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Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry
Background Although anthracycline-based triplets are one of the most widely used schedules to treat advanced gastric cancer (AGC), the benefit of including epirubicin in these therapeutic combinations remains unknown. This study aims to evaluate both the efficacy and tolerance of triplets with epiru...
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Published in: | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2018, Vol.21 (1), p.96-105 |
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creator | Carmona-Bayonas, A. Jiménez-Fonseca, P. Custodio, A. Sánchez Cánovas, M. Hernández, R. Pericay, C. Echavarria, I. Lacalle, A. Visa, L. Rodríguez Palomo, A. Mangas, M. Cano, J. M. Buxo, E. Álvarez-Manceñido, F. García, T. Lorenzo, J. E. Ferrer-Cardona, M. Viudez, A. Azkarate, A. Ramchandani, A. Arias, D. Longo, F. López, C. Sánchez Bayona, R. Limón, M. L. Díaz-Serrano, A. Fernández Montes, A. Sala, P. Cerdá, P. Rivera, F. Gallego, J. |
description | Background
Although anthracycline-based triplets are one of the most widely used schedules to treat advanced gastric cancer (AGC), the benefit of including epirubicin in these therapeutic combinations remains unknown. This study aims to evaluate both the efficacy and tolerance of triplets with epirubicin vs. doublets with platinum-fluoropyrimidine in a national AGC registry.
Methods
Patients with AGC treated with polychemotherapy without trastuzumab at 28 hospitals in Spain between 2008 and 2016 were included. The effect of anthracycline-based triplets against doublets was evaluated by propensity score matching (PSM) and Cox proportional hazards (PH) regression.
Result
A total of 1002 patients were included (doublets,
n
= 653; anthracycline-based triplets,
n
= 349). The multivariable Cox PH regression failed to detect significantly increased OS in favor of triplets with anthracyclines: HR 0.90 (95% CI, 0.78–1.05),
p
=
0.20035. After PSM, the sample contained 325 pairs with similar baseline characteristics. This method was also unable to reveal an increase in OS: 10.5 (95% CI, 9.7–12.3) vs. 9.9 (95% CI, 9.2–11.4) months, HR 0.91 (CI 95%, 0.76–1.083), and (log-rank test,
p
=
0.226). Response rates (42.1 vs. 33.1%,
p
=
0.12) and PFS (HR 0.95, CI 95%, 0.80–1.13, log-rank test,
p
=
0.873) were not significantly higher with epirubicin-based regimens. The triplets were associated with greater grade 3–4 hematological toxicity, and increased hospitalization due to toxicity by 68%. The addition of epirubicin is viable, but 23.7% discontinued treatment because of adverse effects or patient decision.
Conclusion
Anthracyclines added to platinum-fluoropyrimidine doublets did not improve the response rate or survival outcomes in patients with AGC but entailed greater toxicity. |
