Carbon Ion Reirradiation for Recurrent Head and Neck Cancer: A Single-Institutional Experience

被引:43
|
作者
Held, Thomas [1 ,2 ,3 ]
Windisch, Paul [1 ,2 ,3 ]
Akbaba, Sati [1 ,2 ,3 ]
Lang, Kristin [1 ,2 ,3 ]
El Shafie, Rami [1 ,2 ,3 ]
Bernhardt, Denise [1 ,2 ,3 ]
Plinkert, Peter [4 ]
Kargus, Steffen [5 ]
Rieken, Stefan [1 ,2 ,3 ,6 ,7 ,8 ]
Herfarth, Klaus [1 ,2 ,3 ,6 ,7 ,8 ]
Debus, Juergen [1 ,2 ,3 ,6 ,7 ,8 ]
Adeberg, Sebastian [1 ,2 ,3 ,6 ,7 ,8 ]
机构
[1] Heidelberg Univ Hosp, Dept Radiat Oncol, Heidelberg, Germany
[2] HIRO, Heidelberg, Germany
[3] Natl Ctr Tumor Dis NCT, Heidelberg, Germany
[4] Heidelberg Univ, Dept Otorhinolaryngol, Heidelberg, Germany
[5] Univ Hosp Heidelberg, Dept Oral & Maxillofacial Surg, Heidelberg, Germany
[6] German Canc Res Ctr, Clin Cooperat Unit Radiat Oncol, Heidelberg, Germany
[7] Heidelberg Ion Beam Therapy Ctr HIT, Heidelberg, Germany
[8] German Canc Res Ctr, German Canc Consortium DKTK, Partner Site Heidelberg, Heidelberg, Germany
关键词
SQUAMOUS-CELL CARCINOMA; CHEMOTHERAPY; COMBINATION; CISPLATIN;
D O I
10.1016/j.ijrobp.2019.07.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study aimed to assess the feasibility of carbon ion reirradiation (CIR) for recurrent head and neck cancer (HNC). Methods and Materials: This retrospective study included 229 patients with recurrent HNC who were treated with CIR between 2010 and 2017. We assessed progression-free survival, overall survival, pattern of failure, and toxicity. Of the primary tumors, 54.1% were adenoid cystic carcinomas, 26.2% were squamous cell carcinomas, 8.3% were adenocarcinomas, and 11.4% were other tumor entities. Results: The median radiation therapy interval was 3.9 years (range, 0.3-46.5 years), and patients received a median dose of 51 Gy (relative biological effectiveness [RBE]; range, 30-66 Gy [RBE]) in 3 Gy (RBE) fractions. The median cumulative lifetime dose after CIR was 132.8 Gy (range, 88.8-155.0 Gy). The median local progression-free survival after CIR was 24.2 months (95% confidence interval, 19.4-29.0 months), and the median overall survival was 26.1 months (95% confidence interval, 21.9-30.3 months). Serious acute toxicity (grade >= 3) after CIR included laryngeal edema, grade 4 (n = 2; 0.9%); dysphagia, grade 3 (n = 3; 1.3%); fistula, grade 3 (n = 1; 0.4%); and impaired hearing, grade 3 (n = 1; 0.4%). Late toxicities of grades 3 or higher (n = 18; 14.5%) included central nervous system necrosis, grades 4/3 (n = 1; 0.8%/n = 5; 4.0%); optic nerve disorder, grades 4/3 (n = 2; 1.6%/n = 2; 1.6%); impaired hearing, grade 3 (n = 5; 4.0%), osteonecrosis, grade 3 (n = 1; 0.8%); and carotid blowout, grade 4 (n = 1; 0.8%). Conclusions: In patients with locally recurrent HNC, CIR was a feasible, effective treatment with acceptable toxicity and good local control. Thus, CIR represented a valuable alternative to surgical salvage and palliative chemotherapy in selected patients. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:803 / 811
页数:9
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