Randomized Trial of Radiotherapy Plus Concurrent–Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma

Background Current practice of adding concurrent–adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than...

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Veröffentlicht in:JNCI : Journal of the National Cancer Institute 2010-08, Vol.102 (15), p.1188-1198
Hauptverfasser: Lee, Anne W. M., Tung, Stewart Y., Chua, Daniel T. T., Ngan, Roger K. C., Chappell, Rick, Tung, Raymond, Siu, Lillian, Ng, W. T., Sze, W. K., Au, Gordon K. H., Law, Stephen C. K., O'Sullivan, Brian, Yau, T. K., Leung, T. W., Au, Joseph S. K., Sze, W. M., Choi, C. W., Fung, K. K., Lau, Joseph T., Lau, W. H.
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container_end_page 1198
container_issue 15
container_start_page 1188
container_title JNCI : Journal of the National Cancer Institute
container_volume 102
creator Lee, Anne W. M.
Tung, Stewart Y.
Chua, Daniel T. T.
Ngan, Roger K. C.
Chappell, Rick
Tung, Raymond
Siu, Lillian
Ng, W. T.
Sze, W. K.
Au, Gordon K. H.
Law, Stephen C. K.
O'Sullivan, Brian
Yau, T. K.
Leung, T. W.
Au, Joseph S. K.
Sze, W. M.
Choi, C. W.
Fung, K. K.
Lau, Joseph T.
Lau, W. H.
description Background Current practice of adding concurrent–adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than those in other trials, and there were no data on late toxicities. Verification of the long-term therapeutic index of this regimen is needed. Methods Patients with nonkeratinizing nasopharyngeal carcinoma staged T1-4N2-3M0 were randomly assigned to RT (176 patients) or to CRT (172 patients) using cisplatin (100 mg/m2) every 3 weeks for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m2) plus fluorouracil (1000 mg per m2 per day for 4 days) every 4 weeks for three cycles. Primary endpoints included overall failure-free rate (FFR) (the time to first failure at any site) and progression-free survival. Secondary endpoints included overall survival, locoregional FFR, distant FFR, and acute and late toxicity rates. All statistical tests were two-sided. Results The two treatment groups were well balanced in all patient characteristics, tumor factors, and radiotherapy parameters. Adding chemotherapy statistically significantly improved the 5-year FFR (CRT vs RT: 67% vs 55%; P = .014) and 5-year progression-free survival (CRT vs RT: 62% vs 53%; P = .035). Cumulative incidence of acute toxicity increased with chemotherapy by 30% (CRT vs RT: 83% vs 53%; P < .001), but the 5-year late toxicity rate did not increase statistically significantly (CRT vs RT: 30% vs 24%; P = .30). Deaths because of disease progression were reduced statistically significantly by 14% (CRT vs RT: 38% vs 24%; P = .008), but 5-year overall survival was similar (CRT vs RT: 68% vs 64%; P = .22; hazard ratio of CRT = 0.81, 95% confidence interval = 0.58 to 1.13) because deaths due to toxicity or incidental causes increased by 7% (CRT vs RT: 1.7% vs 0, and 8.1% vs 3.4%, respectively; P = .015). Conclusions Adding concurrent–adjuvant chemotherapy statistically significantly reduced failure and cancer-specific deaths when compared with radiotherapy alone. Although there was no statistically significant increase in major late toxicity, increase in noncancer deaths narrowed the resultant gain in overall survival.
