Evaluation of the Cryodestruction of Non Abdominopelvic Desmoid Tumors in Patients Progressing Despite Medical Treatment (CRYODESMO01)
Primary Purpose
Desmoid Tumors
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
"cryoprobes"
Sponsored by
About this trial
This is an interventional treatment trial for Desmoid Tumors
Eligibility Criteria
Inclusion Criteria:
- Extra-abdominal desmoid tumor (confirmed by prior biopsy)
- 18 years of age or older
- Tumor deemed accessible for cryoablation procedure by the operator in the investigator center
- At least one measurable lesion (RECIST v1.1) using MRI (gadolinium injection mandatory)
- 90 % of destruction of the tumor achievable in one procedure of cryoablation with a possible second cryoablation procedure (if a complete treatment must be achieved).
- Progressive disease under standard treatment (after at least two lines of adequate medical therapy, including tamoxifen, non-steroid anti-inflamatory or chemotherapy), with presence of functional symptoms and/or pain The definition of progressing tumors also involves patients with RECIST stable disease, but with persistent functional disability or tumor-induced pain not controlled by adequate pain medication including narcotics.
- Unresectable tumor or tumor amenable only to mutilating surgery, deemed inappropriate, and discussed in multidisciplinary meeting (RCP)
- ECOG performance status 0-2
Biological and hematological parameters:
- neutrophils 1,5.109/L
- platelet count 100.109/L
- No significant hemostatic abnormalities
- Subject affiliated to social security
- Signed informed consent
Exclusion Criteria:
- Any contra-indication for the procedure as stated by the radiologist in terms of tumor size, proximity to neural/vascular structures making the procedure at unacceptable risk
- Impaired hemostasis, that may interfere with the conduct of the cryoablation
- Concurrent participation in other experimental studies that could affect endpoints of this study
- Contraindication to any form of sedation
- Contraindication to MRI or gadolinium injection (proven allergy, subject with impaired renal function (defined by a creatinine clearance below 30 ml/min by MDRD formula))
- Psychiatric disorders and adults under guardianship
- Pregnancy or breastfeeding
- Patients under judicial protection
Sites / Locations
- Service d'Imagerie Interventionnelle
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
cryoablation
Arm Description
patients undergo cryoablation procedure for desmoid tumor
Outcomes
Primary Outcome Measures
Non-progression of non-abdominopelvic desmoid tumor
The success of cryoablation, i.e. non-progression of non-abdominopelvic desmoid tumor, will be declared if the MRI control at 1 year after the last procedure shows:
no suspicious contrast enhancement (the suspicious character is defined by heterogeneous or nodular or crescent-shape contrast enhancement) in the treated zone,
and if the cryolesion (ablation zone) is not increasing in size compared to early post-ablation control (M1)
Secondary Outcome Measures
Full Information
NCT ID
NCT02476305
First Posted
June 4, 2015
Last Updated
November 15, 2017
Sponsor
University Hospital, Strasbourg, France
1. Study Identification
Unique Protocol Identification Number
NCT02476305
Brief Title
Evaluation of the Cryodestruction of Non Abdominopelvic Desmoid Tumors in Patients Progressing Despite Medical Treatment
Acronym
CRYODESMO01
Official Title
Evaluation of the Cryodestruction of Non Abdominopelvic Desmoid Tumors in Patients Progressing Despite Medical
Study Type
Interventional
2. Study Status
Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
May 2015 (Actual)
Primary Completion Date
November 2017 (Actual)
Study Completion Date
November 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Strasbourg, France
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Desmoid tumors (DT) are rare tumors (2-4 cases/million/year) that originate from musculoaponeurotic structures. Although they are benign tumors with no metastatic potential, DT are considered as locally aggressive tumors, with local invasiveness and tissue destruction, leading to pain, and disability. Surgery remains the keystone of therapy, but is limited by the anatomical situation of extra-abdominal desmoid (EAD) tumors (chest wall, root members). In patients where surgery is considered, negative-margin resection (R0) is recommended, but this frequently results in cosmetic/functional impairment. Moreover, prognostic impact of R0 resections remains controversial. The outcome after initial surgery depends upon several factors such as age, tumor site, and tumor size as demonstrated by recent data from the French Sarcoma Group.
Alternative therapies to DT surgery for front-line or recurrence include NSAID's, anti-estrogens alone or in combination, -interferon, chemotherapy, targeted therapies or radiation therapy. All of these medical approaches however may fail to achieve long-term disease control and a number of patients suffer from irreducible pain, and disability from tumor volume.
