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Association details:
Biomarker:IDH1 mutation
Cancer:Glioma
Drug:Tibsovo (ivosidenib) (IDH1 inhibitor)
Direction:Sensitive
Evidence:
Evidence Level:
Sensitive: C1 - Off-label
  (Approved for Cholangiocarcinoma)
New
Excerpt:
TIBSOVO is an isocitrate dehydrogenase-1 (IDH1) inhibitor indicated for the treatment of adult patients with a susceptible IDH1 mutation as detected by an FDA-approved test with...Locally Advanced or Metastatic Cholangiocarcinoma...Locally advanced or metastatic cholangiocarcinoma who have been previously treated.
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

Ivosidenib off-label use for IDH mutant gliomas: The MD Anderson Cancer Center real life experience.

Published date:
05/25/2023
Excerpt:
All patients are still alive as of January 11th, 2023. Disease control rate (all stable disease) was 78%. After a median follow-up of 17.8 (range 15-29) months, mPFS was 3.81 (95% CI: 1.25, 12.78) months. Patients with non-enhancing disease had better PFS than those with enhancing disease...Ivosidenib was successfully approved by third party payers for treatment of nine patients with IDH mutant gliomas. Ivosidenib was well-tolerated with a modest PFS. Patients with non-enhancing disease may trend toward better PFS than those with enhancing disease.
DOI:
10.1200/JCO.2023.41.16_suppl.e14022
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

3D-volumetric assessment of response to ivosidenib in IDH-mutant gliomas

Published date:
05/26/2022
Excerpt:
In the present study we assess our single-institutional experience with the off-label use of ivosidenib to reduce tumor growth rate in patients with IDH mutant gliomas. PFS-6 and PFS-12 were 91% (n = 11), and 88% (n = 8), respectively. The use of ivosidenib in treatment-naïve gliomas was associated with a high response rate…
DOI:
10.1200/JCO.2022.40.16_suppl.2063
Evidence Level:
Sensitive: C3 – Early Trials
Title:

Ivosidenib in Isocitrate Dehydrogenase 1 - Mutated Advanced Glioma

Published date:
10/10/2020
Excerpt:
In patients with mIDH1 advanced glioma, ivosidenib 500 mg once per day was associated with a favorable safety profile, prolonged disease control, and reduced growth of nonenhancing tumors.
DOI:
10.1200/JCO.19.03327
Trial ID: