Advantage of accelerated fractionation regimens in definitive radiotherapy for stage II glottic carcinoma

被引:5
作者
Nomiya, Takuma [1 ]
Nemoto, Kenji [1 ]
Wada, Hitoshi [1 ]
Takai, Yoshihiro [1 ]
Yamada, Shogo [1 ]
机构
[1] Tohoku Univ, Sch Med, Dept Radiat Oncol, Aoba Ku, Sendai, Miyagi 9808574, Japan
关键词
accelerated fractionation; glottic carcinoma; overall treatment time; radiotherapy; T2; cancer; total dose;
D O I
10.1177/000348940611501003
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objectives: We evaluated the prognostic factors for local control of T2 glottic cancer and verified the efficacy of accelerated fractionation regimens such as hyperfractionation and accelerated hyperfractionation. Methods: A total of 86 patients with T2 NO MO glottic squamous cell carcinoma, who were treated with definitive radiotherapy, were analyzed retrospectively by multivariate analysis. Results: Overall treatment time of radiotherapy (p =.0003) and total dose (p = .0036) were the significant prognostic factors for local control on multivariate analysis. The group with a higher total dose (>= 67 Gy versus < 67 Gy) showed a favorable prognosis (5-year local control rate of 91 % versus 60%, respectively; p = .0013, log-rank test). Likewise, the group with a shorter overall treatment time of radiotherapy (<= 54 days versus > 54 days) showed a favorable prognosis (5-year local control rate of 87% versus 71 %, respectively; p = .023). Conclusions: A radiotherapy total dose of >= 67 Gy delivered for a shorter period is required for T2 glottic cancer. The fractionation regimens of hyperfractionation and accelerated hyperfractionation are more effective than conventional fractionation in terms of shortening overall treatment time and delivering a high total dose with acceptable toxicity.
引用
收藏
页码:727 / 732
页数:6
相关论文
共 18 条
[1]  
[Anonymous], 1999, COMM TOX CRIT VERS 2
[2]  
Chatani Masashi, 1993, Strahlentherapie und Onkologie, V169, P102
[3]   Do overall treatment time, field size, and treatment energy influence local control of T1-T2 squamous cell carcinomas of the glottic larynx? [J].
Fein, DA ;
Lee, WR ;
Hanlon, AL ;
Ridge, JA ;
Curran, WJ ;
Coia, LR .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1996, 34 (04) :823-831
[4]  
HARWOOD AR, 1980, CANCER, V45, P991, DOI 10.1002/1097-0142(19800301)45:5<991::AID-CNCR2820450526>3.0.CO
[5]  
2-D
[6]  
KAPLAN MJ, 1984, CANCER, V53, P2641, DOI 10.1002/1097-0142(19840615)53:12<2641::AID-CNCR2820531212>3.0.CO
[7]  
2-H
[8]  
Kitano Masashi, 2002, Nippon Acta Radiologica, V62, P366
[9]  
Krawczyk J, 1991, Clin Oncol (R Coll Radiol), V3, P330, DOI 10.1016/S0936-6555(05)80588-6
[10]   Influence of fraction size, total dose, and overall time on local control of T1-T2 glottic carcinoma [J].
Le, QTX ;
Fu, KK ;
Kroll, S ;
Ryu, JK ;
Quivey, JM ;
Meyler, TS ;
Krieg, RM ;
Phillips, TL .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1997, 39 (01) :115-126