PDL-1 in non-small cell lung cancer (NSCLC): Association with molecular alterations and clinical outcome

Abstract Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. Aims: To correlate clinicopathological...

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Published inIndian journal of cancer Vol. 62; no. 2; pp. 228 - 233
Main Authors Mannan, Khalid Abdul, Fonseca, Daphne, Arya, Sahithi S., Vaishnavi, Kunteepuram, Kodandapani, Suseela, Rajappa, Senthil J.
Format Journal Article
LanguageEnglish
Published India Wolters Kluwer - Medknow 01.04.2025
Medknow Publications and Media Pvt. Ltd
Medknow Publications & Media Pvt. Ltd
Edition2
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ISSN0019-509X
1998-4774
DOI10.4103/ijc.ijc_151_23

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Abstract Abstract Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. Aims: To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1%). Materials and Methods: We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1% and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS). Results: Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group. Conclusions: Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma.
AbstractList The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1). We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1 and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS). Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group. Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma.
Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. Aims: To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1). Materials and Methods: We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1 and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS). Results: Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group. Conclusions: Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma. Keywords: Clinical outcome, molecular alteration, non-small cell lung cancer, PDL-1
AbstractBackground:The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients.Aims:To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1%).Materials and Methods:We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1% and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS).Results:Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group.Conclusions:Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma.
The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1%). We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1% and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS). Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group. Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma.
Abstract Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the association of PDL-1 with molecular alterations in non small cell lung cancer patients. Aims: To correlate clinicopathological features with molecular phenotype across PDL-1 subgroups and analyze survival outcomes for patients having PDL-1 expression (>1%). Materials and Methods: We did a retrospective study of 100 NSCLC cases diagnosed at primary and metastatic sites using a next-generation sequencing (NGS) lung panel and the PDL-1 SP263 clone on the Ventana platform. PDL-1 expression, sample size, sex, histological type, and oncogenic mutation status were analyzed. Patients with PDL-1 expression >1% and managed with immunotherapy (IO), targeted therapy (TT), and conventional chemotherapy (CC) were followed up for a median time of 7 months. The outcome was assessed as overall survival (OS). Results: Fifty-one percent of the cases showed a positive PDL-1 expression. Squamous cell carcinoma (SCC) exhibited higher PDL-1 expression than adenocarcinoma (AC) (P-value = 0.005). The KRAS expression was more frequent in males (P-value = 0.048). There was no difference between the tumor location and the type of sample used. The EGFR mutation was exclusively seen in AC compared with other NSCLCs. The median overall survival in the IO and TT groups was 13 and 11 months, respectively, compared to 7 months in the CC group. Conclusions: Integrating clinical, molecular, and immunological data will enhance the predictive value of PDL-1 biomarkers in lung adenocarcinoma.
Audience Academic
Author Mannan, Khalid Abdul
Kodandapani, Suseela
Arya, Sahithi S.
Vaishnavi, Kunteepuram
Rajappa, Senthil J.
