Evidence map›Paper›PMID 18193223›Full record

ArticleCancer immunology, immunotherapy : CII2008

The effect of anti-VEGF therapy on immature myeloid cell and dendritic cells in cancer patients.

Takuya Osada, Gabriel Chong, Robert Tansik, Timothy Hong, Neil Spector, Rakesh Kumar, Herbert I Hurwitz, Inderjit Dev, Andrew B Nixon, H Kim Lyerly and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 167 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
167citing 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.

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

167 citing papers in PubMed, 2 syntheses or guidelines pooled it, 304 citations in OpenAlex.

  1. Pooled it
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  10. Clinical activity and safety of combination therapy with temsirolimus and bevacizumab for advanced melanoma: a phase II trial (CTEP 7190/Mel47).Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
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  17. The Current Role of Antiangiogenics in Colorectal Cancer.International journal of molecular sciences · 2025
    Review
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107 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 5 institutions in 2 countries.

Takuya OsadaDuke University Medical Center, Box 3233, Durham, NC 27710, USA. osada001@mc.duke.edu
Gabriel Chong
Robert Tansik
Timothy Hong
Neil Spector
Rakesh Kumar
Herbert I Hurwitz
Inderjit Dev
Andrew B Nixon
H Kim Lyerly
Timothy Clay
Michael A Morse
Duke Medical Center · USDuke University Hospital · USGlaxoSmithKline (Netherlands) · NLHartford Hospital · USResearch Triangle Park Foundation · US

Funding

RNA TRASFECTED DENDRITIC CELLS FOR CANCER IMMUNOTHERAPYP01CA078673 · NCI · DUKE UNIVERSITY · PI AMALFITANO, ANDREA NA · 1999 to 2008
$13.2M
Wound Angiogenesis as a Biomarker for Tumor AngiogenesisK24CA113755 · NCI · DUKE UNIVERSITY · PI HURWITZ, HERBERT I · 2006 to 2010
$613k
NCI NIH HHS 5 P01 CA78673.NCI NIH HHS K24 CA113755NCI NIH HHS P01 CA078673
6 · The paper itself

Abstract

Impairment of dendritic cells (DC), the most effective activators of anticancer immune responses, is one mechanism for defective antitumor immunity, but the causes of DC impairment are incompletely understood. We evaluated the association of impaired DC differentiation with angiogenesis-associated molecules D-dimer, vascular endothelial growth factor (VEGF), urokinase plasminogen activator (uPA), and plasminogen activator inhibitor (PAI-1) in peripheral blood from 41 patients with lung, breast, and colorectal carcinoma. Subsequently, we studied the effect of administration of the anti-VEGF antibody (bevacizumab) on DC maturation and function in vivo. Compared with healthy volunteers, cancer patients had a bias toward the immunoregulatory DC2, had deficits in DC maturation after overnight in vitro culture, and had a significant increase in immature myeloid cell progenitors of DC (0.50 +/- 0.31% vs. 0.32 +/- 0.16% of peripheral blood mononuclear cells, respectively, P = 0.011). A positive correlation was found between the percentage of DC2 and PAI-1 (R = 0.50) and between immature myeloid cells and VEGF (R = 0.52). Bevacizumab administration to cancer patients was associated with a decrease in the accumulation of immature progenitor cells (0.39 +/- 0.30% vs. 0.27 +/- 0.24%, P = 0.012) and induced a modest increase in the DC population in peripheral blood (0.47 +/- 0.23% vs. 0.53 +/- 0.30%). Moreover, anti-VEGF antibody treatment enhanced allo-stimulatory capacity of DC and T cell proliferation against recall antigens. These data suggest that DC differentiation is negatively associated with VEGF levels and may be one explanation for impaired anticancer immunity, especially in patients with advanced malignancies.

Indexed as

Angiogenesis InhibitorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBevacizumabBreast NeoplasmsCell DifferentiationCell ProliferationCells, CulturedColorectal NeoplasmsDendritic CellsFibrin Fibrinogen Degradation ProductsHumansImmunotherapyLung NeoplasmsMyeloid Progenitor CellsNeovascularization, PathologicAngiogenesis InhibitorsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedBevacizumabFibrin Fibrinogen Degradation Productsfibrin fragment DPlasminogen Activator Inhibitor 1Urokinase-Type Plasminogen ActivatorVascular Endothelial Growth Factor A

Identifiers

PMID18193223
PMCPMC4110970
OpenAlexW2067969350

What OpenQuestion holds

Textmetadata
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.