Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study
Background: The optimal sequence of chemotherapeutic agents is not firmly established for the treatment of metastatic colorectal cancer (mCRC). This phase II multi-centre study investigated the efficacy and tolerability of a standard capecitabine plus irinotecan (XELIRI) regimen with bevacizumab in...
| Autores: | , , , , , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2015 |
| País: | España |
| Institución: | Universitat de Lleida (UdL) |
| Repositorio: | Repositori Obert UdL |
| OAI Identifier: | oai:repositori.udl.cat:10459.1/56603 |
| Acceso en línea: | https://doi.org/10.1186/s12885-015-1293-y http://hdl.handle.net/10459.1/56603 |
| Access Level: | acceso abierto |
| Palabra clave: | Irinotecan Capecitabine Bevacizumab Metastatic colorectal cancer Chemotherapy |
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Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI studyGarcia-Alfonso, PilarChaves, ManuelMuñoz, AndrésSalud Salvia, Maria AntonietaGarcía-Gonzalez, MariaGrávalos, CristinaMassuti, BartomeuGonzález-Flores, EncarnaQueralt, BernardoLópez-Ladrón, AmeliaLosa, F.Gómez, Maria JoseOltra, AmparoAranda, EnriqueIrinotecanCapecitabineBevacizumabMetastatic colorectal cancerChemotherapyBackground: The optimal sequence of chemotherapeutic agents is not firmly established for the treatment of metastatic colorectal cancer (mCRC). This phase II multi-centre study investigated the efficacy and tolerability of a standard capecitabine plus irinotecan (XELIRI) regimen with bevacizumab in previously untreated patients with mCRC. Methods: Patients received intravenous irinotecan 175 mg/m2 on day 1 and oral capecitabine 1000 mg/m2 (800 mg/m2 for patients >65 years of age) twice daily on days 2–8, followed by a 1-week rest, and bevacizumab 5 mg/kg as an intravenous infusion on day 1 every 2 weeks. Results: Seventy-seven patients were included in the intention-to-treat and safety populations. Progression-free survival at 9 months was 61%. The overall response and disease control rates were 51% and 84%, respectively. Median progression-free and overall survival times were 11.9 and 24.8 months, respectively. 48 patients (62%) had at least one grade 3/4 adverse event, the most common being asthenia, diarrhoea and neutropenia. Quality of life varied little over the study period with mean visual analogue scale general health scores ranging from 71 to 76 over cycles 1–11. Conclusion: Our study found irinotecan and capecitabine administered fortnightly with bevacizumab in patients with mCRC to be an effective and tolerable regimen. Trial registration: clinicaltrials.gov identifier NCT00875771. Trial registration date: 04/02/2009. Keywords: Irinotecan, Capecitabine, Bevacizumab, Metastatic colorectal cancer, ChemotherapyBioMed Central2015info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttps://doi.org/10.1186/s12885-015-1293-yhttp://hdl.handle.net/10459.1/56603reponame:Repositori Obert UdL instname:Universitat de Lleida (UdL)InglésReproducció del document publicat a https://doi.org/10.1186/s12885-015-1293-yBMC Cancer, 2015, vol.15, núm. 327cc-by, (c) Garcia-Alfonso et al., 2015info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/3.0/es/oai:repositori.udl.cat:10459.1/566032026-06-24T12:42:17Z |
| dc.title.none.fl_str_mv |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| title |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| spellingShingle |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study Garcia-Alfonso, Pilar Irinotecan Capecitabine Bevacizumab Metastatic colorectal cancer Chemotherapy |
| title_short |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| title_full |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| title_fullStr |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| title_full_unstemmed |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| title_sort |
Capecitabine and irinotecan with bevacizumab 2-weekly for metastatic colorectal cancer: the phase II AVAXIRI study |
