Superselective intra-arterial cisplatin infusion and concomitant radiotherapy for maxillary sinus cancer

被引:52
|
作者
Homma, A. [1 ]
Sakashita, T. [1 ]
Yoshida, D. [2 ]
Onimaru, R. [2 ]
Tsuchiya, K. [2 ]
Suzuki, F. [1 ]
Yasuda, K. [2 ]
Hatakeyama, H. [1 ]
Furusawa, J. [1 ]
Mizumachi, T. [1 ]
Kano, S. [1 ]
Inamura, N. [1 ]
Taki, S. [1 ]
Shirato, H. [2 ]
Fukuda, S. [1 ]
机构
[1] Hokkaido Univ, Grad Sch Med, Dept Otolaryngol Head & Neck Surg, Kita Ku, Sapporo, Hokkaido 0608638, Japan
[2] Hokkaido Univ, Grad Sch Med, Dept Radiol, Sapporo, Hokkaido 0608638, Japan
关键词
intra-arterial; cisplatin; maxillary sinus; chemotherapy; radiotherapy; HIGH-DOSE CISPLATIN; SQUAMOUS-CELL CARCINOMA; NECK-CANCER; PARANASAL SINUSES; ADVANCED HEAD; NASAL CAVITY; RETROSPECTIVE ANALYSIS; THERAPY; OUTCOMES; CHEMORADIATION;
D O I
10.1038/bjc.2013.663
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The purpose of this study was to evaluate the efficacy of superselective cisplatin infusion with concomitant radiotherapy (RADPLAT) for previously untreated patients with the squamous cell carcinoma of maxillary sinus (SCC-MS). Methods: Between 1999 and 2010, 54 patients were given superselective intra-arterial infusions of cisplatin (100-120mgm(-2) per week) with simultaneous intra-venous infusions of thiosulfate to neutralise cisplatin toxicity and conventional radiotherapy (65-70 Gy). Results: One patient (1.9%) was diagnosed with T2, 14 (25.9%) with T3, 27 (50%) with T4a, and 12 (22.2%) with T4b disease. Lymph-node involvement was present in 12 patients (22.2%). During the median follow-up period of 6.4 years, the 5-year local progression-free and overall survival rates were 65.8 and 67.9% for all patients, respectively. No patient died as a result of treatment toxicity or experienced a cerebrovascular accident. Osteonecrosis (n-5), brain necrosis (n-1), and ocular/ visual problems (n = 14) were observed as late adverse reactions. Conclusion: We have shown excellent overall survival and local progression-free rate in SCC-MS patients treated by RADPLAT with acceptable rates of acute and late toxicity. A multi-institutional trial is needed to prove that this strategy is a feasible and effective approach for the treatment of SCC-MS.
引用
收藏
页码:2980 / 2986
页数:7
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