Evidence map›Paper›PMID 23019074›Full record

Trial reportMolecular medicine (Cambridge, Mass.)2012

T(H)2-like chemokine patterns correlate with disease severity in patients with recurrent respiratory papillomatosis.

David W Rosenthal, James A DeVoti, Bettie M Steinberg, Allan L Abramson, Vincent R Bonagura

Open access · goldAbstract readClinical Trial, Phase IIRandomized Controlled Trial
In one paragraph

Trial report in Molecular medicine (Cambridge, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 24% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Current and future management of recurrent respiratory papillomatosis.Laryngoscope investigative otolaryngology · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Expression of human papillomavirus and prognosis of juvenile laryngeal papilloma.International journal of clinical and experimental medicine · 2015
    Article
  17. Immune therapy for human papillomaviruses-related cancers.World journal of clinical oncology · 2014
    Review
  18. Article
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

5 authors at 2 institutions in 1 country.

David W RosenthalElmezzi Graduate School of Molecular Medicine, Manhasset, New York, USA.
James A DeVoti
Bettie M Steinberg
Allan L Abramson
Vincent R Bonagura
Feinstein Institute for Medical Research · USIcahn School of Medicine at Mount Sinai · US

Funding

HPV-Specific, Immune Suppression in Patients with RRPR01DE017227 · NIDCR · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI BONAGURA, VINCENT ROBERT · 2006 to 2017
$4.5M
Celecoxib therapy for patients with recurrent respiratory papillomatosisU01DC007946 · NIDCD · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI STEINBERG, BETTIE M. · 2007 to 2011
$3.8M
NIDCD NIH HHS U01 DC007946NIDCD NIH HHS U01DC007946NIDCR NIH HHS R01 DE017227NIDCR NIH HHS R01DE017227
6 · The paper itself

Abstract

Recurrent respiratory papillomatosis (RRP), characterized by the recurrent growth of benign tumors of the respiratory tract, is caused by infection with human papillomavirus (HPV), predominantly types 6 and 11. Surgical removal of these lesions can be required as frequently as every 3 to 4 wks to maintain a patent airway. There is no approved medical treatment for this disease. In this study, we have characterized the T(H)2-like chemokine profile (CCL17, CCL18, CCL20, CCL22) in patients with RRP and asked whether it was modulated in patients who had achieved significant clinical improvement. CCL17, CCL18 and CCL22 messenger RNAs (mRNAs) were increased in papillomas compared with clinically normal laryngeal epithelium of the RRP patients. Overall, CCL20 mRNA expression was not increased, but there was intense, selective CCL20 protein expression in the basal layer of the papillomas. Patients with RRP expressed more CCL17 (p = 0.003), CCL18 (p = 0.0003), and CCL22 (p = 0.007) in their plasma than controls. Plasma CCL18 decreased over time in three patients enrolled in a pilot clinical trial of celecoxib, and the decrease occurred in conjunction with clinical improvement. There was a significant correlation between sustained clinical remission in additional patients with RRP and reduced levels of CCL17 (p = 0.01), CCL22 (p = 0.002) and CCL18 (p = 0.05). Thus, the change in expression of these three plasma T(H)2-like chemokines may, with future studies, prove to serve as a useful biomarker for predicting disease prognosis.

Indexed as

Severity of Illness IndexCase-Control StudiesCelecoxibChemokinesHumansLarynxPapillomaPapillomavirus InfectionsPyrazolesRemission InductionRespiratory Tract InfectionsSulfonamidesTh2 CellsCelecoxibChemokinesPyrazolesSulfonamides

Identifiers

PMID23019074
PMCPMC3521785
OpenAlexW219827365

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.