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A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: a Hellenic Cooperative Oncology Group study
Colon cancer is a public health problem worldwide. Adjuvant chemotherapy after surgical resection for stage III colon cancer has been shown to improve both progression-free and overall survival, and is currently recommended as standard therapy. However, its value for patients with stage II disease r...
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Published in: | BMC medicine 2011-01, Vol.9 (1), p.10-10, Article 10 |
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creator | Papadimitriou, Christos A Papakostas, Pavlos Karina, Maria Malettou, Lia Dimopoulos, Meletios A Pentheroudakis, George Samantas, Epaminontas Bamias, Aristotelis Miliaras, Dimosthenis Basdanis, George Xiros, Nikolaos Klouvas, George Bafaloukos, Dimitrios Kafiri, Georgia Papaspirou, Irene Pectasides, Dimitrios Karanikiotis, Charisios Economopoulos, Theofanis Efstratiou, Ioannis Korantzis, Ippokratis Pisanidis, Nikolaos Makatsoris, Thomas Matsiakou, Fotini Aravantinos, Gerasimos Kalofonos, Haralabos P Fountzilas, George |
description | Colon cancer is a public health problem worldwide. Adjuvant chemotherapy after surgical resection for stage III colon cancer has been shown to improve both progression-free and overall survival, and is currently recommended as standard therapy. However, its value for patients with stage II disease remains controversial. When this study was designed 5-fluorouracil (5FU) plus leucovorin (LV) was standard adjuvant treatment for colon cancer. Irinotecan (CPT-11) is a topoisomerase I inhibitor with activity in metastatic disease. In this multicenter adjuvant phase III trial, we evaluated the addition of irinotecan to weekly 5FU plus LV in patients with stage II or III colon cancer.
The study included 873 eligible patients. The treatment consisted of weekly administration of irinotecan 80 mg/m2 intravenously (i.v.), LV 200 mg/m2 and 5FU 450 mg/m2 bolus (Arm A) versus LV 200 mg/m2 and 5FU 500 mg/m2 i.v. bolus (Arm B). In Arm A, treatments were administered weekly for four consecutive weeks, followed by a two-week rest, for a total of six cycles, while in Arm B treatments were administered weekly for six consecutive weeks, followed by a two-week rest, for a total of four cycles. The primary end-point was disease-free survival (DFS) at three years.
The probability of overall survival (OS) at three years was 0.88 for patients in Arm A and 0.86 for those in Arm B, while the five-year OS probability was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.436). Furthermore, the probability of DFS at three years was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.334). With the exception of leucopenia and neutropenia, which were higher in patients in Arm A, there were no significant differences in Grades 3 and 4 toxicities between the two regimens. The most frequently recorded Grade 3/4 toxicity was diarrhea in both treatment arms.
Irinotecan added to weekly bolus 5FU plus LV did not result in improvement in disease-free or overall survival in stage II or III colon cancer, but did increase toxicity.
Australian New Zealand Clinical Trials Registry: ACTRN12610000148077. |
doi_str_mv | 10.1186/1741-7015-9-10 |
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The study included 873 eligible patients. The treatment consisted of weekly administration of irinotecan 80 mg/m2 intravenously (i.v.), LV 200 mg/m2 and 5FU 450 mg/m2 bolus (Arm A) versus LV 200 mg/m2 and 5FU 500 mg/m2 i.v. bolus (Arm B). In Arm A, treatments were administered weekly for four consecutive weeks, followed by a two-week rest, for a total of six cycles, while in Arm B treatments were administered weekly for six consecutive weeks, followed by a two-week rest, for a total of four cycles. The primary end-point was disease-free survival (DFS) at three years.
The probability of overall survival (OS) at three years was 0.88 for patients in Arm A and 0.86 for those in Arm B, while the five-year OS probability was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.436). Furthermore, the probability of DFS at three years was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.334). With the exception of leucopenia and neutropenia, which were higher in patients in Arm A, there were no significant differences in Grades 3 and 4 toxicities between the two regimens. The most frequently recorded Grade 3/4 toxicity was diarrhea in both treatment arms.
Irinotecan added to weekly bolus 5FU plus LV did not result in improvement in disease-free or overall survival in stage II or III colon cancer, but did increase toxicity.
