- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00804830
Avastin and Doxorubicin Postoperatively for Patients With Anaplastic Thyroid Cancer
August 24, 2018 updated by: Region Skane
Phase 2 Study With Avastin and Doxorubicin Postoperatively for Patients With Anaplastic Thyroid Cancer
Anaplastic Thyroid Cancer is a very aggressive disease.
The investigators believe that angiogenesis is very important for these tumors to progress.
Preclinical data is suggesting this.
This is why we we prospectively want to treat these patients with avastin (and doxorubicin).
However, local control is of major concern.
Therefore, patients are initially treated with hyperfractionated radiotherapy and undergo surgery.
Then they can enter this study.
Study Overview
Status
Terminated
Intervention / Treatment
Detailed Description
Patients with Anaplastic Thyroid Cancer have a poor prognosis.
We will treat the patients initially with our standard radiochemotherapy, which consists of doxorubicin 20mg fixed dose/week and hyperfractionated radiotherapy 1,6 Gy twice daily up to 46 Gy in total.
The first week during radiotherapy, they will also receive Avastin 15mg/kg.
1-2 weeks after radiotherapy patients will undergo surgery of their primary tumor.
After this "standard" therapy patients can be included in this study.
Treatment is 20 mg fixed dose doxorubicin q1w and avastin 15mg/kg q3w.
Treatment will continue maximum 6 months or until progress or until intolerable side effects occur.
Study Type
Interventional
Enrollment (Actual)
15
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Göteborg, Sweden, 413 45
- Jubileumskliniken, Sahlgrenska universitetsjukhuset
-
Lund, Sweden, 221 85
- Dep of Oncology, Lund University Hospital
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Stockholm, Sweden, 17176
- Karolinska University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- cytologically or histologically verified anaplastic thyroid cancer
- completed standard therapy
- operated with R0 or R1 surgery
- Performance Status 0-2 (if pulmonary mets PS 0-1)
- normal wound healing
- neutrophils > 1,5 million/ml
- platelets > 100 million/ml
- bilirubin < 2 ULN
- creatinin < 150mikromol/L
Exclusion Criteria:
- PS 3-4 (if pulmonary mets 2-4)
- R2 resection of primary tumor
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: chemotherapy
Treatment with Avastin 15 mg/kg q3w and doxorubicin 20 mg q1w for 6 months.
|
Avastin 15 mg/kg q3w and doxorubicin 20 mg q1w
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Overall Survival
Time Frame: 2-5 years
|
2-5 years
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Response rate
Time Frame: 2-5 years
|
2-5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Jan Tennvall, MD, PhD, Dep of Oncology, Lund University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 1, 2008
Primary Completion (Actual)
December 1, 2012
Study Completion (Actual)
December 1, 2014
Study Registration Dates
First Submitted
December 8, 2008
First Submitted That Met QC Criteria
December 8, 2008
First Posted (Estimate)
December 9, 2008
Study Record Updates
Last Update Posted (Actual)
August 28, 2018
Last Update Submitted That Met QC Criteria
August 24, 2018
Last Verified
August 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Neoplasms by Histologic Type
- Neoplasms
- Neoplasms by Site
- Carcinoma
- Neoplasms, Glandular and Epithelial
- Endocrine System Diseases
- Endocrine Gland Neoplasms
- Head and Neck Neoplasms
- Thyroid Diseases
- Thyroid Neoplasms
- Thyroid Carcinoma, Anaplastic
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Enzyme Inhibitors
- Antineoplastic Agents
- Topoisomerase II Inhibitors
- Topoisomerase Inhibitors
- Antineoplastic Agents, Immunological
- Angiogenesis Inhibitors
- Angiogenesis Modulating Agents
- Growth Substances
- Growth Inhibitors
- Antibiotics, Antineoplastic
- Bevacizumab
- Doxorubicin
Other Study ID Numbers
- 2007-001783-75
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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