Photodynamic therapy (PDT) for lung cancers

被引:218
作者
Usuda, Jitsuo
Kato, Harubumi
Okunaka, Tetsuya
Furukawa, Kinya
Tsutsui, Hidemitsu
Yamada, Kimito
Suga, Yasuhiro
Honda, Hidetoshi
Nagatsuka, Yoshitaka
Ohira, Tatsuo
Tsuboi, Masahiro
Hirano, Takashi
机构
[1] Tokyo Med Univ, Dept Thorac Surg, Tokyo, Japan
[2] Int Univ Hlth & Welf, Sanno Hosp, Resp Dis Ctr, Tokyo, Japan
[3] Tokyo Med Univ, Kasumigaura Hosp, Dept Thorac Surg, Ibaraki, Japan
关键词
photodynamic therapy; lung cancer;
D O I
10.1097/01243894-200606000-00018
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Photodynamic therapy (PDT), a treatment for cancer, uses a photosensitizer and laser irradiation to produce reactive oxygen in cells. In Japan, the United States, and many other countries, PDT is a treatment option for stage 0 (TisN0M0) and stage 1 (T1N0M0) centrally located early stage lung cancer. PDT can preserve lung function, can be repeated, and can be combined with other therapeutic modalities such as chemotherapy. Recently, mono-L-aspartyl chlorine e6 (NPe6, Laserphyrin), a second-generation photosensitizer with lower photosensitivity than Photofrin (porfimer sodium), was approved by the Japanese government and a phase 11 clinical study using NPe6 with a new diode laser demonstrated an excellent antitumor effect and low skin photosensitivity. We expect PDT to be widely employed in many fields and the applications of PDT to be extended because of the decreasing cost of laser equipment and lower systemic photosensitivity induced by the photosensitizer. The purpose of this review is to introduce not only recent clinical trials of PDT for centrally located early lung cancer, but also new applications of PDT for cases of peripheral-type, early-stage lung cancers. We also discuss the applications of PDT for advanced lung cancer and combined therapy using PDT and other treatments for lung cancer.
引用
收藏
页码:489 / 493
页数:5
相关论文
共 44 条
[1]  
Cortese DA, 1997, MAYO CLIN PROC, V72, P595
[2]   PHASE-I STUDY OF DEBULKING SURGERY AND PHOTODYNAMIC THERAPY FOR DISSEMINATED INTRAPERITONEAL TUMORS [J].
DELANEY, TF ;
SINDELAR, WF ;
TOCHNER, Z ;
SMITH, PD ;
FRIAUF, WS ;
THOMAS, G ;
DACHOWSKI, L ;
COLE, JW ;
STEINBERG, SM ;
GLATSTEIN, E .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1993, 25 (03) :445-457
[3]   Efficacy and safety of photodynamic therapy versus Nd-YAG laser resection in NSCLC with airway obstruction [J].
Diaz-Jiménez, JP ;
Martinez-Ballarín, JE ;
Llunell, A ;
Farrero, E ;
Rodríguez, A ;
Castro, MJ .
EUROPEAN RESPIRATORY JOURNAL, 1999, 14 (04) :800-805
[4]   Photodynamic therapy [J].
Dougherty, TJ ;
Gomer, CJ ;
Henderson, BW ;
Jori, G ;
Kessel, D ;
Korbelik, M ;
Moan, J ;
Peng, Q .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1998, 90 (12) :889-905
[5]  
Ferrario A, 2000, CANCER RES, V60, P4066
[6]   The matrix metalloproteinase inhibitor prinomastat enhances photodynamic therapy responsiveness in a mouse tumor model [J].
Ferrario, A ;
Chantrain, CF ;
von Tiehl, K ;
Buckley, S ;
Rucker, N ;
Shalinsky, DR ;
Shimada, H ;
DeClerck, YA ;
Gomer, CJ .
CANCER RESEARCH, 2004, 64 (07) :2328-2332
[7]  
Ferrario A, 2002, CANCER RES, V62, P3956
[8]  
FINGAR VH, 1992, CANCER RES, V52, P4914
[9]  
FUKUKAWA K, 1998, PORPHYRINS, V7, P199
[10]   Locally recurrent central-type early stage lung cancer <1.0 cm in diameter after complete remission by photodynamic therapy [J].
Furakawa, K ;
Kato, H ;
Konaka, C ;
Okunaka, T ;
Usuda, J ;
Ebihara, Y .
CHEST, 2005, 128 (05) :3269-3275