Cryoablation Versus Medical Therapy in Desmoid Tumors Progressing After Watchful Waiting

ConditionDesmoid Tumor
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age13+
SponsorUniversity Hospital, Strasbourg, France

About this trial

"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.

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Trial design

Treatments tested in this trial

  • Cryoablation
  • Chemotherapy drug

Treatment groups

150 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University Hospital, Strasbourg, France

Lead sponsor

Direction Générale de l'Offre des Soins (DGOS)

Collaborator