Programmed cell death ligand 1 (PD-L1) expression in non-small cell lung cancer: Findings from a tertiary care institute in western part of India.


Journal

The Indian journal of tuberculosis
ISSN: 0019-5707
Titre abrégé: Indian J Tuberc
Pays: India
ID NLM: 0373027

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 21 03 2022
accepted: 11 01 2023
medline: 17 11 2023
pubmed: 16 11 2023
entrez: 15 11 2023
Statut: ppublish

Résumé

Immune checkpoint inhibitors targeting either programmed cell death protein 1 (PD-1) or programmed cell death ligand 1 (PD-L1) have been established as a novel target for immunotherapy in non-small cell lung cancer (NSCLC). Prevalence of PD-L1 expression in NSCLC varies from 13% to 70%, with sparse data from the Indian subcontinent. In this study, we looked at PD-L1 expression and its association with demographic, clinical, radiologic and pathologic parameters in NSCLC patients. This was an observational study carried over a period of 18 months in which 65 patients of NSCLC were included. Immunohistochemistry (IHC) for PD-L1 was done using an automated IHC stainer and testing was performed using PD-L1 IHC CAL10. For statistical analysis, unpaired t test, Chi square test, Fisher's exact test and binomial logistic regression were used. P < 0.05 was taken to be statistically significant. Mean age of the patients was 62.9 ± 9.2 years, and majority (87.3%) of them were males. Seventeen (26.2%) patients expressed PD-L1, among whom 10 had high PD-L1 expression (≥50%) and 7 had low PD-L1 expression (1-49%). PD-L1 expression was seen in 13 out of 43 cases of squamous cell carcinoma (SCC) and 4 out of 15 cases of adenocarcinoma. On applying binomial logistic regression analysis, association between smoking and PD-L1 expression was found to be insignificant. Almost a quarter of NSCLC cases were PD-L1 positive without any difference in expression between SCC and adenocarcinoma. PD-L1 status was not associated with any specific demographic, clinical or radiologic parameter including the histologic subtype.

Sections du résumé

BACKGROUND BACKGROUND
Immune checkpoint inhibitors targeting either programmed cell death protein 1 (PD-1) or programmed cell death ligand 1 (PD-L1) have been established as a novel target for immunotherapy in non-small cell lung cancer (NSCLC). Prevalence of PD-L1 expression in NSCLC varies from 13% to 70%, with sparse data from the Indian subcontinent. In this study, we looked at PD-L1 expression and its association with demographic, clinical, radiologic and pathologic parameters in NSCLC patients.
METHODS METHODS
This was an observational study carried over a period of 18 months in which 65 patients of NSCLC were included. Immunohistochemistry (IHC) for PD-L1 was done using an automated IHC stainer and testing was performed using PD-L1 IHC CAL10. For statistical analysis, unpaired t test, Chi square test, Fisher's exact test and binomial logistic regression were used. P < 0.05 was taken to be statistically significant.
RESULTS RESULTS
Mean age of the patients was 62.9 ± 9.2 years, and majority (87.3%) of them were males. Seventeen (26.2%) patients expressed PD-L1, among whom 10 had high PD-L1 expression (≥50%) and 7 had low PD-L1 expression (1-49%). PD-L1 expression was seen in 13 out of 43 cases of squamous cell carcinoma (SCC) and 4 out of 15 cases of adenocarcinoma. On applying binomial logistic regression analysis, association between smoking and PD-L1 expression was found to be insignificant.
CONCLUSION CONCLUSIONS
Almost a quarter of NSCLC cases were PD-L1 positive without any difference in expression between SCC and adenocarcinoma. PD-L1 status was not associated with any specific demographic, clinical or radiologic parameter including the histologic subtype.

Identifiants

pubmed: 37968047
pii: S0019-5707(23)00002-1
doi: 10.1016/j.ijtb.2023.01.001
pii:
doi:

Substances chimiques

B7-H1 Antigen 0
Ligands 0
CD274 protein, human 0

Types de publication

Observational Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

416-421

Informations de copyright

Copyright © 2023 Tuberculosis Association of India. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of interest The authors have none to declare.

Auteurs

Priyank Jain (P)

Department of Respiratory Medicine, Government Medical College, Kota, Rajasthan, India.

Nishant Kumar Chauhan (N)

Department of Pulmonary Medicine, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India. Electronic address: nishant97@gmail.com.

Amartya Chakraborti (A)

Department of Pulmonary Medicine, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Manoj Kumar Gupta (MK)

Department of Community Medicine and Family Medicine, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Naveen Dutt (N)

Department of Pulmonary Medicine, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Ram Niwas Jalandra (RN)

Department of Pulmonary Medicine, All India Institute of Medical Sciences, Bhatinda, Punjab, India.

Poonam Elhence (P)

Department of Pathology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Meenakshi Rao (M)

Department of Pathology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Pushpinder Khera (P)

Department of Diagnostic and Interventional Radiology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Pawan Kumar Garg (PK)

Department of Diagnostic and Interventional Radiology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Puneet Pareek (P)

Department of Radiotherapy, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Jeewan Ram Vishnoi (JR)

Department of Surgical Oncology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

Sanjeev Misra (S)

Department of Surgical Oncology, All India Institute of Medical Sciences, Jodhpur, Rajasthan, India.

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