Evidence map›Paper›PMID 26056480›Full record

ArticleOncoTargets and therapy2015

DDMC-p53 gene therapy with or without cisplatin and microwave ablation.

Wolfgang Hohenforst-Schmidt, Paul Zarogoulidis, Joshua Stopek, Thomas Vogl, Frank Hübner, J Francis Turner, Robert Browning, Konstantinos Zarogoulidis, Antonis Drevelegas, Konstantinos Drevelegas and 3 more

Expression of concernOpen access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 9 institutions in 3 countries.

Wolfgang Hohenforst-SchmidtII Medical Clinic, Coburg Hospital, University of Wuerzburg, Coburg, Germany.
Paul ZarogoulidisPulmonary Department-Oncology Unit, G Papanikolaou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Joshua StopekCovidien, Jersey City, NJ, USA.
Thomas VoglDepartment of Diagnostic and Interventional Radiology, Goethe University of Frankfurt, Frankfurt, Germany.
Frank HübnerII Medical Clinic, Coburg Hospital, University of Wuerzburg, Coburg, Germany.
J Francis TurnerDivision of Interventional Pulmonology, Western Regional Medical Center, Goodyear, AZ ; Medical Oncology, Cancer Treatment Centers of America, Western Regional Medical Center, Goodyear, AZ.
Robert BrowningPulmonary and Critical Care Medicine, Interventional Pulmonology, National Naval Medical Center, Walter Reed Army Medical Center, Bethesda, MD, USA.
Konstantinos ZarogoulidisPulmonary Department-Oncology Unit, G Papanikolaou General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Antonis DrevelegasRadiology Department, Interbalkan European Medical Center, Thessaloniki, Greece.
Konstantinos DrevelegasRadiology Department, Interbalkan European Medical Center, Thessaloniki, Greece.
Kaid DarwicheDepartment of interventional Pneumology, Ruhrlandklinik, University Hospital Essen, University of Essen-Duisburg, Essen, Germany.
Lutz FreitagDepartment of interventional Pneumology, Ruhrlandklinik, University Hospital Essen, University of Essen-Duisburg, Essen, Germany.
Harald RittgerMedical Clinic I, 'Fuerth Hospital, University of Erlangen, Erlangen, Germany.
Interbalkan Medical Center · GRKlinikum Coburg · DERuhrlandklinik · DEAristotle University of Thessaloniki · GRGoethe University Frankfurt · DEG. Papanikolaou General Hospital · GRProvid Pharmaceuticals (United States) · USWalter Reed National Military Medical Center · USWestern Regional Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer remains the leading cause of death in cancer patients. Severe treatment side effects and late stage of disease at diagnosis continue to be an issue. We investigated whether local treatment using 2-diethylaminoethyl-dextran methyl methacrylate copolymer with p53 (DDMC-p53) with or without cisplatin and/or microwave ablation enhances disease control in BALBC mice. We used a Lewis lung carcinoma cell line to inoculate 140 BALBC mice, which were divided into the following seven groups; control, cisplatin, microwave ablation, DDMC-p53, DDMC-p53 plus cisplatin, DDMC-p53 plus microwave, and DDMC-p53 plus cisplatin plus microwave. Microwave ablation energy was administered at 20 W for 10 minutes. Cisplatin was administered as 1 mL/mg and the DDMC-p53 complex delivered was 0.5 mL. Increased toxicity was observed in the group receiving DDMC-p53 plus cisplatin plus microwave followed by the group receiving DDMC-p53 plus cisplatin. Infection after repeated treatment administration was a major issue. We conclude that a combination of gene therapy using DDMC-p53 with or without cisplatin and microwave is an alternative method for local disease control. However, more experiments are required in a larger model to identify the appropriate dosage profile.

Indexed as

carboplatinDDMCmicrowavenon-small cell lung cancerp53

Identifiers

PMID26056480
PMCPMC4446017
OpenAlexW1818333817

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.