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Radiofrequency Ablation. Post-ablation Assessment Using CT Perfusion with Pharmacological Modulation in a Rat Subcutaneous Tumor Model

  • ,
  • Agata A. Exner
    ,
  • Tianyi M. Krupka
    ,
  • Brent D. Weinberg
    ,
  • Ravi Patel
    ,
  • John R. Haaga(corresponding author)
*Corresponding author for this work
  • Case Western Reserve University
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

Rationale and Objectives: Inflammatory reaction surrounding the ablated area is a major confounding factor in the early detection of viable tumor after radiofrequency (RF) ablation. A difference in the responsiveness of normal and tumor blood vessels to vasoactive agents may be used to distinguish these regions in post-ablation follow-up. The goal of this study was to examine longitudinal perfusion changes in untreated viable tumor and the peripheral hyperemic rim of RF-ablated tumor in response to a vasoconstrictor (phenylephrine) or vasodilator (hydralazine) in a subcutaneous rat tumor model. Materials and Methods: Bilateral subcutaneous shoulder tumors were inoculated in 24 BDIX rats and evenly divided into two groups (phenylephrine and hydralazine groups). One tumor in each animal was completely treated with RF ablation (at 90 ± 2°C for 3 minutes), and the other remained untreated. Computed tomographic perfusion scans before and after phenylephrine (10 μg/kg) or hydralazine (5 mg/kg) administration were performed 2, 7, and 14 days after ablation. Four rats per group were euthanized on each scan day, and pathologic evaluation was performed. The changes of blood flow in the peripheral rim of ablated tumor and untreated viable tumor in response to phenylephrine or hydralazine at each time point were compared. The diagnostic accuracy of viable tumor using the percentage change of blood flow in response to phenylephrine and hydralazine was compared using receiver-operating characteristic analysis. Results: The peripheral rim of ablated tumor presented with a hyperemic reaction with dilated vessels and congestion on day 2 after ablation, numerous inflammatory vessels on day 7, and granulation tissue formation on day 14. Phenylephrine significantly decreased the blood flow in the peripheral hyperemic rim of ablated tumor on days 2, 7, and 14 by 16.3 ± 9.7% (P = .001), 24.0 ± 22.6% (P = .007), and 31.1 ± 25.4% (P = .045), respectively. In untreated viable tumor, the change in blood flow after phenylephrine was irregular and insignificant. Hydralazine decreased the blood flow in the peripheral rim of both ablated tumor and untreated viable tumor. Receiver-operating characteristic analysis showed that reliable tumor diagnosis using the percentage change of blood flow in response to phenylephrine was noted on days 2 and 7, for which the areas under the curve were 0.82 (95% confidence interval, 0.64-1.00) and 0.81 (95% confidence interval, 0.56-1.00), respectively. However, tumor diagnosis using the blood flow change in response to hydralazine was unreliable. Conclusion: Phenylephrine markedly decreased blood flow in the peripheral hyperemic rim of ablated tumor but had little effect on the untreated viable tumor. Computed tomographic perfusion with phenylephrine may be useful in the long-term treatment assessment of RF ablation.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 321-331 (11 pages)

Journal (Volume, Issue Number)

Academic Radiology (Volume 16, Issue 3)

Publication milestones

  • Published - 03/2009

Publication status

Published - 03/2009

ISSN

1076-6332

Publication IDs

  • Scopus: 59449087072
  • PubMed: 19201361

Publication metrics

Metrics

SciVal
citations
11
Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1
SciVal
FWCI
0.14
SciVal
Author count
6
SciVal
Paper percentile
64
Scopus
citations

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Citation count
13
Captures
21

Funding Details

FundersFunding numbers
NCI
R21CA131014
NIGMS
T32GM007250