Evidence map›Paper›PMID 17360651›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Programmed cell death 1 ligand 1 and tumor-infiltrating CD8+ T lymphocytes are prognostic factors of human ovarian cancer.

Junzo Hamanishi, Masaki Mandai, Masashi Iwasaki, Taku Okazaki, Yoshimasa Tanaka, Ken Yamaguchi, Toshihiro Higuchi, Haruhiko Yagi, Kenji Takakura, Nagahiro Minato and 2 more

8 registry-linked trialsOpen access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 8 registered trials, which are not on this map. Cited by 817 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
817citing papers in PubMed, 3 pooled it
15.2field-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.

NCT01386502 phase1withdrawnnot on this mapstarted 2011, after this paper: background citation

Phase I Trial of Escalating Doses of Anti-PD1 Monoclonal Antibody (CT-011) in Combination With p53 Vaccine in Adults With Advanced Solid Tumors

TypeinterventionalSponsorNational Cancer Institute (NCI)Ran2011 to 2011Enrolled0ConditionsBreast Cancer, Colon Cancer, Pancreatic Cancer, SarcomaArmsp53: 264-272 peptide, CT-011
NCT01774409 naunknown statusnot on this mapstarted 2013, after this paper: background citation

Program to Establish the Genetic and Immunologic Profile of Patient's Tumor for All Types of Advanced Cancer

TypeinterventionalSponsorCentre Leon BerardRan2013 to 2026Enrolled10,000ConditionsNeoplasmsArmsBlood and tumor samples
NCT02766582 phase2completednot on this mapstarted 2016, after this paper: background citation

Phase II Open Label Nonrandomized Trial of the Anti PD 1 Therapy Pembrolizumab With First Line Platinum Based Chemotherapy Followed by 12 Months Pembrolizumab Monotherapy for Patients With Stage III/IV Epithelial Ovarian Cancer

TypeinterventionalSponsorMedical College of WisconsinRan2016 to 2023Enrolled29ConditionsOvarian CancerArmsPembrolizumab, Carboplatin, Paclitaxel
NCT02771197 phase2completednot on this mapstarted 2016, after this paper: background citation

Phase II Trial of Lymphodepletion and Anti-PD-1 Blockade to Reduce Relapse in High Risk AML Patients Who Are Not Eligible for Allogeneic Stem Cell Transplantation

TypeinterventionalSponsorNorthside Hospital, Inc.Ran2016 to 2023Enrolled20ConditionsAcute Myeloid LeukemiaArmsFludarabine, Melphalan, Pembrolizumab
NCT03447678 phase2unknown statusnot on this mapstarted 2018, after this paper: background citation

Phase II Study to Test Pembrolizumab (MK-3475) in First Line Treatment of Advanced NSCLC Patients With PD-L1 Low Tumors (<50%)_ PEOPLE TRIAL (Pembrolizumab in Pd-L1 Low Expressors).

TypeinterventionalSponsorFondazione IRCCS Istituto Nazionale dei Tumori, MilanoRan2018 to 2022Enrolled65ConditionsNon Small Cell Lung Cancer (NSCLC)ArmsPembrolizumab
NCT03542461 phase3unknown statusnot on this mapstarted 2017, after this paper: background citation

An Open-label, Randomized Phase III Study of Early Switch Maintenance vs DElayed Second-line Nivolumab in Advanced Stage Squamous Non Small-cell Lung Cancer (NSCLC) Patients After Standard First-line Platinum-based Chemotherapy - EDEN Trial

TypeinterventionalSponsorGruppo Oncologico Italiano di Ricerca ClinicaRan2017 to 2023Enrolled125ConditionsSquamous Non-small Cell Lung CancerArmsNivolumab 10 MG/ML Intravenous Solution, Best Supportive Care
NCT04730999 phase2completednot on this mapstarted 2020, after this paper: background citation

A Phase II, Single Arm Study of CarbopLatin Plus Etoposide With Bevacizumab and Atezolizumab in Patients With exTEnded-disease Small-cell Lung Cancer (SCLC)

TypeinterventionalSponsorGruppo Oncologico Italiano di Ricerca ClinicaRan2020 to 2024Enrolled54ConditionsSmall Cell Lung CancerArmsEtoposide, Carboplatin, Bevacizumab, Atezolizumab
NCT04761744 phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

A Phase II Study of Nivolumab in Patients With Genetic Alterations in DNA Damage Repair and Response Who Progressed After Standard Treatment for Metastatic Solid Cancers

TypeinterventionalSponsorKorean Cancer Study GroupRan2019 to 2021Enrolled48ConditionsDDR Gene Mutation, Metastatic Solid TumorArmsNivolumab
3 · Its place in the literature

Who cites it

817 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,365 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Trial
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  11. Intratumoral PD-1Medical oncology (Northwood, London, England) · 2026
    Article
  12. Review
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  14. Review
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757 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

12 authors at 1 institution in 1 country.

Junzo HamanishiDepartment of Gynecology and Obstetrics, Graduate School of Medicine, Kyoto University, 54 Shogoin Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
Masaki Mandai
Masashi Iwasaki
Taku Okazaki
Yoshimasa Tanaka
Ken Yamaguchi
Toshihiro Higuchi
Haruhiko Yagi
Kenji Takakura
Nagahiro Minato
Tasuku Honjo
Shingo Fujii
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ligands for programmed cell death 1 (PD-1), an immunoinhibitory receptor belonging to CD28/cytotoxic T lymphocyte antigen 4 family, are PD-1 ligand 1 and 2 (PD-Ls). Recent reports suggest that the aberrant expression of PD-Ls on tumor cells impairs antitumor immunity, resulting in the immune evasion of the tumor cells. Although an inverse correlation between the expression level of PD-Ls and patients' prognosis has been reported for several malignant tumors, the follow-up period was limited because of the lack of the antibody (Ab) applicable to paraffin-embedded specimens. Here we generated a new Ab against PD-1 ligand 1 (PD-L1) and analyzed the expression level of PD-Ls in human ovarian cancer using paraffin-embedded specimens. Patients with higher expression of PD-L1 had a significantly poorer prognosis than patients with lower expression. Although patients with higher expression of PD-1 ligand 2 also had a poorer prognosis, the difference was not statistically significant. A significant inverse correlation was observed between PD-L1 expression and the intraepithelial CD8(+) T lymphocyte count, suggesting that PD-L1 on tumor cells directly suppresses antitumor CD8(+) T cells. Multivariate analysis showed the expression of PD-L1 on tumor cells and intraepithelial CD8(+) T lymphocyte count are independent prognostic factors. The PD-1/PD-L pathway can be a good target for restoring antitumor immunity in ovarian cancer.

Indexed as

AdultAgedAntibodiesAntigens, CDB7-H1 AntigenCD8-Positive T-LymphocytesFemaleHumansImmunohistochemistryLymphocyte CountMiddle AgedMultivariate AnalysisOvarian NeoplasmsPrognosisAntibodiesAntigens, CDB7-H1 AntigenCD274 protein, human

Identifiers

PMID17360651
PMCPMC1805580
OpenAlexW2136313650

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 2 more above

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.