Cargando…
Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China
BACKGROUND: Anti-angiogenesis Tyrosine kinase inhibitors (TKIs) have been proved to show promising effects on prolonging progression-free survival (PFS) for advanced sarcoma after failure of standard multimodal Therapy. Methylsulfonic apatinib is one of those TKIs which specifically inhibits VEGFR-2...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889565/ https://www.ncbi.nlm.nih.gov/pubmed/29625604 http://dx.doi.org/10.1186/s12885-018-4303-z |
_version_ | 1783312723542540288 |
---|---|
author | Xie, Lu Guo, Wei Wang, Ye Yan, Taiqiang Ji, Tao Xu, Jie |
author_facet | Xie, Lu Guo, Wei Wang, Ye Yan, Taiqiang Ji, Tao Xu, Jie |
author_sort | Xie, Lu |
collection | PubMed |
description | BACKGROUND: Anti-angiogenesis Tyrosine kinase inhibitors (TKIs) have been proved to show promising effects on prolonging progression-free survival (PFS) for advanced sarcoma after failure of standard multimodal Therapy. Methylsulfonic apatinib is one of those TKIs which specifically inhibits VEGFR-2. This paper summarizes the experience of three Peking University affiliated hospitals in off-label use of apatinib in the treatment of extensively pre-treated sarcoma. METHODS: We retrospectively analysed files of patients with advanced sarcoma not amenable to curative treatment, who were receiving an apatinib-containing regimen between June 1, 2015 and December 1, 2016. Fifty-six patients were included: 22 osteosarcoma, 10 Ewing’s sarcoma, 3 chondrosarcoma and 21 soft tissue sarcoma. RESULTS: With median follow-up time of 6 months (range, 0.7–18.0 m), thirty-five (62.5%) patients had partial response, and disease was stable in 11 (19.6%). The 4-month and 6-month progression-free survival rates were 46.3 and 36.5%, respectively. The median duration of response was 3.8 months (95% CI 1.9–5.6 m), with much variability among disease subtypes. The median overall survival was 9.9 months (95% CI 7.6–12.2 m). Grade 3 and 4 toxicities were observed in 8 (14.3%) patients, the most common being hypertension, pneumothorax, wound-healing problems, anorexia, and rash or desquamation. CONCLUSIONS: Apatinib might be effective, with a high objective response rate, in an off-label study of sarcoma patients with advanced, previously treated disease. The duration of response was consistent with reports in different subtypes of sarcomas. Prospective trials of apatinib in the treatment of selected subtypes of sarcomas are needed. TRIAL REGISTRATION: Retrospectively registered in the Medical Ethics Committee of Peking University People’s Hospital, Peking University Shougang Hospital and Peking University International Hospital. The trial registration number is 2017PHB176–03 and the date of registration is January 20th 2017. |
format | Online Article Text |
id | pubmed-5889565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58895652018-04-10 Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China Xie, Lu Guo, Wei Wang, Ye Yan, Taiqiang Ji, Tao Xu, Jie BMC Cancer Research Article BACKGROUND: Anti-angiogenesis Tyrosine kinase inhibitors (TKIs) have been proved to show promising effects on prolonging progression-free survival (PFS) for advanced sarcoma after failure of standard multimodal Therapy. Methylsulfonic apatinib is one of those TKIs which specifically inhibits VEGFR-2. This paper summarizes the experience of three Peking University affiliated hospitals in off-label use of apatinib in the treatment of extensively pre-treated sarcoma. METHODS: We retrospectively analysed files of patients with advanced sarcoma not amenable to curative treatment, who were receiving an apatinib-containing regimen between June 1, 2015 and December 1, 2016. Fifty-six patients were included: 22 osteosarcoma, 10 Ewing’s sarcoma, 3 chondrosarcoma and 21 soft tissue sarcoma. RESULTS: With median follow-up time of 6 months (range, 0.7–18.0 m), thirty-five (62.5%) patients had partial response, and disease was stable in 11 (19.6%). The 4-month and 6-month progression-free survival rates were 46.3 and 36.5%, respectively. The median duration of response was 3.8 months (95% CI 1.9–5.6 m), with much variability among disease subtypes. The median overall survival was 9.9 months (95% CI 7.6–12.2 m). Grade 3 and 4 toxicities were observed in 8 (14.3%) patients, the most common being hypertension, pneumothorax, wound-healing problems, anorexia, and rash or desquamation. CONCLUSIONS: Apatinib might be effective, with a high objective response rate, in an off-label study of sarcoma patients with advanced, previously treated disease. The duration of response was consistent with reports in different subtypes of sarcomas. Prospective trials of apatinib in the treatment of selected subtypes of sarcomas are needed. TRIAL REGISTRATION: Retrospectively registered in the Medical Ethics Committee of Peking University People’s Hospital, Peking University Shougang Hospital and Peking University International Hospital. The trial registration number is 2017PHB176–03 and the date of registration is January 20th 2017. BioMed Central 2018-04-06 /pmc/articles/PMC5889565/ /pubmed/29625604 http://dx.doi.org/10.1186/s12885-018-4303-z Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Xie, Lu Guo, Wei Wang, Ye Yan, Taiqiang Ji, Tao Xu, Jie Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title | Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title_full | Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title_fullStr | Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title_full_unstemmed | Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title_short | Apatinib for advanced sarcoma: results from multiple institutions’ off-label use in China |
title_sort | apatinib for advanced sarcoma: results from multiple institutions’ off-label use in china |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889565/ https://www.ncbi.nlm.nih.gov/pubmed/29625604 http://dx.doi.org/10.1186/s12885-018-4303-z |
work_keys_str_mv | AT xielu apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina AT guowei apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina AT wangye apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina AT yantaiqiang apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina AT jitao apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina AT xujie apatinibforadvancedsarcomaresultsfrommultipleinstitutionsofflabeluseinchina |