Interstitial photodynamic therapy of the canine prostate using intra-arterial administration of photosensitizer and computerized pulsed light delivery

被引:5
作者
Xiao, Zhengwen
Dickey, Dwayne
Owen, Richard J.
Tulip, John
Moore, Ronald
机构
[1] Univ Alberta, 2D2 Walter Mackenzie Hlth Sci Ctr, Dept Surg & Oncol, Edmonton, AB T6G 2B7, Canada
[2] Univ Alberta, Dept Oncol, Edmonton, AB, Canada
关键词
prostate; drug delivery systems; photochemotherapy; dogs; QLT0074;
D O I
10.1016/j.juro.2007.03.008
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Purpose: We determined the feasibility of complete treatment of the canine prostate and long-term effectiveness of interstitial photodynamic therapy using the intra-arterial photosensitizer QLT0074 (benzoporphyrin derivative 1,3-diene C,D-diethylene glycol ester A ring) (QLT, Vancouver, British Columbia, Canada) administration and pulsed light delivery. Materials and Methods: The prostate gland of 11 dogs were infused with QLT0074 via the prostatovesical arteries (2 mg drug per artery bilaterally) under fluoroscopic guidance. Immediately following infusion the prostate was surgically exposed and 7 optical fibers with 1.5 cm cylindrical diffusers in after loading sheaths were inserted into the prostate through a template. Light was delivered sequentially to the optic fibers via a computer driven switch system. One dog was sacrificed 6 days after photodynamic therapy to assess acute tissue effects. The other 10 dogs were monitored for clinical tolerance and urinary function, and sacrificed at between 3 and 11 months. Prostate specimens were examined microscopically to evaluate long-term tissue reactions. Results: Comprehensive destruction of the prostate was noted in the acute dog. Except for urinary retention and mild hematuria no other perioperative complications were observed in the chronic dogs. Urodynamic examination did not reveal deleterious bladder and urethral function. Average prostate volume decreased 71% at 3 months and 56% after 6 months (p = 0.007 and 0.014, respectively). Microscopic evaluation revealed prostate glandular epithelial atrophy, stromal fibrosis and mononuclear cell infiltration. Conclusions: Interstitial photodynamic therapy using intra-arterial QLT0074 and pulsed light delivery is safe and feasible for comprehensive destruction of the canine prostate. Clinical trials are required to confirm it for managing prostate diseases.
引用
收藏
页码:308 / 313
页数:6
相关论文
共 19 条
  • [1] Monte Carlo modelling of angular radiance in tissue phantoms and human prostate: PDT light dosimetry
    Barajas, O
    Ballangrud, AM
    Miller, GG
    Moore, RB
    Tulip, J
    [J]. PHYSICS IN MEDICINE AND BIOLOGY, 1997, 42 (09) : 1675 - 1687
  • [2] Chang SC, 1996, INT J CANCER, V67, P555
  • [3] Changes in in vivo optical properties and light distributions in normal canine prostate during photodynamic therapy
    Chen, Q
    Wilson, BC
    Shetty, SD
    Patterson, MS
    Cerny, JC
    Hetzel, FW
    [J]. RADIATION RESEARCH, 1997, 147 (01) : 86 - 91
  • [4] Laser dosimetry studies in the prostate
    Chen, Q
    Hetzel, FW
    [J]. JOURNAL OF CLINICAL LASER MEDICINE & SURGERY, 1998, 16 (01): : 9 - 12
  • [5] The changing face of low-risk prostate cancer: Trends in clinical presentation and primary management
    Cooperberg, MR
    Lubeck, DP
    Meni, MV
    Mehta, SS
    Carroll, PR
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2004, 22 (11) : 2141 - 2149
  • [6] Light dosimetry for multiple cylindrical diffusing sources for use in photodynamic therapy
    Dickey, DJ
    Partridge, K
    Moore, RB
    Tulip, J
    [J]. PHYSICS IN MEDICINE AND BIOLOGY, 2004, 49 (14) : 3197 - 3208
  • [7] Cancer statistics, 2005
    Jemal, A
    Murray, T
    Ward, E
    Samuels, A
    Tiwari, RC
    Ghafoor, A
    Feuer, EJ
    Thun, MJ
    [J]. CA-A CANCER JOURNAL FOR CLINICIANS, 2005, 55 (01) : 10 - 30
  • [8] Kuriyama M, 1994, CANCER CHEMOTH PHARM, V35, P27
  • [9] MOORE RB, 2006, ANN M W SECT AM UR A
  • [10] Photodynamic therapy for prostate cancer recurrence after radiotherapy: A phase I study
    Nathan, TR
    Whitelaw, DE
    Chang, SC
    Lees, WR
    Ripley, PM
    Payne, H
    Jones, L
    Parkinson, MC
    Emberton, M
    Gillams, AR
    Mundy, AR
    Bown, SG
    [J]. JOURNAL OF UROLOGY, 2002, 168 (04) : 1427 - 1432