI-HER2 THERAPY
RECEPTOR STATUS
Issue Date 28-Oct-2021
Publisher FRONTIERS IN ONCOLOGY
Abstract Introduction: The predictive strength and accuracy of some biomarkers for the pathological complete response (pCR) to neoadjuvant therapy for HER2-positive breast cancer remain unclear. This study aimed to compare the accuracy of the HER2-enriched subtype and the presence of PIK3CA mutations, namely, TILs, HRs, and Ki-67, in predicting the pCR to HER2-positive breast cancer therapy.

Methods: We screened studies that included pCR predicted by one of the following biomarkers: the HER2-enriched subtype and the presence of PIK3CA mutations, TILs, HRs, or Ki-67. We then calculated the pooled sensitivity, specificity, positive and negative predictive values (PPVs and NPVs, respectively), and positive and negative likelihood ratios (LRs). Summary receiver operating characteristic (SROC) curves and areas under the curve (AUCs) were used to estimate the diagnostic accuracy.

Results:& nbsp;The pooled estimates of sensitivity and specificity for the HER2-enriched subtype and the presence of PIK3CA mutations, namely, TILs, HRs, and Ki-67, were 0.66 and 0.62, 0.85 and 0.27, 0.49 and 0.61, 0.54 and 0.64, and 0.68 and 0.51, respectively. The AUC of the HER2-enriched subtype was significantly higher (0.71) than those for the presence of TILs (0.59, p = 0.003), HRs (0.65, p = 0.003), and Ki-67 (0.62, p = 0.005). The AUC of the HER2-enriched subtype had a tendency to be higher than that of the presence of PIK3CA mutations (0.58, p = 0.220). Moreover, it had relatively high PPV (0.58) and LR+ (1.77), similar NPV (0.73), and low LR- (0.54) compared with the other four biomarkers.

Conclusions: The HER2-enriched subtype has a moderate breast cancer diagnostic accuracy, which is better than those of the presence of PIK3CA mutations, TILs, HRs, and Ki-67.

URI http://hdl.handle.net/20.500.11897/629369
ISSN 2234-943X
DOI 10.3389/fonc.2021.731148
Indexed SCI(E)
Appears in Collections: 待认领

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