Evidence map›Paper›PMID 26865127›Full record

ReviewImmunotherapy2016

Rationally combining anti-VEGF therapy with checkpoint inhibitors in hepatocellular carcinoma.

Tai Hato, Andrew X Zhu, Dan G Duda

2 registry-linked trialsAbstract readReview
In one paragraph

Review in Immunotherapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 84 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 2 pooled it
6.1field-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.

NCT03149822 phase1 / phase2completednot on this mapstarted 2017, after this paper: background citation

Phase I/II Study of Pembrolizumab and Cabozantinib in Patients With Metastatic Renal Cell Carcinoma

TypeinterventionalSponsorUniversity of Colorado, DenverRan2017 to 2024Enrolled45ConditionsMetastatic Renal Cell CarcinomaArmsCabozantinib, Pembrolizumab
NCT06584435 phase2active not recruitingnot on this mapstarted 2022, after this paper: background citation

A Single-arm Study of Toripalimab in Adjuvant Therapy After Resection of High-risk Renal Cancer

TypeinterventionalSponsorTianjin Medical University Second HospitalRan2022 to 2027Enrolled100ConditionsHigh-risk Renal Cell CarcinomaArmsToripalimab
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 2 syntheses or guidelines pooled it, 150 citations in OpenAlex.

  1. Pooled it
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  6. Observational
  7. Review
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  14. Medicinal chemistry (Shariqah (United Arab Emirates)) · 2025
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24 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 2 countries.

Tai HatoEdwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Andrew X ZhuHematology/Oncology, Department of Medicine, Massachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA 02114, USA.
Dan G DudaEdwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.
Harvard University · USMassachusetts General Hospital · US

Funding

Vascular Normalization: Rolse of Perivascular CellsP01CA080124 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2000 to 2016
$35.0M
Role of SDF1a pathway in prostate cancer relapse and metastasis post-radiotherapyR01CA159258 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DUDA, DAN GABRIEL · 2011 to 2015
$1.6M
Visualizing Immune Responses in vivo: a systems biology approachR21CA139168 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DUDA, DAN GABRIEL · 2009 to 2010
$412k
NCI NIH HHS P01 CA080124NCI NIH HHS P01-CA080124NCI NIH HHS R01 CA159258NCI NIH HHS R01-CA159258NCI NIH HHS R21 CA139168NCI NIH HHS R21-CA139168
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a fatal disease with rising incidence in the world. For advanced HCC, sorafenib, a multikinase inhibitor, is the only systemic therapy with proven survival benefits. Sorafenib is a pan-VEGF receptor inhibitor, and thus many studies have focused its antivascular effects. But VEGF also acts as an immunosuppressive molecule. VEGF can inhibit maturation of dendritic cells, promote immune suppressive cell infiltration and enhance immune checkpoint molecules expression. On the other hand, potent VEGF inhibition may increase tumor hypoxia, which could hinder antitumor immunity or immunotherapy. Thus, achieving synergy when combining anti-VEGF therapy with immunotherapy may require proper polarization of the tumor microenvironment by dose titration or combination with other immunomodulating agents.

Indexed as

AnimalsCarcinoma, HepatocellularCell CycleCell DifferentiationDendritic CellsHumansImmunosuppression TherapyLiver NeoplasmsNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsReceptors, Vascular Endothelial Growth FactorSorafenibTumor MicroenvironmentNiacinamidePhenylurea CompoundsProtein Kinase InhibitorsReceptors, Vascular Endothelial Growth FactorSorafenibCTLA-4hepatocellular carcinomaimmune checkpointLAG-3PD-1PD-L1TIM-3VEGFVEGFR2

Identifiers

PMID26865127
PMCPMC5619018
OpenAlexW2268557403

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.