The MOTION study: a randomized, phase III study of vimseltinib for the treatment of tenosynovial giant cell tumor.

CSF1R MOTION pigmented villonodular synovitis tenosynovial giant cell tumor tyrosine kinase inhibitor vimseltinib

Journal

Future oncology (London, England)
ISSN: 1744-8301
Titre abrégé: Future Oncol
Pays: England
ID NLM: 101256629

Informations de publication

Date de publication:
Mar 2024
Historique:
pubmed: 18 8 2023
medline: 18 8 2023
entrez: 18 8 2023
Statut: ppublish

Résumé

Tenosynovial giant cell tumor (TGCT) is a rare, locally aggressive neoplasm that occurs in the synovium of joints, bursae, or tendon sheaths and is caused by upregulation of the Tenosynovial giant cell tumor (or TGCT) is a rare, noncancerous tumor that grows in the soft tissue lining the spaces of joints and bursae (fluid-filled sacs that work to reduce friction in the joints). These tumors are linked to increased levels of a protein called CSF1. While this condition is typically treated with surgery, some patients may not be candidates for surgical removal of the tumor due to factors such as location or complexity of the tumor; therefore, drug treatments are needed to help these patients. Vimseltinib is an investigational oral drug specifically designed to inhibit the receptor to which the CSF1 protein binds. In this article, we describe the rationale and design for a phase III clinical trial that will test how well vimseltinib works in participants with TGCT who are not candidates for surgery. In the first part of the study, participants are randomly assigned to receive vimseltinib 30 mg twice weekly or a matching placebo (inactive substance) for up to 24 weeks. This first part is blinded, so participants will not know if they are receiving vimseltinib or the placebo. The second part of the study is a long-term treatment phase in which all participants will receive vimseltinib (unblinded).

Autres résumés

Type: plain-language-summary (eng)
Tenosynovial giant cell tumor (or TGCT) is a rare, noncancerous tumor that grows in the soft tissue lining the spaces of joints and bursae (fluid-filled sacs that work to reduce friction in the joints). These tumors are linked to increased levels of a protein called CSF1. While this condition is typically treated with surgery, some patients may not be candidates for surgical removal of the tumor due to factors such as location or complexity of the tumor; therefore, drug treatments are needed to help these patients. Vimseltinib is an investigational oral drug specifically designed to inhibit the receptor to which the CSF1 protein binds. In this article, we describe the rationale and design for a phase III clinical trial that will test how well vimseltinib works in participants with TGCT who are not candidates for surgery. In the first part of the study, participants are randomly assigned to receive vimseltinib 30 mg twice weekly or a matching placebo (inactive substance) for up to 24 weeks. This first part is blinded, so participants will not know if they are receiving vimseltinib or the placebo. The second part of the study is a long-term treatment phase in which all participants will receive vimseltinib (unblinded).

Identifiants

pubmed: 37593881
doi: 10.2217/fon-2023-0238
doi:

Banques de données

ClinicalTrials.gov
['NCT05059262']

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

593-601

Subventions

Organisme : Deciphera Pharmaceuticals

Auteurs

William D Tap (WD)

Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.

Maitreyi G Sharma (MG)

Clinical Development, Deciphera Pharmaceuticals, LLC, Waltham, MA 02451, USA.

Marc Vallee (M)

Biostatistics, Deciphera Pharmaceuticals, LLC, Waltham, MA 02451, USA.

Bryan D Smith (BD)

Biological Sciences, Deciphera Pharmaceuticals, LLC, Lawrence, KS 66044, USA.

Matthew L Sherman (ML)

Clinical Development, Deciphera Pharmaceuticals, LLC, Waltham, MA 02451, USA.

Rodrigo Ruiz-Soto (R)

Clinical Development, Deciphera Pharmaceuticals, LLC, Waltham, MA 02451, USA.

Michiel van de Sande (MV)

Leiden University Medical Center, Leiden, 2333, The Netherlands.

R Lor Randall (RL)

University of California Davis Medical Center, Sacramento, CA 95817, USA.

Nicholas M Bernthal (NM)

University of California Los Angeles, Los Angeles, CA 90095, USA.

Hans Gelderblom (H)

Leiden University Medical Center, Leiden, 2333, The Netherlands.

Classifications MeSH