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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01486134
Other study ID # P100138/AOM 10266
Secondary ID 2011-A00007-34
Status Terminated
Phase N/A
First received
Last updated
Start date June 20, 2012
Est. completion date December 20, 2016

Study information

Verified date May 2020
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Object of the study:

To assess the effectiveness of MR temperature monitoring of RFA of large hepatocellular carcinomas (HCC) (≥ 5 cm) in terms of complete tumor necrosis rate achieved and in term of reduction of the number of procedure required to obtain complete ablation of the tumors.

Experimental plan :

This pilot study consist to perform in a single center a single procedure of the multipolar RF ablation under MR temperature monitoring for the treatment of up to three HCC with diameter ranging from 5 cm and 10 cm in 20 inoperable patients. The main judgement criterion of the study will be the rate of complete ablation one month after one RFA procedure performed under MR temperature monitoring. The secondary criteria are, the 2-years local recurrence rate (after the first initial RF ablation procedure performed under MR temperature imaging ± additional RF ablation procedures under ultrasound monitoring in case of remnant viable foci of tumor), the potential reduction of the number of RF procedures required to achieve complete necrosis and the complication rate of RF ablation procedure performed under MR temperature monitoring.

In exploratory attempt, the study will include comparative assessment of these criteria with a historic leg of patients previously treated by the same operator in the same center for similar large tumor by multipolar RFA but using exclusively ultrasound monitoring.


Description:

The RF procedure and results assessment:

1. In preparing MR room, the patient will be positioned on MR bed put on dedicated MR compatible trolley. The abdominal antenna will be installed.

2. General anesthesia with tracheal intubation will be performed.

3. Up to six RF electrodes (up to 6 depending on the size and the location of the tumor) will be inserted under ultrasound guidance.

4. The patient will be translated without any direct manipulation in the magnet.

5. With usual T1 and T2 weighted MR morphologic sequences the poisoning of electrode will be checked and if necessary adjusted

6. Adjustment or MR temperature imaging (before RF energy deposition)

7. Starting of RF procedure under MR temperature monitoring

8. According to thermal dose maps data repositioning of electrodes and complementary energy deposition if necessary

9. Hot withdrawal of electrodes

10. Immediate (T0) post procedure MR assessment of the limits of ablation zone (T2 SPIRCHOL, Diffusion B600, In out phase, THRIVE dynamic after intravenous gadolinium injection).

After the procedure patients will be monitored at least 48 h.

MR assessment of treatment response will be performed one month after the procedure (same MR protocol performed at T0).

If the ablation is complete follow up will be ensured by MR every three months. If the ablation appeared incomplete or in case of recurrence additional RF ablation will be performed if the patient stills met the criteria of the treatment. The eventual additional RF ablation will be performed under ultrasound monitoring (the response to each additional RF ablation procedure will be assessed by MR one month after).

At the end of the study patients for whom complete radiological response of the tumor(s) initially treated (not local or distance recurrences) will be never achieved, will be considered in treatment failure.

Local recurrence is defined as the reappearance of viable tumor in contact of ablation zone of a tumor considered at least on one MR post therapeutic examination as completely ablated.

All the adverse effect and complication will be recorded and reported.

Quantitative analysis of 2D and 3D parameters of tumors and their related ablation zones as observed at the end of RF procedures on temperature maps using thermal dose concept (as previously extensively investigated) and with usual morphologic MR imaging (all used sequences) before, during and after the procedure (one month after) will be recorded and compared.

Antibioprophylaxy: will be prescribed in patients with an antecedent of endoscopic sphincterotomy (according to the CLIN protocol of Jean Verdier Hospital) and will be extended in patients : 1 older than 75 years , 2 patient with vesicular lithiasis 3) patients with nodule previously treated by embolization and those with a severe diabetes


Recruitment information / eligibility

Status Terminated
Enrollment 15
Est. completion date December 20, 2016
Est. primary completion date January 20, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patient of 18 year old.