Australian New Zealand Clinical Trials Registry: ACTRN12610000148077.</description><identifier>ISSN: 1741-7015</identifier><identifier>EISSN: 1741-7015</identifier><identifier>DOI: 10.1186/1741-7015-9-10</identifier><identifier>PMID: 21281463</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject><![CDATA[Acquisitions & mergers ; Adult ; Aged ; Antineoplastic Agents - therapeutic use ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Camptothecin - administration & dosage ; Camptothecin - adverse effects ; Camptothecin - analogs & derivatives ; Camptothecin - therapeutic use ; Cancer ; Cancer therapies ; Chemotherapy ; Chemotherapy, Adjuvant ; Clinical medicine ; Clinical trials ; Colon cancer ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - pathology ; Colorectal cancer ; Dose-Response Relationship, Drug ; Drug therapy ; Drug therapy, Combination ; Female ; Fluorouracil ; Fluorouracil - administration & dosage ; Fluorouracil - adverse effects ; Fluorouracil - therapeutic use ; Greece ; Health aspects ; Heart attacks ; Histology ; Hospitals ; Humans ; Kaplan-Meier Estimate ; Leucovorin ; Leucovorin - administration & dosage ; Leucovorin - adverse effects ; Leucovorin - therapeutic use ; Male ; Medical imaging ; Medicine ; Middle Aged ; Mortality ; Neoplasm Staging ; Patient outcomes ; Statistical analysis ; Tomography ; Treatment Outcome ; Young Adult]]></subject><ispartof>BMC medicine, 2011-01, Vol.9 (1), p.10-10, Article 10</ispartof><rights>COPYRIGHT 2011 BioMed Central Ltd.</rights><rights>2011 Papadimitriou et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2011 Papadimitriou et al; licensee BioMed Central Ltd. 2011 Papadimitriou et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b638t-e0283f8aec153e38081c6ac8a9c0d3a5425a8633f00334a5b578dabff83c12433</citedby><cites>FETCH-LOGICAL-b638t-e0283f8aec153e38081c6ac8a9c0d3a5425a8633f00334a5b578dabff83c12433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3038965/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/902280875?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21281463$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Papadimitriou, Christos A</creatorcontrib><creatorcontrib>Papakostas, Pavlos</creatorcontrib><creatorcontrib>Karina, Maria</creatorcontrib><creatorcontrib>Malettou, Lia</creatorcontrib><creatorcontrib>Dimopoulos, Meletios A</creatorcontrib><creatorcontrib>Pentheroudakis, George</creatorcontrib><creatorcontrib>Samantas, Epaminontas</creatorcontrib><creatorcontrib>Bamias, Aristotelis</creatorcontrib><creatorcontrib>Miliaras, Dimosthenis</creatorcontrib><creatorcontrib>Basdanis, George</creatorcontrib><creatorcontrib>Xiros, Nikolaos</creatorcontrib><creatorcontrib>Klouvas, George</creatorcontrib><creatorcontrib>Bafaloukos, Dimitrios</creatorcontrib><creatorcontrib>Kafiri, Georgia</creatorcontrib><creatorcontrib>Papaspirou, Irene</creatorcontrib><creatorcontrib>Pectasides, Dimitrios</creatorcontrib><creatorcontrib>Karanikiotis, Charisios</creatorcontrib><creatorcontrib>Economopoulos, Theofanis</creatorcontrib><creatorcontrib>Efstratiou, Ioannis</creatorcontrib><creatorcontrib>Korantzis, Ippokratis</creatorcontrib><creatorcontrib>Pisanidis, Nikolaos</creatorcontrib><creatorcontrib>Makatsoris, Thomas</creatorcontrib><creatorcontrib>Matsiakou, Fotini</creatorcontrib><creatorcontrib>Aravantinos, Gerasimos</creatorcontrib><creatorcontrib>Kalofonos, Haralabos P</creatorcontrib><creatorcontrib>Fountzilas, George</creatorcontrib><title>A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: a Hellenic Cooperative Oncology Group study</title><title>BMC medicine</title><addtitle>BMC Med</addtitle><description>Colon cancer is a public health problem worldwide. Adjuvant chemotherapy after surgical resection for stage III colon cancer has been shown to improve both progression-free and overall survival, and is currently recommended as standard therapy. However, its value for patients with stage II disease remains controversial. When this study was designed 5-fluorouracil (5FU) plus leucovorin (LV) was standard adjuvant treatment for colon cancer. Irinotecan (CPT-11) is a topoisomerase I inhibitor with activity in metastatic disease. In this multicenter adjuvant phase III trial, we evaluated the addition of irinotecan to weekly 5FU plus LV in patients with stage II or III colon cancer.
The study included 873 eligible patients. The treatment consisted of weekly administration of irinotecan 80 mg/m2 intravenously (i.v.), LV 200 mg/m2 and 5FU 450 mg/m2 bolus (Arm A) versus LV 200 mg/m2 and 5FU 500 mg/m2 i.v. bolus (Arm B). In Arm A, treatments were administered weekly for four consecutive weeks, followed by a two-week rest, for a total of six cycles, while in Arm B treatments were administered weekly for six consecutive weeks, followed by a two-week rest, for a total of four cycles. The primary end-point was disease-free survival (DFS) at three years.
