Cargando…
5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study
BACKGROUND: Sunitinib is an oral inhibitor of tyrosine kinase receptors implicated in tumor proliferation, angiogenesis, and metastasis. In this randomized, multicenter, open-label Phase IIb study, sunitinib plus mFOLFOX6 (oxaliplatin plus leucovorin plus 5-fluorouracil) was compared with bevacizuma...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474399/ https://www.ncbi.nlm.nih.gov/pubmed/26109878 http://dx.doi.org/10.2147/CMAR.S61408 |
_version_ | 1782377266339119104 |
---|---|
author | Hecht, J Randolph Mitchell, Edith P Yoshino, Takayuki Welslau, Manfred Lin, Xun Chow Maneval, Edna Paolini, Jolanda Lechuga, Maria Jose Kretzschmar, Albrecht |
author_facet | Hecht, J Randolph Mitchell, Edith P Yoshino, Takayuki Welslau, Manfred Lin, Xun Chow Maneval, Edna Paolini, Jolanda Lechuga, Maria Jose Kretzschmar, Albrecht |
author_sort | Hecht, J Randolph |
collection | PubMed |
description | BACKGROUND: Sunitinib is an oral inhibitor of tyrosine kinase receptors implicated in tumor proliferation, angiogenesis, and metastasis. In this randomized, multicenter, open-label Phase IIb study, sunitinib plus mFOLFOX6 (oxaliplatin plus leucovorin plus 5-fluorouracil) was compared with bevacizumab plus mFOLFOX6 as first-line therapy in patients with metastatic colorectal cancer. METHODS: Patients were stratified by performance status, baseline lactate dehydrogenase level, and prior adjuvant treatment, and randomized 1:1 to receive sunitinib 37.5 mg/day for 4 weeks on and 2 weeks off plus mFOLFOX6 every 2 weeks or bevacizumab 5 mg/kg every 2 weeks plus mFOLFOX6 every 2 weeks. The primary endpoint was progression-free survival. Secondary endpoints included objective response rate, overall survival, safety, and quality of life. RESULTS: Enrollment was closed early following accrual of 191 patients, based on an interim analysis showing an inferior trend in the primary progression-free survival efficacy endpoint for sunitinib. Ninety-six patients were randomized to sunitinib plus mFOLFOX6 and 95 to bevacizumab plus mFOLFOX6. Median progression-free survival was 9.3 months and 15.4 months, respectively, but the objective response rate was similar between the study arms. Median overall survival was 23.7 months and 34.1 months, respectively. Dose reductions and interruptions were more common with sunitinib. Hematologic toxicity was more common in the sunitinib arm. CONCLUSION: While the results of the sunitinib arm are comparable with those of previously reported FOLFOX combinations, the sunitinib-based combination was associated with more toxicity than that observed with bevacizumab and mFOLFOX6. The bevacizumab arm had an unexpectedly good outcome, and was much better than that seen in the Phase III trials. Combination therapy with sunitinib plus mFOLFOX6 is not recommended for patients with metastatic colorectal cancer. |
format | Online Article Text |
id | pubmed-4474399 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44743992015-06-24 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study Hecht, J Randolph Mitchell, Edith P Yoshino, Takayuki Welslau, Manfred Lin, Xun Chow Maneval, Edna Paolini, Jolanda Lechuga, Maria Jose Kretzschmar, Albrecht Cancer Manag Res Original Research BACKGROUND: Sunitinib is an oral inhibitor of tyrosine kinase receptors implicated in tumor proliferation, angiogenesis, and metastasis. In this randomized, multicenter, open-label Phase IIb study, sunitinib plus mFOLFOX6 (oxaliplatin plus leucovorin plus 5-fluorouracil) was compared with bevacizumab plus mFOLFOX6 as first-line therapy in patients with metastatic colorectal cancer. METHODS: Patients were stratified by performance status, baseline lactate dehydrogenase level, and prior adjuvant treatment, and randomized 1:1 to receive sunitinib 37.5 mg/day for 4 weeks on and 2 weeks off plus mFOLFOX6 every 2 weeks or bevacizumab 5 mg/kg every 2 weeks plus mFOLFOX6 every 2 weeks. The primary endpoint was progression-free survival. Secondary endpoints included objective response rate, overall survival, safety, and quality of life. RESULTS: Enrollment was closed early following accrual of 191 patients, based on an interim analysis showing an inferior trend in the primary progression-free survival efficacy endpoint for sunitinib. Ninety-six patients were randomized to sunitinib plus mFOLFOX6 and 95 to bevacizumab plus mFOLFOX6. Median progression-free survival was 9.3 months and 15.4 months, respectively, but the objective response rate was similar between the study arms. Median overall survival was 23.7 months and 34.1 months, respectively. Dose reductions and interruptions were more common with sunitinib. Hematologic toxicity was more common in the sunitinib arm. CONCLUSION: While the results of the sunitinib arm are comparable with those of previously reported FOLFOX combinations, the sunitinib-based combination was associated with more toxicity than that observed with bevacizumab and mFOLFOX6. The bevacizumab arm had an unexpectedly good outcome, and was much better than that seen in the Phase III trials. Combination therapy with sunitinib plus mFOLFOX6 is not recommended for patients with metastatic colorectal cancer. Dove Medical Press 2015-06-15 /pmc/articles/PMC4474399/ /pubmed/26109878 http://dx.doi.org/10.2147/CMAR.S61408 Text en © 2015 Hecht et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Hecht, J Randolph Mitchell, Edith P Yoshino, Takayuki Welslau, Manfred Lin, Xun Chow Maneval, Edna Paolini, Jolanda Lechuga, Maria Jose Kretzschmar, Albrecht 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title | 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title_full | 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title_fullStr | 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title_full_unstemmed | 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title_short | 5-Fluorouracil, leucovorin, and oxaliplatin (mFOLFOX6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized Phase IIb study |
title_sort | 5-fluorouracil, leucovorin, and oxaliplatin (mfolfox6) plus sunitinib or bevacizumab as first-line treatment for metastatic colorectal cancer: a randomized phase iib study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474399/ https://www.ncbi.nlm.nih.gov/pubmed/26109878 http://dx.doi.org/10.2147/CMAR.S61408 |
work_keys_str_mv | AT hechtjrandolph 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT mitchelledithp 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT yoshinotakayuki 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT welslaumanfred 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT linxun 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT chowmanevaledna 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT paolinijolanda 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT lechugamariajose 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy AT kretzschmaralbrecht 5fluorouracilleucovorinandoxaliplatinmfolfox6plussunitiniborbevacizumabasfirstlinetreatmentformetastaticcolorectalcancerarandomizedphaseiibstudy |