PD-L1 Assay Concordance in Metastatic Renal Cell Carcinoma and Metastatic Urothelial Carcinoma.


Journal

Clinical genitourinary cancer
ISSN: 1938-0682
Titre abrégé: Clin Genitourin Cancer
Pays: United States
ID NLM: 101260955

Informations de publication

Date de publication:
12 2020
Historique:
received: 27 12 2019
revised: 30 03 2020
accepted: 31 03 2020
pubmed: 3 6 2020
medline: 19 8 2021
entrez: 3 6 2020
Statut: ppublish

Résumé

Immune checkpoint inhibitors are now standard of care for many patients with metastatic renal cell carcinoma (mRCC) and metastatic urothelial carcinoma (mUC). Given real-world limitations in programmed death-ligand 1 (PD-L1) testing, concordance studies between PD-L1 assays are needed. We undertook comparisons of Dako 28-8 and Ventana SP142 assays in mRCC and Dako 22C3 and Ventana SP263 assays in mUC. Thirty-two patients with mRCC and 18 patients with mUC who had received immune checkpoint inhibitor therapy were identified. Formalin-fixed paraffin-embedded tumor samples for patients with mRCC were evaluated with Dako 28-8 and Ventana SP142 PD-L1 immunohistochemistry assays. For patients with mUC, formalin-fixed paraffin-embedded tumor samples were evaluated with Dako 22C3 and Ventana SP263 PD-L1 immunohistochemistry assays. The majority (29/32; 91%) of mRCC cases were concordant between assays. The majority (17/18; 94%) of mUC cases were also concordant between assays. There was strong concordance between PD-L1 assays chosen for comparison in both mRCC and mUC, with similar performance characteristics. One limitation is the small number of cases in this study; larger comparison studies are needed for this biomarker in mRCC and mUC.

Sections du résumé

BACKGROUND
Immune checkpoint inhibitors are now standard of care for many patients with metastatic renal cell carcinoma (mRCC) and metastatic urothelial carcinoma (mUC). Given real-world limitations in programmed death-ligand 1 (PD-L1) testing, concordance studies between PD-L1 assays are needed. We undertook comparisons of Dako 28-8 and Ventana SP142 assays in mRCC and Dako 22C3 and Ventana SP263 assays in mUC.
PATIENTS AND METHODS
Thirty-two patients with mRCC and 18 patients with mUC who had received immune checkpoint inhibitor therapy were identified. Formalin-fixed paraffin-embedded tumor samples for patients with mRCC were evaluated with Dako 28-8 and Ventana SP142 PD-L1 immunohistochemistry assays. For patients with mUC, formalin-fixed paraffin-embedded tumor samples were evaluated with Dako 22C3 and Ventana SP263 PD-L1 immunohistochemistry assays.
RESULTS
The majority (29/32; 91%) of mRCC cases were concordant between assays. The majority (17/18; 94%) of mUC cases were also concordant between assays.
CONCLUSIONS
There was strong concordance between PD-L1 assays chosen for comparison in both mRCC and mUC, with similar performance characteristics. One limitation is the small number of cases in this study; larger comparison studies are needed for this biomarker in mRCC and mUC.

Identifiants

pubmed: 32482566
pii: S1558-7673(20)30092-6
doi: 10.1016/j.clgc.2020.03.020
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
Biomarkers, Tumor 0

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

509-513

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Landon C Brown (LC)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Jason Zhu (J)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Matthew K Labriola (MK)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Yuan Wu (Y)

Department of Biostatistics and Bioinformatics, School of Medicine, Duke University, Durham, NC.

Sachica Cheris (S)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Xin Liu (X)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Kathryn Perkinson (K)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Zuowei Su (Z)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Shannon McCall (S)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Jiaoti Huang (J)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Wen-Chi Foo (WC)

Department of Pathology, School of Medicine, Duke University, Durham, NC.

Rajan T Gupta (RT)

Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC; Department of Radiology, School of Medicine, Duke University, Durham, NC.

Andrew J Armstrong (AJ)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Daniel J George (DJ)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Michael R Harrison (MR)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC.

Tian Zhang (T)

Department of Medicine, School of Medicine, Duke University, Durham, NC; Duke Cancer Institute Center for Prostate and Urologic Cancers, Durham, NC. Electronic address: tian.zhang2@duke.edu.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH