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- Publisher Website: 10.1002/1097-0142(20011201)92:11<2856::AID-CNCR10132>3.0.CO;2-6
- Scopus: eid_2-s2.0-0035575766
- PMID: 11753959
- WOS: WOS:000172310400015
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Article: Alternating chemoradiotherapy versus partly accelerated radiotherapy in locally advanced squamous cell carcinoma of the head and neck: Results from a phase III randomized trial
Title | Alternating chemoradiotherapy versus partly accelerated radiotherapy in locally advanced squamous cell carcinoma of the head and neck: Results from a phase III randomized trial |
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Authors | |
Keywords | Accelerated radiotherapy Chemoradiotherapy Head and neck carcinoma Randomized clinical trial Squamous cell carcinoma |
Issue Date | 2001 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 |
Citation | Cancer, 2001, v. 92 n. 11, p. 2856-2867 How to Cite? |
Abstract | BACKGROUND. The authors previously have found that in patients with locally advanced squamous cell carcinoma of the head and neck (SCC-HN), alternating chemoradiotherapy (ALT) was superior to low-total-dose conventional radiotherapy alone. The purpose of this randomized trial was to compare the same chemoradiotherapy approach with high-total-dose partly accelerated radiotherapy. METHODS. During 6 years, 136 consecutive patients with previously untreated unfavorable Stage II or Stage III-IV (International Union Against Cancer) SCC of the oral cavity, pharynx, and larynx were enrolled. They were randomly assigned to chemotherapy consisting of 4 cycles of intravenous cisplatin (20 mg/m2 of body surface area per day for 5 consecutive days) and 5-fluorouracil (200 mg/m2 per day for 5 consecutive days; weeks 1, 4, 7, and 10) alternated with three 2-week courses of radiotherapy (20 grays [Gy] per course, 2 Gy per day, 5 days per week; ALT, 70 patients) or to partly accelerated radiotherapy with final concomitant boost technique (75 Gy/40 fractions in 6 weeks; partly accelerated radiotherapy [PA-RT], 66 patients). RESULTS. At the median follow-up of 60 months (range, 30-102 months), no statistical differences were observed in overall survival, progression free survival, or locoregional control between the 2 treatments. Actuarial 3-year overall survival and progression free survival were 37% and 35%, respectively, in the ALT group and 29% and 27%, respectively, in PA-RT group. The median overall survival and progression free survival were 24 and 15 months, respectively, in the ALT arm and 18 and 11 months, respectively, in PA-RT arm. Actuarial 3-year locoregional control rates were 32% in the ALT group and 27% in the PA-RT group. At multivariate analysis, tumor classification was the only factor that emerged as a significant independent variable affecting overall survival. Patients treated in the PA-RT arm experienced higher Grade 3+ (World Health Organization) acute skin and mucosal reactions than patients in the ALT arm. Moreover, local late mucosal and skin toxicities occurred more often in patients treated with PA-RT. CONCLUSIONS. This trial failed to disclose statistically significant differences in the outcome of patients treated with either ALT or PA-RT. Therefore, definitive conclusions could not be made. However, acute skin effects and late mucosal and skin toxicities above the clavicles appeared to be significantly lower with chemoradiotherapy. © 2001 American Cancer Society. |
Persistent Identifier | http://hdl.handle.net/10722/172796 |
ISSN | 2023 Impact Factor: 6.1 2023 SCImago Journal Rankings: 2.887 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Chua, DTT | en_HK |
dc.contributor.author | Sham, JST | en_HK |
dc.contributor.author | Wei, WI | en_HK |
dc.contributor.author | Ho, WK | en_HK |
dc.contributor.author | Au, GKH | en_HK |
dc.date.accessioned | 2012-10-30T06:24:58Z | - |
dc.date.available | 2012-10-30T06:24:58Z | - |
dc.date.issued | 2001 | en_HK |
dc.identifier.citation | Cancer, 2001, v. 92 n. 11, p. 2856-2867 | en_HK |
dc.identifier.issn | 0008-543X | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/172796 | - |
