Outcomes of Frontline Triplet Regimens With a Hypomethylating Agent, Venetoclax, and Isocitrate Dehydrogenase Inhibitor for Intensive Chemotherapy–Ineligible Patients With Isocitrate Dehydrogenase–Mutated AML

C Courtney D. DiNardo (Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA) J Jennifer Marvin-Peek (2Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) S Sanam Loghavi K Koichi Takahashi G Ghayas C. Issa W Wei-Ying Jen (The University of Texas MD Anderson Cancer Center) N Naval G. Daver (Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA) P Patrick K. Reville (1Division of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) N Nicholas J. Short (1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) K Koji Sasaki (1The University of Texas MD Anderson Cancer Center, Houston, TX) J Jillian K. Mullin (Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) C Corey A. Bradley (Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) G Gautam Borthakur (5MD Anderson Cancer Center, Houston, United States) A Abhishek Maiti (1University of Texas MD Anderson Cancer Center, Leukemia, Houston, United States) Y Yesid Alvarado (1The University of Texas MD Anderson Cancer Center, Leukemia, Houston, United States) N Naveen Pemmaraju (The University of Texas MD Anderson Cancer Center, Houston, Texas, United States) H Hussein A. Abbas (M D Anderson Cancer Center, Houston, Texas, United States) D Danielle E. Hammond (Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) F Fadi Haddad G Guillermo Montalban Bravo (Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) K Kelly S. Chien M Musa Yilmaz S Steven M. Kornblau (8Division of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) E Elias Jabbour (Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA) F Farhad Ravandi (Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA) T Tapan Kadia (2Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX) G Guillermo Garcia-Manero M Marina Y. Konopleva (Department of Leukemia, The University of Texas MD Anderson Cancer Center) H Hagop M. Kantarjian (Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA)

Abstract

PURPOSE The development of targeted therapeutics has revolutionized treatment for elderly patients with AML. Two doublet regimens are approved in the frontline setting for intensive chemotherapy (IC)–ineligible AML: venetoclax (VEN) in combination with hypomethylating agent (HMA) therapy and azacitidine (AZA) plus ivosidenib (IVO) specifically for IDH1 -mutated AML. Although both regimens have improved AML outcomes, most patients will either not respond to frontline therapy or relapse, with dismal salvage outcomes. METHODS We herein report on 60 newly diagnosed IC-ineligible patients treated at our institution with triplet regimens for isocitrate dehydrogenase ( IDH )–mutant AML. Patients received either AZA + VEN + IVO on NCT03471260 ( IDH1 -mutated patients only) or oral decitabine + VEN + IVO/enasidenib on NCT04774393 (arms for IDH1- and IDH2 -mutant disease, respectively). RESULTS The triplet regimens were well tolerated with low early mortality (n = 1 [2%] in 60 days) and a similar safety profile to HMA + VEN and isocitrate dehydrogenase inhibitor doublet regimens. The composite complete remission rate (CRc) was 92% (55/60), with an overall response rate of 95% (57/60). With a median follow-up of 27.4 months, the median overall survival (OS) has not yet been reached. The 2-year OS was 69% with a 2-year cumulative incidence of relapse of 24%. Patients with treated-secondary AML (tsAML) experienced inferior outcomes with a CRc of 71% (12/17) and a 2-year OS of 34%; the 2-year OS was 84% in patients without tsAML. Nineteen patients (32%) transitioned to stem cell transplant, and 51% remain on study. CONCLUSION Given the excellent outcomes of IDH-triplet therapy for newly diagnosed, IC-ineligible IDH -mutant AML, further prospective studies comparing IDH-triplet versus IDH-doublet regimens are warranted.

Article Details

Volume / Issue Vol. 43, Issue 24
Published August 20, 2025
Pages 2692-2699
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (29)

C

Courtney D. DiNardo

Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

J

Jennifer Marvin-Peek

2Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

S

Sanam Loghavi

K

Koichi Takahashi

G

Ghayas C. Issa

W

Wei-Ying Jen

The University of Texas MD Anderson Cancer Center

N

Naval G. Daver

Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

P

Patrick K. Reville

1Division of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

N

Nicholas J. Short

1Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

K

Koji Sasaki

1The University of Texas MD Anderson Cancer Center, Houston, TX

J

Jillian K. Mullin

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

C

Corey A. Bradley

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

G

Gautam Borthakur

5MD Anderson Cancer Center, Houston, United States

A

Abhishek Maiti

1University of Texas MD Anderson Cancer Center, Leukemia, Houston, United States

Y

Yesid Alvarado

1The University of Texas MD Anderson Cancer Center, Leukemia, Houston, United States

N

Naveen Pemmaraju

The University of Texas MD Anderson Cancer Center, Houston, Texas, United States

H

Hussein A. Abbas

M D Anderson Cancer Center, Houston, Texas, United States

D

Danielle E. Hammond

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

F

Fadi Haddad

G

Guillermo Montalban Bravo

Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

K

Kelly S. Chien

M

Musa Yilmaz

S

Steven M. Kornblau

8Division of Cancer Medicine, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

E

Elias Jabbour

Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

F

Farhad Ravandi

Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA

T

Tapan Kadia

2Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX

G

Guillermo Garcia-Manero

M

Marina Y. Konopleva

Department of Leukemia, The University of Texas MD Anderson Cancer Center

H

Hagop M. Kantarjian

Department of Leukemia The University of Texas MD Anderson Cancer Center Houston Texas USA