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NCT Number: NCT06081400

Cryoablation Versus Medical Therapy in Desmoid Tumors Progressing After Watchful Waiting

"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.

Recruiting

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Key information

Age range

13 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Service d'oncologie/CHU de Besançon, Besançon, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Subject (male or female) with extra-peritoneal desmoid tumor (confirmed by prior biopsy by an experienced pathologist within the RRePS network)
  • 13 years of age or older
  • Measurable viable tumor (according to the mRECIST criteria using MRI. The baseline MRI imaging is mandatory in the 2 months prior to treatment initiation (D0).
  • Progressive disease (according to the mRECIST criteria) after the watchful waiting period or significant increase in symptoms requiring an active therapy, as advised in a multidisciplinary sarcoma tumor board
  • Tumor deemed accessible for cryoablation procedure by the operator in a type I center. (In pediatric cases, a careful site tumor analysis will be performed with interventional radiologist to ensure for limited consequence of cryoablation in pediatric patients especially regarding growth plates).
  • 100 % of destruction of the tumor achievable in one procedure of cryoablation with 1cm security margin according to assessment by referral center (type 1) for cryoablation
  • ECOG performance status 0-2 at inclusion visit
  • Biological and hematological parameters (neutrophils ≥ 1,5.109/L ; platelet count ≥ 100.109/L ; no significant hemostatic abnormalities) in the 4 weeks prior to treatment initiation (D0)
  • Subject able to understand the objectives and risks of the research and to give dated and signed informed consent. For minors, the consent of the 2 parents must be obtained.
  • Subject affiliated to a social health insurance plan
  • For a woman of childbearing age: negative blood pregnancy test at screening/inclusion visit
  • Subject agreeing to use a contraceptive method

Exclusion criteria

  • Intra-peritoneal or multifocal desmoid tumor
  • Concurrent or prior use of any antitumor agent for the current desmoid tumor
  • Relapse after surgery for desmoid tumor
  • Any contraindication including known hypersensitivity to vinorelbine or other vinca-alkaloids, or other constituents to navelbine, to vinblastine, to methotrexate or any excipients, such as, but not limited to current or recent (within 2 weeks) severe infection, severe renal failure, severe hepatic injury, chronic respiratory failure
  • Any contraindication including hypersensitivity to gadoteric acid, meglumine or any drug containing gadolinium
  • Concomitant treatment with: yellow fever vaccine, prophylactic treatment with phenytoin, trimethoprim, ciprofloxacin, penicillins, probenecid, acetylsalicylic acid, NSAIDs, PPIs, acitretin, azote protoxide, St John's wort
  • Any contra-indication for the procedure as stated by the interventional radiologist in terms of tumor size, proximity to neural/vascular structures or adjacent organs at risk making the procedure at unacceptable risk
  • Impaired hemostasis, that may interfere with the conduct of the cryoablation
  • Contraindication to any form of sedation
  • Others contra-indications to MRI
  • Pregnancy or breastfeeding
  • Concurrent participation in other experimental studies that could affect endpoints of the present study
  • Impossibility to give the subject informed information (subject in an emergency situation, patient with comprehension difficulties ...)
  • Psychiatric disorders
  • Incompetent subject (subject to a legal protection measure: curatorship, guardianship, future protection mandate, family habilitation)

Treatment and study plan

Cryoablation

Procedure

Percutaneous imaging-guided cryoablation

Chemotherapy drug

Drug

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

Primary outcomes

  1. Rate of non-progressive disease

    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)

Secondary outcomes

  1. Progression-free survival 1

    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

  2. Rate of patients who cross over to the other arm

    Time frame: 24 months after treatment initiation

  3. Rate of complete response

    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

  4. Secondary Progression-free survival 2

    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

  5. Incidence of Treatment-Emergent Adverse Events as assessed by NCI-CTCAE version 5.0 toxicity scale

    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

  6. QUALITY OF LIFE assessed by EUROQOL EQ 5D before and after treatment

    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)

  7. PAIN assessed by brief pain inventory (BPI) before and after treatment

    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)

  8. Health economics assessment

    Time frame: Through study completion, up to 39 months

    cost and incremental cost utility ratio

Study contacts

Contact information is provided by the study sponsor or research team.

Afshin GANGI, MD,PhD

CONTACT

[email protected]

0369550304 ext. 33

Roberto Luigi CAZZATO, MD

CONTACT

[email protected]

0369550304 ext. 33

Sponsors and collaborators

Lead sponsor

University Hospital, Strasbourg, France

Other

Collaborators

  • Direction Générale de l'Offre des Soins (DGOS)

Registry information

Official study title

A Phase II Multicentric, Randomized Trial Assessing Cryoablation Versus Medical Therapy in Desmoid Tumors Progressing After Watchful Waiting

Acronym: CRYODESMO-02

Important dates

Study start
2024
Primary completion
2027
Study completion
2029
First posted
Oct 13, 2023
Registry last updated
Nov 19, 2025

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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