doi_str_mv | 10.1007/s10120-017-0718-5 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1979947203</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1979947203</sourcerecordid><originalsourceid>FETCH-LOGICAL-c439t-5ddd3d82f5aaf93aac40a9d4355e47c0a49e956dbbe454f2d00ba432e411a98e3</originalsourceid><addsrcrecordid>eNp1kc1u1DAUhSMEoqXwAGyQJdamdmxPYnajUSlI_ZEQrKMb-3rqKokH2ymah-SdcGbaig0r2_I537m6p6rec_aJM9acJ854zSjjDWUNb6l6UZ1yKVZUCKZePt1rzU-qNyndM8aV5qvX1UndCi3qpj2t_qynfBfB7M3gJ6Q9JLQkR78bMCdiA5lCJn7cxfCAJN8hQee8KXoSHNkNkP00j9QNc4hht49-9LZwinHuDwQ_EedjynTBFzBCHnHKixvsA0ymxG0hlURDzPKMn0kRDfR3iIMlFjIQF8N4yF5frq8vrm9vyE3JDRMMZHOwkO-49YWxf1u9cjAkfPd4nlU_v1z82HylV7eX3zbrK2qk0Jkqa62wbe0UgNMCwEgG2kqhFMrGMJAatVrZvkeppKstYz1IUaPkHHSL4qz6eOSWvfyaMeXuPsyxDJQ6rhutZVMzUVT8qDIxpBTRdbuyIIj7jrNuKbA7FtiVArulwE4Vz4dH8tyPaJ8dT40VQX0UpPI1bTH-E_1f6l8At6sY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1979947203</pqid></control><display><type>article</type><title>Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry</title><source>Springer Nature</source><creator>Carmona-Bayonas, A. ; Jiménez-Fonseca, P. ; Custodio, A. ; Sánchez Cánovas, M. ; Hernández, R. ; Pericay, C. ; Echavarria, I. ; Lacalle, A. ; Visa, L. ; Rodríguez Palomo, A. ; Mangas, M. ; Cano, J. M. ; Buxo, E. ; Álvarez-Manceñido, F. ; García, T. ; Lorenzo, J. E. ; Ferrer-Cardona, M. ; Viudez, A. ; Azkarate, A. ; Ramchandani, A. ; Arias, D. ; Longo, F. ; López, C. ; Sánchez Bayona, R. ; Limón, M. L. ; Díaz-Serrano, A. ; Fernández Montes, A. ; Sala, P. ; Cerdá, P. ; Rivera, F. ; Gallego, J.</creator><creatorcontrib>Carmona-Bayonas, A. ; Jiménez-Fonseca, P. ; Custodio, A. ; Sánchez Cánovas, M. ; Hernández, R. ; Pericay, C. ; Echavarria, I. ; Lacalle, A. ; Visa, L. ; Rodríguez Palomo, A. ; Mangas, M. ; Cano, J. M. ; Buxo, E. ; Álvarez-Manceñido, F. ; García, T. ; Lorenzo, J. E. ; Ferrer-Cardona, M. ; Viudez, A. ; Azkarate, A. ; Ramchandani, A. ; Arias, D. ; Longo, F. ; López, C. ; Sánchez Bayona, R. ; Limón, M. L. ; Díaz-Serrano, A. ; Fernández Montes, A. ; Sala, P. ; Cerdá, P. ; Rivera, F. ; Gallego, J. ; AGAMENON study group ; AGAMENON study group</creatorcontrib><description>Background
Although anthracycline-based triplets are one of the most widely used schedules to treat advanced gastric cancer (AGC), the benefit of including epirubicin in these therapeutic combinations remains unknown. This study aims to evaluate both the efficacy and tolerance of triplets with epirubicin vs. doublets with platinum-fluoropyrimidine in a national AGC registry.
Methods
Patients with AGC treated with polychemotherapy without trastuzumab at 28 hospitals in Spain between 2008 and 2016 were included. The effect of anthracycline-based triplets against doublets was evaluated by propensity score matching (PSM) and Cox proportional hazards (PH) regression.
Result
A total of 1002 patients were included (doublets,
n
= 653; anthracycline-based triplets,
n
= 349). The multivariable Cox PH regression failed to detect significantly increased OS in favor of triplets with anthracyclines: HR 0.90 (95% CI, 0.78–1.05),
p
=
0.20035. After PSM, the sample contained 325 pairs with similar baseline characteristics. This method was also unable to reveal an increase in OS: 10.5 (95% CI, 9.7–12.3) vs. 9.9 (95% CI, 9.2–11.4) months, HR 0.91 (CI 95%, 0.76–1.083), and (log-rank test,
p
=
0.226). Response rates (42.1 vs. 33.1%,
p
=
0.12) and PFS (HR 0.95, CI 95%, 0.80–1.13, log-rank test,
p
=
0.873) were not significantly higher with epirubicin-based regimens. The triplets were associated with greater grade 3–4 hematological toxicity, and increased hospitalization due to toxicity by 68%. The addition of epirubicin is viable, but 23.7% discontinued treatment because of adverse effects or patient decision.
