Ixazomib in addition to chemotherapy for the treatment of acute lymphoblastic leukemia in older adults.


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
06 2022
Historique:
pubmed: 26 1 2022
medline: 3 6 2022
entrez: 25 1 2022
Statut: ppublish

Résumé

We sought to assess the safety of adding ixazomib, an oral proteasome inhibitor, to a multi-agent treatment regimen for older adults with acute lymphoblastic leukemia (ALL). Patients 51 to 75 years of age with newly diagnosed ALL were screened. Induction consisted of prednisone (P), vincristine (V), and doxorubicin (D). For BCR-ABL1+ patients, dasatinib was added. On Days 1, 8, 15 of induction, ixazomib was given orally. After induction patients received 1 cycle of consolidation in which ixazomib was given on Days 1, 8, 15. After consolidation, patients in remission (CR) were offered stem cell transplantation. Among the 19 patients treated, 15 (79%) [90% CI, 58-92%] achieved CR or CRi. At 2 years, the overall survival was 47% [95%CI, 29-72%]. In this study the dose of 2.3 mg of ixazomib in combination was the MTD for older patients with ALL and is the recommended dose for future phase 2 studies.

Identifiants

pubmed: 35075985
doi: 10.1080/10428194.2021.2018582
doi:

Substances chimiques

Boron Compounds 0
Vincristine 5J49Q6B70F
ixazomib 71050168A2
Glycine TE7660XO1C

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1428-1435

Auteurs

Philip Amrein (P)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Karen Ballen (K)

Division of Hematology-Oncology, University of Virginia School of Medicine, Charlottsville, VA.

Kristen Stevenson (K)

Data Science, Dana-Farber Cancer Institute, Boston, MA.

Andrew Brunner (A)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Gabriela Hobbs (G)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Hanno Hock (H)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Steven McAfee (S)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Jenna Moran (J)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Meghan Bergeron (M)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Julia Foster (J)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Christina Bertoli (C)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Kristin McGreggor (K)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Molly Macrea (M)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Meghan Burke (M)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Tanya Behnam (T)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Tina Som (T)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Aura Ramos (A)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Megan Vartanian (M)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Jennifer Lombardi Story (J)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Christine Connolly (C)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

Traci Blonquist (T)

Data Science, Dana-Farber Cancer Institute, Boston, MA.

Donna Neuberg (D)

Data Science, Dana-Farber Cancer Institute, Boston, MA.

Amir Fathi (A)

Division of Hematology-Oncology, Massachusetts General Hospital, Boston, MA.

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Classifications MeSH