Chemoradiation paradigm for the treatment of lung cancer
For the treatment of advanced non-small-cell lung cancer, randomized controlled trials have shown that platinum-based chemotherapy and radiotherapy provide a measurable survival benefit compared with radiotherapy alone. Newer drugs that target growth factor receptors might further synergize with ion...
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Veröffentlicht in: | Nature clinical practice. Oncology 2006-04, Vol.3 (4), p.188-199 |
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description | For the treatment of advanced non-small-cell lung cancer, randomized controlled trials have shown that platinum-based chemotherapy and radiotherapy provide a measurable survival benefit compared with radiotherapy alone. Newer drugs that target growth factor receptors might further synergize with ionizing irradiation, although convincing data from multicenter phase III are currently lacking. The authors discuss why concurrent chemoradiation followed by consolidation platinum-based chemotherapy is an attractive approach for treating patients with inoperable tumors.
For the treatment of locoregional advanced stage III non-small-cell lung cancer, when chemotherapy is added sequentially to radiotherapy it acts systemically and is aimed at reducing distant metastases. Concurrent chemotherapy and radiation, however, is intended to enhance the locoregional efficacy of this modality. Combined effects of these modalities are based on their different toxicity profiles, leading to a reduced toxicity : efficacy ratio of the combination. Controlled trials investigating this additive approach indicate that concurrent application of chemotherapy and radiotherapy results in a small but significant benefit for locoregional control, which translates into a small but measurable survival benefit. This benefit is most evident when looking at 3-year or 5-year overall survival rates, when it is of clinical significance. The use of single-agent cisplatin has already demonstrated major radiosensitizing effects whereas the radiosensitizing properties of concurrent application of the single-agent carboplatin have not been observed in controlled trials. Newer drugs such as vinorelbine, the taxanes and gemcitabine might enhance this effect, although no improvement has been observed in randomized controlled trials comparing such regimens with single-agent cisplatin. New 'targeted' agents might synergize with ionizing irradiation and provide an interesting rationale concerning combined modality therapy, but this hypothesis awaits prospective clinical evidence from randomized controlled trials.
Key Points
Based on data from multicenter phase III trials, combining platinum-based chemotherapy and radiotherapy to treat patients with locally advanced and inoperable NSCLC improves median and long-term survival
Sequential administration of chemotherapy prior to radiotherapy compared with radiotherapy alone improves median as well as long-term survival by increasing systemic control
Combining co |
doi_str_mv | 10.1038/ncponc0461 |
format | Article |
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For the treatment of locoregional advanced stage III non-small-cell lung cancer, when chemotherapy is added sequentially to radiotherapy it acts systemically and is aimed at reducing distant metastases. Concurrent chemotherapy and radiation, however, is intended to enhance the locoregional efficacy of this modality. Combined effects of these modalities are based on their different toxicity profiles, leading to a reduced toxicity : efficacy ratio of the combination. Controlled trials investigating this additive approach indicate that concurrent application of chemotherapy and radiotherapy results in a small but significant benefit for locoregional control, which translates into a small but measurable survival benefit. This benefit is most evident when looking at 3-year or 5-year overall survival rates, when it is of clinical significance. The use of single-agent cisplatin has already demonstrated major radiosensitizing effects whereas the radiosensitizing properties of concurrent application of the single-agent carboplatin have not been observed in controlled trials. Newer drugs such as vinorelbine, the taxanes and gemcitabine might enhance this effect, although no improvement has been observed in randomized controlled trials comparing such regimens with single-agent cisplatin. New 'targeted' agents might synergize with ionizing irradiation and provide an interesting rationale concerning combined modality therapy, but this hypothesis awaits prospective clinical evidence from randomized controlled trials.