doi_str_mv 10.1093/jnci/djq258
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M. ; Tung, Stewart Y. ; Chua, Daniel T. T. ; Ngan, Roger K. C. ; Chappell, Rick ; Tung, Raymond ; Siu, Lillian ; Ng, W. T. ; Sze, W. K. ; Au, Gordon K. H. ; Law, Stephen C. K. ; O'Sullivan, Brian ; Yau, T. K. ; Leung, T. W. ; Au, Joseph S. K. ; Sze, W. M. ; Choi, C. W. ; Fung, K. K. ; Lau, Joseph T. ; Lau, W. H.</creator><creatorcontrib>Lee, Anne W. M. ; Tung, Stewart Y. ; Chua, Daniel T. T. ; Ngan, Roger K. C. ; Chappell, Rick ; Tung, Raymond ; Siu, Lillian ; Ng, W. T. ; Sze, W. K. ; Au, Gordon K. H. ; Law, Stephen C. K. ; O'Sullivan, Brian ; Yau, T. K. ; Leung, T. W. ; Au, Joseph S. K. ; Sze, W. M. ; Choi, C. W. ; Fung, K. K. ; Lau, Joseph T. ; Lau, W. H.</creatorcontrib><description>Background Current practice of adding concurrent–adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than those in other trials, and there were no data on late toxicities. Verification of the long-term therapeutic index of this regimen is needed. Methods Patients with nonkeratinizing nasopharyngeal carcinoma staged T1-4N2-3M0 were randomly assigned to RT (176 patients) or to CRT (172 patients) using cisplatin (100 mg/m2) every 3 weeks for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m2) plus fluorouracil (1000 mg per m2 per day for 4 days) every 4 weeks for three cycles. Primary endpoints included overall failure-free rate (FFR) (the time to first failure at any site) and progression-free survival. Secondary endpoints included overall survival, locoregional FFR, distant FFR, and acute and late toxicity rates. All statistical tests were two-sided. Results The two treatment groups were well balanced in all patient characteristics, tumor factors, and radiotherapy parameters. Adding chemotherapy statistically significantly improved the 5-year FFR (CRT vs RT: 67% vs 55%; P = .014) and 5-year progression-free survival (CRT vs RT: 62% vs 53%; P = .035). Cumulative incidence of acute toxicity increased with chemotherapy by 30% (CRT vs RT: 83% vs 53%; P &lt; .001), but the 5-year late toxicity rate did not increase statistically significantly (CRT vs RT: 30% vs 24%; P = .30). Deaths because of disease progression were reduced statistically significantly by 14% (CRT vs RT: 38% vs 24%; P = .008), but 5-year overall survival was similar (CRT vs RT: 68% vs 64%; P = .22; hazard ratio of CRT = 0.81, 95% confidence interval = 0.58 to 1.13) because deaths due to toxicity or incidental causes increased by 7% (CRT vs RT: 1.7% vs 0, and 8.1% vs 3.4%, respectively; P = .015). Conclusions Adding concurrent–adjuvant chemotherapy statistically significantly reduced failure and cancer-specific deaths when compared with radiotherapy alone. 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M.</creatorcontrib><creatorcontrib>Tung, Stewart Y.</creatorcontrib><creatorcontrib>Chua, Daniel T. T.</creatorcontrib><creatorcontrib>Ngan, Roger K. C.</creatorcontrib><creatorcontrib>Chappell, Rick</creatorcontrib><creatorcontrib>Tung, Raymond</creatorcontrib><creatorcontrib>Siu, Lillian</creatorcontrib><creatorcontrib>Ng, W. T.</creatorcontrib><creatorcontrib>Sze, W. K.</creatorcontrib><creatorcontrib>Au, Gordon K. H.</creatorcontrib><creatorcontrib>Law, Stephen C. K.</creatorcontrib><creatorcontrib>O'Sullivan, Brian</creatorcontrib><creatorcontrib>Yau, T. K.</creatorcontrib><creatorcontrib>Leung, T. W.</creatorcontrib><creatorcontrib>Au, Joseph S. K.</creatorcontrib><creatorcontrib>Sze, W. M.</creatorcontrib><creatorcontrib>Choi, C. W.</creatorcontrib><creatorcontrib>Fung, K. K.</creatorcontrib><creatorcontrib>Lau, Joseph T.</creatorcontrib><creatorcontrib>Lau, W. H.</creatorcontrib><title>Randomized Trial of Radiotherapy Plus Concurrent–Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>J Natl Cancer Inst</addtitle><description>Background Current practice of adding concurrent–adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than those in other trials, and there were no data on late toxicities. Verification of the long-term therapeutic index of this regimen is needed. Methods Patients with nonkeratinizing nasopharyngeal carcinoma staged T1-4N2-3M0 were randomly assigned to RT (176 patients) or to CRT (172 patients) using cisplatin (100 mg/m2) every 3 weeks for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m2) plus fluorouracil (1000 mg per m2 per day for 4 days) every 4 weeks for three cycles. Primary endpoints included overall failure-free rate (FFR) (the time to first failure at any site) and progression-free