Alternating bortezomib-dexamethasone and lenalidomide-dexamethasone in patients with newly diagnosed multiple myeloma aged over 75 years.


Journal

Nagoya journal of medical science
ISSN: 2186-3326
Titre abrégé: Nagoya J Med Sci
Pays: Japan
ID NLM: 0412011

Informations de publication

Date de publication:
Feb 2022
Historique:
received: 25 11 2020
accepted: 21 05 2021
entrez: 8 4 2022
pubmed: 9 4 2022
medline: 12 4 2022
Statut: ppublish

Résumé

More than 40% of Japanese patients with multiple myeloma (MM) are over 75 years of age at diagnosis. Regardless of the treatment benefits, complications and relapses obstruct long-term survival. We conducted a phase II, open-label, single-arm, multicenter clinical trial to assess the efficacy and safety of alternating bortezomib-dexamethasone (Bd) and lenalidomide-dexamethasone (Ld) (Bd/Ld) treatment in MM patients aged over 75 years (MARBLE trial). Patients received Bd therapy from days 1 to 35 and Ld therapy from days 36 to 63. For Bd therapy, patients were administered bortezomib 1.3 mg/m

Identifiants

pubmed: 35392014
doi: 10.18999/nagjms.84.1.80
pmc: PMC8971029
doi:

Substances chimiques

Bortezomib 69G8BD63PP
Dexamethasone 7S5I7G3JQL
Lenalidomide F0P408N6V4

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

80-90

Déclaration de conflit d'intérêts

AK reports personal fees from Bayer Yakuhin, Ltd., as a member of the independent data monitoring committee of clinical trials outside the submitted work. KS received research funding from Ono Pharmaceutical, MSD, Celgene, AbbVie, Takeda Pharmaceutical, Sanofi, Bristol-Myers Squibb, Daiichi Sankyo, Janssen, Novartis, Alexion Pharma, and GlaxoSmithKline and received honoraria from Ono Pharmaceutical, Celgene, Takeda Pharmaceutical, and Bristol-Myers Squibb. The other authors have no conflicts of interest to declare.

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Auteurs

Akihiro Yokoyama (A)

Division of Hematology, Department of Internal Medicine, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Division of Transfusion Medicine, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.

Akiko Kada (A)

Department of Clinical Trials and Research, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Toshiya Kagoo (T)

Division of Hematology, Department of Internal Medicine, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.

Michihiro Hidaka (M)

Department of Hematology, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.

Hiroatsu Iida (H)

Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Yasuhiko Miyata (Y)

Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Akiko M Saito (AM)

Department of Clinical Trials and Research, Clinical Research Center, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

Morio Sawamura (M)

Department of Hematology, National Hospital Organization Shibukawa Medical Center, Shibukawa, Japan.

Takuya Komeno (T)

Department of Hematology, National Hospital Organization Mito Medical Center, Ibaraki, Japan.

Kazutaka Sunami (K)

Department of Hematology, National Hospital Organization Okayama Medical Center, Okayama, Japan.

Naoki Takezako (N)

Department of Hematology, National Hospital Organization Disaster Medical Center of Japan, Tachikawa, Japan.

Hirokazu Nagai (H)

Department of Hematology, National Hospital Organization Nagoya Medical Center, Nagoya, Japan.

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Classifications MeSH