Evidence map›Paper›PMID 24514954›Full record

ArticleCancer immunology, immunotherapy : CII2014

PD-1(+) immune cell infiltration inversely correlates with survival of operable breast cancer patients.

Shenyou Sun, Xiaochun Fei, Yan Mao, Xiumin Wang, David H Garfield, Ou Huang, Jinglong Wang, Fei Yuan, Long Sun, Qixiang Yu and 3 more

Registry-linked trialOpen access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06576921 (Efficacy and Safety of Serplulimab Combined With Nab-paclitaxel and SOX as Neoadjuvant Treatment for Locally Advanced Gastric Cancer or Adenocarcinoma of Esophagogastric Junction), which is not on this map. Cited by 90 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed, 11 pooled it
8.8field-weighted citation impact, top 1% 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.

NCT06576921 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

Efficacy and Safety of Serplulimab Combined With Nab-paclitaxel and SOX as Neoadjuvant Treatment for Locally Advanced Gastric Cancer or Adenocarcinoma of Esophagogastric Junction: A Multicenter Randomized Controlled Trial

TypeinterventionalSponsorXijing HospitalRan2024 to 2026Enrolled116ConditionsStomach Neoplasms, Immune Checkpoint InhibitorsArmsSerplulimab Combined With Chemotherapy, Placebo combined with Chemotherapy
3 · Its place in the literature

Who cites it

90 citing papers in PubMed, 11 syntheses or guidelines pooled it, 154 citations in OpenAlex.

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  7. Prognostic and predictive value of tumor-infiltrating lymphocytes in breast cancer: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2016
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30 more citing papers are in PubMed but not listed here.

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

13 authors at 3 institutions in 1 country.

Shenyou SunShanghai Ruijin Hospital, Comprehensive Breast Health Center, Shanghai, 200025, China.
Xiaochun Fei
Yan Mao
Xiumin Wang
David H Garfield
Ou Huang
Jinglong Wang
Fei Yuan
Long Sun
Qixiang Yu
Xiaolong Jin
Jianhua Wang
Kunwei Shen
Ruijin Hospital · CNShanghai Jiao Tong University · CNShanghai Cancer Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The programmed death-1 (PD-1) molecule is mainly expressed on functionally "exhausted" CD8(+) T cells, dampening the host antitumor immune response. We evaluated the ratio between effective and regulatory T cells (Tregs) and PD-1 expression as a prognostic factor for operable breast cancer patients. A series of 218 newly diagnosed invasive breast cancer patients who had undergone primary surgery at Ruijin Hospital were identified. The influence of CD8(+) cytotoxic T lymphocytes, FOXP3(+) (Treg cell marker), and PD-1(+) immune cell counts on prognosis was analyzed utilizing immunohistochemistry. Both PD-1(+) immune cells and FOXP3(+) Tregs counts were significantly associated with unfavorable prognostic factors. In bivariate, but not multivariate analysis, high tumor infiltrating PD-1(+) cell counts correlated with significantly shorter patient survival. Our results suggest a prognostic value of the PD-1(+) immune cell population in such breast cancer patients. Targeting the PD-1 pathway may be a feasible approach to treating patients with breast cancer.

Indexed as

AdultAgedAged, 80 and overAntigens, Differentiation, T-LymphocyteApoptosisBreast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, LobularCD8-Positive T-LymphocytesCombined Modality TherapyDisease-Free SurvivalFemaleFollow-Up StudiesForkhead Transcription FactorsHumansKaplan-Meier EstimateAntigens, Differentiation, T-LymphocyteForkhead Transcription FactorsFOXP3 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID24514954
PMCPMC11029035
OpenAlexW2080780959

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.