Evidence map›Paper›PMID 28522811›Full record

ArticleScientific reports2017

PD-L1 expression in Xp11.2 translocation renal cell carcinoma: Indicator of tumor aggressiveness.

Kun Chang, Yuanyuan Qu, Bo Dai, Jian-Yuan Zhao, Hualei Gan, Guohai Shi, Yiping Zhu, Yijun Shen, Yao Zhu, Hailiang Zhang and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  11. Role of HPV status and PD-L1 expression in prognosis of laryngeal squamous cell carcinoma.International journal of clinical and experimental pathology · 2021
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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

11 authors.

Kun ChangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yuanyuan QuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Bo DaiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Jian-Yuan ZhaoThe State Key Laboratory of Genetic Engineering and Collaborative Innovation Center of Genetics & Development, School of Life Sciences, Fudan University, Shanghai, 200433, China.
Hualei GanDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Guohai ShiDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yiping ZhuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yijun ShenDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Yao ZhuDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. maizhuyao@163.com.
Hailiang ZhangDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. zhanghl918@163.com.
Dingwei YeDepartment of Urology, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. dwyeli@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Programmed death ligand-1 (PD-L1), a promising antitumor target, has proven clinical value against many malignancies. However, the PD-L1 content of Xp11.2 translocation renal cell carcinoma (Xp11.2 RCC) and its correlation with clinical outcomes remain unclear. This study aimed to investigate PD-L1 expression in Xp11.2 RCC and to assess its prognostic value. Formalin-fixed paraffin-embedded specimens from 36 adult patients that were histologically confirmed (by fluorescence in situ hybridization) were subjected to immunohistochemical analysis. Of the 36 Xp11.2 RCC patients, 9 (25.0%) had tumors with positive PD-L1 expression and 27 (75.0%) had tumors with negative PD-L1 expression. Positive PD-L1 expression correlated with advanced tumor stage (P = 0.001), regional lymph node metastasis (P < 0.001), and distant metastasis (P < 0.001). A multivariate analysis identified positive PD-L1 expression was an independent adverse prognostic factor for both progression free survival (hazard ratio: 3.7, P = 0.018) and overall survival (hazard ratio: 4.5, P = 0.034). The median PFS and OS for the whole cohort were 13.0 months (95% confidence interval [CI], 9.4-16.6 months) and 36.0 months (95% CI, 23.9-48.1 months), respectively. Our findings suggest that positive PD-L1 expression is indicative of worse clinical outcome in Xp11.2 RCC. Further studies are needed to explore the potential efficacy of targeting PD-L1 in Xp11.2 RCC.

Indexed as

Translocation, GeneticAdolescentAdultB7-H1 AntigenBiomarkers, TumorCarcinoma, Renal CellChromosomes, Human, XFemaleHumansKidney NeoplasmsMaleMiddle AgedNeoplasm MetastasisB7-H1 AntigenBiomarkers, TumorCD274 protein, human

Identifiers

PMID28522811
PMCPMC5437001

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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.