Fonseca, Daphne
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Cites_doi 10.1016/j.cllc.2019.05.009
10.1093/annonc/mdy126
10.1016/j.annonc.2020.01.065
10.1016/j.lungcan.2021.04.007
10.3390/ijms23094517
10.1016/j.jtho.2019.12.107
10.1007/s00432-020-03444-y
10.1016/j.prp.2021.153497
10.1111/resp.13614
10.1038/bjc.2015.356
10.21037/tlcr.2019.08.04
10.1016/j.jtho.2021.03.028
10.1016/j.lungcan.2021.04.001
10.3389/pore.2021.592997
10.1159/000517078
10.1186/s12885-020-06851-z
10.1016/j.lungcan.2019.03.012
10.2147/ITT.S125070
10.1371/journal.pone.0206370
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molecular alteration
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PDL-1
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References Schoenfeld (R11-20250812) 2020; 31
Mansour (R17-20250812) 2021; 65
Li (R4-20250812) 2019; 8
Mansour (R14-20250812) 2022; 23
Kuan (R18-20250812) 2015; 113
Velcheti (R7-20250812) 2018; 13
Grosu (R15-20250812) 2019; 24
Noordhof (R5-20250812) 2021; 155
Kim (R19-20250812) 2019; 20
Jain (R12-20250812) 2021; 228
Zheng (R9-20250812) 2021; 147
Raju (R1-20250812) 2018; 7
Lantuejoul (R2-20250812) 2020; 15
Wang (R13-20250812) 2018; 29
Zou (R16-20250812) 2020; 20
Kerr (R3-20250812) 2019; 131
Hwang (R8-20250812) 2021; 16
Waterhouse (R6-20250812) 2021; 156
Huang (R10-20250812) 2021; 27
References_xml – volume: 20
  start-page: 331
  year: 2019
  ident: R19-20250812
  article-title: First-line pembrolizumab versus pembrolizumab plus chemotherapy versus chemotherapy alone in non–small-cell lung cancer:A systematic review and network meta-analysis
  publication-title: Clin Lung Cancer
  doi: 10.1016/j.cllc.2019.05.009
– volume: 29
  start-page: 1417
  year: 2018
  ident: R13-20250812
  article-title: Cytology cell blocks are suitable for immunohistochemical testing for PD-L1 in lung cancer
  publication-title: Ann Oncol
  doi: 10.1093/annonc/mdy126
– volume: 31
  start-page: 599
  year: 2020
  ident: R11-20250812
  article-title: Clinical and molecular correlates of PD-L1 expression in patients with lung adenocarcinomas
  publication-title: Ann Oncol
  doi: 10.1016/j.annonc.2020.01.065
– volume: 156
  start-page: 41
  year: 2021
  ident: R6-20250812
  article-title: Real-world outcomes of immunotherapy-based regimens in first-line advanced non-small cell lung cancer
  publication-title: Lung Cancer
  doi: 10.1016/j.lungcan.2021.04.007
– volume: 23
  start-page: 4517
  year: 2022
  ident: R14-20250812
  article-title: PD-L1 Expression in non-small cell lung cancer specimens:Association with clinicopathological factors and molecular alterations
  publication-title: Int J Mol Sci
  doi: 10.3390/ijms23094517
– volume: 15
  start-page: 499
  year: 2020
  ident: R2-20250812
  article-title: PD-L1 testing for lung cancer in 2019:Perspective from the IASLC pathology committee
  publication-title: J Thorac Oncol
  doi: 10.1016/j.jtho.2019.12.107
– volume: 147
  start-page: 1547
  year: 2021
  ident: R9-20250812
  article-title: Clinicopathological and molecular characteristics associated with PD-L1 expression in non-small cell lung cancer:A large-scale, multi-center, real-world study in China
  publication-title: J Cancer Res Clin Oncol
  doi: 10.1007/s00432-020-03444-y
– volume: 228
  start-page: 153497
  year: 2021
  ident: R12-20250812
  article-title: PD-L1 expression and its clinicopathologic and genomic correlation in the non-small cell lung carcinoma patients:An Indian perspective
  publication-title: Pathol Res Pract
  doi: 10.1016/j.prp.2021.153497
– volume: 24
  start-page: 1198
  year: 2019
  ident: R15-20250812
  article-title: PD-L1 detection in histology specimens and matched pleural fluid cell blocks of patients with NSCLC
  publication-title: Respirology
  doi: 10.1111/resp.13614
– volume: 113
  start-page: 1519
  year: 2015
  ident: R18-20250812
  article-title: Overall survival benefits of first-line EGFR tyrosine kinase inhibitors in EGFR-mutated non-small-cell lung cancers:A systematic review and meta-analysis
  publication-title: Br J Cancer
  doi: 10.1038/bjc.2015.356
