Preoperative chemoradiation in rectal cancer: Retrospective comparison between capecitabine and continuous infusion of 5-fluorouracil

Background We compared the efficacy and toxicity of oral capecitabine and continuous infusion of 5‐fluorouracil (5‐FU) in the preoperative chemoradiation treatment of patients with rectal cancer. Patients and Methods The files of 89 patients with rectal cancer, 43 treated preoperatively with oral ca...

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Veröffentlicht in:Journal of surgical oncology 2006-06, Vol.93 (7), p.529-533
Hauptverfasser: Yerushalmi, Rinat, Idelevich, Efraim, Dror, Ygael, Stemmer, Salomon M., Figer, Arie, Sulkes, Aaron, Brenner, Baruch, Loven, David, Dreznik, Zeev, Nudelman, Israel, Shani, Adi, Fenig, Eyal
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container_end_page 533
container_issue 7
container_start_page 529
container_title Journal of surgical oncology
container_volume 93
creator Yerushalmi, Rinat
Idelevich, Efraim
Dror, Ygael
Stemmer, Salomon M.
Figer, Arie
Sulkes, Aaron
Brenner, Baruch
Loven, David
Dreznik, Zeev
Nudelman, Israel
Shani, Adi
Fenig, Eyal
description Background We compared the efficacy and toxicity of oral capecitabine and continuous infusion of 5‐fluorouracil (5‐FU) in the preoperative chemoradiation treatment of patients with rectal cancer. Patients and Methods The files of 89 patients with rectal cancer, 43 treated preoperatively with oral capecitabine and 46 with intravenous 5‐FU, were reviewed, and the outcome of the groups was compared. Results There was no statistically significant difference in the complete pathological response rate between the capecitabine and the 5‐FU groups (30% vs. 17%, P = 0.15). The downstaging rate was higher in the capecitabine group (77% vs. 50%, P = 0.009). Toxicity was mild in both groups. The rate of Grade 3 gastrointestinal toxicity was similar in the two groups (diarrhea 2% vs. 4%, proctitis 5% vs. 7%), except for one patient in the 5‐FU group (2%) who developed a rectovaginal fistula. In the capecitabine group, one patient (2%) had Grade 3 hand‐foot syndrome, and another had an acute myocardial infarction. In the 5‐FU group, two patients (4%) had Grade 3 hematological toxicity, and three (6%) had complications from Port‐a‐Cath insertion. Conclusion Preoperative chemoradiation with oral capecitabine appears to be safe and well tolerated, and at least as good as continuous 5‐FU. J. Surg. Oncol. 2006;93:529–533. © 2006 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jso.20503
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Patients and Methods The files of 89 patients with rectal cancer, 43 treated preoperatively with oral capecitabine and 46 with intravenous 5‐FU, were reviewed, and the outcome of the groups was compared. Results There was no statistically significant difference in the complete pathological response rate between the capecitabine and the 5‐FU groups (30% vs. 17%, P = 0.15). The downstaging rate was higher in the capecitabine group (77% vs. 50%, P = 0.009). Toxicity was mild in both groups. The rate of Grade 3 gastrointestinal toxicity was similar in the two groups (diarrhea 2% vs. 4%, proctitis 5% vs. 7%), except for one patient in the 5‐FU group (2%) who developed a rectovaginal fistula. In the capecitabine group, one patient (2%) had Grade 3 hand‐foot syndrome, and another had an acute myocardial infarction. In the 5‐FU group, two patients (4%) had Grade 3 hematological toxicity, and three (6%) had complications from Port‐a‐Cath insertion. Conclusion Preoperative chemoradiation with oral capecitabine appears to be safe and well tolerated, and at least as good as continuous 5‐FU. J. Surg. Oncol. 2006;93:529–533. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0022-4790</identifier><identifier>EISSN: 1096-9098</identifier><identifier>DOI: 10.1002/jso.20503</identifier><identifier>PMID: 16705722</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Administration, Oral ; Adult ; Aged ; Aged, 80 and over ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Capecitabine ; continuous-infusion 5-FU ; Deoxycytidine - administration &amp; dosage ; Deoxycytidine - adverse effects ; Deoxycytidine - analogs &amp; derivatives ; Diarrhea - chemically induced ; Drug Administration Schedule ; Female ; Fluorouracil - administration &amp; dosage ; Fluorouracil - adverse effects ; Humans ; Infusions, Intravenous ; Male ; Middle Aged ; Neoadjuvant Therapy ; preoperative chemoradiation ; rectal cancer ; Rectal Neoplasms - drug therapy ; Rectal Neoplasms - pathology ; Rectal Neoplasms - radiotherapy ; Rectal