The probability of overall survival (OS) at three years was 0.88 for patients in Arm A and 0.86 for those in Arm B, while the five-year OS probability was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.436). Furthermore, the probability of DFS at three years was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.334). With the exception of leucopenia and neutropenia, which were higher in patients in Arm A, there were no significant differences in Grades 3 and 4 toxicities between the two regimens. The most frequently recorded Grade 3/4 toxicity was diarrhea in both treatment arms.
Irinotecan added to weekly bolus 5FU plus LV did not result in improvement in disease-free or overall survival in stage II or III colon cancer, but did increase toxicity.
Australian New Zealand Clinical Trials Registry: ACTRN12610000148077.</description><subject>Acquisitions & mergers</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Camptothecin - administration & dosage</subject><subject>Camptothecin - adverse effects</subject><subject>Camptothecin - analogs & derivatives</subject><subject>Camptothecin - therapeutic use</subject><subject>Cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Clinical medicine</subject><subject>Clinical trials</subject><subject>Colon cancer</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug therapy</subject><subject>Drug therapy, Combination</subject><subject>Female</subject><subject>Fluorouracil</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - adverse effects</subject><subject>Fluorouracil - therapeutic use</subject><subject>Greece</subject><subject>Health aspects</subject><subject>Heart attacks</subject><subject>Histology</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Leucovorin</subject><subject>Leucovorin - administration & dosage</subject><subject>Leucovorin - adverse effects</subject><subject>Leucovorin - therapeutic use</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Medicine</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Neoplasm Staging</subject><subject>Patient outcomes</subject><subject>Statistical analysis</subject><subject>Tomography</subject><subject>Treatment Outcome</subject><subject>Young 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Combination</topic><topic>Female</topic><topic>Fluorouracil</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - adverse effects</topic><topic>Fluorouracil - therapeutic use</topic><topic>Greece</topic><topic>Health aspects</topic><topic>Heart attacks</topic><topic>Histology</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Leucovorin</topic><topic>Leucovorin - administration & dosage</topic><topic>Leucovorin - adverse effects</topic><topic>Leucovorin - therapeutic use</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Medicine</topic><topic>Middle Aged</topic><topic>Mortality</topic><topic>Neoplasm Staging</topic><topic>Patient outcomes</topic><topic>Statistical analysis</topic><topic>Tomography</topic><topic>Treatment Outcome</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Papadimitriou, Christos A</creatorcontrib><creatorcontrib>Papakostas, Pavlos</creatorcontrib><creatorcontrib>Karina, Maria</creatorcontrib><creatorcontrib>Malettou, Lia</creatorcontrib><creatorcontrib>Dimopoulos, Meletios A</creatorcontrib><creatorcontrib>Pentheroudakis, George</creatorcontrib><creatorcontrib>Samantas, Epaminontas</creatorcontrib><creatorcontrib>Bamias, Aristotelis</creatorcontrib><creatorcontrib>Miliaras, Dimosthenis</creatorcontrib><creatorcontrib>Basdanis, George</creatorcontrib><creatorcontrib>Xiros, Nikolaos</creatorcontrib><creatorcontrib>Klouvas, George</creatorcontrib><creatorcontrib>Bafaloukos, Dimitrios</creatorcontrib><creatorcontrib>Kafiri, Georgia</creatorcontrib><creatorcontrib>Papaspirou, Irene</creatorcontrib><creatorcontrib>Pectasides, Dimitrios</creatorcontrib><creatorcontrib>Karanikiotis, Charisios</creatorcontrib><creatorcontrib>Economopoulos, Theofanis</creatorcontrib><creatorcontrib>Efstratiou, Ioannis</creatorcontrib><creatorcontrib>Korantzis, Ippokratis</creatorcontrib><creatorcontrib>Pisanidis, Nikolaos</creatorcontrib><creatorcontrib>Makatsoris, Thomas</creatorcontrib><creatorcontrib>Matsiakou, Fotini</creatorcontrib><creatorcontrib>Aravantinos, Gerasimos</creatorcontrib><creatorcontrib>Kalofonos, Haralabos P</creatorcontrib><creatorcontrib>Fountzilas, George</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Virology and AIDS Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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 UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Publicly Available Content 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><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Papadimitriou, Christos A</au><au>Papakostas, Pavlos</au><au>Karina, Maria</au><au>Malettou, Lia</au><au>Dimopoulos, Meletios