– volume: 8
  start-page: 429
  year: 2019
  ident: R4-20250812
  article-title: The clinicopathological and prognostic significance of PD-L1 expression assessed by immunohistochemistry in lung cancer:A meta-analysis of 50 studies with 11,383 patients
  publication-title: Transl Lung Cancer Res
  doi: 10.21037/tlcr.2019.08.04
– volume: 16
  start-page: 1490
  year: 2021
  ident: R8-20250812
  article-title: Prevalence and heterogeneity of PD-L1 expression by 22C3 assay in routine population-based and reflexive clinical testing in lung cancer
  publication-title: J Thorac Oncol
  doi: 10.1016/j.jtho.2021.03.028
– volume: 155
  start-page: 163
  year: 2021
  ident: R5-20250812
  article-title: Prognostic impact of KRAS mutation status for patients with stage IV adenocarcinoma of the lung treated with first-line pembrolizumab monotherapy
  publication-title: Lung Cancer
  doi: 10.1016/j.lungcan.2021.04.001
– volume: 27
  start-page: 592997
  year: 2021
  ident: R10-20250812
  article-title: Landscape of biomarkers in non-small cell lung cancer using comprehensive genomic profiling and PD-L1 immunohistochemistry
  publication-title: Pathol Oncol Res
  doi: 10.3389/pore.2021.592997
– volume: 65
  start-page: 501
  year: 2021
  ident: R17-20250812
  article-title: PD-L1 Testing in cytological non-small cell lung cancer specimens:A comparison with biopsies and review of the literature
  publication-title: Acta Cytol
  doi: 10.1159/000517078
– volume: 20
  start-page: 344
  year: 2020
  ident: R16-20250812
  article-title: Cytology cell blocks from malignant pleural effusion are good candidates for PD-L1 detection in advanced NSCLC compared with matched histology samples
  publication-title: BMC Cancer
  doi: 10.1186/s12885-020-06851-z
– volume: 131
  start-page: 95
  year: 2019
  ident: R3-20250812
  article-title: A retrospective cohort study of PD-L1 prevalence, molecular associations and clinical outcomes in patients with NSCLC:Results from the European Thoracic Oncology Platform (ETOP) lungscape project
  publication-title: Lung Cancer
  doi: 10.1016/j.lungcan.2019.03.012
– volume: 7
  start-page: 63
  year: 2018
  ident: R1-20250812
  article-title: Review of checkpoint immunotherapy for the management of non-small cell lung cancer
  publication-title: Immunotargets Ther
  doi: 10.2147/ITT.S125070
– volume: 13
  start-page: e0206370
  year: 2018
  ident: R7-20250812
  article-title: Real-world PD-L1 testing and distribution of PD-L1 tumor expression by immunohistochemistry assay type among patients with metastatic non-small cell lung cancer in the United States
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0206370
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Snippet Abstract Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to...
The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand the...
Background: The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to understand...
AbstractBackground:The Immune checkpoint inhibitors (ICI) targeting PDL-1 show improved outcomes in lung adenocarcinoma patients. This study is intended to...
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SubjectTerms Adult
Aged
Aged, 80 and over
B7-H1 Antigen - genetics
B7-H1 Antigen - metabolism
Biomarkers, Tumor - genetics
Cancer
Carcinoma, Non-Small-Cell Lung - drug therapy
Carcinoma, Non-Small-Cell Lung - genetics
Carcinoma, Non-Small-Cell Lung - pathology
Chemotherapy
Female
Humans
Immunotherapy
Lung cancer
Lung cancer, Non-small cell
Lung cancer, Small cell
Lung Neoplasms - drug therapy
Lung Neoplasms - genetics
Lung Neoplasms - pathology
Male
Medical research
Medicine, Experimental
Metastasis
Middle Aged
Mutation
Original Article
Patient outcomes
Pemetrexed
Prognosis
Retrospective Studies
Squamous cell carcinoma
Title PDL-1 in non-small cell lung cancer (NSCLC): Association with molecular alterations and clinical outcome
URI https://doi.org/10.4103/ijc.ijc_151_23
https://www.ncbi.nlm.nih.gov/pubmed/40788737
https://www.proquest.com/docview/3238301362
Volume 62
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