Conclusion
Anthracyclines added to platinum-fluoropyrimidine doublets did not improve the response rate or survival outcomes in patients with AGC but entailed greater toxicity.</description><identifier>ISSN: 1436-3291</identifier><identifier>EISSN: 1436-3305</identifier><identifier>DOI: 10.1007/s10120-017-0718-5</identifier><identifier>PMID: 28393278</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Abdominal Surgery ; Anthracycline ; Cancer Research ; Epirubicin ; Gastric cancer ; Gastroenterology ; Medicine ; Medicine & Public Health ; Monoclonal antibodies ; Oncology ; Original Article ; Platinum ; Surgical Oncology ; Targeted cancer therapy ; Toxicity ; Trastuzumab</subject><ispartof>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2018, Vol.21 (1), p.96-105</ispartof><rights>The International Gastric Cancer Association and The Japanese Gastric Cancer Association 2017</rights><rights>Gastric Cancer is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c439t-5ddd3d82f5aaf93aac40a9d4355e47c0a49e956dbbe454f2d00ba432e411a98e3</citedby><cites>FETCH-LOGICAL-c439t-5ddd3d82f5aaf93aac40a9d4355e47c0a49e956dbbe454f2d00ba432e411a98e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28393278$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Carmona-Bayonas, A.</creatorcontrib><creatorcontrib>Jiménez-Fonseca, P.</creatorcontrib><creatorcontrib>Custodio, A.</creatorcontrib><creatorcontrib>Sánchez Cánovas, M.</creatorcontrib><creatorcontrib>Hernández, R.</creatorcontrib><creatorcontrib>Pericay, C.</creatorcontrib><creatorcontrib>Echavarria, I.</creatorcontrib><creatorcontrib>Lacalle, A.</creatorcontrib><creatorcontrib>Visa, L.</creatorcontrib><creatorcontrib>Rodríguez Palomo, A.</creatorcontrib><creatorcontrib>Mangas, M.</creatorcontrib><creatorcontrib>Cano, J. M.</creatorcontrib><creatorcontrib>Buxo, E.</creatorcontrib><creatorcontrib>Álvarez-Manceñido, F.</creatorcontrib><creatorcontrib>García, T.</creatorcontrib><creatorcontrib>Lorenzo, J. E.</creatorcontrib><creatorcontrib>Ferrer-Cardona, M.</creatorcontrib><creatorcontrib>Viudez, A.</creatorcontrib><creatorcontrib>Azkarate, A.</creatorcontrib><creatorcontrib>Ramchandani, A.</creatorcontrib><creatorcontrib>Arias, D.</creatorcontrib><creatorcontrib>Longo, F.</creatorcontrib><creatorcontrib>López, C.</creatorcontrib><creatorcontrib>Sánchez Bayona, R.</creatorcontrib><creatorcontrib>Limón, M. L.</creatorcontrib><creatorcontrib>Díaz-Serrano, A.</creatorcontrib><creatorcontrib>Fernández Montes, A.</creatorcontrib><creatorcontrib>Sala, P.</creatorcontrib><creatorcontrib>Cerdá, P.</creatorcontrib><creatorcontrib>Rivera, F.</creatorcontrib><creatorcontrib>Gallego, J.</creatorcontrib><creatorcontrib>AGAMENON study group</creatorcontrib><creatorcontrib>AGAMENON study group</creatorcontrib><title>Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry</title><title>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</title><addtitle>Gastric Cancer</addtitle><addtitle>Gastric Cancer</addtitle><description>Background
Although anthracycline-based triplets are one of the most widely used schedules to treat advanced gastric cancer (AGC), the benefit of including epirubicin in these therapeutic combinations remains unknown. This study aims to evaluate both the efficacy and tolerance of triplets with epirubicin vs. doublets with platinum-fluoropyrimidine in a national AGC registry.
Methods
Patients with AGC treated with polychemotherapy without trastuzumab at 28 hospitals in Spain between 2008 and 2016 were included. The effect of anthracycline-based triplets against doublets was evaluated by propensity score matching (PSM) and Cox proportional hazards (PH) regression.
