Cargando…

Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study

BACKGROUND: The effects of sorafenib in the treatment of advanced renal cell carcinoma (RCC) have been confirmed in an international collaborative phase III trial. This study aims to confirm similar efficacy and treatment-induced toxicities of sorafenib in the treatment of metastatic RCC in ethnic C...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Hailiang, Dong, Baijun, Lu, Jiade J, Yao, Xudong, Zhang, Shilin, Dai, Bo, Shen, Yijun, Zhu, Yao, Ye, Dingwei, Huang, Yiran
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724546/
https://www.ncbi.nlm.nih.gov/pubmed/19622166
http://dx.doi.org/10.1186/1471-2407-9-249
_version_ 1782170435592388608
author Zhang, Hailiang
Dong, Baijun
Lu, Jiade J
Yao, Xudong
Zhang, Shilin
Dai, Bo
Shen, Yijun
Zhu, Yao
Ye, Dingwei
Huang, Yiran
author_facet Zhang, Hailiang
Dong, Baijun
Lu, Jiade J
Yao, Xudong
Zhang, Shilin
Dai, Bo
Shen, Yijun
Zhu, Yao
Ye, Dingwei
Huang, Yiran
author_sort Zhang, Hailiang
collection PubMed
description BACKGROUND: The effects of sorafenib in the treatment of advanced renal cell carcinoma (RCC) have been confirmed in an international collaborative phase III trial. This study aims to confirm similar efficacy and treatment-induced toxicities of sorafenib in the treatment of metastatic RCC in ethnic Chinese patients. METHODS: Ninety-eight consecutive and non-selected patients with pathologically confirmed metastatic RCC were treated according to an institutional treatment protocol. All patients were treated with 400 mg of sorafenib orally twice daily on a continuous basis until disease progression or intolerance to treatment occurred. Dose reduction to 400 mg once daily was required if grade 3 or 4 toxicities occurred. All patients except for 7 received nephrectomy in the course of their disease. All patients were assessed for tumor response, progression-free survival (PFS), overall survival (OS), and treatment-induced toxicities. RESULTS: The median follow-up time was 76 weeks (range 2–296 weeks) for the entire group of patients. Radiologically confirmed complete response (CR), partial response (PR), stable disease (SD) of more than 4 months, and disease progression as best objective responses were observed in 1 (1%), 23 (23.5%), 62 (63.3%), and 12 (12.2%) patients, respectively. The tumor control rate (CR+PR+SD of >4 months) was 87.8%. The 1-year estimated PFS and OS were 58.4% and 64.6%, respectively. The median progression-free survival (PFS) time was 60 weeks (95% CI 41–79); and the median overall survival (OS) time was not reached with a follow-up of 76 weeks. Reduction of sorafenib dose was required in 26 patients who developed grade 3 or 4 treatment-cause adverse-effects. An additional 9 patients discontinued sorafenib treatment due to severe adverse-effects. No grade 5 toxicity occurred. Multivariate analysis revealed that independent predictive factors for tumor response to sorafenib treatment included ECOG status, presence of lymph node metastasis, and nephrectomy prior to the development of metastasis. CONCLUSION: Sorafenib produced an 87.8% disease control rate for metastatic renal cell carcinoma in Chinese patients, with acceptable rates of toxicity. The medication dosed at 400 mg twice daily is both efficacious and safe in the treatment of metastatic renal cell carcinoma in Chinese patients.
format Text
id pubmed-2724546
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-27245462009-08-11 Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study Zhang, Hailiang Dong, Baijun Lu, Jiade J Yao, Xudong Zhang, Shilin Dai, Bo Shen, Yijun Zhu, Yao Ye, Dingwei Huang, Yiran BMC Cancer Research Article BACKGROUND: The effects of sorafenib in the treatment of advanced renal cell carcinoma (RCC) have been confirmed in an international collaborative phase III trial. This study aims to confirm similar efficacy and treatment-induced toxicities of sorafenib in the treatment of metastatic RCC in ethnic Chinese patients. METHODS: Ninety-eight consecutive and non-selected patients with pathologically confirmed metastatic RCC were treated according to an institutional treatment protocol. All patients were treated with 400 mg of sorafenib orally twice daily on a continuous basis until disease progression or intolerance to treatment occurred. Dose reduction to 400 mg once daily was required if grade 3 or 4 toxicities occurred. All patients except for 7 received nephrectomy in the course of their disease. All patients were assessed for tumor response, progression-free survival (PFS), overall survival (OS), and treatment-induced toxicities. RESULTS: The median follow-up time was 76 weeks (range 2–296 weeks) for the entire group of patients. Radiologically confirmed complete response (CR), partial response (PR), stable disease (SD) of more than 4 months, and disease progression as best objective responses were observed in 1 (1%), 23 (23.5%), 62 (63.3%), and 12 (12.2%) patients, respectively. The tumor control rate (CR+PR+SD of >4 months) was 87.8%. The 1-year estimated PFS and OS were 58.4% and 64.6%, respectively. The median progression-free survival (PFS) time was 60 weeks (95% CI 41–79); and the median overall survival (OS) time was not reached with a follow-up of 76 weeks. Reduction of sorafenib dose was required in 26 patients who developed grade 3 or 4 treatment-cause adverse-effects. An additional 9 patients discontinued sorafenib treatment due to severe adverse-effects. No grade 5 toxicity occurred. Multivariate analysis revealed that independent predictive factors for tumor response to sorafenib treatment included ECOG status, presence of lymph node metastasis, and nephrectomy prior to the development of metastasis. CONCLUSION: Sorafenib produced an 87.8% disease control rate for metastatic renal cell carcinoma in Chinese patients, with acceptable rates of toxicity. The medication dosed at 400 mg twice daily is both efficacious and safe in the treatment of metastatic renal cell carcinoma in Chinese patients. BioMed Central 2009-07-21 /pmc/articles/PMC2724546/ /pubmed/19622166 http://dx.doi.org/10.1186/1471-2407-9-249 Text en Copyright ©2009 Zhang et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhang, Hailiang
Dong, Baijun
Lu, Jiade J
Yao, Xudong
Zhang, Shilin
Dai, Bo
Shen, Yijun
Zhu, Yao
Ye, Dingwei
Huang, Yiran
Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title_full Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title_fullStr Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title_full_unstemmed Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title_short Efficacy of sorafenib on metastatic renal cell carcinoma in Asian patients: Results from a multicenter study
title_sort efficacy of sorafenib on metastatic renal cell carcinoma in asian patients: results from a multicenter study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724546/
https://www.ncbi.nlm.nih.gov/pubmed/19622166
http://dx.doi.org/10.1186/1471-2407-9-249
work_keys_str_mv AT zhanghailiang efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT dongbaijun efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT lujiadej efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT yaoxudong efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT zhangshilin efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT daibo efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT shenyijun efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT zhuyao efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT yedingwei efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy
AT huangyiran efficacyofsorafenibonmetastaticrenalcellcarcinomainasianpatientsresultsfromamulticenterstudy