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The value of trabectedin in the treatment of soft tissue sarcoma
Soft tissue sarcomas (STSs) are a group of rare tumors accounting for less than 1% of all adult malignant tumors, a heterogeneous group of more than 50 histological subtypes. Five percent to 30% of STS patients experience local recurrence and 10%–38% present with clinically detectable metastases. Do...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716771/ https://www.ncbi.nlm.nih.gov/pubmed/26834480 http://dx.doi.org/10.2147/TCRM.S84789 |
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author | Nakamura, Tomoki Matsumine, Akihiko Sudo, Akihiro |
author_facet | Nakamura, Tomoki Matsumine, Akihiko Sudo, Akihiro |
author_sort | Nakamura, Tomoki |
collection | PubMed |
description | Soft tissue sarcomas (STSs) are a group of rare tumors accounting for less than 1% of all adult malignant tumors, a heterogeneous group of more than 50 histological subtypes. Five percent to 30% of STS patients experience local recurrence and 10%–38% present with clinically detectable metastases. Doxorubicin either alone or in combination with ifosfamide has been used as first-line chemotherapy for advanced disease. After failure of first-line chemotherapy, high-dose ifosfamide, gemcitabine + docetaxel, and dacarbazine may be applicable, although high-level evidence is lacking. Trabectedin is a synthetic, marine-derived alkylating agent derived from the Caribbean tunicate, Ecteinascidia turbinata. Several clinical trials have shown that trabectedin has a favorable toxicity profile and is an alternative therapeutic option in adult patients with advanced STS who have not responded to treatment with doxorubicin and ifosfamide. Several clinical trials also recommend the 24-hour intravenous infusion every 3 weeks regimen. The most frequently reported grade 3/4 adverse events were neutropenia and elevated serum levels of AST/ALT. Steroid pretreatment is an effective way of reducing the extent of hepatotoxicity, and steroids are now given routinely before trabectedin administration. Further studies are ongoing to evaluate the efficacy and safety of combination therapy of trabectedin with other agents. |
format | Online Article Text |
id | pubmed-4716771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47167712016-02-01 The value of trabectedin in the treatment of soft tissue sarcoma Nakamura, Tomoki Matsumine, Akihiko Sudo, Akihiro Ther Clin Risk Manag Review Soft tissue sarcomas (STSs) are a group of rare tumors accounting for less than 1% of all adult malignant tumors, a heterogeneous group of more than 50 histological subtypes. Five percent to 30% of STS patients experience local recurrence and 10%–38% present with clinically detectable metastases. Doxorubicin either alone or in combination with ifosfamide has been used as first-line chemotherapy for advanced disease. After failure of first-line chemotherapy, high-dose ifosfamide, gemcitabine + docetaxel, and dacarbazine may be applicable, although high-level evidence is lacking. Trabectedin is a synthetic, marine-derived alkylating agent derived from the Caribbean tunicate, Ecteinascidia turbinata. Several clinical trials have shown that trabectedin has a favorable toxicity profile and is an alternative therapeutic option in adult patients with advanced STS who have not responded to treatment with doxorubicin and ifosfamide. Several clinical trials also recommend the 24-hour intravenous infusion every 3 weeks regimen. The most frequently reported grade 3/4 adverse events were neutropenia and elevated serum levels of AST/ALT. Steroid pretreatment is an effective way of reducing the extent of hepatotoxicity, and steroids are now given routinely before trabectedin administration. Further studies are ongoing to evaluate the efficacy and safety of combination therapy of trabectedin with other agents. Dove Medical Press 2016-01-13 /pmc/articles/PMC4716771/ /pubmed/26834480 http://dx.doi.org/10.2147/TCRM.S84789 Text en © 2016 Nakamura et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Nakamura, Tomoki Matsumine, Akihiko Sudo, Akihiro The value of trabectedin in the treatment of soft tissue sarcoma |
title | The value of trabectedin in the treatment of soft tissue sarcoma |
title_full | The value of trabectedin in the treatment of soft tissue sarcoma |
title_fullStr | The value of trabectedin in the treatment of soft tissue sarcoma |
title_full_unstemmed | The value of trabectedin in the treatment of soft tissue sarcoma |
title_short | The value of trabectedin in the treatment of soft tissue sarcoma |
title_sort | value of trabectedin in the treatment of soft tissue sarcoma |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716771/ https://www.ncbi.nlm.nih.gov/pubmed/26834480 http://dx.doi.org/10.2147/TCRM.S84789 |
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