Result
A total of 1002 patients were included (doublets,
n
= 653; anthracycline-based triplets,
n
= 349). The multivariable Cox PH regression failed to detect significantly increased OS in favor of triplets with anthracyclines: HR 0.90 (95% CI, 0.78–1.05),
p
=
0.20035. After PSM, the sample contained 325 pairs with similar baseline characteristics. This method was also unable to reveal an increase in OS: 10.5 (95% CI, 9.7–12.3) vs. 9.9 (95% CI, 9.2–11.4) months, HR 0.91 (CI 95%, 0.76–1.083), and (log-rank test,
p
=
0.226). Response rates (42.1 vs. 33.1%,
p
=
0.12) and PFS (HR 0.95, CI 95%, 0.80–1.13, log-rank test,
p
=
0.873) were not significantly higher with epirubicin-based regimens. The triplets were associated with greater grade 3–4 hematological toxicity, and increased hospitalization due to toxicity by 68%. The addition of epirubicin is viable, but 23.7% discontinued treatment because of adverse effects or patient decision.
Conclusion
Anthracyclines added to platinum-fluoropyrimidine doublets did not improve the response rate or survival outcomes in patients with AGC but entailed greater toxicity.</description><subject>Abdominal Surgery</subject><subject>Anthracycline</subject><subject>Cancer Research</subject><subject>Epirubicin</subject><subject>Gastric cancer</subject><subject>Gastroenterology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Platinum</subject><subject>Surgical Oncology</subject><subject>Targeted cancer therapy</subject><subject>Toxicity</subject><subject>Trastuzumab</subject><issn>1436-3291</issn><issn>1436-3305</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kc1u1DAUhSMEoqXwAGyQJdamdmxPYnajUSlI_ZEQrKMb-3rqKokH2ymah-SdcGbaig0r2_I537m6p6rec_aJM9acJ854zSjjDWUNb6l6UZ1yKVZUCKZePt1rzU-qNyndM8aV5qvX1UndCi3qpj2t_qynfBfB7M3gJ6Q9JLQkR78bMCdiA5lCJn7cxfCAJN8hQee8KXoSHNkNkP00j9QNc4hht49-9LZwinHuDwQ_EedjynTBFzBCHnHKixvsA0ymxG0hlURDzPKMn0kRDfR3iIMlFjIQF8N4yF5frq8vrm9vyE3JDRMMZHOwkO-49YWxf1u9cjAkfPd4nlU_v1z82HylV7eX3zbrK2qk0Jkqa62wbe0UgNMCwEgG2kqhFMrGMJAatVrZvkeppKstYz1IUaPkHHSL4qz6eOSWvfyaMeXuPsyxDJQ6rhutZVMzUVT8qDIxpBTRdbuyIIj7jrNuKbA7FtiVArulwE4Vz4dH8tyPaJ8dT40VQX0UpPI1bTH-E_1f6l8At6sY</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Carmona-Bayonas, A.</creator><creator>Jiménez-Fonseca, P.</creator><creator>Custodio, A.</creator><creator>Sánchez Cánovas, M.</creator><creator>Hernández, R.</creator><creator>Pericay, C.</creator><creator>Echavarria, I.</creator><creator>Lacalle, A.</creator><creator>Visa, L.</creator><creator>Rodríguez Palomo, A.</creator><creator>Mangas, M.</creator><creator>Cano, J. M.</creator><creator>Buxo, E.</creator><creator>Álvarez-Manceñido, F.</creator><creator>García, T.</creator><creator>Lorenzo, J. E.</creator><creator>Ferrer-Cardona, M.</creator><creator>Viudez, A.</creator><creator>Azkarate, A.</creator><creator>Ramchandani, A.</creator><creator>Arias, D.</creator><creator>Longo, F.</creator><creator>López, C.</creator><creator>Sánchez Bayona, R.</creator><creator>Limón, M. L.</creator><creator>Díaz-Serrano, A.</creator><creator>Fernández Montes, A.</creator><creator>Sala, P.</creator><creator>Cerdá, P.</creator><creator>Rivera, F.</creator><creator>Gallego, J.