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The use of cytological material in melanoma for programmed death ligand 1 immunostaining.

Authors :
Bashover E
Arriola AG
Joseph CT
Staerkel G
Wang WB
Roy-Chowdhuri S
Source :
Cytopathology : official journal of the British Society for Clinical Cytology [Cytopathology] 2019 Jan; Vol. 30 (1), pp. 61-67. Date of Electronic Publication: 2018 Oct 23.
Publication Year :
2019

Abstract

Objective: Interest in immune therapies has exploded since the 2014 approval of first-generation programmed cell death 1 blocking antibodies for use in advanced melanoma. Clinical trials have focused primarily on histological material as the gold standard for evaluating programmed death ligand 1 (PD-L1) by immunoperoxidase (IPOX) studies. Studies validating the use of cytological specimens in the assessment of PD-L1 by IPOX staining are needed to optimise tissue utilisation in complementary diagnostic testing.<br />Methods: Twenty-three melanoma surgical biopsies (SBx) with an IPOX stain for PD-L1 clone 28-8, and a corresponding cytological specimen from the same patient, adequate for PD-L1 evaluation, were selected. Cell-transfer cell blocks (CBs) and conventional CBs were used to perform PD-L1 testing. Tumour proportion scores (TPS) were generated and the results were correlated with the corresponding SBx.<br />Results: Overall agreement (OA) using a ≥1% TPS cut-off for SBx compared to CB was 88.9%, positive percent agreement (PPA) was 87.5%, and negative percent agreement (NPA) was 100%, OA using a ≥5% TPS cut-off was 55.6%, PPA was 42.9%, and NPA was 100%. SBx compared to cell-transfer CB using a ≥1% TPS cut-off had an OA of 65.2%, a PPA of 55.6%, and a NPA of 100%, while a ≥5% TPS cut-off generated an OA of 52.2%, a PPA of 35.7%, and a NPA of 77.8%.<br />Conclusion: Our results demonstrate that cytological material, particularly conventional CB, is a viable alternative for evaluating PD-L1 in melanoma cases and suggest that a lower threshold (≥1%) may be beneficial when evaluating cytological material.<br /> (© 2018 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2303
Volume :
30
Issue :
1
Database :
MEDLINE
Journal :
Cytopathology : official journal of the British Society for Clinical Cytology
Publication Type :
Academic Journal
Accession number :
30244524
Full Text :
https://doi.org/10.1111/cyt.12634