Evidence map›Paper›PMID 27105512›Full record

ArticleOncotarget2016

High post-treatment serum levels of soluble programmed cell death ligand 1 predict early relapse and poor prognosis in extranodal NK/T cell lymphoma patients.

Hua Wang, Liang Wang, Wen-Jian Liu, Zhong-Jun Xia, Hui-Qiang Huang, Wen-Qi Jiang, Zhi-Ming Li, Yue Lu

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 5 pooled it
5.9field-weighted citation impact, top 3% 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

36 citing papers in PubMed, 5 syntheses or guidelines pooled it, 53 citations in OpenAlex.

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  17. Immune subtyping of extranodal NK/T-cell lymphoma: a new biomarker and an immune shift during disease progression.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
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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

8 authors at 3 institutions in 1 country.

Hua WangDepartment of Hematological Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Liang WangDepartment of Hematological Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Wen-Jian LiuDepartment of Hematological Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Zhong-Jun XiaDepartment of Hematological Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Hui-Qiang HuangDepartment of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Wen-Qi JiangDepartment of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Zhi-Ming LiDepartment of Medical Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
Yue LuDepartment of Hematological Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China.
State Key Laboratory of Oncology in South ChinaSun Yat-sen University · CNSun Yat-sen University Cancer Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The impact of serum levels of soluble programmed cell death ligand 1 (sPD-L1) on prognosis in patients with Epstein-Barr virus-associated malignancies has never been investigated. We prospectively measured pre- and post-treatment serum sPD-L1 levels and evaluated their prognostic value in 97 patients with newly diagnosed, early stage extranodal NK/T-cell lymphoma (ENKTCL) treated with asparaginase-based chemotherapy followed by radiotherapy. For predicting survival outcomes, serum sPD-L1 levels of 3.23 ng/mL and 1.12 ng/mL were respectively identified for pre- and post-treatment cut-off levels. Patients with high pretreatment (>3.23 ng/mL) had shorter progression-free survival (PFS) and overall survival (OS). In a multivariate survival analysis, post-treatment sPD-L1 >1.12 ng/mL, treatment response (complete vs. non-complete response), and stage II disease were independent prognostic factors for shorter PFS and OS. In patients with a complete response, post-treatment sPD-L1 >1.12 ng/mL was associated with shorter PFS and OS. In patients with high pretreatment sPD-L1 levels (>3.23 ng/mL), low post-treatment sPD-L1 level (≤1.12 ng/mL) correlated with longer PFS and OS. Our data suggest the post-treatment sPD-L1 level is a potent biomarker for predicting early relapse and poor prognosis in early stage ENKTCL patients treated with asparaginase, and may be a useful marker of minimal residual disease.

Indexed as

AdultB7-H1 AntigenBiomarkers, TumorFemaleHumansLymphoma, Extranodal NK-T-CellMalePrognosisRecurrenceSurvival RateB7-H1 AntigenBiomarkers, TumorCD274 protein, humanasparaginaseextranodal NK/T cell lymphomaminimal residual diseaseprognosissoluble programmed cell death ligand 1

Identifiers

PMID27105512
PMCPMC5078073
OpenAlexW2336088551

What OpenQuestion holds

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LicenceCC BY
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.