Pomalidomide-bortezomib-dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM.


Journal

Cancer science
ISSN: 1349-7006
Titre abrégé: Cancer Sci
Pays: England
ID NLM: 101168776

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 07 01 2020
revised: 26 03 2020
accepted: 02 04 2020
pubmed: 17 4 2020
medline: 20 6 2020
entrez: 17 4 2020
Statut: ppublish

Résumé

In the phase 3 OPTIMISMM trial, pomalidomide, bortezomib and dexamethasone (PVd) significantly improved the progression-free survival (PFS) and the overall response rate (ORR) vs bortezomib and dexamethasone (Vd) in patients with relapsed or refractory multiple myeloma. All patients were previously treated with lenalidomide (70% refractory to lenalidomide) and had received one to three prior regimens. Here we report the first efficacy and safety analysis of PVd vs Vd in Japanese patients with relapsed or refractory multiple myeloma. Seventeen patients enrolled in the OPTIMISMM trial in Japan. With a median follow-up of 14.8 months, the median PFS was 17.6 months with PVd (n = 12) vs 4.4 months with Vd (n = 5), and the ORR was 100% vs 60.0%, respectively. The safety profile was as expected for PVd. Toxicities were managed with dose reductions and interruptions, and no patients discontinued PVd due to treatment-emergent adverse events. These results are consistent with those in the overall OPTIMISMM patient population and confirm the clinical benefit of PVd in Japanese patients.

Identifiants

pubmed: 32297407
doi: 10.1111/cas.14415
pmc: PMC7293071
doi:

Substances chimiques

Thalidomide 4Z8R6ORS6L
Bortezomib 69G8BD63PP
Dexamethasone 7S5I7G3JQL
pomalidomide D2UX06XLB5

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

2116-2122

Subventions

Organisme : Celgene
Organisme : Bristol-Myers Squibb Company

Informations de copyright

© 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.

Références

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Auteurs

Kazutaka Sunami (K)

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

Kosei Matsue (K)

Department of Hematology, Kameda Medical Center, Chiba, Japan.

Kenshi Suzuki (K)

Department of Hematology, Japanese Red Cross Medical Center, Tokyo, Japan.

Naoki Takezako (N)

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

Atsushi Shinagawa (A)

Department of Hemato-Oncology, Hitachi General Hospital, Ibaraki, Japan.

Sanae Sakurai (S)

Department of Clinical Research & Development Study, Celgene KK, a Bristol-Myers Squibb Company, Tokyo, Japan.

Hiromi Tamakoshi (H)

Department of Clinical Research & Development Study, Celgene KK, a Bristol-Myers Squibb Company, Tokyo, Japan.

Tsvetan Biyukov (T)

Department of Clinical R&D Management, Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland.

Teresa Peluso (T)

Department of Clinical R&D Management, Celgene International Sàrl, a Bristol-Myers Squibb Company, Boudry, Switzerland.

Paul Richardson (P)

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

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