Evidence map›Paper›PMID 21748755›Full record

Trial reportThe Prostate2012

Lenalidomide modulates IL-8 and anti-prostate antibody levels in men with biochemically recurrent prostate cancer.

Daniel J Zabransky, Heath A Smith, Christopher J Thoburn, Marianna Zahurak, Daniel Keizman, Michael Carducci, Mario A Eisenberger, Douglas G McNeel, Charles G Drake, Emmanuel S Antonarakis

Abstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in The Prostate, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
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  8. Targeting angiogenesis for the treatment of prostate cancer.Expert opinion on therapeutic targets · 2012
    Review
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

10 authors at 3 institutions in 1 country.

Daniel J ZabranskyJohns Hopkins Kimmel Cancer Center, Johns Hopkins University, Baltimore, MD, USA.
Heath A Smith
Christopher J Thoburn
Marianna Zahurak
Daniel Keizman
Michael Carducci
Mario A Eisenberger
Douglas G McNeel
Charles G Drake
Emmanuel S Antonarakis
Sidney Kimmel Cancer Center · USJohns Hopkins University · USUniversity of Wisconsin Carbone Cancer Center · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
TRANSGENIC MODELS FOR PROSTATE CANCER AND AUTOIMMUNITYP50CA058236 · NCI · JOHNS HOPKINS UNIVERSITY · PI DENMEADE, SAMUEL R · 1992 to 2020
$43.9M
Training in Cancer Biology Training GrantT32CA009135 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI SUGDEN, WILLIAM M. · 1985 to 2024
$10.4M
Analysis of Lag-3 in Regulatory T Cell Function and Immune SupressionR01CA127153 · NCI · JOHNS HOPKINS UNIVERSITY · PI DRAKE, CHARLES G. · 2008 to 2012
$1.7M
NCI NIH HHS 1P50CA58236-15NCI NIH HHS P30 CA006973NCI NIH HHS P50 CA058236NCI NIH HHS R01 CA127153NCI NIH HHS R01CA127153
6 · The paper itself

Abstract

backgroundWe retrospectively explored changes in immunological parameters in men with biochemically recurrent prostate cancer treated with either 5 or 25 mg of lenalidomide in a randomized phase 2 trial, and determined whether those changes correlated with disease progression.

methodsCytokine levels were compared for each patient at baseline and after 6 months of treatment with lenalidomide. Regression models for correlated data were used to assess associations of cytokine levels with lenalidomide treatment effect. Estimates were obtained using generalized estimating equations. Changes in circulating anti-prostate antibodies were evaluated using a high-throughput immunoblot technique.

resultsTreatment with lenalidomide was associated with global changes in immunoreactivity to a number of prostate-associated antigens, as well as with changes in circulating levels of the T(H) 2 cytokines IL-4, IL-5, IL-10, and IL-13. Disease progression in treated patients was associated with an increase in circulating IL-8 levels, while IL-8 levels decreased significantly in non-progressors.

conclusionsLenalidomide demonstrates immunomodulatory properties in patients with biochemically recurrent prostate cancer. The induction of novel anti-prostate antibodies is a potential mechanism for lenalidomide response. Changes in serum IL-8 levels may serve as a potential biomarker in treated patients. These hypotheses require formal testing in future prospective trials.

Indexed as

AdenocarcinomaAgedAged, 80 and overAntigens, SurfaceAntineoplastic AgentsBiomarkers, TumorDisease ProgressionHumansImmunomodulationInterleukin-8LenalidomideMaleMiddle AgedNeoplasm Recurrence, LocalProstatectomyProstate-Specific AntigenAntigens, SurfaceAntineoplastic AgentsBiomarkers, TumorInterleukin-8LenalidomideProstate-Specific AntigenThalidomide

Identifiers

PMID21748755
PMCPMC3248613
OpenAlexW2042576072

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.