Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP)
The objectives of this study were to evaluate the safety profile of aflibercept and health-related quality of life (HRQL) in patients with metastatic colorectal cancer (mCRC) provided with aflibercept access before marketing authorization. Patients received aflibercept followed by FOLFIRI (fluoroura...
Gespeichert in:
Veröffentlicht in: | Clinical colorectal cancer 2019-09, Vol.18 (3), p.183-191.e3 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 191.e3 |
---|---|
container_issue | 3 |
container_start_page | 183 |
container_title | Clinical colorectal cancer |
container_volume | 18 |
creator | Riechelmann, Rachel P. Srimuninnimit, Vichien Bordonaro, Roberto Kavan, Petr Di Bartolomeo, Maria Maiello, Evaristo Cicin, Irfan García-Alfonso, Pilar Chau, Ian Fedyanin, Mikhail Y. Martos, Carlos Fernández Ter-Ovanesov, Mikhail Peeters, Marc Ko, Yoo-Joung Yalcin, Suayib Karthaus, Meinolf Aparicio, Jorge Heinemann, Volker Picard, Pascaline Bury, Denise Drea, Edward Sobrero, Alberto |
description | The objectives of this study were to evaluate the safety profile of aflibercept and health-related quality of life (HRQL) in patients with metastatic colorectal cancer (mCRC) provided with aflibercept access before marketing authorization.
Patients received aflibercept followed by FOLFIRI (fluorouracil, leucovorin, irinotecan) on day 1 of a 2-week cycle until disease progression, unacceptable toxicity, death, or patient/investigator decision to discontinue. Treatment-emergent adverse events (TEAEs) were evaluated, and HRQL was assessed at baseline, cycle 3, and every other cycle using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, EORTC QLQ-CR29, and EuroQol 5-Dimensions 3-Levels questionnaires (NCT01571284).
Overall, 779 adult patients with mCRC, who received ≥ 1 prior oxaliplatin-based regimen and had disease progression during or following their last administration of oxaliplatin-based chemotherapy, were enrolled. At data cutoff, all patients had discontinued treatment, mainly owing to disease progression (51.7%). The most common TEAEs of any grade were diarrhea (61.6%), hypertension (48.4%), and nausea (43.3%). The most common grade 3/4 TEAEs were hypertension (24.1%), neutropenia (23.1%), and diarrhea (15.3%). Clinically meaningful changes in HRQL were reported for all measures. Most patients either had an improvement in their HRQL scores or remained stable during the treatment period based on patient-reported outcomes.
The data from this study support the tolerability of the combination of aflibercept and FOLFIRI in a setting that more closely approximates real life in patients with mCRC who failed to respond to oxaliplatin-based chemotherapy, and also suggest an improvement in HRQL.
This study evaluated safety and quality of life in patients with metastatic colorectal cancer undergoing treatment with aflibercept and FOLFIRI (fluorouracil, leucovorin, irinotecan). Most patients treated with this combination experienced either improvement or stability in quality of life scores. Aflibercept plus FOLFIRI is tolerable in the treatment of patients with metastatic colorectal cancer with a safety profile similar to that seen in previous studies of these individual medications. |
