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- Publisher Website: 10.1093/jnci/djq258
- Scopus: eid_2-s2.0-77955445967
- PMID: 20634482
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Article: Randomized trial of radiotherapy plus concurrent-adjuvant chemotherapy vs radiotherapy alone for regionally advanced nasopharyngeal carcinoma
Title | Randomized trial of radiotherapy plus concurrent-adjuvant chemotherapy vs radiotherapy alone for regionally advanced nasopharyngeal carcinoma |
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Authors | |
Issue Date | 2010 |
Citation | Journal of the National Cancer Institute, 2010, v. 102, n. 15, p. 1188-1198 How to Cite? |
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 <. 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. © 2010 The Author. Published by Oxford University Press. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/213936 |
ISSN | 2023 Impact Factor: 9.9 2023 SCImago Journal Rankings: 4.986 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lee, Anne W M | - |
dc.contributor.author | Tung, Stewart Y. | - |
dc.contributor.author | Chua, Daniel T T | - |
dc.contributor.author | Ngan, Roger K C | - |
dc.contributor.author | Chappell, Rick | - |
dc.contributor.author | Tung, Raymond | - |
dc.contributor.author | Siu, Lillian | - |
dc.contributor.author | Ng, W. T. | - |
dc.contributor.author | Sze, W. K. | - |
dc.contributor.author | Au, Gordon K H | - |
dc.contributor.author | Law, Stephen C K | - |
dc.contributor.author | O'Sullivan, Brian | - |
dc.contributor.author | Yau, T. K. | - |
dc.contributor.author | Leung, T. W. | - |
dc.contributor.author | Au, Joseph S K | - |
dc.contributor.author | Sze, W. M. | - |
dc.contributor.author | Choi, C. W. | - |
dc.contributor.author | Fung, K. K. | - |
dc.contributor.author | Lau, Joseph T. | - |
dc.contributor.author | Lau, W. H. | - |
dc.date.accessioned | 2015-08-19T13:41:17Z | - |
dc.date.available | 2015-08-19T13:41:17Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Journal of the National Cancer Institute, 2010, v. 102, n. 15, p. 1188-1198 | - |
dc.identifier.issn | 0027-8874 | - |
dc.identifier.uri | http://hdl.handle.net/10722/213936 | - |
dc.description.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 <. 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. © 2010 The Author. Published by Oxford University Press. All rights reserved. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of the National Cancer Institute | - |
dc.title | Randomized trial of radiotherapy plus concurrent-adjuvant chemotherapy vs radiotherapy alone for regionally advanced nasopharyngeal carcinoma | - |
dc.type | Article | - |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.doi | 10.1093/jnci/djq258 | - |
dc.identifier.pmid | 20634482 | - |
dc.identifier.scopus | eid_2-s2.0-77955445967 | - |
dc.identifier.hkuros | 266198 | - |
dc.identifier.volume | 102 | - |
dc.identifier.issue | 15 | - |
dc.identifier.spage | 1188 | - |
dc.identifier.epage | 1198 | - |
dc.identifier.eissn | 1460-2105 | - |
dc.identifier.isi | WOS:000280705500012 | - |
dc.identifier.f1000 | 5793956 | - |
dc.identifier.issnl | 0027-8874 | - |