Clinical and radiological response of Maffucci related enchondromas to mutant IDH1 inhibitor Ivosidenib.

Bone

Department of Neurosurgery, Lariboisière Hospital, APHP.Nord, France; Frontlab, CNRS UMR 7225, INSERM U1127, Paris Brain Institute (ICM), Paris, France; Université Paris Cité, Paris, France.

Published: November 2024

AI Article Synopsis

  • - Ollier Disease (OD) and Maffucci syndrome (MS) are rare bone disorders linked to genetic mutations and affect bone growth, with a prevalence of 1 in 100,000 people.
  • - Ivosidenib, a treatment for certain cancers, was used in the first reported case of a patient with MS, resulting in tumor size stabilization and notable improvement in the patient's painful enchondromas.
  • - This case suggests potential benefits of IDH inhibitors for OD and MS patients, highlighting the need for further research on their long-term effects in these conditions.

Article Abstract

Ollier Disease (OD) and Maffucci syndrome (MS) is a rare bone disorder that affects the growth and development of the bones, with an estimated prevalence of 1 in 100,000 people. It is associated with somatic mosaicism of isocitrate dehydrogenase-1 (IDH1) or 2 (IDH2) pathogenic variants. Ivosidenib is indicated for the treatment of acute myeloid leukemia and locally advanced or metastatic cholangiocarcinoma and is currently investigated in low-grade glioma with a susceptible isocitrate dehydrogenase-1 (IDH1) pathogenic variant, but its effects in patients with OD or MS are unknown. We here report the first case of a patient with MS who was treated with Ivosidenib for recurrent IDH-1 mutated glioma. Besides the stabilization of the tumor size, the patient observed significant improvement in his enchondromas that became stiffer, with reduced pain, and significant modification of the mineralization of the enchondromas observed on X-rays. This first case report provides hope for the medical management of patients suffering because of OD or MS. Future clinical research is urgently needed to evaluate long-term benefit risk profile of IDH inhibitors in these rare diseases.

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http://dx.doi.org/10.1016/j.bone.2024.117221DOI Listing

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