survival. Secondary endpoints included overall survival, locoregional FFR, distant FFR, and acute and late toxicity rates. All statistical tests were two-sided. Results The two treatment groups were well balanced in all patient characteristics, tumor factors, and radiotherapy parameters. Adding chemotherapy statistically significantly improved the 5-year FFR (CRT vs RT: 67% vs 55%; P = .014) and 5-year progression-free survival (CRT vs RT: 62% vs 53%; P = .035). Cumulative incidence of acute toxicity increased with chemotherapy by 30% (CRT vs RT: 83% vs 53%; P &lt; .001), but the 5-year late toxicity rate did not increase statistically significantly (CRT vs RT: 30% vs 24%; P = .30). Deaths because of disease progression were reduced statistically significantly by 14% (CRT vs RT: 38% vs 24%; P = .008), but 5-year overall survival was similar (CRT vs RT: 68% vs 64%; P = .22; hazard ratio of CRT = 0.81, 95% confidence interval = 0.58 to 1.13) because deaths due to toxicity or incidental causes increased by 7% (CRT vs RT: 1.7% vs 0, and 8.1% vs 3.4%, respectively; P = .015). Conclusions Adding concurrent–adjuvant chemotherapy statistically significantly reduced failure and cancer-specific deaths when compared with radiotherapy alone. Although there was no statistically significant increase in major late toxicity, increase in noncancer deaths narrowed the resultant gain in overall survival.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer</subject><subject>Carcinoma - drug therapy</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma - radiotherapy</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant</subject><subject>Cisplatin - administration &amp; dosage</subject><subject>Clinical trials</subject><subject>Disease-Free Survival</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Fluorouracil - administration &amp; dosage</subject><subject>Follow-Up Studies</subject><subject>Hong Kong - epidemiology</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Nasopharyngeal Neoplasms - drug therapy</subject><subject>Nasopharyngeal Neoplasms - pathology</subject><subject>Nasopharyngeal Neoplasms - radiotherapy</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Staging</subject><subject>Neoplasms, Second Primary - epidemiology</subject><subject>Neoplasms, Second Primary - etiology</subject><subject>Odds Ratio</subject><subject>Oncology</subject><subject>Radiation therapy</subject><subject>Radiotherapy, Adjuvant</subject><subject>Suicide - statistics &amp; numerical data</subject><subject>Treatment Outcome</subject><issn>0027-8874</issn><issn>1460-2105</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpd0c1u1DAQB3ALgehSOHFHERcOVVondvxxXIWWUlWAVoUiLtbEdroJib21k4py4g048IY8Ca62rAS-WLJ_M6PRH6HnBT4ssCRHvdPdkemvy0o8QIuCMpyXBa4eogXGJc-F4HQPPYmxx-nIkj5GeyVmhFJRLtDPFTjjx-67NdlF6GDIfJutwHR-WtsAm9vswzDHrPZOzyFYN_3-8Wtp-vkG3JTVazvu3E38t245eGez1odsZa8672AY0qNJhTrNegfRb9YQbt2VTUNrCLpzfoSn6FELQ7TP7u999PHk-KI-zc_fv3lbL89zTYWY8oZrW1nRcMHKFjctYEOMZqYCTLgsmsJYoNASRqluKK5EBbIRWFBMjMSSk330att3E_z1bOOkxi5qOwzgrJ-jEpxXknHGknz5n-z9HNI6UXHKJS1IKRM62CIdfIzBtmoTujGtpwqs7lJSdympbUpJv7hvOTejNTv7N5YE8i3o4mS_7f4hfFWME16p089f1OtLfnnCPlF1Rv4Adhyh3w</recordid><startdate>20100804</startdate><enddate>20100804</enddate><creator>Lee, Anne W. M.</creator><creator>Tung, Stewart Y.</creator><creator>Chua, Daniel T. T.</creator><creator>Ngan, Roger K. C.</creator><creator>Chappell, Rick</creator><creator>Tung, Raymond</creator><creator>Siu, Lillian</creator><creator>Ng, W. T.</creator><creator>Sze, W. K.</creator><creator>Au, Gordon K. H.</creator><creator>Law, Stephen C. K.</creator><creator>O'Sullivan, Brian</creator><creator>Yau, T. K.</creator><creator>Leung, T. W.</creator><creator>Au, Joseph S. K.</creator><creator>Sze, W. M.</creator><creator>Choi, C. W.</creator><creator>Fung, K. K.</creator><creator>Lau, Joseph T.</creator><creator>Lau, W. H.</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</general><scope>BSCLL</scope><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>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope></search><sort><creationdate>20100804</creationdate><title>Randomized Trial of Radiotherapy Plus Concurrent–Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma</title><author>Lee, Anne W. M. ; Tung, Stewart Y. ; Chua, Daniel T. T. ; Ngan, Roger K. C. ; Chappell, Rick ; Tung, Raymond ; Siu, Lillian ; Ng, W. T. ; Sze, W. K. ; Au, Gordon K. H. ; Law, Stephen C. K. ; O'Sullivan, Brian ; Yau, T. K. ; Leung, T. W. ; Au, Joseph S. K. ; Sze, W. M. ; Choi, C. W. ; Fung, K. K. ; Lau, Joseph T. ; Lau, W. 