An interstitial light assembly for photodynamic therapy in prostatic carcinoma

Objective  To develop an interstitial laser light delivery system using multiple optical fibres for photodynamic therapy (PDT) in the treatment of prostate cancer. Patients and methods  A laser beam was divided equally with a 1×4 fibre splitter to deliver PDT simultaneously through four 2‐cm long, f...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:BJU international 1999-11, Vol.84 (7), p.821-826
Hauptverfasser: LEE, L. K, WHITEHURST, C, PANTELIDES, M. L, MOORE, J. V
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective  To develop an interstitial laser light delivery system using multiple optical fibres for photodynamic therapy (PDT) in the treatment of prostate cancer. Patients and methods  A laser beam was divided equally with a 1×4 fibre splitter to deliver PDT simultaneously through four 2‐cm long, flexible cylindrical optical diffusers. Biplanar transrectal ultrasonography (TRUS) and a template were used to position the optical fibres percutaneously. In vivo measurements of light penetration depth (1/μeff ) in prostate tissue were made in seven patients, using a sheathed isoprobe to measure light fluence rates at varying radial distances from the diffuser. The prostate was fixed with stabilization needles to minimize displacement during needle placement. Results  The mean (sd, range) μeff in the prostates of the seven patients was 0.35 (0.07, 0.22–0.44) mm−1 , which produced closely parallel slopes of light attenuation. However, there was up to a 10‐fold variation in absolute light levels at the same diffuser–detector separation distances amongst the seven patients, probably caused by blood pooling around the diffuser light source. A similar problem around the isoprobe detector was overcome by sheathing the probe in clear plastic tubing. By stabilizing the prostate, the optical fibre positioning was precise to within 2 mm. Conclusion  Although this light delivery and TRUS assembly were developed for clinical PDT in the prostate, the same instrumentation can be used reliably for in vivo light‐penetration studies. Haemorrhage was unpredictable and highlighted one of the main problems which needs to be overcome.
ISSN:1464-4096
1464-410X
DOI:10.1046/j.1464-410x.1999.00314.x