Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study
The concurrent administration of adjuvant chemotherapy and radiotherapy in breast cancer treatment might lead to an increased incidence of side-effects. In this prospective, non-randomised, comparative study, the acute toxicity of radiotherapy alone (RT) and radiotherapy concurrent with doxorubicin-...
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Veröffentlicht in: | European journal of cancer (1990) 2003-05, Vol.39 (8), p.1081-1088 |
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description | The concurrent administration of adjuvant chemotherapy and radiotherapy in breast cancer treatment might lead to an increased incidence of side-effects. In this prospective, non-randomised, comparative study, the acute toxicity of radiotherapy alone (RT) and radiotherapy concurrent with doxorubicin-cyclophosphamide (AC/RT) and radiotherapy concurrent with cyclophosphamide-methotrexate-5-fluorouracil (CMF/RT) was compared. We used the common toxicity criteria (CTC) to score the level of acute toxicity before, during and 6 months after the completion of the period of irradiation. The number of hospital admissions, as well as the compliance of chemotherapy, were noted. We observed that patients treated with AC/RT and CMF/RT had significant higher incidences of (high-grade) skin-toxicity, oesophagitis, dyspnoea, malaise, anorexia, nausea and hospital admission compared with those treated with RT only. The target-volume of radiotherapy was the main predictor of (high-grade) acute skin toxicity and oesophagitis. AC/RT was associated with significant more (high-grade) skin toxicity than CMF/RT. The dose of chemotherapy was reduced to less than 85% of the planned dose in 11% of patients, 17% of patients treated with concurrent chemotherapy and radiotherapy needed admission to hospital. From the results of our study, we conclude that the concurrent administration of adjuvant chemotherapy and radiotherapy leads to an unacceptably high level of acute toxicity. |
doi_str_mv | 10.1016/S0959-8049(03)00178-3 |
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In this prospective, non-randomised, comparative study, the acute toxicity of radiotherapy alone (RT) and radiotherapy concurrent with doxorubicin-cyclophosphamide (AC/RT) and radiotherapy concurrent with cyclophosphamide-methotrexate-5-fluorouracil (CMF/RT) was compared. We used the common toxicity criteria (CTC) to score the level of acute toxicity before, during and 6 months after the completion of the period of irradiation. The number of hospital admissions, as well as the compliance of chemotherapy, were noted. We observed that patients treated with AC/RT and CMF/RT had significant higher incidences of (high-grade) skin-toxicity, oesophagitis, dyspnoea, malaise, anorexia, nausea and hospital admission compared with those treated with RT only. The target-volume of radiotherapy was the main predictor of (high-grade) acute skin toxicity and oesophagitis. AC/RT was associated with significant more (high-grade) skin toxicity than CMF/RT. The dose of chemotherapy was reduced to less than 85% of the planned dose in 11% of patients, 17% of patients treated with concurrent chemotherapy and radiotherapy needed admission to hospital. From the results of our study, we conclude that the concurrent administration of adjuvant chemotherapy and radiotherapy leads to an unacceptably high level of acute toxicity.</description><identifier>ISSN: 0959-8049</identifier><identifier>EISSN: 1879-0852</identifier><identifier>DOI: 10.1016/S0959-8049(03)00178-3</identifier><identifier>PMID: 12736107</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Acute toxicity ; Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Biological and medical sciences ; Breast cancer ; Breast Neoplasms - drug therapy ; Breast Neoplasms - radiotherapy ; Breast Neoplasms - surgery ; Chemotherapy, Adjuvant - adverse effects ; Combined modality therapy ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - adverse effects ; Doxorubicin - administration & dosage ; Doxorubicin - adverse effects ; Female ; Fluorouracil - administration & dosage ; Fluorouracil - adverse effects ; Gynecology. Andrology. Obstetrics ; Hospitalization ; Humans ; Mammary gland diseases ; Mastectomy, Radical ; Medical sciences ; Methotrexate - administration & dosage ; Methotrexate - adverse effects ; Middle Aged ; Prognosis ; Prospective Studies ; Radiotherapy, Adjuvant - adverse effects ; Risk