doi_str_mv | 10.1016/j.clcc.2019.05.003 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2245632415</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1533002819300234</els_id><sourcerecordid>2245632415</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-798a272bf5d1d93a43ef62ac60d7a36141c8eb8d3bc829ab81406e7002da66bf3</originalsourceid><addsrcrecordid>eNp9kU1vEzEQhlcIRNvAH-CAfCyHXfyxn4hLFJE2UlDSppwtrz2mjrzrYHsr5Y_x--ooBXHiNCPNO-9o3ifLPhBcEEzqz_tCWikLiklX4KrAmL3KLknH2hzXTfk69RVjOca0vciuQtinrmaEvM0uGKGUVCW9zH7PtTU9eAmHiLZ2Cmi5WS9X9yuknUc7kG5UuTUjoAcPIg4wRuQ0-g5RhCiikWjhrPMgo7BoIUYJ_gva9AH8U5q6MSDt3YDiI6Ab6_ok-vfgTmiIRyRGhW5B2PiY34MVERS6m4Q18Zg7na-NBrT17qcXA7qe7-7c9tO77I0WNsD7lzrLfiy_PSxu8_XmZrWYr3NZYhzzpmsFbWivK0VUx0TJQNdUyBqrRrCalES20LeK9bKlnehbUuIamhSUEnXdazbLrs--B-9-TRAiH0yQYK0YwU2BU1pWNaNlSnqW0bNUeheCB80P3gzCHznB_MSL7_mJFz_x4rjiiVda-vjiP_UDqL8rfwAlwdezANKXTwY8D9JAilmZU-hcOfM__2cdq6fq</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2245632415</pqid></control><display><type>article</type><title>Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP)</title><source>ScienceDirect Journals (5 years ago - present)</source><creator>Riechelmann, Rachel P. ; Srimuninnimit, Vichien ; Bordonaro, Roberto ; Kavan, Petr ; Di Bartolomeo, Maria ; Maiello, Evaristo ; Cicin, Irfan ; García-Alfonso, Pilar ; Chau, Ian ; Fedyanin, Mikhail Y. ; Martos, Carlos Fernández ; Ter-Ovanesov, Mikhail ; Peeters, Marc ; Ko, Yoo-Joung ; Yalcin, Suayib ; Karthaus, Meinolf ; Aparicio, Jorge ; Heinemann, Volker ; Picard, Pascaline ; Bury, Denise ; Drea, Edward ; Sobrero, Alberto</creator><creatorcontrib>Riechelmann, Rachel P. ; Srimuninnimit, Vichien ; Bordonaro, Roberto ; Kavan, Petr ; Di Bartolomeo, Maria ; Maiello, Evaristo ; Cicin, Irfan ; García-Alfonso, Pilar ; Chau, Ian ; Fedyanin, Mikhail Y. ; Martos, Carlos Fernández ; Ter-Ovanesov, Mikhail ; Peeters, Marc ; Ko, Yoo-Joung ; Yalcin, Suayib ; Karthaus, Meinolf ; Aparicio, Jorge ; Heinemann, Volker ; Picard, Pascaline ; Bury, Denise ; Drea, Edward ; Sobrero, Alberto</creatorcontrib><description>The objectives of this study were to evaluate the safety profile of aflibercept and health-related quality of life (HRQL) in patients with metastatic colorectal cancer (mCRC) provided with aflibercept access before marketing authorization.
Patients received aflibercept followed by FOLFIRI (fluorouracil, leucovorin, irinotecan) on day 1 of a 2-week cycle until disease progression, unacceptable toxicity, death, or patient/investigator decision to discontinue. Treatment-emergent adverse events (TEAEs) were evaluated, and HRQL was assessed at baseline, cycle 3, and every other cycle using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, EORTC QLQ-CR29, and EuroQol 5-Dimensions 3-Levels questionnaires (NCT01571284).
Overall, 779 adult patients with mCRC, who received ≥ 1 prior oxaliplatin-based regimen and had disease progression during or following their last administration of oxaliplatin-based chemotherapy, were enrolled. At data cutoff, all patients had discontinued treatment, mainly owing to disease progression (51.7%). The most common TEAEs of any grade were diarrhea (61.6%), hypertension (48.4%), and nausea (43.3%). The most common grade 3/4 TEAEs were hypertension (24.1%), neutropenia (23.1%), and diarrhea (15.3%). Clinically meaningful changes in HRQL were reported for all measures. Most patients either had an improvement in their HRQL scores or remained stable during the treatment period based on patient-reported outcomes.
The data from this study support the tolerability of the combination of aflibercept and FOLFIRI in a setting that more closely approximates real life in patients with mCRC who failed to respond to oxaliplatin-based chemotherapy, and also suggest an improvement in HRQL.
