Intraoperative radiotherapy for locally advanced prostate cancer: The experience of the European institute of oncology
Abstract
Data di Pubblicazione:
2008
Citazione:
Intraoperative radiotherapy for locally advanced prostate cancer: The experience of the European institute of oncology / Vavassori, Andrea; Ciocca, Mario; Jereczek, Barbara; Zerini, Dario; Ivaldi, Giovanni; Fodor, Cristiana; Lazzari, Roberta; Cattani, Federica; Rondi, Elena; Garibaldi, Cristina; Cambria, Raffaella; Matei, Victor; Scardino, Epifanio; Verweij, Fabrizio; Musi, Gennaro; Rocco, Bernardo Maria Cesare; De Cobelli, Ottavio; Orecchia, Roberto. - In: THE JOURNAL OF UROLOGY. - ISSN 0022-5347. - 179:4(2008), pp. 183-183. [10.1016/S0022-5347(08)60529-7]
Abstract:
INTRODUCTION AND OBJECTIVE: To present the technique
adopted for intraoperative radiotherapy (IORT) for locally advanced
prostate cancer.
METHODS: Between June 2005 and February 2007, 24
patients (pts) with non-metastatic prostate cancer were treated with
IORT before prostatectomy as part of their surgical procedure. Median
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median bioptic Gleason Score was 7. According to NCCN 2007, risk
group distribution was as follows: intermediate risk 2 pts (8.33%) and
high risk 22 pts (91.67%). A total of 11 pts (45.83%) were treated with
neoadjuvant hormones. Immediately before IORT prostate dimensions
and rectum depth were measured with intraoperative ultrasound. IORT
was delivered by a mobile linear accelerator in the operating room.
The prescribed dose was 12 Gy at the 90% isodose. In vivo dosimetry
was performed. Three months later, postoperative external beam
radiotherapy (EBRT) of 45-50,4 Gy in 25-28 fractions was prescribed
to the prostatic bed alone and whole pelvis in case of pT3-4 pN0 and
pN1, respectively.
RESULTS: According to the MSKCC nomograms, the mean
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and lymph node involvement were 8%, 40% and 25% respectively.
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6-9), pT2 7 pts (29,2%), pT3 14 pts (58,3), pT4 3 (12,5%), pN0 12 pts,
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pts (16.6%) and no further radiation treatment was prescribed. Based
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bed EBRT is planned in 12 and 8 pts, respectively. After a median
follow up of 9.2 months (range 3.3-15.7) only 1 patient had evidence of
biochemical relapse. No patients had major acute rectal toxicity. No acute
urinary toxicity was observed in 6 patients, 17 patients had G1 toxicity.
No increased risk of urinary incontinence was recorded.
CONCLUSIONS: IORT delivered before prostatectomy
appeared a feasible and safe approach for prostate cancer, showing
a satisfactory dose coverage to the prostate bed with relatively low
rectal wall dose. Longer follow-up is needed to evaluate late toxicity
and clinical control.
Tipologia CRIS:
Abstract in Rivista
Elenco autori:
Vavassori, Andrea; Ciocca, Mario; Jereczek, Barbara; Zerini, Dario; Ivaldi, Giovanni; Fodor, Cristiana; Lazzari, Roberta; Cattani, Federica; Rondi, Elena; Garibaldi, Cristina; Cambria, Raffaella; Matei, Victor; Scardino, Epifanio; Verweij, Fabrizio; Musi, Gennaro; Rocco, Bernardo Maria Cesare; De Cobelli, Ottavio; Orecchia, Roberto
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