Key Points
Based on data from multicenter phase III trials, combining platinum-based chemotherapy and radiotherapy to treat patients with locally advanced and inoperable NSCLC improves median and long-term survival
Sequential administration of chemotherapy prior to radiotherapy compared with radiotherapy alone improves median as well as long-term survival by increasing systemic control
Combining concurrent cisplatin-based or platinum-based chemotherapy to radiation increases median survival and long-term survival by improvement of local control
Data from phase III randomized trials indicate that a cisplatin-based combination chemoradiotherapy regimen is the preferable choice when using a concurrent chemoradiation protocol
Combining chemotherapy and radiotherapy increases both hematological and nonhematological toxicities, but with adequate supportive measures treatment compliance is generally good
Future prospective randomized studies should evaluate newer chemotherapeutic and molecular targeted agents, as well as innovative, more intensive and conformal radiation schedules within these multimodality protocols</description><identifier>ISSN: 1743-4254</identifier><identifier>ISSN: 1759-4774</identifier><identifier>EISSN: 1743-4262</identifier><identifier>EISSN: 1759-4782</identifier><identifier>DOI: 10.1038/ncponc0461</identifier><identifier>PMID: 16596143</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer ; Carboplatin ; Carboplatin - administration & dosage ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - radiotherapy ; Care and treatment ; Chemoradiotherapy ; Chemotherapy ; Cisplatin ; Cisplatin - administration & dosage ; Clinical trials ; Clinical Trials, Phase III as Topic ; Combined Modality Therapy ; Diagnosis ; Etoposide - administration & dosage ; Gemcitabine ; Health aspects ; Humans ; Lung cancer ; Lung Neoplasms - drug therapy ; Lung Neoplasms - radiotherapy ; Medicine ; Medicine & Public Health ; Metastases ; Methods ; Multicenter Studies as Topic ; Oncology ; Paclitaxel - administration & dosage ; Radiation therapy ; Radiotherapy ; Randomized Controlled Trials as Topic ; review-article ; Synergism ; Taxanes ; Toxicity ; Vinorelbine</subject><ispartof>Nature clinical practice. Oncology, 2006-04, Vol.3 (4), p.188-199</ispartof><rights>Springer Nature Limited 2006</rights><rights>COPYRIGHT 2006 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Apr 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c441t-c47b35478bf871204d6e1754d9e5603495502878ae16cd8d3dadec031b7564973</citedby><cites>FETCH-LOGICAL-c441t-c47b35478bf871204d6e1754d9e5603495502878ae16cd8d3dadec031b7564973</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2727,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16596143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eberhardt, Wilfried</creatorcontrib><creatorcontrib>Pöttgen, Christoph</creatorcontrib><creatorcontrib>Stuschke, Martin</creatorcontrib><title>Chemoradiation paradigm for the treatment of lung cancer</title><title>Nature clinical practice. Oncology</title><addtitle>Nat Rev Clin Oncol</addtitle><addtitle>Nat Clin Pract Oncol</addtitle><description>For the treatment of advanced non-small-cell lung cancer, randomized controlled trials have shown that platinum-based chemotherapy and radiotherapy provide a measurable survival benefit compared with radiotherapy alone. Newer drugs that target growth factor receptors might further synergize with ionizing irradiation, although convincing data from multicenter phase III are currently lacking. The authors discuss why concurrent chemoradiation followed by consolidation platinum-based chemotherapy is an attractive approach for treating patients with inoperable tumors.
For the treatment of locoregional advanced stage III non-small-cell lung cancer, when chemotherapy is added sequentially to radiotherapy it acts systemically and is aimed at reducing distant metastases. Concurrent chemotherapy and radiation, however, is intended to enhance the locoregional efficacy of this modality. Combined effects of these modalities are based on their different toxicity profiles, leading to a reduced toxicity : efficacy ratio of the combination. Controlled trials investigating this additive approach indicate that concurrent application of chemotherapy and radiotherapy results in a small but significant benefit for locoregional control, which translates into a small but measurable survival benefit. This benefit is most evident when looking at 3-year or 5-year overall survival rates, when it is of clinical significance. The use of single-agent cisplatin has already demonstrated major radiosensitizing effects whereas the radiosensitizing properties of concurrent application of the single-agent carboplatin have not been observed in controlled trials. Newer drugs such as vinorelbine, the taxanes and gemcitabine might enhance this effect, although no improvement has been observed in randomized controlled trials comparing such regimens with single-agent cisplatin. New 'targeted' agents might synergize with ionizing irradiation and provide an interesting rationale concerning combined modality therapy, but this hypothesis awaits prospective clinical evidence from randomized controlled trials.