| dc.creator.none.fl_str_mv |
Garcia-Alfonso, Pilar Chaves, Manuel Muñoz, Andrés Salud Salvia, Maria Antonieta García-Gonzalez, Maria Grávalos, Cristina Massuti, Bartomeu González-Flores, Encarna Queralt, Bernardo López-Ladrón, Amelia Losa, F. Gómez, Maria Jose Oltra, Amparo Aranda, Enrique |
| author |
Garcia-Alfonso, Pilar |
| author_facet |
Garcia-Alfonso, Pilar Chaves, Manuel Muñoz, Andrés Salud Salvia, Maria Antonieta García-Gonzalez, Maria Grávalos, Cristina Massuti, Bartomeu González-Flores, Encarna Queralt, Bernardo López-Ladrón, Amelia Losa, F. Gómez, Maria Jose Oltra, Amparo Aranda, Enrique |
| author_role |
author |
| author2 |
Chaves, Manuel Muñoz, Andrés Salud Salvia, Maria Antonieta García-Gonzalez, Maria Grávalos, Cristina Massuti, Bartomeu González-Flores, Encarna Queralt, Bernardo López-Ladrón, Amelia Losa, F. Gómez, Maria Jose Oltra, Amparo Aranda, Enrique |
| author2_role |
author author author author author author author author author author author author author |
| dc.subject.none.fl_str_mv |
Irinotecan Capecitabine Bevacizumab Metastatic colorectal cancer Chemotherapy |
| topic |
Irinotecan Capecitabine Bevacizumab Metastatic colorectal cancer Chemotherapy |
| description |
Background: The optimal sequence of chemotherapeutic agents is not firmly established for the treatment of metastatic colorectal cancer (mCRC). This phase II multi-centre study investigated the efficacy and tolerability of a standard capecitabine plus irinotecan (XELIRI) regimen with bevacizumab in previously untreated patients with mCRC. Methods: Patients received intravenous irinotecan 175 mg/m2 on day 1 and oral capecitabine 1000 mg/m2 (800 mg/m2 for patients >65 years of age) twice daily on days 2–8, followed by a 1-week rest, and bevacizumab 5 mg/kg as an intravenous infusion on day 1 every 2 weeks. Results: Seventy-seven patients were included in the intention-to-treat and safety populations. Progression-free survival at 9 months was 61%. The overall response and disease control rates were 51% and 84%, respectively. Median progression-free and overall survival times were 11.9 and 24.8 months, respectively. 48 patients (62%) had at least one grade 3/4 adverse event, the most common being asthenia, diarrhoea and neutropenia. Quality of life varied little over the study period with mean visual analogue scale general health scores ranging from 71 to 76 over cycles 1–11. Conclusion: Our study found irinotecan and capecitabine administered fortnightly with bevacizumab in patients with mCRC to be an effective and tolerable regimen. Trial registration: clinicaltrials.gov identifier NCT00875771. Trial registration date: 04/02/2009. Keywords: Irinotecan, Capecitabine, Bevacizumab, Metastatic colorectal cancer, Chemotherapy |
| publishDate |
2015 |
| dc.date.none.fl_str_mv |
2015 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://doi.org/10.1186/s12885-015-1293-y http://hdl.handle.net/10459.1/56603 |
| url |
https://doi.org/10.1186/s12885-015-1293-y http://hdl.handle.net/10459.1/56603 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a https://doi.org/10.1186/s12885-015-1293-y BMC Cancer, 2015, vol.15, núm. 327 |
| dc.rights.none.fl_str_mv |
cc-by, (c) Garcia-Alfonso et al., 2015 info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/3.0/es/ |
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cc-by, (c) Garcia-Alfonso et al., 2015 http://creativecommons.org/licenses/by/3.0/es/ |
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openAccess |
| dc.publisher.none.fl_str_mv |
BioMed Central |
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BioMed Central |
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reponame:Repositori Obert UdL instname:Universitat de Lleida (UdL) |
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Universitat de Lleida (UdL) |
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Repositori Obert UdL |
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