Eastern Ablation Registry for Solid Tumor (EAST)

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT03362749
Collaborator
(none)
500
1
31.9
15.7

Study Details

Study Description

Brief Summary

Local tumor ablation is among the major anti-tumor modalities worldwide. Given the number of changes that have taken place in the field of tumor ablation in the past 10 years, it is our intention to ensure that this highly utilized standardization continues to remain relevant as it unites all investigators and clinicians practicing interventional oncology by providing a common language to describe therapies and outcomes, develop studies, and communicate with other medical specialties. In an attempt to attain greater Asian-wide adoption, the investigators will initiate the registry system for local tumor ablation in Taiwan, China, Korea, Singapore, Hong Kong and Thailand.

Condition or Disease Intervention/Treatment Phase
  • Other: RFA, MWA, cryo and IRE

Detailed Description

Local tumor ablation is among the major anti-tumor modalities worldwide. Although surgical resection is potentially curative and beneficial to long-term patient survival, the majority of patients are deemed unresectable.

In 2003, the International Working Group on Image-Guided Tumor Ablation published a document titled "Image-Guided Tumor Ablation: Proposal for Standardization of Terms and Reporting Criteria". Ten years later, the field of tumor ablation continues to evolve. Tumor ablation modalities that were still being developed at the time of original preparation, such as microwave, irreversible electroporation (IRE), have been introduced and clinical niches are being defined. Preliminary clinical studies have matured into larger longer-term series with 5- and 10-year follow-up data on par with the surgical and medical oncology literature. Over the interim, our initial document has also given rise to several additional position statements within the field of interventional oncology and been the source for more focused societal statements on tumor ablation of liver, kidney, pancreas and musculoskeletal tumors.

Given the number of changes that have taken place in the field of tumor ablation in the past 10 years, it is our intention to ensure that this highly utilized standardization continues to remain relevant as it unites all investigators and clinicians practicing interventional oncology by providing a common language to describe therapies and outcomes, develop studies, and communicate with other medical specialties. In an attempt to attain greater Asian-wide adoption, the investigators will initiate the registry system for local tumor ablation in Taiwan, China, Korea, Singapore, Hong Kong and Thailand.

The main objective of the registry will be "improved precision and communication in this field that leads to more accurate comparison of technologies and results and ultimately to improved patient outcomes". This study aims to establish a local tumor ablation registry in Taiwan and collect real-life data regarding the safety, efficacy, changes in clinical presentation, and practice pattern of treatment in patients with clinically confirmed solid tumor including thyroid, bone, liver, pancreas and those which are scheduated to be treated by local tumor ablation including radiofrequency ablation, microwave ablation, cryoablation and irreversible electroporation The results collected from this registry and the analyses generated will be valuable reference for physicians in choosing treatment strategy in the future.

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Eastern Ablation Registry for Solid Tumor (EAST)
Actual Study Start Date :
Sep 1, 2017
Anticipated Primary Completion Date :
Apr 30, 2020
Anticipated Study Completion Date :
Apr 30, 2020

Outcome Measures

Primary Outcome Measures

  1. To observe the efficacy of local tumor ablation [through study completion, an average of 1 year]

    Response rate (RR) to local tumor ablation

Secondary Outcome Measures

  1. The effect of local tumor ablation [up to 3 years]

    time-to-progression

  2. To observe the survival rate [up to 3 years]

    overall survival (OS)

  3. To observe the progression-free survival rate [up to 3 years]

    to observe the progression-free survival

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients who meet all inclusion criteria will be included:
  1. Males or non-pregnant females, at least 18 years of age (inclusive)

  2. Patients with clinically confirmed solid tumor including thyroid, bone, liver, pancreas and those which are scheduated to be treated by local tumor ablation including radiofrequency ablation, microwave ablation, cryoablation and irreversible electroporation

  3. Patients who have provided written informed consent

  4. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 1

  5. American Society of Anaesthesiologists (ASA) score ≤ 3

Exclusion Criteria:
Patients who meet any exclusion criteria will be excluded:
  1. The procedure of local ablation is not completed due to machine or patient problem

  2. Received treatment with an investigational agent/ procedure within 30 days prior to local ablation

  3. Known history of HIV infection

  4. Women who are pregnant

  5. Life expectancy is less than 3 months

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Taiwan University Hospital Taipei Taiwan

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

  • Principal Investigator: Kai-Wen Huang, M.D. Ph.D, National Taiwan University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT03362749
Other Study ID Numbers:
  • 201703032RIND
First Posted:
Dec 5, 2017
Last Update Posted:
Dec 5, 2017
Last Verified:
Apr 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2017