dc.description.abstract | BACKGROUND. The authors previously have found that in patients with locally advanced squamous cell carcinoma of the head and neck (SCC-HN), alternating chemoradiotherapy (ALT) was superior to low-total-dose conventional radiotherapy alone. The purpose of this randomized trial was to compare the same chemoradiotherapy approach with high-total-dose partly accelerated radiotherapy. METHODS. During 6 years, 136 consecutive patients with previously untreated unfavorable Stage II or Stage III-IV (International Union Against Cancer) SCC of the oral cavity, pharynx, and larynx were enrolled. They were randomly assigned to chemotherapy consisting of 4 cycles of intravenous cisplatin (20 mg/m2 of body surface area per day for 5 consecutive days) and 5-fluorouracil (200 mg/m2 per day for 5 consecutive days; weeks 1, 4, 7, and 10) alternated with three 2-week courses of radiotherapy (20 grays [Gy] per course, 2 Gy per day, 5 days per week; ALT, 70 patients) or to partly accelerated radiotherapy with final concomitant boost technique (75 Gy/40 fractions in 6 weeks; partly accelerated radiotherapy [PA-RT], 66 patients). RESULTS. At the median follow-up of 60 months (range, 30-102 months), no statistical differences were observed in overall survival, progression free survival, or locoregional control between the 2 treatments. Actuarial 3-year overall survival and progression free survival were 37% and 35%, respectively, in the ALT group and 29% and 27%, respectively, in PA-RT group. The median overall survival and progression free survival were 24 and 15 months, respectively, in the ALT arm and 18 and 11 months, respectively, in PA-RT arm. Actuarial 3-year locoregional control rates were 32% in the ALT group and 27% in the PA-RT group. At multivariate analysis, tumor classification was the only factor that emerged as a significant independent variable affecting overall survival. Patients treated in the PA-RT arm experienced higher Grade 3+ (World Health Organization) acute skin and mucosal reactions than patients in the ALT arm. Moreover, local late mucosal and skin toxicities occurred more often in patients treated with PA-RT. CONCLUSIONS. This trial failed to disclose statistically significant differences in the outcome of patients treated with either ALT or PA-RT. Therefore, definitive conclusions could not be made. However, acute skin effects and late mucosal and skin toxicities above the clavicles appeared to be significantly lower with chemoradiotherapy. © 2001 American Cancer Society. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/28741 | en_HK |
dc.relation.ispartof | Cancer | en_HK |
dc.subject | Accelerated radiotherapy | en_HK |
dc.subject | Chemoradiotherapy | en_HK |
dc.subject | Head and neck carcinoma | en_HK |
dc.subject | Randomized clinical trial | en_HK |
dc.subject | Squamous cell carcinoma | en_HK |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Carcinoma, Squamous Cell - Drug Therapy - Mortality - Radiotherapy | en_US |
dc.subject.mesh | Combined Modality Therapy | en_US |
dc.subject.mesh | Disease-Free Survival | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Head And Neck Neoplasms - Drug Therapy - Mortality - Radiotherapy | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Neoplasm Metastasis | en_US |
dc.subject.mesh | Neoplasm Staging | en_US |
dc.subject.mesh | Neoplasms, Second Primary - Etiology | en_US |
dc.subject.mesh | Patient Compliance | en_US |
dc.subject.mesh | Regression Analysis | en_US |
dc.subject.mesh | Treatment Outcome | en_US |
dc.title | Alternating chemoradiotherapy versus partly accelerated radiotherapy in locally advanced squamous cell carcinoma of the head and neck: Results from a phase III randomized trial | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Chua, DTT: dttchua@hkucc.hku.hk | en_HK |
dc.identifier.email | Wei, WI: hrmswwi@hku.hk | en_HK |
dc.identifier.authority | Chua, DTT=rp00415 | en_HK |
dc.identifier.authority | Wei, WI=rp00323 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/1097-0142(20011201)92:11<2856::AID-CNCR10132>3.0.CO;2-6 | en_HK |
dc.identifier.pmid | 11753959 | - |
dc.identifier.scopus | eid_2-s2.0-0035575766 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035575766&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 92 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 2856 | en_HK |
dc.identifier.epage | 2867 | en_HK |
dc.identifier.isi | WOS:000172310400015 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Chua, DTT=7006773480 | en_HK |
dc.identifier.scopusauthorid | Sham, JST=7101655565 | en_HK |
dc.identifier.scopusauthorid | Wei, WI=7403321552 | en_HK |
dc.identifier.scopusauthorid | Ho, WK=7402968844 | en_HK |
dc.identifier.scopusauthorid | Au, GKH=7003748615 | en_HK |
dc.identifier.issnl | 0008-543X | - |