This study evaluated safety and quality of life in patients with metastatic colorectal cancer undergoing treatment with aflibercept and FOLFIRI (fluorouracil, leucovorin, irinotecan). Most patients treated with this combination experienced either improvement or stability in quality of life scores. Aflibercept plus FOLFIRI is tolerable in the treatment of patients with metastatic colorectal cancer with a safety profile similar to that seen in previous studies of these individual medications.</description><identifier>ISSN: 1533-0028</identifier><identifier>EISSN: 1938-0674</identifier><identifier>DOI: 10.1016/j.clcc.2019.05.003</identifier><identifier>PMID: 31221542</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Antiangiogenic ; Colorectal neoplasms ; Patient-reported outcome measures ; Receptors ; Vascular endothelial growth factor</subject><ispartof>Clinical colorectal cancer, 2019-09, Vol.18 (3), p.183-191.e3</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-798a272bf5d1d93a43ef62ac60d7a36141c8eb8d3bc829ab81406e7002da66bf3</citedby><cites>FETCH-LOGICAL-c400t-798a272bf5d1d93a43ef62ac60d7a36141c8eb8d3bc829ab81406e7002da66bf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.clcc.2019.05.003$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31221542$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Riechelmann, Rachel P.</creatorcontrib><creatorcontrib>Srimuninnimit, Vichien</creatorcontrib><creatorcontrib>Bordonaro, Roberto</creatorcontrib><creatorcontrib>Kavan, Petr</creatorcontrib><creatorcontrib>Di Bartolomeo, Maria</creatorcontrib><creatorcontrib>Maiello, Evaristo</creatorcontrib><creatorcontrib>Cicin, Irfan</creatorcontrib><creatorcontrib>García-Alfonso, Pilar</creatorcontrib><creatorcontrib>Chau, Ian</creatorcontrib><creatorcontrib>Fedyanin, Mikhail Y.</creatorcontrib><creatorcontrib>Martos, Carlos Fernández</creatorcontrib><creatorcontrib>Ter-Ovanesov, Mikhail</creatorcontrib><creatorcontrib>Peeters, Marc</creatorcontrib><creatorcontrib>Ko, Yoo-Joung</creatorcontrib><creatorcontrib>Yalcin, Suayib</creatorcontrib><creatorcontrib>Karthaus, Meinolf</creatorcontrib><creatorcontrib>Aparicio, Jorge</creatorcontrib><creatorcontrib>Heinemann, Volker</creatorcontrib><creatorcontrib>Picard, Pascaline</creatorcontrib><creatorcontrib>Bury, Denise</creatorcontrib><creatorcontrib>Drea, Edward</creatorcontrib><creatorcontrib>Sobrero, Alberto</creatorcontrib><title>Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP)</title><title>Clinical colorectal cancer</title><addtitle>Clin Colorectal Cancer</addtitle><description>The objectives of this study were to evaluate the safety profile of aflibercept and health-related quality of life (HRQL) in patients with metastatic colorectal cancer (mCRC) provided with aflibercept access before marketing authorization.
Patients received aflibercept followed by FOLFIRI (fluorouracil, leucovorin, irinotecan) on day 1 of a 2-week cycle until disease progression, unacceptable toxicity, death, or patient/investigator decision to discontinue. Treatment-emergent adverse events (TEAEs) were evaluated, and HRQL was assessed at baseline, cycle 3, and every other cycle using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, EORTC QLQ-CR29, and EuroQol 5-Dimensions 3-Levels questionnaires (NCT01571284).
Overall, 779 adult patients with mCRC, who received ≥ 1 prior oxaliplatin-based regimen and had disease progression during or following their last administration of oxaliplatin-based chemotherapy, were enrolled. At data cutoff, all patients had discontinued treatment, mainly owing to disease progression (51.7%). The most common TEAEs of any grade were diarrhea (61.6%), hypertension (48.4%), and nausea (43.3%). The most common grade 3/4 TEAEs were hypertension (24.1%), neutropenia (23.1%), and diarrhea (15.3%). Clinically meaningful changes in HRQL were reported for all measures. Most patients either had an improvement in their HRQL scores or remained stable during the treatment period based on patient-reported outcomes.
The data from this study support the tolerability of the combination of aflibercept and FOLFIRI in a setting that more closely approximates real life in patients with mCRC who failed to respond to oxaliplatin-based chemotherapy, and also suggest an improvement in HRQL.
