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Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride

Lung cancer is the leading cause of cancer death, and approximately 15% of all lung cancer patients have small-cell lung cancer (SCLC). Although second-line chemotherapy can produce tumor regression, the prognosis is poor. Amrubicin hydrochloride (AMR) is a synthetic anthracycline anticancer agent a...

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Detalles Bibliográficos
Autores principales: Kimura, Tatsuo, Kudoh, Shinzoh, Hirata, Kazuto
Formato: Texto
Lenguaje:English
Publicado: Libertas Academica 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076041/
https://www.ncbi.nlm.nih.gov/pubmed/21499556
http://dx.doi.org/10.4137/CMO.S5072
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author Kimura, Tatsuo
Kudoh, Shinzoh
Hirata, Kazuto
author_facet Kimura, Tatsuo
Kudoh, Shinzoh
Hirata, Kazuto
author_sort Kimura, Tatsuo
collection PubMed
description Lung cancer is the leading cause of cancer death, and approximately 15% of all lung cancer patients have small-cell lung cancer (SCLC). Although second-line chemotherapy can produce tumor regression, the prognosis is poor. Amrubicin hydrochloride (AMR) is a synthetic anthracycline anticancer agent and a potent topoisomerase II inhibitor. Here, we discuss the features of SCLC, the chemistry, pharmacokinetics, and pharmacodynamics of AMR, the results of in vitro and in vivo studies, and the efficacy and safety of AMR monotherapy and combination therapy in clinical trials. With its predictable and manageable toxicities, AMR is one of the most attractive agents for the treatment of chemotherapy-sensitive and -refractory relapsed SCLC. Numerous studies are ongoing to define the applicability of AMR therapy for patients with SCLC. These clinical trials, including phase III studies, will clarify the status of AMR in the treatment of SCLC.
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spelling pubmed-30760412011-04-15 Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride Kimura, Tatsuo Kudoh, Shinzoh Hirata, Kazuto Clin Med Insights Oncol Review Lung cancer is the leading cause of cancer death, and approximately 15% of all lung cancer patients have small-cell lung cancer (SCLC). Although second-line chemotherapy can produce tumor regression, the prognosis is poor. Amrubicin hydrochloride (AMR) is a synthetic anthracycline anticancer agent and a potent topoisomerase II inhibitor. Here, we discuss the features of SCLC, the chemistry, pharmacokinetics, and pharmacodynamics of AMR, the results of in vitro and in vivo studies, and the efficacy and safety of AMR monotherapy and combination therapy in clinical trials. With its predictable and manageable toxicities, AMR is one of the most attractive agents for the treatment of chemotherapy-sensitive and -refractory relapsed SCLC. Numerous studies are ongoing to define the applicability of AMR therapy for patients with SCLC. These clinical trials, including phase III studies, will clarify the status of AMR in the treatment of SCLC. Libertas Academica 2011-03-03 /pmc/articles/PMC3076041/ /pubmed/21499556 http://dx.doi.org/10.4137/CMO.S5072 Text en © the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Review
Kimura, Tatsuo
Kudoh, Shinzoh
Hirata, Kazuto
Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title_full Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title_fullStr Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title_full_unstemmed Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title_short Review of the Management of Relapsed Small-Cell Lung Cancer with Amrubicin Hydrochloride
title_sort review of the management of relapsed small-cell lung cancer with amrubicin hydrochloride
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3076041/
https://www.ncbi.nlm.nih.gov/pubmed/21499556
http://dx.doi.org/10.4137/CMO.S5072
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