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Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients
The present study investigated the safety and efficacy of neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcoma in adult and older patients. A total of 18 consecutive patients with bone sarcoma (American Joint Committee on Cancer stage II in 14 patients and stage IV...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214507/ https://www.ncbi.nlm.nih.gov/pubmed/25364412 http://dx.doi.org/10.3892/ol.2014.2567 |
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author | URAKAWA, HIROSHI TSUKUSHI, SATOSHI SUGIURA, HIDESHI YAMADA, KENJI YAMADA, YOSHIHISA KOZAWA, EIJI ARAI, EISUKE FUTAMURA, NAOHISA ISHIGURO, NAOKI NISHIDA, YOSHIHIRO |
author_facet | URAKAWA, HIROSHI TSUKUSHI, SATOSHI SUGIURA, HIDESHI YAMADA, KENJI YAMADA, YOSHIHISA KOZAWA, EIJI ARAI, EISUKE FUTAMURA, NAOHISA ISHIGURO, NAOKI NISHIDA, YOSHIHIRO |
author_sort | URAKAWA, HIROSHI |
collection | PubMed |
description | The present study investigated the safety and efficacy of neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcoma in adult and older patients. A total of 18 consecutive patients with bone sarcoma (American Joint Committee on Cancer stage II in 14 patients and stage IV in four) treated with neoadjuvant and adjuvant chemotherapy at Nagoya Musculoskeletal Oncology Group hospitals in Japan between 2004 and 2011 were reviewed. The treatment efficacy and side-effects were evaluated. The responses to neoadjuvant chemotherapy were stable disease in 11 patients and progressive disease in three. Among the 12 evaluable patients, there were five with ≥90% tumor necrosis. The estimated overall survival (OS) rate at five years for the patients without metastasis prior to treatment was 56%. Major grade 3 or 4 side-effects included leukopenia in 14 cases, anemia in seven, thrombocytopenia in three, nausea in two and febrile neutropenia in two. One patient discontinued chemotherapy due to a temporarily depressed level of consciousness with arrhythmia (grade 2). The estimated five-year OS rate in this study was acceptable in patients without metastasis prior to treatment. A better coordinated prospective study of this combination regimen for older patients with bone sarcoma will be required to clarify its efficacy and tolerability. |
format | Online Article Text |
id | pubmed-4214507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-42145072014-10-31 Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients URAKAWA, HIROSHI TSUKUSHI, SATOSHI SUGIURA, HIDESHI YAMADA, KENJI YAMADA, YOSHIHISA KOZAWA, EIJI ARAI, EISUKE FUTAMURA, NAOHISA ISHIGURO, NAOKI NISHIDA, YOSHIHIRO Oncol Lett Articles The present study investigated the safety and efficacy of neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcoma in adult and older patients. A total of 18 consecutive patients with bone sarcoma (American Joint Committee on Cancer stage II in 14 patients and stage IV in four) treated with neoadjuvant and adjuvant chemotherapy at Nagoya Musculoskeletal Oncology Group hospitals in Japan between 2004 and 2011 were reviewed. The treatment efficacy and side-effects were evaluated. The responses to neoadjuvant chemotherapy were stable disease in 11 patients and progressive disease in three. Among the 12 evaluable patients, there were five with ≥90% tumor necrosis. The estimated overall survival (OS) rate at five years for the patients without metastasis prior to treatment was 56%. Major grade 3 or 4 side-effects included leukopenia in 14 cases, anemia in seven, thrombocytopenia in three, nausea in two and febrile neutropenia in two. One patient discontinued chemotherapy due to a temporarily depressed level of consciousness with arrhythmia (grade 2). The estimated five-year OS rate in this study was acceptable in patients without metastasis prior to treatment. A better coordinated prospective study of this combination regimen for older patients with bone sarcoma will be required to clarify its efficacy and tolerability. D.A. Spandidos 2014-12 2014-09-26 /pmc/articles/PMC4214507/ /pubmed/25364412 http://dx.doi.org/10.3892/ol.2014.2567 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles URAKAWA, HIROSHI TSUKUSHI, SATOSHI SUGIURA, HIDESHI YAMADA, KENJI YAMADA, YOSHIHISA KOZAWA, EIJI ARAI, EISUKE FUTAMURA, NAOHISA ISHIGURO, NAOKI NISHIDA, YOSHIHIRO Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title | Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title_full | Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title_fullStr | Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title_full_unstemmed | Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title_short | Neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
title_sort | neoadjuvant and adjuvant chemotherapy with doxorubicin and ifosfamide for bone sarcomas in adult and older patients |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4214507/ https://www.ncbi.nlm.nih.gov/pubmed/25364412 http://dx.doi.org/10.3892/ol.2014.2567 |
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