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A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma
Recent clinical trials showed that bortezomib, a novel proteasome inhibitor, had therapeutic activity in multiple myeloma. However, there was no data about the feasibility of bortezomib in Korean patients. We performed a pilot study of bortezomib in patients with relapsed or refractory myeloma (1.3...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782154/ https://www.ncbi.nlm.nih.gov/pubmed/16100450 http://dx.doi.org/10.3346/jkms.2005.20.4.598 |
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author | Lee, Keun-Wook Yun, Tak Song, Eun Kee Na, Im il Shin, Hyunchoon Bang, Soo-Mee Lee, Jae Hoon Lee, Seung Tae Kim, Jee Hyun Yoon, Sung-Soo Lee, Jong Seok Park, Seonyang Kim, Byoung Kook Kim, Noe Kyeong |
author_facet | Lee, Keun-Wook Yun, Tak Song, Eun Kee Na, Im il Shin, Hyunchoon Bang, Soo-Mee Lee, Jae Hoon Lee, Seung Tae Kim, Jee Hyun Yoon, Sung-Soo Lee, Jong Seok Park, Seonyang Kim, Byoung Kook Kim, Noe Kyeong |
author_sort | Lee, Keun-Wook |
collection | PubMed |
description | Recent clinical trials showed that bortezomib, a novel proteasome inhibitor, had therapeutic activity in multiple myeloma. However, there was no data about the feasibility of bortezomib in Korean patients. We performed a pilot study of bortezomib in patients with relapsed or refractory myeloma (1.3 mg/m(2) twice weekly for 2 week in a 3-week cycle). Seven patients were enrolled. The median age of patients was 59 yr. All patients previously received VAD (vincristine, doxorubicin and dexamethasone) and thalidomide chemotherapy. Three patients previously received alkylator-containing chemotherapy and 4 patients, autologous stem cell transplantation. Bortezomib monotherapy resulted in 3 partial remissions (43%), 3 no changes (43%) and 1 progressive disease (14%). One patient who had no response to bortezomib monotherapy experienced partial remission after addition of dexamethasone to bortezomib. The most common serious toxicity was thrombocytopenia (grade 3/4, 10 of 20 cycles (50%)) and grade 3 peripheral neuropathy was developed in 2 of 20 cycles (10%). Drug-related adverse event led to discontinuation of bortezomib in 1 patient. There was no treatment related mortality. Overall, bortezomib seems to be effective and feasible. Conduction of larger clinical studies on Korean patients is necessary to characterize clinical efficacy and safety of bortezomib more precisely. |
format | Text |
id | pubmed-2782154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-27821542009-11-25 A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma Lee, Keun-Wook Yun, Tak Song, Eun Kee Na, Im il Shin, Hyunchoon Bang, Soo-Mee Lee, Jae Hoon Lee, Seung Tae Kim, Jee Hyun Yoon, Sung-Soo Lee, Jong Seok Park, Seonyang Kim, Byoung Kook Kim, Noe Kyeong J Korean Med Sci Original Article Recent clinical trials showed that bortezomib, a novel proteasome inhibitor, had therapeutic activity in multiple myeloma. However, there was no data about the feasibility of bortezomib in Korean patients. We performed a pilot study of bortezomib in patients with relapsed or refractory myeloma (1.3 mg/m(2) twice weekly for 2 week in a 3-week cycle). Seven patients were enrolled. The median age of patients was 59 yr. All patients previously received VAD (vincristine, doxorubicin and dexamethasone) and thalidomide chemotherapy. Three patients previously received alkylator-containing chemotherapy and 4 patients, autologous stem cell transplantation. Bortezomib monotherapy resulted in 3 partial remissions (43%), 3 no changes (43%) and 1 progressive disease (14%). One patient who had no response to bortezomib monotherapy experienced partial remission after addition of dexamethasone to bortezomib. The most common serious toxicity was thrombocytopenia (grade 3/4, 10 of 20 cycles (50%)) and grade 3 peripheral neuropathy was developed in 2 of 20 cycles (10%). Drug-related adverse event led to discontinuation of bortezomib in 1 patient. There was no treatment related mortality. Overall, bortezomib seems to be effective and feasible. Conduction of larger clinical studies on Korean patients is necessary to characterize clinical efficacy and safety of bortezomib more precisely. The Korean Academy of Medical Sciences 2005-08 2005-08-31 /pmc/articles/PMC2782154/ /pubmed/16100450 http://dx.doi.org/10.3346/jkms.2005.20.4.598 Text en Copyright © 2005 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Keun-Wook Yun, Tak Song, Eun Kee Na, Im il Shin, Hyunchoon Bang, Soo-Mee Lee, Jae Hoon Lee, Seung Tae Kim, Jee Hyun Yoon, Sung-Soo Lee, Jong Seok Park, Seonyang Kim, Byoung Kook Kim, Noe Kyeong A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title | A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title_full | A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title_fullStr | A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title_full_unstemmed | A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title_short | A Pilot Study of Bortezomib in Korean Patients with Relapsed or Refractory Myeloma |
title_sort | pilot study of bortezomib in korean patients with relapsed or refractory myeloma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2782154/ https://www.ncbi.nlm.nih.gov/pubmed/16100450 http://dx.doi.org/10.3346/jkms.2005.20.4.598 |
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