-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
- Cosmetic Ingredient
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
Intensive induction chemotherapy containing cytarabine and anthracyclines is still the most effective treatment for newly diagnosed adult patients with acute myeloid leukemia (AML).
Isocitrate dehydrogenase (IDH) 1 or 2 gene mutations are seen in about 20% of AML patients .
Isocitrate dehydrogenase (IDH) 1 or 2 gene mutations are seen in about 20% of AML patients
Ivosidenib (AG-120) and Enasidenib (AG-221) are targeted oral small molecule inhibitors of mutant isocitrate dehydrogenase (mIDH1) 1 and 2 enzymes, respectively .
Ivosidenib (AG-120) and Enasidenib (AG-221) are targeted oral small molecule inhibitors of mutant isocitrate dehydrogenase (mIDH1) 1 and 2, respectively.
Ivosidenib 500 mg (1/day) and Enasidenib 100 mg (1/day) are well tolerated under the conditions of the study, and their safety is consistent with that of single induction and consolidation chemotherapy
Overall survival rate
Overall survival rateIn patients receiving Ivosidenib+ intensive chemotherapy, the frequency and grade of QT interval prolongation were similar to those observed during Ivosidenib monotherapy .
In patients receiving Ivosidenib+ intensive chemotherapy, the frequency and grade of QT interval prolongation are similar to those observed during Ivosidenib monotherapy
Basic mutation profile and best overall clinical response
Basic mutation profile and best overall clinical responseIn patients receiving Ivosidenib (n=60) or Enasidenib (n=91), the complete remission rate after induction was 55% and 47%, respectively, with CR/CR with incomplete neutrophil or platelet recovery (CR/CRi/ CRp) rates were 72% and 63%, respectively .
In patients receiving Ivosidenib (n=60) or Enasidenib (n=91), the complete remission rate after induction was 55% and 47%, respectively, with CR/CR with incomplete neutrophil or platelet recovery (CR/CRi/ CRp) rates were 72% and 63%, respectively.
Among the patients with the best overall CR/CRi/CRp response, 16/41 (39%) patients in the Ivosidenib group had IDH1 mutation clearance, while 15/64 (23%) in the Enasidenib group had IDH2 mutations Removal (PCR); In addition, 16/20 (80%) and 10/16 (63%) patients had detectable residual disease turned negative (multi-parameter loss cytometry).
In conclusion, Ivosidenib or Enasidenib combined with intensive chemotherapy can improve the prognosis of newly diagnosed adult patients with mIDH1/2 AML.
Original source:
Eytan M.
org/10.
1182/blood.
2020007233" target="_blank" rel="noopener">Ivosidenib or enasidenib combined with intensive chemotherapy in patients with newly diagnosed AML: a phase 1 study in this message