Ixazomib maintenance therapy in newly diagnosed multiple myeloma: An integrated analysis of four phase I/II studies.


Journal

European journal of haematology
ISSN: 1600-0609
Titre abrégé: Eur J Haematol
Pays: England
ID NLM: 8703985

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 02 01 2019
revised: 18 03 2019
accepted: 20 03 2019
pubmed: 4 4 2019
medline: 16 11 2019
entrez: 4 4 2019
Statut: ppublish

Résumé

To evaluate the safety and efficacy of maintenance therapy with the oral proteasome inhibitor ixazomib in patients with newly diagnosed multiple myeloma (NDMM) not undergoing transplantation. Data were pooled from four NDMM phase I/II studies; patients received induction therapy with once- or twice-weekly ixazomib plus lenalidomide-dexamethasone (IRd), melphalan-prednisone (IMP), or cyclophosphamide-dexamethasone (ICd), followed by single-agent ixazomib maintenance, given at the last tolerated dose during induction, until disease progression, death, or unacceptable toxicity. A total of 121 patients achieved stable disease or better after induction (weekly IRd, n = 25; twice-weekly IRd, n = 18; weekly or twice-weekly IMP, n = 35; weekly ICd, n = 43) and received ≥ 1 dose of ixazomib maintenance. Grade ≥ 3 drug-related adverse events occurred in 24% of patients during maintenance; each event was reported in ≤2% of patients. Rates of complete response were 22% after induction and 35% after maintenance. A total of 28 patients (23%) improved their response during maintenance. Ixazomib maintenance following ixazomib-based induction is associated with deepening of responses and a positive safety profile with no cumulative toxicity in patients with NDMM not undergoing transplantation, suggesting that ixazomib is feasible for long-term administration. Phase III investigation of ixazomib maintenance is ongoing.

Identifiants

pubmed: 30943323
doi: 10.1111/ejh.13231
doi:

Substances chimiques

Antineoplastic Agents 0
Boron Compounds 0
Protease Inhibitors 0
ixazomib 71050168A2
Glycine TE7660XO1C

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

494-503

Subventions

Organisme : Millennium Pharmaceuticals, Inc., Cambridge, MA, USA, a wholly owned subsidiary of Takeda Pharmaceutical Company Limited

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Auteurs

Meletios A Dimopoulos (MA)

Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.

Jacob P Laubach (JP)

Dana-Farber Cancer Institute, Boston, Massachusetts.

Maria Asunción Echeveste Gutierrez (MA)

Hospital Universitario Donostia, San Sebastián, Spain.

Norbert Grzasko (N)

Department of Hematology, St. John's Cancer Center and Medical University of Lublin, Lublin, Poland.

Craig C Hofmeister (CC)

The Ohio State University, Columbus, Ohio.
Winship Cancer Institute of Emory University, Atlanta, Georgia.

Jesus F San-Miguel (JF)

Clinica Universidad de Navarra, Centro Investigación Medica Aplicada (CIMA), IDISNA, CIBERONC, Pamplona, Spain.

Shaji Kumar (S)

Division of Hematology, Mayo Clinic, Rochester, Minnesota.

Richard Labotka (R)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Vickie Lu (V)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Deborah Berg (D)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Catriona Byrne (C)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Zhaoyang Teng (Z)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Guohui Liu (G)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Helgi van de Velde (H)

Millennium Pharmaceuticals, Inc., Cambridge, MA, USA.

Paul G Richardson (PG)

Dana-Farber Cancer Institute, Boston, Massachusetts.

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Classifications MeSH