Cryoablation is a promising technique that is suitable for patients experiencing extra-abdominal DT. The procedure is based on repeated cycles of freezing/passive thawing of the tumor, leading to cell death. The technique has many advantages, among which: the accurate control of iceball under real-time MRI or CT-scan monitoring (that is not possible with other techniques such as radiofrequency), the lack of mutilation, the possibility of repeating the procedure. The cryoablation procedure has proven to be beneficial for the treatment of various tumors (liver metastases, breast, kidney). Recently, percutaneous cryotherapy has been reported in the treatment of EAD tumors poorly suited to surgery, with promising results.
In the light of these encouraging data, it is believed that patients with extra-abdominal DT not amenable to surgery unless unacceptable surgical sequel and progressing after at least two lines of adequate medical therapy (tamoxifen, NSAID or chemotherapy), could benefit from the cryoablation procedure. Tumor cryotherapy-induced regression should allow symptoms relief, prolonged progression-free survival and a better quality of life.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Desmoid Tumors
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
cryoablation
Arm Type
Experimental
Arm Description
patients undergo cryoablation procedure for desmoid tumor
Intervention Type
Device
Intervention Name(s)
"cryoprobes"
Intervention Description
Patient undergo percutaneous cryoablation of desmoid tumor, with cryoprobes
Primary Outcome Measure Information:
Title
Non-progression of non-abdominopelvic desmoid tumor
Description
The success of cryoablation, i.e. non-progression of non-abdominopelvic desmoid tumor, will be declared if the MRI control at 1 year after the last procedure shows:
no suspicious contrast enhancement (the suspicious character is defined by heterogeneous or nodular or crescent-shape contrast enhancement) in the treated zone,
and if the cryolesion (ablation zone) is not increasing in size compared to early post-ablation control (M1)
Time Frame
12 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Extra-abdominal desmoid tumor (confirmed by prior biopsy)
18 years of age or older
Tumor deemed accessible for cryoablation procedure by the operator in the investigator center
At least one measurable lesion (RECIST v1.1) using MRI (gadolinium injection mandatory)
90 % of destruction of the tumor achievable in one procedure of cryoablation with a possible second cryoablation procedure (if a complete treatment must be achieved).
Progressive disease under standard treatment (after at least two lines of adequate medical therapy, including tamoxifen, non-steroid anti-inflamatory or chemotherapy), with presence of functional symptoms and/or pain The definition of progressing tumors also involves patients with RECIST stable disease, but with persistent functional disability or tumor-induced pain not controlled by adequate pain medication including narcotics.
Unresectable tumor or tumor amenable only to mutilating surgery, deemed inappropriate, and discussed in multidisciplinary meeting (RCP)
ECOG performance status 0-2
Biological and hematological parameters:
neutrophils 1,5.109/L
platelet count 100.109/L
No significant hemostatic abnormalities
Subject affiliated to social security
Signed informed consent
Exclusion Criteria:
Any contra-indication for the procedure as stated by the radiologist in terms of tumor size, proximity to neural/vascular structures making the procedure at unacceptable risk
Impaired hemostasis, that may interfere with the conduct of the cryoablation
Concurrent participation in other experimental studies that could affect endpoints of this study
Contraindication to any form of sedation
Contraindication to MRI or gadolinium injection (proven allergy, subject with impaired renal function (defined by a creatinine clearance below 30 ml/min by MDRD formula))
Psychiatric disorders and adults under guardianship
Pregnancy or breastfeeding
Patients under judicial protection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Afshin GANGI, MD
Organizational Affiliation
Strasbourg's University Hospitals
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service d'Imagerie Interventionnelle
City
Strasbourg
State/Province
Alsace
ZIP/Postal Code
67091
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
33290994
Citation
Kurtz JE, Buy X, Deschamps F, Sauleau E, Bouhamama A, Toulmonde M, Honore C, Bertucci F, Brahmi M, Chevreau C, Duffaud F, Gantzer J, Garnon J, Blay JY, Gangi A. CRYODESMO-O1: A prospective, open phase II study of cryoablation in desmoid tumour patients progressing after medical treatment. Eur J Cancer. 2021 Jan;143:78-87. doi: 10.1016/j.ejca.2020.10.035. Epub 2020 Dec 5.
Results Reference
derived
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Evaluation of the Cryodestruction of Non Abdominopelvic Desmoid Tumors in Patients Progressing Despite Medical Treatment
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