Abstract

Introduction.The goal of the CLOVER study performed by the Russian Society of Clinical Oncology, was a pairwise comparison of three validated PD-L1 immunohistochemical (IHC) tests (Ventana SP142, Ventana SP263, Dako 22C3) in the patient population with non-small cell lung cancer (NSCLC). This study is the first large Russian comparative study to evaluate PD-L1 expression levels using immunohistochemistry methods.Materials and methods.The study was conducted on 473 NSCLC samples from Biobank. The IHC tests were carried out with 3 antibody clones. Four trained pathologists independently evaluated the percentage of positively stained tumor cells (TC) and immune cells (IC). To assess the correlation of TC and IC between different runs and the prognostic values of one test for another, a concordant analysis was used.Results.The number of PD-L1‑positive cells (≥1 %) was higher among IC compared with TC in all three IHC tests. Pearson correlation coefficients (PCC) for TCs were 0.71, 0.87, and 0.75 for 22C3 / SP142, 22C3 / SP263 and SP263 / SP142, respectively. PCC values for ICs were 0.45, 0.61, and 0.68 for the same pairs. A high coincidence of positive and negative results (>91 %) was obtained between the staining with antibodies 22C3 and SP263 of immunooncological agents in the 1st line.Conclusions.The highest correlation between IHC tests was obtained by pairwise comparison of 22C3 and SP263. Clone 22C3 can be considered as a substitute for SP263 in the first-line treatment of NSCLC. Clone SP142 showed weaker expression in TC and IC compared to the other two tests in patients with non-small cell lung cancer.

Highlights

  • The goal of the CLOVER study performed by the Russian Society of Clinical Oncology, was a pairwise comparison of three validated PD-L1 immunohistochemical (IHC) tests (Ventana SP142, Ventana SP263, Dako 22C3) in the patient population with non-small cell lung cancer (NSCLC)

  • Four trained pathologists independently evaluated the percentage of positively stained tumor cells (TC) and immune cells (IC)

  • The number of PD-L1‐positive cells (≥1 %) was higher among IC compared with TC in all three IHC tests

Read more

Summary

Собственные исследования

Целью исследования CLOVER, проведенного Российским обществом клинической онкологии, было попарное сравнение трех валидированныхиммуногистохимических (ИГХ) тестов PD-L1 (Ventana SP142, Ventana SP263, Dako 22C3) на одной и той же популяции пациентов с немелкоклеточным раком легкого (НМРЛ). Пембролизумаб, анти-PD-1 гуманизированное анти‐ тело, рекомендуется в качестве препарата первой линии для пациентов с метастатическим НМРЛ с уровнем экс‐ прессии PD-L1 более 50 %, выявляемым иммуногистохи‐ мическим (ИГХ) методом с диагностическим антителом 22C3 (Agilent) [2,3]. Недавно пембролизумаб был одобрен к применению в качестве препарата первой линии для ЗЛОКАЧЕСТВЕННЫЕ ОПУХОЛИ Российское общество клинической онкологии том / vol 9 No 4 2019. Атезолизумаб, анти-PD-L1 гуманизированное антитело, одобрен в комбинации с химиотерапией и бевацизумабом в качестве терапии первой линии для пациентов с мета‐ статическим НМРЛ независимо от уровня экспрессии PD-L1 [6]. Целью исследования «CLOVER», проведенного Рос‐ сийским обществом клинической онкологии (RUSSCO), было попарное сравнение трехвалидированных ИГХ тестов PDL1 (22C3, SP142 и SP263) на одной и той же популяции пациентов

МАТЕРИАЛЫ И МЕТОДЫ
АНАЛИЗ ДАННЫХ
EGFR негативный
Вероятность позитивного теста B при позитивном тесте A
ИНФОРМАЦИЯ ОБ АВТОРАХ
Materials and methods
Results
Conclusions
INFORMATION ABOUT THE AUTHORS
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.