Factors ; Tumors</subject><ispartof>European journal of cancer (1990), 2003-05, Vol.39 (8), p.1081-1088</ispartof><rights>2003 Elsevier Science Ltd</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0959-8049(03)00178-3$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14750050$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12736107$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fiets, W.E</creatorcontrib><creatorcontrib>van Helvoirt, R.P</creatorcontrib><creatorcontrib>Nortier, J.W.R</creatorcontrib><creatorcontrib>van der Tweel, I</creatorcontrib><creatorcontrib>Struikmans, H</creatorcontrib><title>Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study</title><title>European journal of cancer (1990)</title><addtitle>Eur J Cancer</addtitle><description>The concurrent administration of adjuvant chemotherapy and radiotherapy in breast cancer treatment might lead to an increased incidence of side-effects. In this prospective, non-randomised, comparative study, the acute toxicity of radiotherapy alone (RT) and radiotherapy concurrent with doxorubicin-cyclophosphamide (AC/RT) and radiotherapy concurrent with cyclophosphamide-methotrexate-5-fluorouracil (CMF/RT) was compared. We used the common toxicity criteria (CTC) to score the level of acute toxicity before, during and 6 months after the completion of the period of irradiation. The number of hospital admissions, as well as the compliance of chemotherapy, were noted. We observed that patients treated with AC/RT and CMF/RT had significant higher incidences of (high-grade) skin-toxicity, oesophagitis, dyspnoea, malaise, anorexia, nausea and hospital admission compared with those treated with RT only. The target-volume of radiotherapy was the main predictor of (high-grade) acute skin toxicity and oesophagitis. AC/RT was associated with significant more (high-grade) skin toxicity than CMF/RT. The dose of chemotherapy was reduced to less than 85% of the planned dose in 11% of patients, 17% of patients treated with concurrent chemotherapy and radiotherapy needed admission to hospital. From the results of our study, we conclude that the concurrent administration of adjuvant chemotherapy and radiotherapy leads to an unacceptably high level of acute toxicity.</description><subject>Acute toxicity</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - radiotherapy</subject><subject>Breast Neoplasms - surgery</subject><subject>Chemotherapy, Adjuvant - adverse effects</subject><subject>Combined modality therapy</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Cyclophosphamide - adverse effects</subject><subject>Doxorubicin - administration & dosage</subject><subject>Doxorubicin - adverse effects</subject><subject>Female</subject><subject>Fluorouracil - administration & dosage</subject><subject>Fluorouracil - adverse effects</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Mammary gland diseases</subject><subject>Mastectomy, Radical</subject><subject>Medical sciences</subject><subject>Methotrexate - administration & dosage</subject><subject>Methotrexate - adverse effects</subject><subject>Middle Aged</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Radiotherapy, Adjuvant - adverse effects</subject><subject>Risk Factors</subject><subject>Tumors</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkdtqFTEUhoModlt9BCU3QguOrkzmlN7IZmNVqHihXoeVZA1N6UyGJLNxP4sva9pd69U68PGvw8_YawHvBYjuww9QraoGaNQZyHMA0Q-VfMI2YuhVBUNbP2WbR-SEvUjpBgD6oYHn7ETUvewE9Bv2Z2vXTDyH3976fOBh5DbMdo2R5szR3ax7LElE50O-pojLgePsuL2m6bFxtvt2yUPk29059zM3kTBlbnG2FPmC2RetdMGRLzGkhWz2e3pX5kwLRjwWc5irWITD5BM5nvLqDi_ZsxFvE716iKfs1-Wnn7sv1dX3z19326uKaiVzhbJTtUXVGwuuVa10gpRqetPJYaR2HA0qMwoyXYND3bUEZrRG2K5zcpQg5Sl7c9RdVjOR00v0E8aD_velArx9ADBZvB3Lotan_1zTtwAtFO7jkaOy7d5T1MmW2y05H8vV2gWvBeg7__S9f_rOHA1S3_unpfwLJy-PKg</recordid><startdate>20030501</startdate><enddate>20030501</enddate><creator>Fiets, W.E</creator><creator>van Helvoirt, R.P</creator><creator>Nortier, J.W.R</creator><creator>van der Tweel, I</creator><creator>Struikmans, H</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20030501</creationdate><title>Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study</title><author>Fiets, W.E ; van Helvoirt, R.P ; Nortier, J.W.R ; van der Tweel, I ; Struikmans, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e293t-a3692ca97bc0d5953d1e9947b638fe5ffba9bf1eb64a8265e0bfcb1c66d3f3033</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Acute toxicity</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - radiotherapy</topic><topic>Breast