Evidence map›Paper›PMID 25858804›Full record

ReviewCancer cell2015

Immune checkpoint blockade: a common denominator approach to cancer therapy.

Suzanne L Topalian, Charles G Drake, Drew M Pardoll

4 registry-linked trialsOpen access · bronzeAbstract readReview
In one paragraph

Review in Cancer cell, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 2,425 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2,425citing papers in PubMed, 3 pooled it
160.8field-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.

NCT03792724 phase1 / phase2unknown statusnot on this mapstarted 2019, after this paper: background citation

Phase I-II Study of Intratumoral Urelumab Combined With Nivolumab in Patients With Solid Tumors

TypeinterventionalSponsorClinica Universidad de Navarra, Universidad de NavarraRan2019 to 2023Enrolled32ConditionsNeoplasmsArmsUrelumab + Nivolumab
NCT03895970 phase2completednot on this mapstarted 2019, after this paper: background citation

Lenvatinib Combined Pembrolizumab as a Second-line Treatment in Advanced Hepatobiliary Tumors: a Single-center, Single-arm, Non-randomized Clinical Study

TypeinterventionalSponsorPeking Union Medical College HospitalRan2019 to 2021Enrolled32ConditionsLiver Neoplasm Malignant Primary, Cholangiocarcinoma, Combinational Immunotherapy, BiomarkerArmsLenvatinib plus Pembrolizumab
NCT04010071 phase2unknown statusnot on this mapstarted 2020, after this paper: background citation

Axitinib Plus Toripalimab as Second-line Treatment in Hepatobiliary Malignant Tumors: a Single-arm, Non-randomized, Single-center Phase II Trial

TypeinterventionalSponsorPeking Union Medical College HospitalRan2020 to 2024Enrolled60ConditionsHepatobiliary Neoplasm, Liver Neoplasm, Biliary Tract NeoplasmsArmsaxitinib plus toripalimab
NCT05048017 phase2unknown statusnot on this mapstarted 2021, after this paper: background citation

Regorafenib Combined With PD-1 Inhibitor Therapy for Second-line Treatment of Hepatocellular Carcinoma: A Single Arm, Nonrandomized, Single Center Clinical Study

TypeinterventionalSponsorPeking Union Medical College HospitalRan2021 to 2025Enrolled20ConditionsHepatocellular Carcinoma, Regorafenib, PD-1 InhibitorArmsRegorafenib, PD-1 inhibitor
3 · Its place in the literature

Who cites it

2,425 citing papers in PubMed, 3 syntheses or guidelines pooled it, 4,168 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Review
  7. CD112 Lactylation Drives Dual Immune Evasion From CD8+ T Cells and NK Cells.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  8. Review
  9. Article
  10. Review
  11. Article
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  13. Dendritic cell PD-L2 restrains intratumoral CD8bioRxiv : the preprint server for biology · 2026
    Article
  14. Interpreting vaccine-associated survival differences in immune checkpoint inhibitor therapy.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  15. Article
  16. Review
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  19. Article
  20. Review

2,365 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

3 authors at 2 institutions in 1 country.

Suzanne L TopalianDepartment of Surgery, Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. Electronic address: stopali1@jhmi.edu.
Charles G DrakeThe Brady Urological Institute, Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA; Department of Oncology, Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Drew M PardollDepartment of Oncology, Sidney Kimmel Comprehensive Cancer Center and Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
Sidney Kimmel Comprehensive Cancer Center · USJohns Hopkins University · US

Funding

PD-1/PD-L1 modulation in cancer therapyR01CA142779 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M., TAUBE, JANIS M · 2010 to 2025
$8.2M
Role of Tc17 cells in tumor immunotherapyR01CA154555 · NCI · JOHNS HOPKINS UNIVERSITY · PI PARDOLL, DREW M. · 2012 to 2016
$1.7M
NCI NIH HHS R01 CA142779NCI NIH HHS R01CA142779NCI NIH HHS R01 CA154555
6 · The paper itself

Abstract

The immune system recognizes and is poised to eliminate cancer but is held in check by inhibitory receptors and ligands. These immune checkpoint pathways, which normally maintain self-tolerance and limit collateral tissue damage during anti-microbial immune responses, can be co-opted by cancer to evade immune destruction. Drugs interrupting immune checkpoints, such as anti-CTLA-4, anti-PD-1, anti-PD-L1, and others in early development, can unleash anti-tumor immunity and mediate durable cancer regressions. The complex biology of immune checkpoint pathways still contains many mysteries, and the full activity spectrum of checkpoint-blocking drugs, used alone or in combination, is currently the subject of intense study.

Indexed as

Models, ImmunologicalAntibodies, MonoclonalAntineoplastic AgentsCD28 AntigensCTLA-4 AntigenHumansImmunotherapyNeoplasmsProgrammed Cell Death 1 ReceptorAntibodies, MonoclonalAntineoplastic AgentsCD28 AntigensCTLA-4 AntigenProgrammed Cell Death 1 Receptor

Identifiers

PMID25858804
PMCPMC4400238
OpenAlexW2143772132

What OpenQuestion holds

Textmetadata
LicenceTDM
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.