A</au><au>Pentheroudakis, George</au><au>Samantas, Epaminontas</au><au>Bamias, Aristotelis</au><au>Miliaras, Dimosthenis</au><au>Basdanis, George</au><au>Xiros, Nikolaos</au><au>Klouvas, George</au><au>Bafaloukos, Dimitrios</au><au>Kafiri, Georgia</au><au>Papaspirou, Irene</au><au>Pectasides, Dimitrios</au><au>Karanikiotis, Charisios</au><au>Economopoulos, Theofanis</au><au>Efstratiou, Ioannis</au><au>Korantzis, Ippokratis</au><au>Pisanidis, Nikolaos</au><au>Makatsoris, Thomas</au><au>Matsiakou, Fotini</au><au>Aravantinos, Gerasimos</au><au>Kalofonos, Haralabos P</au><au>Fountzilas, George</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: a Hellenic Cooperative Oncology Group study</atitle><jtitle>BMC medicine</jtitle><addtitle>BMC Med</addtitle><date>2011-01-31</date><risdate>2011</risdate><volume>9</volume><issue>1</issue><spage>10</spage><epage>10</epage><pages>10-10</pages><artnum>10</artnum><issn>1741-7015</issn><eissn>1741-7015</eissn><abstract>Colon cancer is a public health problem worldwide. Adjuvant chemotherapy after surgical resection for stage III colon cancer has been shown to improve both progression-free and overall survival, and is currently recommended as standard therapy. However, its value for patients with stage II disease remains controversial. When this study was designed 5-fluorouracil (5FU) plus leucovorin (LV) was standard adjuvant treatment for colon cancer. Irinotecan (CPT-11) is a topoisomerase I inhibitor with activity in metastatic disease. In this multicenter adjuvant phase III trial, we evaluated the addition of irinotecan to weekly 5FU plus LV in patients with stage II or III colon cancer.
The study included 873 eligible patients. The treatment consisted of weekly administration of irinotecan 80 mg/m2 intravenously (i.v.), LV 200 mg/m2 and 5FU 450 mg/m2 bolus (Arm A) versus LV 200 mg/m2 and 5FU 500 mg/m2 i.v. bolus (Arm B). In Arm A, treatments were administered weekly for four consecutive weeks, followed by a two-week rest, for a total of six cycles, while in Arm B treatments were administered weekly for six consecutive weeks, followed by a two-week rest, for a total of four cycles. The primary end-point was disease-free survival (DFS) at three years.
The probability of overall survival (OS) at three years was 0.88 for patients in Arm A and 0.86 for those in Arm B, while the five-year OS probability was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.436). Furthermore, the probability of DFS at three years was 0.78 and 0.76 for patients in Arm A and Arm B, respectively (P = 0.334). With the exception of leucopenia and neutropenia, which were higher in patients in Arm A, there were no significant differences in Grades 3 and 4 toxicities between the two regimens. The most frequently recorded Grade 3/4 toxicity was diarrhea in both treatment arms.
Irinotecan added to weekly bolus 5FU plus LV did not result in improvement in disease-free or overall survival in stage II or III colon cancer, but did increase toxicity.
Australian New Zealand Clinical Trials Registry: ACTRN12610000148077.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>21281463</pmid><doi>10.1186/1741-7015-9-10</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1741-7015 |
ispartof | BMC medicine, 2011-01, Vol.9 (1), p.10-10, Article 10 |
issn | 1741-7015 1741-7015 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_abe5201e2693437496d37ad7a36329c5 |
source | Publicly Available Content Database; PubMed Central |
subjects | Acquisitions & mergers Adult Aged Antineoplastic Agents - therapeutic use Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Antineoplastic Combined Chemotherapy Protocols - therapeutic use Camptothecin - administration & dosage Camptothecin - adverse effects Camptothecin - analogs & derivatives Camptothecin - therapeutic use Cancer Cancer therapies Chemotherapy Chemotherapy, Adjuvant Clinical medicine Clinical trials Colon cancer Colonic Neoplasms - drug therapy Colonic Neoplasms - pathology Colorectal cancer Dose-Response Relationship, Drug Drug therapy Drug therapy, Combination Female Fluorouracil Fluorouracil - administration & dosage Fluorouracil - adverse effects Fluorouracil - therapeutic use Greece Health aspects Heart attacks Histology Hospitals Humans Kaplan-Meier Estimate Leucovorin Leucovorin - administration & dosage Leucovorin - adverse effects Leucovorin - therapeutic use Male Medical imaging Medicine Middle Aged Mortality Neoplasm Staging Patient outcomes Statistical analysis Tomography Treatment Outcome Young Adult |
title | A randomized phase III trial of adjuvant chemotherapy with irinotecan, leucovorin and fluorouracil versus leucovorin and fluorouracil for stage II and III colon cancer: a Hellenic Cooperative Oncology Group study |
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