Phase 2 study of lenalidomide maintenance for patients with high-risk acute myeloid leukemia in remission.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 06 2021
Historique:
revised: 12 10 2020
received: 21 07 2020
accepted: 27 11 2020
pubmed: 16 1 2021
medline: 31 12 2021
entrez: 15 1 2021
Statut: ppublish

Résumé

New drug combinations have led to significant improvements in remission rates for patients with acute myeloid leukemia (AML). However, many patients with high-risk AML who respond to their initial treatment and are not candidates for allogeneic stem cell transplantation (ASCT) will eventually relapse with poor outcomes. In this phase 2 trial, the efficacy of lenalidomide maintenance was evaluated in patients with high-risk AML who had achieved their first or second remission after induction chemotherapy and at least 1 consolidation cycle and who were not candidates for immediate ASCT. Lenalidomide was given orally at 10 to 20 mg daily on days 1 to 28 of a 28-day cycle for up to 24 cycles. A total of 28 patients were enrolled in this study with a median age of 61 years (range, 24-87 years). The median number of cycles was 8 (range, 1-24 cycles). Ten patients (36%) completed 24 months of maintenance treatment. With a median follow-up of 22.5 months (range, 2.6-55 months), 12 patients (43%) relapsed after a median of 3 months (range, 0.7-23 months). The median duration of remission for all patients was 18.7 months (range, 0.7-55.1 months). The 2-year overall survival and relapse-free survival rates from the time of enrollment were 63% and 50%, respectively. Overall, lenalidomide was well tolerated; serious adverse events of grade 3 or 4, including rash (n = 5), thrombocytopenia (n = 4), neutropenia (n = 4), and fatigue (n = 2), were observed in 13 patients (46%). Lenalidomide is a safe and feasible maintenance strategy in patients with high-risk AML who are not candidates for ASCT, and it has beneficial effects for patients with negative measurable residual disease.

Sections du résumé

BACKGROUND
New drug combinations have led to significant improvements in remission rates for patients with acute myeloid leukemia (AML). However, many patients with high-risk AML who respond to their initial treatment and are not candidates for allogeneic stem cell transplantation (ASCT) will eventually relapse with poor outcomes.
METHODS
In this phase 2 trial, the efficacy of lenalidomide maintenance was evaluated in patients with high-risk AML who had achieved their first or second remission after induction chemotherapy and at least 1 consolidation cycle and who were not candidates for immediate ASCT. Lenalidomide was given orally at 10 to 20 mg daily on days 1 to 28 of a 28-day cycle for up to 24 cycles.
RESULTS
A total of 28 patients were enrolled in this study with a median age of 61 years (range, 24-87 years). The median number of cycles was 8 (range, 1-24 cycles). Ten patients (36%) completed 24 months of maintenance treatment. With a median follow-up of 22.5 months (range, 2.6-55 months), 12 patients (43%) relapsed after a median of 3 months (range, 0.7-23 months). The median duration of remission for all patients was 18.7 months (range, 0.7-55.1 months). The 2-year overall survival and relapse-free survival rates from the time of enrollment were 63% and 50%, respectively. Overall, lenalidomide was well tolerated; serious adverse events of grade 3 or 4, including rash (n = 5), thrombocytopenia (n = 4), neutropenia (n = 4), and fatigue (n = 2), were observed in 13 patients (46%).
CONCLUSIONS
Lenalidomide is a safe and feasible maintenance strategy in patients with high-risk AML who are not candidates for ASCT, and it has beneficial effects for patients with negative measurable residual disease.

Identifiants

pubmed: 33449377
doi: 10.1002/cncr.33409
doi:

Substances chimiques

Angiogenesis Inhibitors 0
Lenalidomide F0P408N6V4

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1894-1900

Subventions

Organisme : Celgene
Organisme : NIH HHS
ID : P30 CA016672
Pays : United States

Informations de copyright

© 2020 American Cancer Society.

Références

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Auteurs

Iman Abou Dalle (I)

Hematology-Oncology Division, Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Hagop M Kantarjian (HM)

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

Farhad Ravandi (F)

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

Naval Daver (N)

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

Xuemei Wang (X)

Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Elias Jabbour (E)

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

Zeev Estrov (Z)

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

Courtney D DiNardo (CD)

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

Naveen Pemmaraju (N)

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

Alessandra Ferrajoli (A)

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

Nitin Jain (N)

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

Sa A Wang (SA)

Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Nadya Jammal (N)

Department of Pharmacy, The University of Texas MD Anderson Cancer Center, Houston, Texas.

Gautam Borthakur (G)

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

Kiran Naqvi (K)

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

Sarah Pelletier (S)

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

Sherry Pierce (S)

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

Michael Andreeff (M)

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

Guillermo Garcia-Manero (G)

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

Jorge E Cortes (JE)

Georgia Cancer Center, Augusta, Georgia.

Tapan M Kadia (TM)

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

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