Global Ring Study to Investigate the Comparability of Total Assay Performance of Commercial Claudin 18 Antibodies for Evaluation in Gastric Cancer

被引:7
作者
Jasani, Bharat [1 ]
Taniere, Philippe [2 ]
Schildhaus, Hans-Ulrich [1 ]
Blighe, Kevin [3 ]
Parry, Suzanne [4 ]
Wilkinson, Dawn [4 ]
Atkey, Neil [5 ]
Clare-Antony, Scott [5 ]
McCabe, Clare [5 ]
Quinn, Christine [5 ]
Dodson, Andrew [4 ]
机构
[1] Discovery Life Sci DLS Biomarker Serv GmbH, Dept Social Sci, Kassel, Germany
[2] Univ Hosp Birmingham NHS Fdn Trust, Birmingham, England
[3] Clin Bioinformat Res Ltd, London, England
[4] UK Natl External Qual Assessment Scheme Immunocyto, London, England
[5] Diaceutics Plc, Belfast, North Ireland
关键词
Claudin-18.2; CLDN18.2; zolbetuximab; gastroesophageal junction; adenocarcinoma; gastric adenocarcinoma; POSITIVE SOLID TUMORS; GASTROESOPHAGEAL JUNCTION; OPEN-LABEL; IMMUNOHISTOCHEMISTRY; EFFICACY; LUNG;
D O I
10.1016/j.labinv.2023.100284
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Claudin 18.2 (CLDN18.2), the dominant isoform of CLDN18 in gastric tissues, is a highly specific tight junction protein of the gastric mucosa with variably retained expressions in gastric and gastroesophageal junction cancers. Additionally, CLDN18.2-targeted treatment with zolbetuximab, in combination with chemotherapy, has recently been assessed in 2 phase-III studies of patients with HER2-negative, locally advanced, unresectable, or metastatic gastric or gastroesophageal junction adenocarcinoma. These trials used the investigational VENTANA CLDN18 (43-14A) RxDx immunohistochemistry (IHC) assay on the Ventana BenchMark platform to identify patients eligible for CLDN18.2-targeted treatment. We report the findings of a global ring study evaluating the analytical comparability of concordance of the results of 3 CLDN18 antibodies (Ventana, LSBio, and Novus) stained on 3 IHC-staining platforms (Ventana, Dako, and Leica). A tissue microarray (TMA), comprising 15 gastric cancer cases, was stained by 27 laboratories across 11 countries. Each laboratory stained the TMAs using at least 2 of the 3 evaluated CLDN18 antibodies. Stained TMAs were assessed and scored using an agreed IHC-scoring algorithm, and the results were collated for statistical analysis. The data confirmed a high level of concordance for the VENTANA CLDN18 (43-14A; Ventana platform only) and LSBio antibodies on both the Dako and Leica platforms, with accuracy, precision, sensitivity, and specificity rates all reaching a minimum acceptable >85% threshold and good-to-excellent levels of concordance as measured by Cohen's kappa coefficient. The Novus antibody showed the highest level of variability against the reference central laboratory results for the same antibody/platform combinations. It also failed to meet the threshold for accuracy and sensitivity when used on either the Dako or Leica platform. These results demonstrated the reliability of IHC testing for CLDN18 expression in gastric tumor samples when using commercially available platforms with an appropriate methodology and primary antibody selection. (c) 2023 THE AUTHORS. Published by Elsevier Inc. on behalf of the United States & Canadian Academy of Pathology.
引用
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页数:11
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