This study evaluated safety and quality of life in patients with metastatic colorectal cancer undergoing treatment with aflibercept and FOLFIRI (fluorouracil, leucovorin, irinotecan). Most patients treated with this combination experienced either improvement or stability in quality of life scores. Aflibercept plus FOLFIRI is tolerable in the treatment of patients with metastatic colorectal cancer with a safety profile similar to that seen in previous studies of these individual medications.</description><subject>Antiangiogenic</subject><subject>Colorectal neoplasms</subject><subject>Patient-reported outcome measures</subject><subject>Receptors</subject><subject>Vascular endothelial growth factor</subject><issn>1533-0028</issn><issn>1938-0674</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kU1vEzEQhlcIRNvAH-CAfCyHXfyxn4hLFJE2UlDSppwtrz2mjrzrYHsr5Y_x--ooBXHiNCPNO-9o3ifLPhBcEEzqz_tCWikLiklX4KrAmL3KLknH2hzXTfk69RVjOca0vciuQtinrmaEvM0uGKGUVCW9zH7PtTU9eAmHiLZ2Cmi5WS9X9yuknUc7kG5UuTUjoAcPIg4wRuQ0-g5RhCiikWjhrPMgo7BoIUYJ_gva9AH8U5q6MSDt3YDiI6Ab6_ok-vfgTmiIRyRGhW5B2PiY34MVERS6m4Q18Zg7na-NBrT17qcXA7qe7-7c9tO77I0WNsD7lzrLfiy_PSxu8_XmZrWYr3NZYhzzpmsFbWivK0VUx0TJQNdUyBqrRrCalES20LeK9bKlnehbUuIamhSUEnXdazbLrs--B-9-TRAiH0yQYK0YwU2BU1pWNaNlSnqW0bNUeheCB80P3gzCHznB_MSL7_mJFz_x4rjiiVda-vjiP_UDqL8rfwAlwdezANKXTwY8D9JAilmZU-hcOfM__2cdq6fq</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Riechelmann, Rachel P.</creator><creator>Srimuninnimit, Vichien</creator><creator>Bordonaro, Roberto</creator><creator>Kavan, Petr</creator><creator>Di Bartolomeo, Maria</creator><creator>Maiello, Evaristo</creator><creator>Cicin, Irfan</creator><creator>García-Alfonso, Pilar</creator><creator>Chau, Ian</creator><creator>Fedyanin, Mikhail Y.</creator><creator>Martos, Carlos Fernández</creator><creator>Ter-Ovanesov, Mikhail</creator><creator>Peeters, Marc</creator><creator>Ko, Yoo-Joung</creator><creator>Yalcin, Suayib</creator><creator>Karthaus, Meinolf</creator><creator>Aparicio, Jorge</creator><creator>Heinemann, Volker</creator><creator>Picard, Pascaline</creator><creator>Bury, Denise</creator><creator>Drea, Edward</creator><creator>Sobrero, Alberto</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201909</creationdate><title>Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP)</title><author>Riechelmann, Rachel P. ; Srimuninnimit, Vichien ; Bordonaro, Roberto ; Kavan, Petr ; Di Bartolomeo, Maria ; Maiello, Evaristo ; Cicin, Irfan ; García-Alfonso, Pilar ; Chau, Ian ; Fedyanin, Mikhail Y. ; Martos, Carlos Fernández ; Ter-Ovanesov, Mikhail ; Peeters, Marc ; Ko, Yoo-Joung ; Yalcin, Suayib ; Karthaus, Meinolf ; Aparicio, Jorge ; Heinemann, Volker ; Picard, Pascaline ; Bury, Denise ; Drea, Edward ; Sobrero, Alberto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-798a272bf5d1d93a43ef62ac60d7a36141c8eb8d3bc829ab81406e7002da66bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antiangiogenic</topic><topic>Colorectal neoplasms</topic><topic>Patient-reported outcome measures</topic><topic>Receptors</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Riechelmann, Rachel P.</creatorcontrib><creatorcontrib>Srimuninnimit, Vichien</creatorcontrib><creatorcontrib>Bordonaro, Roberto</creatorcontrib><creatorcontrib>Kavan, Petr</creatorcontrib><creatorcontrib>Di Bartolomeo, Maria</creatorcontrib><creatorcontrib>Maiello, Evaristo</creatorcontrib><creatorcontrib>Cicin, Irfan</creatorcontrib><creatorcontrib>García-Alfonso, Pilar</creatorcontrib><creatorcontrib>Chau, Ian</creatorcontrib><creatorcontrib>Fedyanin, Mikhail Y.</creatorcontrib><creatorcontrib>Martos, Carlos Fernández</creatorcontrib><creatorcontrib>Ter-Ovanesov, Mikhail</creatorcontrib><creatorcontrib>Peeters, Marc</creatorcontrib><creatorcontrib>Ko, Yoo-Joung</creatorcontrib><creatorcontrib>Yalcin, Suayib</creatorcontrib><creatorcontrib>Karthaus, Meinolf</creatorcontrib><creatorcontrib>Aparicio, Jorge</creatorcontrib><creatorcontrib>Heinemann, Volker</creatorcontrib><creatorcontrib>Picard, Pascaline</creatorcontrib><creatorcontrib>Bury, Denise</creatorcontrib><creatorcontrib>Drea, Edward</creatorcontrib><creatorcontrib>Sobrero, Alberto</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical colorectal cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riechelmann, Rachel P.</au><au>Srimuninnimit, Vichien</au><au>Bordonaro, Roberto</au><au>Kavan, Petr</au><au>Di Bartolomeo, Maria</au><au>Maiello, Evaristo</au><au>Cicin, Irfan</au><au>García-Alfonso, Pilar</au><au>Chau, Ian</au><au>Fedyanin, Mikhail Y.</au><au>Martos, Carlos Fernández</au><au>Ter-Ovanesov, Mikhail</au><au>Peeters, Marc</au><au>Ko, Yoo-Joung</au><au>Yalcin, Suayib</au><au>Karthaus, Meinolf</au><au>Aparicio, Jorge</au><au>Heinemann, Volker</au><au>Picard, Pascaline</au><au>Bury, Denise</au><au>Drea, Edward</au><au>Sobrero, Alberto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP)</atitle><jtitle>Clinical colorectal cancer</jtitle><addtitle>Clin Colorectal Cancer</addtitle><date>2019-09</date><risdate>2019</risdate><volume>18</volume><issue>3</issue><spage>183</spage><epage>191.e3</epage><pages>183-191.e3</pages><issn>1533-0028</issn><eissn>1938-0674</eissn><abstract>The objectives of this study were to evaluate the safety profile of aflibercept and health-related quality of life (HRQL) in patients with metastatic colorectal cancer (mCRC) provided with aflibercept access before marketing authorization.
