Stereotactic Liver Ablation Assisted With Intra-Arterial CT Hepatic Arteriography and Ablation Confirmation Software Assessment (STEREOLAB)

NCT ID: NCT05361551

Last Updated: 2025-10-14

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-02-21
• Study Completion Date: 2026-08-31

Brief Summary

To achieve adequate tumor treatment coverage with sufficient minimal ablation margins, several steps are required: firstly, it is critical to define tumor boundaries and extent on intra-procedural CT image; secondly, accurate planning, targeting, and confirmation of ablation probe placement within the tumor; thirdly, the use of an intra-procedural imaging assessment method to evaluate minimal ablation margins is required to define whether sufficient minimal ablation margins was obtained or if additional ablation is needed. Taking all together, those factors points to the need of having a high-precision ablation methodology for intra-procedural planning, monitoring, and ablation margin assessment. Currently, such methods are only utilized in isolation and the benefit of a combined and standardized procedure workflow is unknown. Therefore, our primary goal of this single-arm clinical trial is to investigate the technical efficacy of a high-precision liver ablation technique comprised by stereotactic-guidance, CT during hepatic arteriography-based imaging analysis, and computer-based software assessment of ablation margins for the treatment of patients referred to ablation for the treatment of primary and secondary liver cancers.

Detailed Description

Primary Objective:

To evaluate the technical efficacy and Local Tumor Progression-free survival [LTPFS] of a high-precision liver ablation technique comprised by stereotactic-guidance, CT during hepatic arteriography-based imaging analysis, and computer-based software assessment of ablation margins, for the treatment of patients with colorectal liver metastasis referred to percutaneous liver ablation.

Secondary Objectives:

To evaluate the impact of this high-precision liver ablation technique on:

1. Impact of minimally ablated margins on LTPFS

2. 3D Minimal ablation margins;

3. Adverse events;

4. Liver function;

5. Tissue properties from US elastography;

6. Contrast-media utilization and radiation exposure;

7. Overall oncological outcomes (disease-free and overall survival, and ability to provide salvage local therapy at the time of recurrence).

8. Anesthesia/procedural time

9. Response and Duration of response

10. Assessing whether ringenhancing hypervascular liver micronodules represent metastasis

Conditions

Liver Ablation; Hepatic

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Liver ablation

The ablation procedure will be performed in 1 day

Group Type: EXPERIMENTAL

Liver ablation

Intervention Type: PROCEDURE

Ablation needle placement An image-guidance device be used for planning of the procedure and for placement of the ablation needle

Interventions

Liver ablation

Ablation needle placement An image-guidance device be used for planning of the procedure and for placement of the ablation needle

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

1. Patients presenting with up to 5 colorectal liver metastasis measuring up to 5 cm who are referred to percutaneous ablation;

2. Ability to completely cover the target tumor with at least a 5 mm ablation margin as determined per pre-procedure cross-sectional imaging;

3. Distance to central bile ducts > 1 cm;

4. Adequate glomerular filtration rate (GFR > 40) and no severe allergies to iodine contrast-media;

5. Ability to understand and the willingness to sign written informed consent;

6. Age > 18 years-old;

7. Performance status 0-2 (Eastern Cooperative Oncology Group Classification [ECOG]);

8. Expected survival > 12 months.

Exclusion Criteria

1. Use of other prior or concomitant local therapy at the target tumor(s).

2. Active bacterial infection or fungal infection on the day of the ablation.

3. Platelet < 50,000/mm3.

4. INR > 1.5

5. Patients with uncorrectable coagulopathy.

6. Currently breastfeeding or pregnant (latter confirmed by serum pregnancy test).

7. Physical or psychological condition which would impair study participation.

8. ASA (American Society of Anesthesiologists) score of ≥ 4.

9. Any other loco-regional therapies at the target lesion(s).

10. Anatomical variations in the arterial-hepatic blood supply of the liver that preclude the use of CTHA imaging.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

M.D. Anderson Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bruno Odisio, MD

Role: PRINCIPAL_INVESTIGATOR

M.D. Anderson Cancer Center

Locations

M D Anderson Cancer Center

Houston, Texas, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Bruno Odisio, MD

Role: CONTACT

bcodisio@mdanderson.org

(713) 563-1066

Facility Contacts

Bruno Odisio, MD

Role: primary

bcodisio@mdanderson.org

713-563-1066

References

Paolucci I, Albuquerque Marques Silva J, Lin YM, Fellman BM, Jones KA, Tatsui CE, Weinberg JS, Ruiz J, Tan J, Brock KK, Bale R, Odisio BC. Study Protocol STEREOLAB: Stereotactic Liver Ablation Assisted with Intra-Arterial CT Hepatic Arteriography and Ablation Confirmation Software Assessment. Cardiovasc Intervent Radiol. 2023 Dec;46(12):1748-1754. doi: 10.1007/s00270-023-03524-9. Epub 2023 Aug 10.

Reference Type: DERIVED

PMID: 37563313 (View on PubMed)

Related Links

http://www.mdanderson.org

M D Anderson Cancer Center

Other Identifiers

NCI-2022-03903

Identifier Type: OTHER

Identifier Source: secondary_id

2022-0221

Identifier Type: -

Identifier Source: org_study_id