Cryoablation
ProcedurePercutaneous imaging-guided cryoablation
NCT Number: NCT06081400
"Wait & see" is currently the standard of care of recently diagnosed desmoid tumors (DT). In case of progression or symptomatic disease, medical therapy is nowadays widely used including chemotherapy.
Cryoablation has proven to be beneficial for the treatment of large, progressive and symptomatic DT.
This randomized phase II trial aims to compare cryoablation versus medical therapy in DT patients progressing after the "wait & see" period. Moreover, a cross-over design has been anticipated to allow all patients to undergo cryoablation if necessary.
Interested in participating?
Request Info13 year and older
All sexes
Interventional
Not applicable
Service d'oncologie/CHU de Besançon, Besançon, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Percutaneous imaging-guided cryoablation
Either :
methotrexate 30mg/m² + vinblastine 6mg/m² (IV infusion) once/week for 6 months, then every other week from months 7 to 12, or vinorelbine : for adults : 90mg/week (per os: 3x30mg, soft capsules) for 12 months; for adolescents: 60mg/m2/week (capped at 90mg/week) for 12 months
Time frame: 12 months after treatment initiation (Day 0+12months)
Rates of non-progressive disease (sum of complete response (CR), partial response (PR), and stable disease (SD) according to modified RECIST criteria)
Time frame: from treatment initiation to PD or 24 months whichever comes first
Progression-free survival 1 (PFS1: from the beginning of cryoablation or medical therapy to first disease progression) in cryoablation and medical therapy group
Time frame: 24 months after treatment initiation
Time frame: 12 months after treatment initiation and 12 months after cross-over
Rate of complete response at 12 months in cryoablation and medical therapy group with and without a cross-over treatment
Time frame: Through study completion, up to 39 months
Secondary Progression-free survival 2 (PFS 2: from the cross-over to second disease progression) in cryoablation and medical therapy group
Time frame: Through study completion, up to 39 months
The occurrence of complications and adverse reactions according to the classification of the NCI-CTCAE version 5.0 toxicity scale
Time frame: Screening visit, Month 1, Month 2, Month 3, Month 6, Month 9 and Month 12 after treatment initiation
EUROQOL EQ 5D will be used; score ranging from 1 (good quality of life) to 5 (poor quality of life)
Time frame: Screening visit, Day 0/Day 1, Month 1, Month 2, Month 3, Month 6, Month 9 and Month 12 after treatment initiation
BPI will be used; score ranging from 0 (no pain) to 10 (high pain)
Time frame: Through study completion, up to 39 months
cost and incremental cost utility ratio
Contact information is provided by the study sponsor or research team.
Afshin GANGI, MD,PhD
CONTACT
0369550304 ext. 33
Roberto Luigi CAZZATO, MD
CONTACT
0369550304 ext. 33
University Hospital, Strasbourg, France
Other
A Phase II Multicentric, Randomized Trial Assessing Cryoablation Versus Medical Therapy in Desmoid Tumors Progressing After Watchful Waiting
Acronym: CRYODESMO-02
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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