Key Points
Based on data from multicenter phase III trials, combining platinum-based chemotherapy and radiotherapy to treat patients with locally advanced and inoperable NSCLC improves median and long-term survival
Sequential administration of chemotherapy prior to radiotherapy compared with radiotherapy alone improves median as well as long-term survival by increasing systemic control
Combining concurrent cisplatin-based or platinum-based chemotherapy to radiation increases median survival and long-term survival by improvement of local control
Data from phase III randomized trials indicate that a cisplatin-based combination chemoradiotherapy regimen is the preferable choice when using a concurrent chemoradiation protocol
Combining chemotherapy and radiotherapy increases both hematological and nonhematological toxicities, but with adequate supportive measures treatment compliance is generally good
Future prospective randomized studies should evaluate newer chemotherapeutic and molecular targeted agents, as well as innovative, more intensive and conformal radiation schedules within these multimodality protocols</description><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer</subject><subject>Carboplatin</subject><subject>Carboplatin - administration & dosage</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - radiotherapy</subject><subject>Care and treatment</subject><subject>Chemoradiotherapy</subject><subject>Chemotherapy</subject><subject>Cisplatin</subject><subject>Cisplatin - administration & dosage</subject><subject>Clinical trials</subject><subject>Clinical Trials, Phase III as Topic</subject><subject>Combined Modality Therapy</subject><subject>Diagnosis</subject><subject>Etoposide - administration & dosage</subject><subject>Gemcitabine</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - radiotherapy</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Methods</subject><subject>Multicenter Studies as Topic</subject><subject>Oncology</subject><subject>Paclitaxel - administration & dosage</subject><subject>Radiation therapy</subject><subject>Radiotherapy</subject><subject>Randomized Controlled Trials as Topic</subject><subject>review-article</subject><subject>Synergism</subject><subject>Taxanes</subject><subject>Toxicity</subject><subject>Vinorelbine</subject><issn>1743-4254</issn><issn>1759-4774</issn><issn>1743-4262</issn><issn>1759-4782</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNptkN9LwzAQx4Mobk5f_AOk4JuymTRpkj6O4S8Y-KLPJU2uXcea1DR98L-3o2NVGAe5I_e5b3JfhG4JXhBM5ZPVjbMaM07O0JQIRucs5vH5sU7YBF217RZjKgTDl2hCeJJywugUydUGaueVqVSonI0ata_LOiqcj8IGouBBhRpsiFwR7TpbRlpZDf4aXRRq18LNIc_Q18vz5-ptvv54fV8t13PNGAn9KXKaMCHzQgoSY2Y4EJEwk0LCMWVpkuBYCqmAcG2koUYZ0JiSXCScpYLO0P2g23j33UEbsq3rvO2fzGJMUxlzIclIlWoHWWULF7zSddXqbEkkpZwRKXtqcYLqw0BdaWehqPr7fwMPw4D2rm09FFnjq1r5n4zgbO99Nnrfw3eHn3Z5DWZED2b3wOMAtH3LluDHVU7KRQNtVeg8HOX-IL_rFJbI</recordid><startdate>200604</startdate><enddate>200604</enddate><creator>Eberhardt, Wilfried</creator><creator>Pöttgen, Christoph</creator><creator>Stuschke, Martin</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>200604</creationdate><title>Chemoradiation paradigm for the treatment of lung cancer</title><author>Eberhardt, Wilfried ; Pöttgen, Christoph ; Stuschke, Martin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c441t-c47b35478bf871204d6e1754d9e5603495502878ae16cd8d3dadec031b7564973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cancer</topic><topic>Carboplatin</topic><topic>Carboplatin - administration & dosage</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - radiotherapy</topic><topic>Care and treatment</topic><topic>Chemoradiotherapy</topic><topic>Chemotherapy</topic><topic>Cisplatin</topic><topic>Cisplatin - administration & dosage</topic><topic>Clinical trials</topic><topic>Clinical Trials, Phase III as Topic</topic><topic>Combined Modality Therapy</topic><topic>Diagnosis</topic><topic>Etoposide - administration & dosage</topic><topic>Gemcitabine</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - radiotherapy</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metastases</topic><topic>Methods</topic><topic>Multicenter Studies as Topic</topic><topic>Oncology</topic><topic>Paclitaxel - administration & dosage</topic><topic>Radiation therapy</topic><topic>Radiotherapy</topic><topic>Randomized Controlled Trials as Topic</topic><topic>review-article</topic><topic>Synergism</topic><topic>Taxanes</topic><topic>Toxicity</topic><topic>Vinorelbine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Eberhardt, Wilfried</creatorcontrib><creatorcontrib>Pöttgen, Christoph</creatorcontrib><creatorcontrib>Stuschke, Martin</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>Nursing & Allied Health Database</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</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>Nature clinical practice. Oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eberhardt, Wilfried</au><au>Pöttgen, Christoph</au><au>Stuschke, Martin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemoradiation paradigm for the treatment of lung cancer</atitle><jtitle>Nature clinical practice. Oncology</jtitle><stitle>Nat Rev Clin Oncol</stitle><addtitle>Nat Clin Pract Oncol</addtitle><date>2006-04</date><risdate>2006</risdate><volume>3</volume><issue>4</issue><spage>188</spage><epage>199</epage><pages>188-199</pages><issn>1743-4254</issn><issn>1759-4774</issn><eissn>1743-4262</eissn><eissn>1759-4782</eissn><abstract>For the treatment of advanced non-small-cell lung cancer, randomized controlled trials have shown that platinum-based chemotherapy and radiotherapy provide a measurable survival benefit compared with radiotherapy alone. Newer drugs that target growth factor receptors might further synergize with ionizing irradiation, although convincing data from multicenter phase III are currently lacking. The authors discuss why concurrent chemoradiation followed by consolidation platinum-based chemotherapy is an attractive approach for treating patients with inoperable tumors.
