Feasibility and radiation induced toxicity regarding the first application of transperineal implementation of biocompatible balloon for high dose radiotherapy in patients with prostate carcinoma

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3109508 14 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
Feasibility and radiation induced toxicity regarding the first application of transperineal implementation of biocompatible balloon for high dose radiotherapy in patients with prostate carcinoma
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Objective: To evaluate the feasibility of the transperineal implementation of biocompatible balloon (Prospace) and the acute toxicity of high dose 3DCRT in patients with localized low risk prostate cancer. Materials and methods: Between December 2011 and April 2012, fifteen patients were treated with external 3DCRT consisted of 76-78 Gy in 38-39 daily fractions (2.0 Gy/ fraction). Before 3DCRT, we placed the Prospace though the perineum by a minimally invasive procedure in the intermediate space between the rectum and the prostate. The primary study endpoint was the evaluation of acute toxicity according to the EORTC/RTOG radiation toxicity scale. Erectile function was evaluated with the IIEF-5 questionnaire. Rectosigmoidoscopy was performed at baseline, at the end of 3DCRT and 3 months thereafter in order to assess also the rectal toxicity according to Subjective-RectoSigmoid (S-RS) scale. The evaluation of pain related to Prospace implementation was done with the visual analogue score (VAS).Results: The acute toxicities were as follows: grade I GI toxicity in two patients and for GU toxicity, three patients with grade I of nocturia, four patients with grade I of frequency, two patients with grade I and two patients with grade II of dysouria. The mean score of rectal toxicity according to S-RS score was 1.8(±0.6). The mean VAS score related to Prospace was 1.4(±0.5). Erectile function was unchanged. The Prospace device was found stable in sequential CTs during irradiation.Conclusions: The implementation of PROSPACE was feasible, while the acute radiation toxicity was low and comparable with IMRT techniques. © 2013 Kouloulias et al.; licensee BioMed Central Ltd.
Έτος δημοσίευσης:
2013
Συγγραφείς:
Kouloulias, V.
Kalogeropoulos, T.
Platoni, K.
Georgakopoulos, J.
Matsopoulos, G.
Chaldeopoulos, D.
Beli, I.
Pantelakos, P.
Asimakopoulos, C.
Kouvaris, J.
Kelekis, N.
Περιοδικό:
Journal of Radiation Oncology
Τόμος:
8
Αριθμός / τεύχος:
1
Λέξεις-κλειδιά:
nonsteroid antiinflammatory agent; prostate specific antigen, aged; article; biocompatibility; cancer localization; cancer radiotherapy; clinical article; controlled study; dysuria; feasibility study; gastrointestinal toxicity; hematuria; human; male; nocturia; outcome assessment; penis erection; perineum; prostate carcinoma; questionnaire; radiation dose; radiation dose fractionation; radiation injury; rectum; rectum disease; retrospective study; sigmoidoscopy; tenesmus; transrectal ultrasonography; urinary urgency; urogenital tract disease; visual analog scale, Adenocarcinoma; Aged; Feasibility Studies; Humans; Male; Prostatic Neoplasms; Radiation Injuries; Radiotherapy, Conformal; Rectum
Επίσημο URL (Εκδότης):
DOI:
10.1186/1748-717X-8-82
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