</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>2018</creationdate><title>Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry</title><author>Carmona-Bayonas, A. ; Jiménez-Fonseca, P. ; Custodio, A. ; Sánchez Cánovas, M. ; Hernández, R. ; Pericay, C. ; Echavarria, I. ; Lacalle, A. ; Visa, L. ; Rodríguez Palomo, A. ; Mangas, M. ; Cano, J. M. ; Buxo, E. ; Álvarez-Manceñido, F. ; García, T. ; Lorenzo, J. E. ; Ferrer-Cardona, M. ; Viudez, A. ; Azkarate, A. ; Ramchandani, A. ; Arias, D. ; Longo, F. ; López, C. ; Sánchez Bayona, R. ; Limón, M. L. ; Díaz-Serrano, A. ; Fernández Montes, A. ; Sala, P. ; Cerdá, P. ; Rivera, F. ; Gallego, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c439t-5ddd3d82f5aaf93aac40a9d4355e47c0a49e956dbbe454f2d00ba432e411a98e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Abdominal Surgery</topic><topic>Anthracycline</topic><topic>Cancer Research</topic><topic>Epirubicin</topic><topic>Gastric cancer</topic><topic>Gastroenterology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Monoclonal antibodies</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Platinum</topic><topic>Surgical Oncology</topic><topic>Targeted cancer therapy</topic><topic>Toxicity</topic><topic>Trastuzumab</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Carmona-Bayonas, A.</creatorcontrib><creatorcontrib>Jiménez-Fonseca, P.</creatorcontrib><creatorcontrib>Custodio, A.</creatorcontrib><creatorcontrib>Sánchez Cánovas, M.</creatorcontrib><creatorcontrib>Hernández, R.</creatorcontrib><creatorcontrib>Pericay, C.</creatorcontrib><creatorcontrib>Echavarria, I.</creatorcontrib><creatorcontrib>Lacalle, A.</creatorcontrib><creatorcontrib>Visa, L.</creatorcontrib><creatorcontrib>Rodríguez Palomo, A.</creatorcontrib><creatorcontrib>Mangas, M.</creatorcontrib><creatorcontrib>Cano, J. M.</creatorcontrib><creatorcontrib>Buxo, E.</creatorcontrib><creatorcontrib>Álvarez-Manceñido, F.</creatorcontrib><creatorcontrib>García, T.</creatorcontrib><creatorcontrib>Lorenzo, J. E.</creatorcontrib><creatorcontrib>Ferrer-Cardona, M.</creatorcontrib><creatorcontrib>Viudez, A.</creatorcontrib><creatorcontrib>Azkarate, A.</creatorcontrib><creatorcontrib>Ramchandani, A.</creatorcontrib><creatorcontrib>Arias, D.</creatorcontrib><creatorcontrib>Longo, F.</creatorcontrib><creatorcontrib>López, C.</creatorcontrib><creatorcontrib>Sánchez Bayona, R.</creatorcontrib><creatorcontrib>Limón, M. L.</creatorcontrib><creatorcontrib>Díaz-Serrano, A.</creatorcontrib><creatorcontrib>Fernández Montes, A.</creatorcontrib><creatorcontrib>Sala, P.</creatorcontrib><creatorcontrib>Cerdá, P.</creatorcontrib><creatorcontrib>Rivera, F.</creatorcontrib><creatorcontrib>Gallego, J.</creatorcontrib><creatorcontrib>AGAMENON study group</creatorcontrib><creatorcontrib>AGAMENON study group</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Carmona-Bayonas, A.</au><au>Jiménez-Fonseca, P.</au><au>Custodio, A.</au><au>Sánchez Cánovas, M.</au><au>Hernández, R.</au><au>Pericay, C.</au><au>Echavarria, I.</au><au>Lacalle, A.</au><au>Visa, L.</au><au>Rodríguez Palomo, A.</au><au>Mangas, M.</au><au>Cano, J. M.</au><au>Buxo, E.</au><au>Álvarez-Manceñido, F.</au><au>García, T.</au><au>Lorenzo, J. E.</au><au>Ferrer-Cardona, M.</au><au>Viudez, A.</au><au>Azkarate, A.</au><au>Ramchandani, A.</au><au>Arias, D.</au><au>Longo, F.</au><au>López, C.</au><au>Sánchez Bayona, R.</au><au>Limón, M. L.</au><au>Díaz-Serrano, A.