Impact of Neoadjuvant Chemotherapy on Concordance of PD-L1 Staining Fidelity between the Primary Tumor and Lymph Node Metastases in Bladder Cancer.


Journal

Urology
ISSN: 1527-9995
Titre abrégé: Urology
Pays: United States
ID NLM: 0366151

Informations de publication

Date de publication:
Sep 2019
Historique:
received: 12 03 2019
revised: 29 05 2019
accepted: 31 05 2019
pubmed: 16 6 2019
medline: 17 1 2020
entrez: 16 6 2019
Statut: ppublish

Résumé

To evaluate programmed death ligand 1 (PD-L1) staining fidelity between the primary tumor and associated lymph node metastases in bladder cancer. To secondarily evaluate whether neoadjuvant chemotherapy (NAC) affects this relationship. Sixty-seven subjects with residual bladder cancer on cystectomy and associated positive lymph nodes were identified between 2008 and 2015. PD-L1 staining of tumor cells was evaluated using H score and 49 specimens were also evaluated using combined positive score (CPS). Univariable and multivariable logistic regression analysis were used to assess how various clinical variables affected odds of PD-L1 fidelity between primary and metastatic tumors. Tumor PD-L1 staining was concordant in 79.1% of cases and CPS was concordant in 79.6% of cases. NAC did not significantly impact odds of PD-L1 or CPS fidelity (OR 1.974, 95% CI 0.673-5.784, OR 0.500, 95% CI 0.093-2.700). Among clinical variables analyzed on univariable analysis of tumor PD-L1 fidelity, H-score, and PD-L1 staining intensity were associated with significantly increased odds of PD-L1 fidelity and the association with staining intensity was confirmed on multivariable analysis. PD-L1 fidelity between primary bladder tumors and nodal metastases was observed in >75% of cases in this study. Additionally, NAC was not shown to diminish this propensity to maintain PD-L1 staining status. Further standardization of immunohistochemistry of tumor and infiltrating imsmune cells in metastatic bladder cancer is needed to improve application of therapeutics.

Identifiants

pubmed: 31201825
pii: S0090-4295(19)30528-X
doi: 10.1016/j.urology.2019.05.039
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
CD274 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

150-156

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

Kinnari R Patel (KR)

Division of Urology, Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Benjamin L Taylor (BL)

Departments of Urology, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY.

Francesca Khani (F)

Departments of Urology, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY; Departments of Pathology and Laboratory Medicine, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY.

Thomas J Guzzo (TJ)

Division of Urology, Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Douglas S Scherr (DS)

Departments of Urology, Weill Cornell Medicine, New York Presbyterian Hospital, New York, NY.

Roshan Ravishankar (R)

Division of Urology, Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Priti Lal (P)

Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Stanley Bruce Malkowicz (SB)

Division of Urology, Department of Surgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA. Electronic address: bruce.malkowicz@uphs.upenn.edu.

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Classifications MeSH