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Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM
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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293071/ https://www.ncbi.nlm.nih.gov/pubmed/32297407 http://dx.doi.org/10.1111/cas.14415 |
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author | Sunami, Kazutaka Matsue, Kosei Suzuki, Kenshi Takezako, Naoki Shinagawa, Atsushi Sakurai, Sanae Tamakoshi, Hiromi Biyukov, Tsvetan Peluso, Teresa Richardson, Paul |
author_facet | Sunami, Kazutaka Matsue, Kosei Suzuki, Kenshi Takezako, Naoki Shinagawa, Atsushi Sakurai, Sanae Tamakoshi, Hiromi Biyukov, Tsvetan Peluso, Teresa Richardson, Paul |
author_sort | Sunami, Kazutaka |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7293071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72930712020-06-15 Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM Sunami, Kazutaka Matsue, Kosei Suzuki, Kenshi Takezako, Naoki Shinagawa, Atsushi Sakurai, Sanae Tamakoshi, Hiromi Biyukov, Tsvetan Peluso, Teresa Richardson, Paul Cancer Sci Original Articles 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. John Wiley and Sons Inc. 2020-05-13 2020-06 /pmc/articles/PMC7293071/ /pubmed/32297407 http://dx.doi.org/10.1111/cas.14415 Text en © 2020 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Sunami, Kazutaka Matsue, Kosei Suzuki, Kenshi Takezako, Naoki Shinagawa, Atsushi Sakurai, Sanae Tamakoshi, Hiromi Biyukov, Tsvetan Peluso, Teresa Richardson, Paul Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title | Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title_full | Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title_fullStr | Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title_full_unstemmed | Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title_short | Pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: Japanese subset analysis of OPTIMISMM |
title_sort | pomalidomide‐bortezomib‐dexamethasone in relapsed or refractory multiple myeloma: japanese subset analysis of optimismm |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7293071/ https://www.ncbi.nlm.nih.gov/pubmed/32297407 http://dx.doi.org/10.1111/cas.14415 |
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