Helical Tomotherapy in Head and Neck Cancer: A European Single-Center Experience

被引:6
作者
Van Gestel, Dirk [1 ]
Van den Weyngaert, Danielle [1 ,6 ]
De Kerf, Geert [1 ]
De Ost, Bie [1 ]
Vanderveken, Olivier [2 ,6 ]
Van Laer, Carl [2 ,6 ]
Specenier, Pol [3 ,6 ]
Geussens, Yasmyne [7 ]
Wouters, Kristien [3 ,4 ]
Meulemans, Els [5 ]
Cheung, Kin Jip [5 ]
Gregoire, Vincent [8 ,9 ]
Vermorken, Jan B. [3 ,6 ]
机构
[1] Univ Radiotherapy Antwerp UZA ZNA, Dept Radiotherapy, Antwerp, Belgium
[2] Univ Antwerp Hosp, Dept Otolaryngol & Head & Neck Surg, Edegem, Belgium
[3] Univ Antwerp Hosp, Dept Med Oncol, Edegem, Belgium
[4] Univ Antwerp Hosp, Sci Coordinat & Biostat, Edegem, Belgium
[5] Univ Antwerp Hosp, Data Management Multidisciplinair Oncol Ctr Antwe, Edegem, Belgium
[6] Univ Antwerp, Fac Med & Hlth Sci, B-2020 Antwerp, Belgium
[7] Iridium Kankernetwerk, St Niklaas, Belgium
[8] St Luc Univ Hosp, Dept Radiat Oncol, Brussels, Belgium
[9] St Luc Univ Hosp, Ctr Mol Imaging & Expt Radiotherapy, Brussels, Belgium
关键词
Head and neck cancer; Helical tomotherapy; Retrospective analysis; Systemic therapy; INTENSITY-MODULATED RADIOTHERAPY; SQUAMOUS-CELL CARCINOMA; LOCALLY ADVANCED HEAD; STAGE NASOPHARYNGEAL CARCINOMA; RADIATION-THERAPY; HUMAN-PAPILLOMAVIRUS; REFERENCE DOSIMETRY; UNRESECTABLE HEAD; CHEMOTHERAPY; CISPLATIN;
D O I
10.1634/theoncologist.2014-0337
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. We report on a retrospective analysis of 147 patients with early and locoregionally advanced squamous cell head and neck cancer (SCCHN) treated with helical tomotherapy (HT). Patients and Methods. Included were patients with SCCHN of theoral cavity (OC), oropharynx (OP), hypopharynx (HP), or larynx (L) consecutively treated in one radiotherapy center in 2008 and 2009. The prescribed HT dose was 60-66 Gy in the postoperative setting (group A) and 66-70 Gy when given as primary treatment (group B). HT was given alone, concurrent with systemic therapy (ST), that is, chemotherapy, biotherapy, or both, and with or without induction therapy (IT). Acute and late toxicities are reported using standard criteria; locoregional failure/progression (LRF), distant metastases (DM), and second primary tumors (SPT) were documented, and event-free survival (EFS) and overall survival (OS) were calculated from the start of HT. Results. Group A patients received HT alone in 22 cases and HT+ST in 20 cases; group B patients received HT alone in 17 cases and HT 1 ST in 88 cases. Severe (grade >= 3) acute mucosal toxicity and swallowing problems increased with more additional ST. After a median follow-up of 44 months, grade >= 2 late toxicity after HT+ST was approximately twice that of HT alone for skin, subcutis, pharynx, and larynx. Forty percent had grade >= 2 late xerostomia, and 29% hadmucosal toxicity. At 3 years, LRF/DM/SPT occurred in 7%/7%/17% and 25%/13%/5% in groups A and B, respectively, leading to a 3-year EFS/OS of 64%/74% and 56%/63% in groups A and B, respectively. Conclusion. The use of HT alone or in combination with ST is feasible and promising and has a low late fatality rate. However, late toxicity is nearly twice as high when ST is added to HT.
引用
收藏
页码:279 / 290
页数:12
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