Evidence map›Paper›PMID 26314410›Full record

ReviewImmunotherapy2015

Antibody-based immunotherapy of solid cancers: progress and possibilities.

Christopher F Nicodemus

Abstract readReview
In one paragraph

Review in Immunotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  10. Effect of Stromal Cells in Tumor Microenvironment on Metastasis Initiation.International journal of biological sciences · 2018
    Review
  11. Article
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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

1 author.

Christopher F NicodemusAIT Strategies, POB 429 Sunset Lane, Franconia, NH 03580, USA.

Funding

Development of an anti-PSA IgE to treat prostate cancerR41CA137881 · NCI · ADVANCED IMMUNE THERAPEUTICS, INC. · PI PENICHET, MANUEL L, SCHULTES, BIRGIT C · 2009 to 2009
$159k
NCI NIH HHS R41 CA137881PHS HHS R41A137881
6 · The paper itself

Abstract

Monoclonal antibodies remain a primary product option for novel cancer treatment. The properties of an antibody are a function of the antigen specificity and constant region incorporated. The rapid advance in molecular understanding of cancer biology and the host-tumor interaction has defined a new range of targets for antibody development. The clinical success of the checkpoint inhibitors has validated immune modulation and mobilization as a therapeutic approach. Solid cancers are distinguished from hematologic malignancies because the solid tumor stroma contains significant tumor promoting and immune dampening elements less prominent in hematologic cancer. This review highlights how engineered monoclonal antibody products are emerging as potential cornerstones of new more personalized cancer treatment paradigms that target both tumor and the stromal environment.

Indexed as

Antibodies, MonoclonalHomeostasisHumansImmune SystemImmunotherapyModels, ImmunologicalMolecular Targeted TherapyNeoplasmsNeovascularization, PathologicAntibodies, Monoclonalcheck pointIgEIgGipilimumabmacrophagemonocytemyeloidnivolumaboregovomabPD-1second signalT celltumor stroma

Identifiers

PMID26314410
PMCPMC4623823
OpenAlexW2181036135

What OpenQuestion holds

Textmetadata
LicenceTDM
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.