Evidence map›Paper›PMID 31317055›Full record

ArticleAmerican journal of clinical and experimental urology2019

PD-L1 instead of PD-1 status is associated with the clinical features in human primary prostate tumors.

Peng Xian, Dongxia Ge, Victor J Wu, Avi Patel, Wendell W Tang, Xiaocheng Wu, Kun Zhang, Li Li, Zongbing You

Open access · greenAbstract read
In one paragraph

Article in American journal of clinical and experimental urology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 6 pooled it
2.0field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 6 syntheses or guidelines pooled it, 23 citations in OpenAlex.

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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

9 authors at 4 institutions in 2 countries.

Peng XianDepartment of Structural and Cellular Biology, Tulane University New Orleans, LA 70112, USA.
Dongxia GeDepartment of Structural and Cellular Biology, Tulane University New Orleans, LA 70112, USA.
Victor J WuDepartment of Structural and Cellular Biology, Tulane University New Orleans, LA 70112, USA.
Avi PatelLaboratory of Translational Cancer Research, Ochsner Clinic Foundation New Orleans, LA 70121, USA.
Wendell W TangDepartment of Pathology, Ochsner Clinic Foundation New Orleans, LA 70121, USA.
Xiaocheng WuEpidemiology Program/Louisiana Tumor Registry, School of Public Health, Louisiana State University Health Sciences Center New Orleans, LA 70112, USA.
Kun ZhangDepartment of Computer Science and Biostatistics Facility of RCMI Cancer Research Center, Xavier University of Louisiana New Orleans, LA 70125, USA.
Li LiLaboratory of Translational Cancer Research, Ochsner Clinic Foundation New Orleans, LA 70121, USA.
Zongbing YouDepartment of Structural and Cellular Biology, Tulane University New Orleans, LA 70112, USA.
Tulane University · USOchsner Medical Center · USLouisiana State University Health Sciences Center New Orleans · USXavier University of Louisiana · US

Funding

STABILITY' (symptomatic review during biologic therapy) Review in Inflammatory Bowel DiseaseP20GM103424 · NIGMS · LOUISIANA STATE UNIV A&M COL BATON ROUGE · PI Konstantin G Kousoulas · 2012 to 2026
$57.4M
The role of IL-17 in prostate cancerR01CA174714 · NCI · TULANE UNIVERSITY OF LOUISIANA · PI YOU, ZONGBING · 2013 to 2017
$1.6M
The role of IL-17 in obesity-associated prostate cancer progressionI01BX004158 · VA · SOUTHEAST LOUISIANA VETERANS HEALTH CARE · PI YOU, ZONGBING · 2019 to 2023
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BLRD VA I01 BX004158NCI NIH HHS R01 CA174714NIGMS NIH HHS P20 GM103424
6 · The paper itself

Abstract

Immunotherapy targeting programmed cell death protein 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) has shown efficacy in a variety of solid tumors. However, prostate cancer has often been a non-responder to anti-PD-1/PD-L1 therapies. The objective of this study was to determine PD-1 and PD-L1 expression status and its correlation with clinical features of the patients. A total of 279 patients who underwent radical prostatectomy for prostate cancer were included in this study. PD-1 and PD-L1 expression in primary prostate tumors was detected using immunohistochemical staining. Analyses were made between PD-1/PD-L1 status and patients' age, ethnicity, body mass index (BMI), diabetes mellitus, tumor stage, lymph node metastasis, prostate-specific antigen (PSA), Gleason score, grade group, and survival. We found that 6.5 (standard deviation 14.3; range 0-161.6) tumor-infiltrating lymphocytes per high power field were positive for PD-1 staining and 50/279 (17.9%) tumors were positive for PD-L1 staining. PD-L1-positive tumors had significantly more PD-1-positive lymphocytes than PD-L1-negative tumors. The number of PD-1-positive lymphocytes was not correlated with any clinical features except that patients with diabetes had significantly less PD-1-positive lymphocytes than patients without diabetes. In contrast, more PD-L1-positive tumors were found in older patients (≥ 65 years), obese patients (BMI ≥ 30), and patients with advanced tumor stage, lymph node metastasis, and high Gleason score. Neither PD-1 nor PD-L1 status was correlated with ethnicity, PSA, or survival. Our findings suggest that PD-L1 instead of PD-1 status is associated with the clinical features in human primary prostate tumors.

Indexed as

correlationimmunohistochemical stainingPD-1PD-L1prostate tumor

Identifiers

PMID31317055
PMCPMC6627547
OpenAlexW2967781020

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.