Preliminary results of interstitial motexafin lutetium-mediated PDT for prostate cancer

被引:81
作者
Du, K. L.
Mick, R.
Busch, T. M.
Zhu, T. C.
Finlay, J. C.
Yu, G.
Yodh, A. G.
Malkowicz, S. B.
Smith, D.
Whittington, R.
Stripp, D.
Hahn, S. M.
机构
[1] Hosp Univ Penn, Dept Radiat Oncol, Sch Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Biostat & Epidemiol, Philadelphia, PA 19104 USA
[3] Hosp Univ Penn, Sch Med, Dept Urol, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Phys & Astron, Philadelphia, PA 19104 USA
关键词
photodynamic therapy; prostate cancer; adenocarcinoma; motexafin lutetium;
D O I
10.1002/lsm.20341
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background and Objectives: Interstitial photodynamic therapy (PDT) is an emerging modality for the treatment of solid organ disease. Our group at the University of Pennsylvania has performed extensive studies that demonstrate the feasibility of interstitial PDT for prostate cancer. Our preclinical and clinical experience is herein detailed. Study Design/Materials and Methods: We have treated 16 canines in preclinical studies, and 16 human subjects in a Phase I study, using motexafin lutetium-mediated PDT for recurrent prostate adenocarcinoma. Dosimetry of light fluence, drug level and oxygen distribution for these patients were performed. Results: We demonstrate the safe and comprehensive treatment of the prostate using PDT. However, there is significant variability in the dose distribution and the subsequent tissue necrosis throughout the prostate. Conclusions: PDT is an attractive option for the treatment of prostate adenocarcinoma. However, the observed variation in PDT dose distribution translates into uncertain therapeutic reproducibility. Our future focus will be on the development of an integrated system that is able to both detect and compensate for dose variations in real-time, in order to deliver a consistent overall PDT dose distribution.
引用
收藏
页码:427 / 434
页数:8
相关论文
共 62 条
[1]   OPTICAL DOSIMETRY FOR INTERSTITIAL PHOTODYNAMIC THERAPY [J].
ARNFIELD, MR ;
TULIP, J ;
CHETNER, M ;
MCPHEE, MS .
MEDICAL PHYSICS, 1989, 16 (04) :602-608
[2]   Photodynamic therapy as adjuvant therapy in surgically treated pleural malignancies [J].
Baas, P ;
Murrer, L ;
Zoetmulder, FAN ;
Stewart, FA ;
Ris, HB ;
vanZandwijk, N ;
Peterse, JL ;
Rutgers, EJT .
BRITISH JOURNAL OF CANCER, 1997, 76 (06) :819-826
[3]   THE CONTRASTING MECHANISMS OF COLONIC COLLAGEN DAMAGE BETWEEN PHOTODYNAMIC THERAPY AND THERMAL-INJURY [J].
BARR, H ;
TRALAU, CJ ;
BOULOS, PB ;
MACROBERT, AJ ;
TILLY, R ;
BOWN, SG .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (05) :795-800
[4]   Complications after radical retropubic prostatectomy in the Medicare population [J].
Benoit, RM ;
Naslund, MJ ;
Cohen, JK .
UROLOGY, 2000, 56 (01) :116-120
[5]  
Busch TM, 2000, CANCER RES, V60, P2636
[6]  
Busch TM, 2002, CANCER RES, V62, P7273
[7]  
Chang SC, 1996, INT J CANCER, V67, P555
[8]  
Chang SC, 1997, PROSTATE, V32, P89, DOI 10.1002/(SICI)1097-0045(19970701)32:2<89::AID-PROS3>3.0.CO
[9]  
2-A
[10]  
Chang Shi-Chung, 1999, Proceedings of the National Science Council Republic of China Part B Life Sciences, V23, P158