For the treatment of locoregional advanced stage III non-small-cell lung cancer, when chemotherapy is added sequentially to radiotherapy it acts systemically and is aimed at reducing distant metastases. Concurrent chemotherapy and radiation, however, is intended to enhance the locoregional efficacy of this modality. Combined effects of these modalities are based on their different toxicity profiles, leading to a reduced toxicity : efficacy ratio of the combination. Controlled trials investigating this additive approach indicate that concurrent application of chemotherapy and radiotherapy results in a small but significant benefit for locoregional control, which translates into a small but measurable survival benefit. This benefit is most evident when looking at 3-year or 5-year overall survival rates, when it is of clinical significance. The use of single-agent cisplatin has already demonstrated major radiosensitizing effects whereas the radiosensitizing properties of concurrent application of the single-agent carboplatin have not been observed in controlled trials. Newer drugs such as vinorelbine, the taxanes and gemcitabine might enhance this effect, although no improvement has been observed in randomized controlled trials comparing such regimens with single-agent cisplatin. New 'targeted' agents might synergize with ionizing irradiation and provide an interesting rationale concerning combined modality therapy, but this hypothesis awaits prospective clinical evidence from randomized controlled trials.
Key Points
Based on data from multicenter phase III trials, combining platinum-based chemotherapy and radiotherapy to treat patients with locally advanced and inoperable NSCLC improves median and long-term survival
Sequential administration of chemotherapy prior to radiotherapy compared with radiotherapy alone improves median as well as long-term survival by increasing systemic control
Combining concurrent cisplatin-based or platinum-based chemotherapy to radiation increases median survival and long-term survival by improvement of local control
Data from phase III randomized trials indicate that a cisplatin-based combination chemoradiotherapy regimen is the preferable choice when using a concurrent chemoradiation protocol
Combining chemotherapy and radiotherapy increases both hematological and nonhematological toxicities, but with adequate supportive measures treatment compliance is generally good
Future prospective randomized studies should evaluate newer chemotherapeutic and molecular targeted agents, as well as innovative, more intensive and conformal radiation schedules within these multimodality protocols</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>16596143</pmid><doi>10.1038/ncponc0461</doi><tpages>12</tpages></addata></record> |
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subjects | Antineoplastic Combined Chemotherapy Protocols - therapeutic use Cancer Carboplatin Carboplatin - administration & dosage Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - radiotherapy Care and treatment Chemoradiotherapy Chemotherapy Cisplatin Cisplatin - administration & dosage Clinical trials Clinical Trials, Phase III as Topic Combined Modality Therapy Diagnosis Etoposide - administration & dosage Gemcitabine Health aspects Humans Lung cancer Lung Neoplasms - drug therapy Lung Neoplasms - radiotherapy Medicine Medicine & Public Health Metastases Methods Multicenter Studies as Topic Oncology Paclitaxel - administration & dosage Radiation therapy Radiotherapy Randomized Controlled Trials as Topic review-article Synergism Taxanes Toxicity Vinorelbine |
title | Chemoradiation paradigm for the treatment of lung cancer |
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