Evidence map›Paper›PMID 35755570›Full record

ArticleCureus2022

Immunoexpression of Programmed Death-1 Receptor (PD-1) and Programmed Death-Ligand 1 (PD-L1) in Non-Small-Cell Lung Carcinoma and Its Correlation With Other Clinicopathological Parameters: A Cross-Sectional Study From North India.

Michael L Anthony, Nilotpal Chowdhury, Mayank Mishra, Sudheer Tale, Kunnumbrath Arathi, Shalinee Rao

Open access · diamondAbstract read
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Article in Cureus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
–field-weighted citation impact, top 92% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Michael L AnthonyPathology, All India Institute of Medical Sciences (AIIMS) Mangalagiri, Mangalagiri, IND.
Nilotpal ChowdhuryPathology, All India Institute of Medical Sciences (AIIMS) Rishikesh, Rishikesh, IND.
Mayank MishraPulmonary Medicine, All India Institute of Medical Sciences (AIIMS) Rishikesh, Rishikesh, IND.
Sudheer TalePulmonary Medicine, Fortis Healthcare, Vijayawada, IND.
Kunnumbrath ArathiPathology, Employees' State Insurance Corporation (ESIC) Medical College and Post Graduate Institutes for Medical Sciences and Research (PGIMSR), Chennai, IND.
Shalinee RaoPathology, All India Institute of Medical Sciences (AIIMS) Rishikesh, Rishikesh, IND.
Seema Dental College and Hospital · INAll India Institute of Medical Sciences · INAll India Institute of Medical Sciences RishikeshEmployees State Insurance Post Graduate Institute of Medical Sciences and Research · INFortis Healthcare · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim To study the prevalence of programmed death-1 receptor (PD-1) and programmed death-ligand 1 (PD-L1) positive cases in non-small-cell lung carcinoma (NSCLC) and their association with other clinicopathological parameters in a tertiary care setting in North India. Material and methods One hundred histologically proven NSCLC cases having sufficient tumor material from July 2016 to July 2018 were examined, and the prevalence of PD-1 and PD-L1 positivity in NSCLC was studied. In addition, H&E-stained sections were reviewed, and 100 consecutive cases meeting study criteria were identified as study cases. Histopathological categorization was done using a panel of immunohistochemical markers. Statistical analysis and results The PD-1 positivity in lymphocytes was 29% (95% CI: 20.4%-38.9%). Membranous positivity for PD-L1 in tumor cells was 27% (95% CI: 18.6%-36.8%) and in tumor-infiltrating lymphocytes was 22% (95% CI: 14.3%-31.4%). There was no statistically significant association between PD-1 or PD-L1 status with age, gender, smoking, pleural effusion, clinical stage, histological type, or lymphocyte infiltration. Conclusion The moderately high prevalence may justify routine testing for PD-1 or PD-L1 in NSCLC, which should preferably be carried out in all cases rather than any selected subsets. However, there was no significant correlation between PD-1 and PD-L1 with the clinical parameters studied.

Indexed as

immunotherapynon-small cell lung carcinomapd-1pd-l1tumor-infiltrating lymphocytes

Identifiers

PMID35755570
PMCPMC9217682
OpenAlexW4281285340

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.