Neoplasms - surgery ; Retrospective Studies ; Treatment Outcome</subject><ispartof>Journal of surgical oncology, 2006-06, Vol.93 (7), p.529-533</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>Copyright 2006 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4273-86ce037c37711459e40e76f44497493137e7148a036087dafc25275de16ae4e43</citedby><cites>FETCH-LOGICAL-c4273-86ce037c37711459e40e76f44497493137e7148a036087dafc25275de16ae4e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjso.20503$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjso.20503$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16705722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yerushalmi, Rinat</creatorcontrib><creatorcontrib>Idelevich, Efraim</creatorcontrib><creatorcontrib>Dror, Ygael</creatorcontrib><creatorcontrib>Stemmer, Salomon M.</creatorcontrib><creatorcontrib>Figer, Arie</creatorcontrib><creatorcontrib>Sulkes, Aaron</creatorcontrib><creatorcontrib>Brenner, Baruch</creatorcontrib><creatorcontrib>Loven, David</creatorcontrib><creatorcontrib>Dreznik, Zeev</creatorcontrib><creatorcontrib>Nudelman, Israel</creatorcontrib><creatorcontrib>Shani, Adi</creatorcontrib><creatorcontrib>Fenig, Eyal</creatorcontrib><title>Preoperative chemoradiation in rectal cancer: Retrospective comparison between capecitabine and continuous infusion of 5-fluorouracil</title><title>Journal of surgical oncology</title><addtitle>J. Surg. Oncol</addtitle><description>Background We compared the efficacy and toxicity of oral capecitabine and continuous infusion of 5‐fluorouracil (5‐FU) in the preoperative chemoradiation treatment of patients with rectal cancer. Patients and Methods The files of 89 patients with rectal cancer, 43 treated preoperatively with oral capecitabine and 46 with intravenous 5‐FU, were reviewed, and the outcome of the groups was compared. Results There was no statistically significant difference in the complete pathological response rate between the capecitabine and the 5‐FU groups (30% vs. 17%, P = 0.15). The downstaging rate was higher in the capecitabine group (77% vs. 50%, P = 0.009). Toxicity was mild in both groups. The rate of Grade 3 gastrointestinal toxicity was similar in the two groups (diarrhea 2% vs. 4%, proctitis 5% vs. 7%), except for one patient in the 5‐FU group (2%) who developed a rectovaginal fistula. In the capecitabine group, one patient (2%) had Grade 3 hand‐foot syndrome, and another had an acute myocardial infarction. In the 5‐FU group, two patients (4%) had Grade 3 hematological toxicity, and three (6%) had complications from Port‐a‐Cath insertion. Conclusion Preoperative chemoradiation with oral capecitabine appears to be safe and well tolerated, and at least as good as continuous 5‐FU. J. Surg. 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Surg. Oncol</addtitle><date>2006-06-01</date><risdate>2006</risdate><volume>93</volume><issue>7</issue><spage>529</spage><epage>533</epage><pages>529-533</pages><issn>0022-4790</issn><eissn>1096-9098</eissn><abstract>Background We compared the efficacy and toxicity of oral capecitabine and continuous infusion of 5‐fluorouracil (5‐FU) in the preoperative chemoradiation treatment of patients with rectal cancer. Patients and Methods The files of 89 patients with rectal cancer, 43 treated preoperatively with oral capecitabine and 46 with intravenous 5‐FU, were reviewed, and the outcome of the groups was compared. Results There was no statistically significant difference in the complete pathological response rate between the capecitabine and the 5‐FU groups (30% vs. 17%, P = 0.15). The downstaging rate was higher in the capecitabine group (77% vs. 50%, P = 0.009). Toxicity was mild in both groups. 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subjects Administration, Oral
Adult
Aged
Aged, 80 and over
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Capecitabine
continuous-infusion 5-FU
Deoxycytidine - administration & dosage
Deoxycytidine - adverse effects
Deoxycytidine - analogs & derivatives
Diarrhea - chemically induced
Drug Administration Schedule
Female
Fluorouracil - administration & dosage
Fluorouracil - adverse effects
Humans
Infusions, Intravenous
Male
Middle Aged
Neoadjuvant Therapy
preoperative chemoradiation
rectal cancer
Rectal Neoplasms - drug therapy
Rectal Neoplasms - pathology
Rectal Neoplasms - radiotherapy
Rectal Neoplasms - surgery
Retrospective Studies
Treatment Outcome
title Preoperative chemoradiation in rectal cancer: Retrospective comparison between capecitabine and continuous infusion of 5-fluorouracil
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