Evaluation of HER2 immunohistochemistry expression in non-standard solid tumors from a Single-Institution Prospective Cohort.

HER2 IHC biomarker solid tumors

Journal

Exploration of targeted anti-tumor therapy
ISSN: 2692-3114
Titre abrégé: Explor Target Antitumor Ther
Pays: United States
ID NLM: 101770662

Informations de publication

Date de publication:
2024
Historique:
received: 14 03 2024
accepted: 29 07 2024
medline: 1 10 2024
pubmed: 1 10 2024
entrez: 1 10 2024
Statut: ppublish

Résumé

Human epidermal growth factor receptor-2 (HER2) is a well-established prognostic and predictive biomarker. It is an FDA-approved therapeutic target for HER2 positive breast, gastroesophageal, and more recently, lung and colon cancers. It is an emerging biomarker in biliary tract, bladder, cervical, endometrial, ovarian, and pancreatic cancers. The emergence of new indications warrants further characterization of HER2 expression in diverse cancer populations. This study investigated HER2 expression in solid tumour samples and the feasibility of obtaining these results. Prospective consent was obtained at a Canadian tertiary academic cancer center from adult oncology patients who were referred for molecular genetic testing of malignant tissue samples. Standard HER2-targeted malignancies were considered breast and gastroesophageal, and were excluded from this study. Between July 2020 and November 2023, 499 samples of solid tumors underwent immunohistochemistry (IHC) HER2 staining. A median turnaround time (TAT) of 14 days would be considered feasible for clinical decision making. The mean age (± SD) of participants was 67 ± 12.5 years, with 270 (54%) male and 229 (46%) female. HER2 protein expression was measured in 42 unique cancer types. IHC levels of 0, 1+, 2+, and 3+ were reported and were 43%, 12%, 35%, and 10% of all analyzable samples respectively (tissue inadequate in 3% of samples). The median TAT for HER2 expression results from time of request to result in release was 18 (interquartile range, 11 to 30) days. HER2 protein expression varies widely between different cancer types. TAT for HER2 IHC results was a median of 18 days, which is close to our feasibility cut-off.

Identifiants

pubmed: 39351438
doi: 10.37349/etat.2024.00265
pmc: PMC11438559
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1100-1109

Informations de copyright

© The Author(s) 2024.

Déclaration de conflit d'intérêts

DB has accepted honoraria and/or speaking fees from Astra Zeneca, Amgen, Bristol-Myers Squibb, Takeda, Bayer, Guardant, Roche, Janssen and Merck. The rest of the authors have no conflict of interest.

Auteurs

Saurav Verma (S)

Division of Medical Oncology, Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.
Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Amanda Chapman (A)

Department of Medicine, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.

Lee-Anne Pickard (LA)

Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Danielle Porplycia (D)

Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Haley McConkey (H)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.
Department of Pathology and Laboratory Medicine, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.

Patricia Jarosz (P)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.

James Sinfield (J)

Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Carolyn Lauzon-Young (C)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.
Department of Pathology and Laboratory Medicine, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.

Matthew J Cecchini (MJ)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Christopher Howlett (C)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Natalie Grindrod (N)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Bekim Sadikovic (B)

Department of Pathology and Laboratory Medicine, London Health Sciences Centre, London, ON N6A 5W9, Canada.
Department of Pathology and Laboratory Medicine, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.

Stephen A Welch (SA)

Division of Medical Oncology, Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.
Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Daniel Breadner (D)

Division of Medical Oncology, Department of Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.
Verspeeten Family Cancer Centre, London Health Sciences Centre, London, ON N6A 5W9, Canada.

Classifications MeSH