</au><au>Fernández Montes, A.</au><au>Sala, P.</au><au>Cerdá, P.</au><au>Rivera, F.</au><au>Gallego, J.</au><aucorp>AGAMENON study group</aucorp><aucorp>AGAMENON study group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry</atitle><jtitle>Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association</jtitle><stitle>Gastric Cancer</stitle><addtitle>Gastric Cancer</addtitle><date>2018</date><risdate>2018</risdate><volume>21</volume><issue>1</issue><spage>96</spage><epage>105</epage><pages>96-105</pages><issn>1436-3291</issn><eissn>1436-3305</eissn><abstract>Background
Although anthracycline-based triplets are one of the most widely used schedules to treat advanced gastric cancer (AGC), the benefit of including epirubicin in these therapeutic combinations remains unknown. This study aims to evaluate both the efficacy and tolerance of triplets with epirubicin vs. doublets with platinum-fluoropyrimidine in a national AGC registry.
Methods
Patients with AGC treated with polychemotherapy without trastuzumab at 28 hospitals in Spain between 2008 and 2016 were included. The effect of anthracycline-based triplets against doublets was evaluated by propensity score matching (PSM) and Cox proportional hazards (PH) regression.
Result
A total of 1002 patients were included (doublets,
n
= 653; anthracycline-based triplets,
n
= 349). The multivariable Cox PH regression failed to detect significantly increased OS in favor of triplets with anthracyclines: HR 0.90 (95% CI, 0.78–1.05),
p
=
0.20035. After PSM, the sample contained 325 pairs with similar baseline characteristics. This method was also unable to reveal an increase in OS: 10.5 (95% CI, 9.7–12.3) vs. 9.9 (95% CI, 9.2–11.4) months, HR 0.91 (CI 95%, 0.76–1.083), and (log-rank test,
p
=
0.226). Response rates (42.1 vs. 33.1%,
p
=
0.12) and PFS (HR 0.95, CI 95%, 0.80–1.13, log-rank test,
p
=
0.873) were not significantly higher with epirubicin-based regimens. The triplets were associated with greater grade 3–4 hematological toxicity, and increased hospitalization due to toxicity by 68%. The addition of epirubicin is viable, but 23.7% discontinued treatment because of adverse effects or patient decision.
Conclusion
Anthracyclines added to platinum-fluoropyrimidine doublets did not improve the response rate or survival outcomes in patients with AGC but entailed greater toxicity.</abstract><cop>Tokyo</cop><pub>Springer Japan</pub><pmid>28393278</pmid><doi>10.1007/s10120-017-0718-5</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1436-3291 |
ispartof | Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association, 2018, Vol.21 (1), p.96-105 |
issn | 1436-3291 1436-3305 |
language | eng |
recordid | cdi_proquest_journals_1979947203 |
source | Springer Nature |
subjects | Abdominal Surgery Anthracycline Cancer Research Epirubicin Gastric cancer Gastroenterology Medicine Medicine & Public Health Monoclonal antibodies Oncology Original Article Platinum Surgical Oncology Targeted cancer therapy Toxicity Trastuzumab |
title | Anthracycline-based triplets do not improve the efficacy of platinum-fluoropyrimidine doublets in first-line treatment of advanced gastric cancer: real-world data from the AGAMEMON National Cancer Registry |
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