Neoplasms - surgery</topic><topic>Chemotherapy, Adjuvant - adverse effects</topic><topic>Combined modality therapy</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Cyclophosphamide - adverse effects</topic><topic>Doxorubicin - administration & dosage</topic><topic>Doxorubicin - adverse effects</topic><topic>Female</topic><topic>Fluorouracil - administration & dosage</topic><topic>Fluorouracil - adverse effects</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Hospitalization</topic><topic>Humans</topic><topic>Mammary gland diseases</topic><topic>Mastectomy, Radical</topic><topic>Medical sciences</topic><topic>Methotrexate - administration & dosage</topic><topic>Methotrexate - adverse effects</topic><topic>Middle Aged</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Radiotherapy, Adjuvant - adverse effects</topic><topic>Risk Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fiets, W.E</creatorcontrib><creatorcontrib>van Helvoirt, R.P</creatorcontrib><creatorcontrib>Nortier, J.W.R</creatorcontrib><creatorcontrib>van der Tweel, I</creatorcontrib><creatorcontrib>Struikmans, H</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>European journal of cancer (1990)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fiets, W.E</au><au>van Helvoirt, R.P</au><au>Nortier, J.W.R</au><au>van der Tweel, I</au><au>Struikmans, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study</atitle><jtitle>European journal of cancer (1990)</jtitle><addtitle>Eur J Cancer</addtitle><date>2003-05-01</date><risdate>2003</risdate><volume>39</volume><issue>8</issue><spage>1081</spage><epage>1088</epage><pages>1081-1088</pages><issn>0959-8049</issn><eissn>1879-0852</eissn><abstract>The concurrent administration of adjuvant chemotherapy and radiotherapy in breast cancer treatment might lead to an increased incidence of side-effects. In this prospective, non-randomised, comparative study, the acute toxicity of radiotherapy alone (RT) and radiotherapy concurrent with doxorubicin-cyclophosphamide (AC/RT) and radiotherapy concurrent with cyclophosphamide-methotrexate-5-fluorouracil (CMF/RT) was compared. We used the common toxicity criteria (CTC) to score the level of acute toxicity before, during and 6 months after the completion of the period of irradiation. The number of hospital admissions, as well as the compliance of chemotherapy, were noted. We observed that patients treated with AC/RT and CMF/RT had significant higher incidences of (high-grade) skin-toxicity, oesophagitis, dyspnoea, malaise, anorexia, nausea and hospital admission compared with those treated with RT only. The target-volume of radiotherapy was the main predictor of (high-grade) acute skin toxicity and oesophagitis. AC/RT was associated with significant more (high-grade) skin toxicity than CMF/RT. The dose of chemotherapy was reduced to less than 85% of the planned dose in 11% of patients, 17% of patients treated with concurrent chemotherapy and radiotherapy needed admission to hospital. From the results of our study, we conclude that the concurrent administration of adjuvant chemotherapy and radiotherapy leads to an unacceptably high level of acute toxicity.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12736107</pmid><doi>10.1016/S0959-8049(03)00178-3</doi><tpages>8</tpages></addata></record> |
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subjects | Acute toxicity Adult Aged Antineoplastic Combined Chemotherapy Protocols - administration & dosage Antineoplastic Combined Chemotherapy Protocols - adverse effects Biological and medical sciences Breast cancer Breast Neoplasms - drug therapy Breast Neoplasms - radiotherapy Breast Neoplasms - surgery Chemotherapy, Adjuvant - adverse effects Combined modality therapy Cyclophosphamide - administration & dosage Cyclophosphamide - adverse effects Doxorubicin - administration & dosage Doxorubicin - adverse effects Female Fluorouracil - administration & dosage Fluorouracil - adverse effects Gynecology. Andrology. Obstetrics Hospitalization Humans Mammary gland diseases Mastectomy, Radical Medical sciences Methotrexate - administration & dosage Methotrexate - adverse effects Middle Aged Prognosis Prospective Studies Radiotherapy, Adjuvant - adverse effects Risk Factors Tumors |
title | Acute toxicity of concurrent adjuvant radiotherapy and chemotherapy (CMF or AC) in breast cancer patients: a prospective, comparative, non-randomised study |
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