Evidence map›Paper›PMID 32952659›Full record

ArticleOncology letters2020

Integrative assessment of clinicopathological parameters and the expression of PD-L1, PD-L2 and PD-1 in tumor cells of retroperitoneal sarcoma.

Makito Miyake, Yuki Oda, Nobutaka Nishimura, Yosuke Morizawa, Sayuri Ohnishi, Kinta Hatakeyama, Tomomi Fujii, Shunta Hori, Daisuke Gotoh, Yasushi Nakai and 10 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 13 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

20 authors at 3 institutions in 1 country.

Makito MiyakeDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yuki OdaDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Nobutaka NishimuraDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yosuke MorizawaDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Sayuri OhnishiDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kinta HatakeyamaDepartment of Diagnostic Pathology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Tomomi FujiiDepartment of Diagnostic Pathology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Shunta HoriDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Daisuke GotohDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yasushi NakaiDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Satoshi AnaiDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kazumasa TorimotoDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Shinji TsukamotoDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hiromasa FujiiDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Akira KidoDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kanya HonokiDepartment of Orthopedic Surgery, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yoshiaki MatsumuraDepartment of Urology, Nara Prefecture General Medical Center, Nara 630-8581, Japan.
Eijiro OkajimaDepartment of Urology, Nara City Hospital, Nara 630-8305, Japan.
Nobumichi TanakaDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kiyohide FujimotoDepartment of Urology, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Nara Medical University · JPNara City Hospital · JPNara Prefecture General Medical Center

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence is limited regarding the immunologic profile and immune microenvironment of soft tissue sarcoma subtypes. The aim of the present study was to describe the clinical significance and prognostic implications of PD-L1, PD-L2, and PD-1 in patients with retroperitoneal sarcoma (RSar). In this retrospective, multicenter, collaborative study, medical charts were reviewed and the immunohistochemical staining results of resected tissue specimens from 51 patients with RSar were examined. Immunohistochemical staining was performed with primary antibodies against PD-L1, PD-L2, PD-1, and Ki-67. The correlations between the baseline clinical parameters and expression levels of the four molecules in sarcoma cells were evaluated, and their prognostic values after tumor resection were assessed. Dedifferentiated liposarcoma (41%), leiomyosarcoma (20%), and undifferentiated pleomorphic sarcoma (16%) were the three major types identified. Dedifferentiated liposarcoma and leiomyosarcoma showed higher levels of PD-L1 expression than did other sarcomas. The Spearman correlation analysis revealed that baseline serum lactate dehydrogenase levels were moderately and positively correlated with PD-L1 (P=0.02, r=0.41) and PD-L2 (P=0.006, r=0.47) expression. The median recurrence-free and disease-specific survival was 58 and 16 months, respectively, during the 29-month median follow-up after surgery. On univariate analysis, a higher expression level of PD-1 was associated with a higher risk of recurrence, whereas multivariate analyses revealed that independent predictors of recurrence-free and disease-specific survival indicated a high expression of Ki-67 (P=0.03; hazard ratio, 2.29 vs. low expression) and prognostic stage IIIB (P=0.04; hazard ratio, 5.11 vs. stage I-II), respectively. Findings of the current study provide novel insights about the prognostic value of PD-L1, PD-L2, and PD-1 expression in RSar. Serum lactate dehydrogenase levels constitute a potential predictor of PD-L1 and PD-L2 expression levels in RSar. Further investigations are needed to determine the immunologic landscape of RSar and provide a foundation for therapeutic intervention using immune checkpoint inhibitors.

Indexed as

Ki-67leiomyosarcomaliposarcomaprognosisprogram cell death ligand-1program cell death ligand-2programmed cell death-1retroperitoneal sarcomasurgeryundifferentiated pleomorphic sarcoma

Identifiers

PMID32952659
PMCPMC7479533
OpenAlexW3083690508

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.