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H.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><jtitle>JNCI : Journal of the National Cancer Institute</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Anne W. M.</au><au>Tung, Stewart Y.</au><au>Chua, Daniel T. T.</au><au>Ngan, Roger K. C.</au><au>Chappell, Rick</au><au>Tung, Raymond</au><au>Siu, Lillian</au><au>Ng, W. T.</au><au>Sze, W. K.</au><au>Au, Gordon K. H.</au><au>Law, Stephen C. K.</au><au>O'Sullivan, Brian</au><au>Yau, T. K.</au><au>Leung, T. W.</au><au>Au, Joseph S. K.</au><au>Sze, W. M.</au><au>Choi, C. W.</au><au>Fung, K. K.</au><au>Lau, Joseph T.</au><au>Lau, W. H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Randomized Trial of Radiotherapy Plus Concurrent–Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma</atitle><jtitle>JNCI : Journal of the National Cancer Institute</jtitle><addtitle>J Natl Cancer Inst</addtitle><date>2010-08-04</date><risdate>2010</risdate><volume>102</volume><issue>15</issue><spage>1188</spage><epage>1198</epage><pages>1188-1198</pages><issn>0027-8874</issn><eissn>1460-2105</eissn><coden>JNCIEQ</coden><abstract>Background Current practice of adding concurrent–adjuvant chemotherapy to radiotherapy (CRT) for treating advanced nasopharyngeal carcinoma is based on the Intergroup-0099 Study published in 1998. However, the outcome for the radiotherapy-alone (RT) group in that trial was substantially poorer than those in other trials, and there were no data on late toxicities. Verification of the long-term therapeutic index of this regimen is needed. Methods Patients with nonkeratinizing nasopharyngeal carcinoma staged T1-4N2-3M0 were randomly assigned to RT (176 patients) or to CRT (172 patients) using cisplatin (100 mg/m2) every 3 weeks for three cycles in concurrence with radiotherapy, followed by cisplatin (80 mg/m2) plus fluorouracil (1000 mg per m2 per day for 4 days) every 4 weeks for three cycles. Primary endpoints included overall failure-free rate (FFR) (the time to first failure at any site) and progression-free survival. Secondary endpoints included overall survival, locoregional FFR, distant FFR, and acute and late toxicity rates. All statistical tests were two-sided. Results The two treatment groups were well balanced in all patient characteristics, tumor factors, and radiotherapy parameters. Adding chemotherapy statistically significantly improved the 5-year FFR (CRT vs RT: 67% vs 55%; P = .014) and 5-year progression-free survival (CRT vs RT: 62% vs 53%; P = .035). Cumulative incidence of acute toxicity increased with chemotherapy by 30% (CRT vs RT: 83% vs 53%; P &lt; .001), but the 5-year late toxicity rate did not increase statistically significantly (CRT vs RT: 30% vs 24%; P = .30). Deaths because of disease progression were reduced statistically significantly by 14% (CRT vs RT: 38% vs 24%; P = .008), but 5-year overall survival was similar (CRT vs RT: 68% vs 64%; P = .22; hazard ratio of CRT = 0.81, 95% confidence interval = 0.58 to 1.13) because deaths due to toxicity or incidental causes increased by 7% (CRT vs RT: 1.7% vs 0, and 8.1% vs 3.4%, respectively; P = .015). Conclusions Adding concurrent–adjuvant chemotherapy statistically significantly reduced failure and cancer-specific deaths when compared with radiotherapy alone. Although there was no statistically significant increase in major late toxicity, increase in noncancer deaths narrowed the resultant gain in overall survival.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>20634482</pmid><doi>10.1093/jnci/djq258</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Cancer
Carcinoma - drug therapy
Carcinoma - pathology
Carcinoma - radiotherapy
Chemotherapy
Chemotherapy, Adjuvant
Cisplatin - administration & dosage
Clinical trials
Disease-Free Survival
Drug Administration Schedule
Female
Fluorouracil - administration & dosage
Follow-Up Studies
Hong Kong - epidemiology
Humans
Kaplan-Meier Estimate
Male
Middle Aged
Nasopharyngeal Neoplasms - drug therapy
Nasopharyngeal Neoplasms - pathology
Nasopharyngeal Neoplasms - radiotherapy
Neoplasm Invasiveness
Neoplasm Staging
Neoplasms, Second Primary - epidemiology
Neoplasms, Second Primary - etiology
Odds Ratio
Oncology
Radiation therapy
Radiotherapy, Adjuvant
Suicide - statistics & numerical data
Treatment Outcome
title Randomized Trial of Radiotherapy Plus Concurrent–Adjuvant Chemotherapy vs Radiotherapy Alone for Regionally Advanced Nasopharyngeal Carcinoma
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