- Up to 3 tumors unresectable suspected to be HCC according the criteria as previously defined by EASL and recently revised by AASLD among them at least one having a maximal diameter equal or larger than 5 cm.

- Proof of underlying cirrhosis.

- Multidisciplinary decision of RF ablation treatment

- Informed consent of patient

- Available healthcare insurance

Exclusion Criteria:

- Patient with short term life training uncontrollable disease

- Pregnancy

- Follow up Impossible

- Contra indication for general anesthesia

- Contra indication for MR examination with gadolinium injection

- Tumor located at less than 10 mm from colonic wall or main biliary tract

- Tumor invisible on MR examination

- Absence of safe percutaneous course to puncture the tumor

- Child - Pugh B or C cirrhosis

- Abundant ascites

- PROTHROMBIN activity < 50 %

- Platelet count < 40 .10 3/ml

- Antecedent of ascitis decompensation

- Severe portal hypertension defined by the presence of large oesophageal variceal (grade 2) , of radiological ascitis or umbilical vein repermeabilisation

- Elevation of transaminases (>3 upper limit normal range)

- Antecedent of biliodigestive anastomosis

- Antecedent of endoscopic sphincterotomy

Study Design


Intervention

Procedure:
Multipolar Radiofrequency ablation
Percutaneous multipolar radiofrequency ablation.

Locations

Country Name City State
France CHU Jean VERDIER Bondy

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

References & Publications (5)

Lepetit-Coiffé M, Laumonier H, Seror O, Quesson B, Sesay MB, Moonen CT, Grenier N, Trillaud H. Real-time monitoring of radiofrequency ablation of liver tumors using thermal-dose calculation by MR temperature imaging: initial results in nine patients, including follow-up. Eur Radiol. 2010 Jan;20(1):193-201. doi: 10.1007/s00330-009-1532-1. Epub 2009 Aug 6. — View Citation

N'Kontchou G, Mahamoudi A, Aout M, Ganne-Carrié N, Grando V, Coderc E, Vicaut E, Trinchet JC, Sellier N, Beaugrand M, Seror O. Radiofrequency ablation of hepatocellular carcinoma: long-term results and prognostic factors in 235 Western patients with cirrhosis. Hepatology. 2009 Nov;50(5):1475-83. doi: 10.1002/hep.23181. — View Citation

Seror O, Lepetit-Coiffé M, Le Bail B, de Senneville BD, Trillaud H, Moonen C, Quesson B. Real time monitoring of radiofrequency ablation based on MR thermometry and thermal dose in the pig liver in vivo. Eur Radiol. 2008 Feb;18(2):408-16. Epub 2007 Sep 26. — View Citation

Seror O, Lepetit-Coiffé M, Quesson B, Trillaud H, Moonen CT. Quantitative magnetic resonance temperature mapping for real-time monitoring of radiofrequency ablation of the liver: an ex vivo study. Eur Radiol. 2006 Oct;16(10):2265-74. Epub 2006 Apr 11. — View Citation

Seror O, N'Kontchou G, Ibraheem M, Ajavon Y, Barrucand C, Ganne N, Coderc E, Trinchet JC, Beaugrand M, Sellier N. Large (>or=5.0-cm) HCCs: multipolar RF ablation with three internally cooled bipolar electrodes--initial experience in 26 patients. Radiology. 2008 Jul;248(1):288-96. doi: 10.1148/radiol.2481071101. Epub 2008 May 15. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of complete ablation one month after one RFA procedure One month after one RFA procedure
Secondary 2-years local recurrence rate 2 years
Secondary Number of procedure required to achieve complete ablation One month after completion of treatment course
Secondary Primary treatment effectiveness (assessed 1 month after completion of treatment course which can include up to 3 RFA procedures performed monthly) 1 month after completion of treatment
Secondary Complication rate per RF procedure under MR temperature monitoring 2 years
Secondary Agreement of 2D and 3D measurements of ablations zones on IRMT° images and those measured on conventional magnitude MR images. during and after the procedure (one month after)
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