Treatment outcome of Photofrin-based photodynamic therapy for T1 and T2 oral squamous cell carcinoma and dysplasia

被引:36
作者
Ikeda, Hisazumi [1 ]
Tobita, Takayoshi [1 ]
Ohba, Seigo [2 ]
Uehara, Masataka [3 ]
Asahina, Izumi [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Unit Translat Med, Dept Regenerat Oral Surg, Nagasaki 8528501, Japan
[2] Univ Fukui, Fac Med Sci, Dept Sensory & Locomotor Med, Div Dent & Oral Surg, Fukui, Japan
[3] Kyushu Dent Coll, Dept Sci Phys Funct, Div Maxillofacial Surg, Fukuoka, Japan
关键词
Photodynamic therapy (PDT); Photofrin; Squamous cell carcinoma dysplasia; PREMALIGNANT LESIONS; NECK CANCERS; LASER-LIGHT; HEAD; RADIOTHERAPY; SURGERY; CAVITY; TUMORS;
D O I
10.1016/j.pdpdt.2013.01.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Photodynamic therapy (PDT) is a minimally invasive treatment modality for early and superficial malignancy or premalignancy in the head and neck regions. However, few studies have examined the use of Photofrin-mediated PDT to manage early carcinoma and dysplasia in the oral cavity. Methods: Between January 2004 and November 2008, 25 T1 to T2 patients with NO oral squamous cell carcinoma and mucosal dysplasia in the oral cavity were treated by Porfimer sodium (Photofrin (R))-mediated PDT at Nagasaki University Hospital. Clinical responses were evaluated according to the guidelines of the Response Evaluation Criteria in Solid Tumors (RECIST). After the PDT and a 2-year follow-up period, disease specific survival rates were then calculated. Results: A total of 30 regions in 25 patients (18 with squamous cell carcinoma and 7 with epithelial dysplasia with hyperkeratosis in the oral cavity) were treated by PDT. Complete response was achieved in 24 of the 25 patients (96%), with a partial response found in the remaining patient. For the three patients who exhibited recurrence at 4, 5, and 15 months after PDT, salvage surgery or a second PDT was performed. Of these three patients, one died due to another disease, while one died due to local lymphatic metastasis that occurred during the follow-up period. Overall, the disease specific survival rate was 95.8%. Treatment-related edema and pain emerged within 24 h after irradiation. Pain control using non-steroid anti-inflammatory drugs and opiates was required for 3-4 weeks in all patients. Complete healing was attained at 4-6 weeks after the treatment. No persistent problems related to functional or esthetic outcomes were noted. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
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