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Association of ERBB2 Copy Number and Gene Coalterations With Trastuzumab Efficacy and Resistance in Human Epidermal Growth Factor Receptor 2–Positive Esophagogastric and Gastric Cancer.

Authors :
Hino, Kaori
Nishina, Tomohiro
Kajiwara, Takeshi
Bando, Hideaki
Nakamura, Maho
Kadowaki, Shigenori
Minashi, Keiko
Yuki, Satoshi
Ohta, Takashi
Hara, Hiroki
Mizukami, Takuro
Moriwaki, Toshikazu
Ohtsubo, Koushiro
Komoda, Masato
Mitani, Seiichiro
Nagashima, Fumio
Kato, Ken
Yamada, Takanobu
Hasegawa, Hiroko
Yamazaki, Kentaro
Source :
JCO Precision Oncology; 8/11/2022, Vol. 6, p1-11, 11p
Publication Year :
2022

Abstract

PURPOSE: ERBB2 copy number (CN), measured using next-generation sequencing, is a predictive biomarker for trastuzumab efficacy in human epidermal growth factor receptor 2 (HER2)–positive advanced esophagogastric and gastric cancer (AGC). We aimed to investigate the association of ERBB2 amplification and gene coalterations with response and resistance to trastuzumab-combined chemotherapy. METHODS: The SCRUM-Japan GI-SCREEN was a comprehensive genomic profiling project of GI cancer tissues using Oncomine Cancer Research Panel and Oncomine Comprehensive Assay. From 885 patients with AGC who successfully underwent gene profiling, 74 with ERBB2 amplification (CN ≥ 4.0) and who received first-line trastuzumab-combined chemotherapy were selected, and ERBB2 CN and gene coalterations were assessed. RESULTS: ERBB2 CN did not differ in tumor response to trastuzumab-combined chemotherapy (one-way analysis of variance test, P =.37). Multivariate analysis using the Cox proportional hazard model revealed that ERBB2 CN (continuous log<subscript>2</subscript>-converted CN, hazard ratio, 0.76; 95% CI, 0.62 to 0.93; P <.01) and receptor/oncogene amplifications in the HER2 signaling pathway (hazard ratio, 2.5; 95% CI, 1.2 to 5.3; P =.01) were significant predictors for progression-free survival (PFS). ERBB2 variants coexisted in five patients (7%) and were missense mutations. Two patients with low variant allele frequencies (VAFs; 8%, 12%) showed high ERBB2 CN (55, 80) and durable response (≥ 20 months), whereas three patients with high VAFs (66%–90%) showed low ERBB2 CN (8-11) and no response with short PFS (1-10 months). CONCLUSION: ERBB2 CN and gene coamplification in the HER2 signaling pathway were positive and negative predictors of PFS in trastuzumab-treated HER2-positive AGC patients, respectively. HER2-positive AGC patients with a high VAF of ERBB2 showed poor outcomes and may need HER2 tyrosine kinase inhibitors and trastuzumab deruxtecan. ERBB2 CN and gene coamplification on the HER2 pathway in gastric cancer are predictors for trastuzumab response. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
24734284
Volume :
6
Database :
Complementary Index
Journal :
JCO Precision Oncology
Publication Type :
Academic Journal
Accession number :
158484332
Full Text :
https://doi.org/10.1200/PO.22.00135