Evidence map›Paper›PMID 28514898›Full record

ArticleTechnology in cancer research & treatment2017

Assessment of Cryosurgical Device Performance Using a 3D Tissue-Engineered Cancer Model.

John M Baust, Anthony Robilotto, Kristi K Snyder, Kimberly Santucci, Jennie Stewart, Robert Van Buskirk, John G Baust

Open access · hybridAbstract read
In one paragraph

Article in Technology in cancer research & treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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  12. Dose Escalation of Vitamin DCancer control : journal of the Moffitt Cancer Center
    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

7 authors at 1 institution in 1 country.

John M BaustCPSI Biotect, Owego, NY, USA.
Anthony RobilottoCPSI Biotect, Owego, NY, USA.
Kristi K SnyderCPSI Biotect, Owego, NY, USA.
Kimberly SantucciCPSI Biotect, Owego, NY, USA.
Jennie StewartCPSI Biotect, Owego, NY, USA.
Robert Van BuskirkCPSI Biotect, Owego, NY, USA.
John G BaustInstitute of Biomedical Technology, Binghamton University, Binghamton, NY, USA.
Binghamton University · US

Funding

ERASE - A new dual thermal ablation/SCN device system for treating pancreatic cancerR43CA206581 · NCI · CELL PRESERVATION SERVICES, INC. · PI VAN BUSKIRK, ROBERT G · 2016 to 2016
$295k
6 · The paper itself

Abstract

As the clinical use of cryoablation for the treatment of cancer has increased, so too has the need for knowledge on the dynamic environment within the frozen mass created by a cryoprobe. While a number of factors exist, an understanding of the iceball size, critical isotherm distribution/penetration, and the resultant lethal zone created by a cryoprobe are critical for clinical application. To this end, cryoprobe performance is typically characterized based on the iceball size and temperature penetration in phantom gel models. Although informative, these models do not provide information as to the impact of heat input from surrounding tissue nor give any information on the ablative zone created. As such, we evaluated the use of a tissue-engineered tumor model (TEM) to assess cryoprobe performance including iceball size, real-time thermal profile distribution, and resultant ablative zone. Studies were conducted using an Endocare V-probe cryoprobe, with a 10/5/10 double freeze-thaw protocol using prostate and renal cancer TEMs. The data demonstrate the generation of a 33- to 38-cm3 frozen mass with the V-Probe cryoprobe following the double freeze of which ∼12.7 and 6.5 cm3 was at or below -20°C and -40°C, respectively. Analysis of ablation zone using fluorescence microscopy 24 hours postthaw demonstrated that the internal ∼40% of the frozen mass was completely ablated, whereas in the periphery of the iceball (outer 1 cm region), a gradient of partial to minimal destruction was observed. These findings correlated well with clinical reports on renal and prostate cancer cryoablation. Overall, this study demonstrates that TEMs provide an effective model for a more complete characterization of cryoablation device performance. The data demonstrate that while the overall iceball size generated in the TEM was consistent with published reports from phantom models, the integration of an external heat load, circulation, and cellular components more closely reflect an

Indexed as

cell deathCryoCare CS systemcryosurgeryprostate cancerrenal cancerthermal ablationtissue-engineered modelV-Probe cryoprobe

Identifiers

PMID28514898
PMCPMC5762047
OpenAlexW2616866935

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.