Evidence map›Paper›PMID 25440090›Full record

ReviewTrends in molecular medicine2015

Human cancer immunotherapy with antibodies to the PD-1 and PD-L1 pathway.

Kim C Ohaegbulam, Amer Assal, Eszter Lazar-Molnar, Yu Yao, Xingxing Zang

Abstract readReview
In one paragraph

Review in Trends in molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 467 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
467citing papers in PubMed, 7 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

467 citing papers in PubMed, 7 syntheses or guidelines pooled it.

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  11. Characterizing risk groups in papillary thyroid carcinoma through T-Cell mediated tumor cell killing-related genes: a pathway to therapeutic predictions.European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery · 2026
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407 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

5 authors.

Kim C OhaegbulamDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY 10461, USA.
Amer AssalDepartment of Oncology, Montefiore Medical Center, New York, NY 10467, USA.
Eszter Lazar-MolnarDepartment of Pathology, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.
Yu YaoDepartment of Neurosurgery, Huashan Hospital, Fudan University, Shanghai 200040, China.
Xingxing ZangDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY 10461, USA; Department of Oncology, Montefiore Medical Center, New York, NY 10467, USA. Electronic address: xing-xing.zang@einstein.yu.edu.

Funding

Core-010UL1TR001073 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI KELLER, MARLA J, SHAMOON, HARRY · 2013 to 2017
$21.3M
Tumor-expressed immune checkpoint B7x-mediated resistance to anti-CTLA-4 therapy.R01CA175495 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2014 to 2025
$5.1M
Mechanisms and Therapies of B7x and B7-H3 in T1DR01DK100525 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2015 to 2019
$1.9M
NRSA Training CoreTL1TR002557 · NCATS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MARANTZ, PAUL R · 2018 to 2022
$1.0M
Tumor expressed B7x accelerates disease and is a novel target for immunotherapyF31CA183493 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI OHAEGBULAM, KIM C · 2014 to 2017
$193k
NCATS NIH HHS TL1 TR002557NCATS NIH HHS UL1 TR001073NCI NIH HHS F31 CA183493NCI NIH HHS F31CA183493NCI NIH HHS R01 CA175495NCI NIH HHS R01CA175495NIDDK NIH HHS R01 DK100525
6 · The paper itself

Abstract

The programmed death 1 (PD-1) receptor and its ligands programmed death ligand 1 (PD-L1) and PD-L2, members of the CD28 and B7 families, play critical roles in T cell coinhibition and exhaustion. Overexpression of PD-L1 and PD-1 on tumor cells and tumor-infiltrating lymphocytes, respectively, correlates with poor disease outcome in some human cancers. Monoclonal antibodies (mAbs) blockading the PD-1/PD-L1 pathway have been developed for cancer immunotherapy via enhancing T cell functions. Clinical trials with mAbs to PD-1 and PD-L1 have shown impressive response rates in patients, particularly for melanoma, non-small-cell lung cancer (NSCLC), renal cell carcinoma (RCC), and bladder cancer. Further studies are needed to dissect the mechanisms of variable response rate, to identify biomarkers for clinical response, to develop small-molecule inhibitors, and to combine these treatments with other therapies.

Indexed as

ImmunotherapyAnimalsAntibodiesB7-H1 AntigenHumansNeoplasmsProgrammed Cell Death 1 ReceptorT-LymphocytesAntibodiesB7-H1 AntigenCD274 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Receptorhuman cancerimmunotherapymonoclonal antibodyPD-1PD-L1PD-L2

Identifiers

PMID25440090
PMCPMC4282825

What OpenQuestion holds

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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.