Patients received aflibercept followed by FOLFIRI (fluorouracil, leucovorin, irinotecan) on day 1 of a 2-week cycle until disease progression, unacceptable toxicity, death, or patient/investigator decision to discontinue. Treatment-emergent adverse events (TEAEs) were evaluated, and HRQL was assessed at baseline, cycle 3, and every other cycle using the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, EORTC QLQ-CR29, and EuroQol 5-Dimensions 3-Levels questionnaires (NCT01571284).
Overall, 779 adult patients with mCRC, who received ≥ 1 prior oxaliplatin-based regimen and had disease progression during or following their last administration of oxaliplatin-based chemotherapy, were enrolled. At data cutoff, all patients had discontinued treatment, mainly owing to disease progression (51.7%). The most common TEAEs of any grade were diarrhea (61.6%), hypertension (48.4%), and nausea (43.3%). The most common grade 3/4 TEAEs were hypertension (24.1%), neutropenia (23.1%), and diarrhea (15.3%). Clinically meaningful changes in HRQL were reported for all measures. Most patients either had an improvement in their HRQL scores or remained stable during the treatment period based on patient-reported outcomes.
The data from this study support the tolerability of the combination of aflibercept and FOLFIRI in a setting that more closely approximates real life in patients with mCRC who failed to respond to oxaliplatin-based chemotherapy, and also suggest an improvement in HRQL.
This study evaluated safety and quality of life in patients with metastatic colorectal cancer undergoing treatment with aflibercept and FOLFIRI (fluorouracil, leucovorin, irinotecan). Most patients treated with this combination experienced either improvement or stability in quality of life scores. Aflibercept plus FOLFIRI is tolerable in the treatment of patients with metastatic colorectal cancer with a safety profile similar to that seen in previous studies of these individual medications.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>31221542</pmid><doi>10.1016/j.clcc.2019.05.003</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1533-0028 |
ispartof | Clinical colorectal cancer, 2019-09, Vol.18 (3), p.183-191.e3 |
issn | 1533-0028 1938-0674 |
language | eng |
recordid | cdi_proquest_miscellaneous_2245632415 |
source | ScienceDirect Journals (5 years ago - present) |
subjects | Antiangiogenic Colorectal neoplasms Patient-reported outcome measures Receptors Vascular endothelial growth factor |
title | Aflibercept Plus FOLFIRI for Second-line Treatment of Metastatic Colorectal Cancer: Observations from the Global Aflibercept Safety and Health-Related Quality-of-Life Program (ASQoP) |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-12T03%3A22%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Aflibercept%20Plus%20FOLFIRI%20for%20Second-line%20Treatment%20of%20Metastatic%20Colorectal%20Cancer:%20Observations%20from%20the%20Global%20Aflibercept%20Safety%20and%20Health-Related%20Quality-of-Life%20Program%20(ASQoP)&rft.jtitle=Clinical%20colorectal%20cancer&rft.au=Riechelmann,%20Rachel%20P.&rft.date=2019-09&rft.volume=18&rft.issue=3&rft.spage=183&rft.epage=191.e3&rft.pages=183-191.e3&rft.issn=1533-0028&rft.eissn=1938-0674&rft_id=info:doi/10.1016/j.clcc.2019.05.003&rft_dat=%3Cproquest_cross%3E2245632415%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2245632415&rft_id=info:pmid/31221542&rft_els_id=S1533002819300234&rfr_iscdi=true |