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The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study

BACKGROUND: Because the efficacy and safety of pazopanib in Japanese patients with soft tissue sarcoma (STS) had not been evaluated previously in a large‐scale cohort, the authors investigated the efficacy and safety of pazopanib in 156 Japanese patients with relapsed STS. This was a retrospective s...

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Autores principales: Nakamura, Tomoki, Matsumine, Akihiko, Kawai, Akira, Araki, Nobuhito, Goto, Takahiro, Yonemoto, Tsukasa, Sugiura, Hideshi, Nishida, Yoshihiro, Hiraga, Hiroaki, Honoki, Kanya, Yasuda, Taketoshi, Boku, Shogen, Sudo, Akihiro, Ueda, Takafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069581/
https://www.ncbi.nlm.nih.gov/pubmed/26970174
http://dx.doi.org/10.1002/cncr.29961
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author Nakamura, Tomoki
Matsumine, Akihiko
Kawai, Akira
Araki, Nobuhito
Goto, Takahiro
Yonemoto, Tsukasa
Sugiura, Hideshi
Nishida, Yoshihiro
Hiraga, Hiroaki
Honoki, Kanya
Yasuda, Taketoshi
Boku, Shogen
Sudo, Akihiro
Ueda, Takafumi
author_facet Nakamura, Tomoki
Matsumine, Akihiko
Kawai, Akira
Araki, Nobuhito
Goto, Takahiro
Yonemoto, Tsukasa
Sugiura, Hideshi
Nishida, Yoshihiro
Hiraga, Hiroaki
Honoki, Kanya
Yasuda, Taketoshi
Boku, Shogen
Sudo, Akihiro
Ueda, Takafumi
author_sort Nakamura, Tomoki
collection PubMed
description BACKGROUND: Because the efficacy and safety of pazopanib in Japanese patients with soft tissue sarcoma (STS) had not been evaluated previously in a large‐scale cohort, the authors investigated the efficacy and safety of pazopanib in 156 Japanese patients with relapsed STS. This was a retrospective study based on the collection of real‐life, postmarketing surveillance data. METHODS: Patients received pazopanib with the objective of treating local recurrence (n = 20), metastasis (n = 104), and both (n = 32). The patient median age was 53.8 years. The primary objective of this study was to clarify the efficacy of pazopanib for patients with STS. RESULTS: The median treatment duration was 28.7 weeks, and the average dose intensity of pazopanib was 609 mg. Adverse events occurred in 127 patients (81.4%). In addition to the main common toxicities, such as hypertension and liver disorder, pneumothorax (n = 11) and thrombocytopenia (n = 16) also were observed. The median progression‐free survival for all patients was 15.4 weeks. The median progression‐free survival for patients with leiomyosarcoma, synovial sarcoma, undifferentiated pleomorphic sarcoma, and liposarcoma was 18.6 weeks, 16.4 weeks, 15.3 weeks, and 8 weeks, respectively. The median survival for all patients was 11.2 months. The median survival for patients with leiomyosarcoma, synovial sarcoma, undifferentiated pleomorphic sarcoma, and liposarcoma was 20.1 months, 10.6 months, 9.5 months, and 7.3 months, respectively. CONCLUSIONS: There were apparent differences in the efficacy of pazopanib treatment among histologic types of STS. Pazopanib treatment is a new treatment option; however, adverse events like pneumothorax and thrombocytopenia, which did not occur frequently in the PALETTE study (pazopanib for metastatic soft‐tissue sarcoma), should be taken into consideration. Cancer 2016;122:1408‐16. © 2016 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society.
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spelling pubmed-50695812016-11-01 The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study Nakamura, Tomoki Matsumine, Akihiko Kawai, Akira Araki, Nobuhito Goto, Takahiro Yonemoto, Tsukasa Sugiura, Hideshi Nishida, Yoshihiro Hiraga, Hiroaki Honoki, Kanya Yasuda, Taketoshi Boku, Shogen Sudo, Akihiro Ueda, Takafumi Cancer Original Articles BACKGROUND: Because the efficacy and safety of pazopanib in Japanese patients with soft tissue sarcoma (STS) had not been evaluated previously in a large‐scale cohort, the authors investigated the efficacy and safety of pazopanib in 156 Japanese patients with relapsed STS. This was a retrospective study based on the collection of real‐life, postmarketing surveillance data. METHODS: Patients received pazopanib with the objective of treating local recurrence (n = 20), metastasis (n = 104), and both (n = 32). The patient median age was 53.8 years. The primary objective of this study was to clarify the efficacy of pazopanib for patients with STS. RESULTS: The median treatment duration was 28.7 weeks, and the average dose intensity of pazopanib was 609 mg. Adverse events occurred in 127 patients (81.4%). In addition to the main common toxicities, such as hypertension and liver disorder, pneumothorax (n = 11) and thrombocytopenia (n = 16) also were observed. The median progression‐free survival for all patients was 15.4 weeks. The median progression‐free survival for patients with leiomyosarcoma, synovial sarcoma, undifferentiated pleomorphic sarcoma, and liposarcoma was 18.6 weeks, 16.4 weeks, 15.3 weeks, and 8 weeks, respectively. The median survival for all patients was 11.2 months. The median survival for patients with leiomyosarcoma, synovial sarcoma, undifferentiated pleomorphic sarcoma, and liposarcoma was 20.1 months, 10.6 months, 9.5 months, and 7.3 months, respectively. CONCLUSIONS: There were apparent differences in the efficacy of pazopanib treatment among histologic types of STS. Pazopanib treatment is a new treatment option; however, adverse events like pneumothorax and thrombocytopenia, which did not occur frequently in the PALETTE study (pazopanib for metastatic soft‐tissue sarcoma), should be taken into consideration. Cancer 2016;122:1408‐16. © 2016 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. John Wiley and Sons Inc. 2016-03-11 2016-05-01 /pmc/articles/PMC5069581/ /pubmed/26970174 http://dx.doi.org/10.1002/cncr.29961 Text en © 2016 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (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
Nakamura, Tomoki
Matsumine, Akihiko
Kawai, Akira
Araki, Nobuhito
Goto, Takahiro
Yonemoto, Tsukasa
Sugiura, Hideshi
Nishida, Yoshihiro
Hiraga, Hiroaki
Honoki, Kanya
Yasuda, Taketoshi
Boku, Shogen
Sudo, Akihiro
Ueda, Takafumi
The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title_full The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title_fullStr The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title_full_unstemmed The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title_short The clinical outcome of pazopanib treatment in Japanese patients with relapsed soft tissue sarcoma: A Japanese Musculoskeletal Oncology Group (JMOG) study
title_sort clinical outcome of pazopanib treatment in japanese patients with relapsed soft tissue sarcoma: a japanese musculoskeletal oncology group (jmog) study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069581/
https://www.ncbi.nlm.nih.gov/pubmed/26970174
http://dx.doi.org/10.1002/cncr.29961
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