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ABSTRACTS OF THE 21st ANNUAL MEETING OF THE ITALIAN ...

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Abstracts of the <strong>21st</strong> Annual Meeting of the Italian Society of Uro-Oncology (SIUrO), 22-24 June, 2011, Naples, Italy<br />

Aim: To evaluate acute urinary and rectal toxicities in patients<br />

with prostate cancer submitted to image-guided radiotherapy<br />

(IGRT). Patients and Methods: From June 2009 to March<br />

2010, 29 patients (median age: 70 years, range: 48-82 years;<br />

median Gleason score: 7, range: 5-10) underwent radical<br />

radiotherapy and 12 patients (median age: 67 years, range: 54-<br />

78 years; median Gleason score: 7, range: 5-9) underwent<br />

adjuvant radiotherapy. All patients underwent simulation<br />

computed tomography (CT) without contrast injection in<br />

supine position. The CT scans were used to delineate the<br />

organs at risk, namely bladder, rectum, coxo-femoral joints<br />

and penis bulb. For patients receiving radical radiotherapy, the<br />

seminal vesicles were excluded at an absorbed dose of 66 Gy.<br />

For this group of patients, the total delivered dose was 74 Gy,<br />

while for patients who underwent adjuvant radiotherapy, the<br />

total delivered dose was 66 Gy. The planning target volume<br />

(PTV) was obtained from the expansion of the clinical target<br />

volume (CTV) by 8 mm anteriorly, laterally and caudally, 10<br />

mm cranially and 5 mm posteriorly. The isocenter positioncheck<br />

protocol was performed with the use of MV cone-beam<br />

CT on the first, second and third day, successively, once a<br />

week. Correct positioning was evaluated using the bone<br />

structures of the pelvis as reference. Corrections of isocenter<br />

position were made with a semi-automatic modality. Acute<br />

urinary and rectal toxicities were evaluated administering IPSS<br />

before radiotherapy, during the weekly clinical examinations<br />

and at the end of the radiotherapy. At the same time, we used<br />

the RTOG scale for acute and late adverse events to evaluate<br />

toxicities. We also calculated the median error of isocenter<br />

position indicated by virtual simulation and cone-beam<br />

existing in the left-right (L-R), cranial-caudal (C-C) and<br />

anterior-posterior (A-P) directions. Results: At the end of<br />

IGRT, we found a median IPSS score of 8 (range: 0-14) for<br />

the 12 patients treated with adjuvant radiotherapy; 50% of<br />

patients had IPSS scores between 0-7. The worst scores<br />

corresponded to the first, fourth and seventh questions. In<br />

addition, we recorded prevalent G1 rectal toxicity and G2<br />

urinary toxicity at end of treatment. In the group of patients<br />

who underwent radical radiotherapy, the median IPSS score at<br />

the end of treatment was 9 (range: 1-28) and 58.6% of patients<br />

had IPSS scores between 0-7. The worst scores corresponded<br />

to the second and seventh questions. There was prevalent G1<br />

rectal toxicity and G2 urinary toxicity in 93.1% and 44.8% of<br />

patients, respectively, at the end of treatment. At the last<br />

follow-up (March 2010), in both groups, rectal and urinary<br />

toxicities were G0, while IPSS scores between 0-7 were<br />

observed in 82.6 and 100% of patients in the radical and<br />

adjuvant radiotherapy groups, respectively. Median values of<br />

L-R, C-C and A-P directions were 3, 2 and 3 mm,<br />

respectively. In order to match precision and workload criteria,<br />

thresholds for the standard deviation of the corrections were<br />

set as: 2.96, 3.78 and 2.78 mm in the L-R, C-C and A-P<br />

directions, respectively. Conclusion: Treatment was well<br />

tolerated. We observed low toxicity rates and a high<br />

compliance to treatment. IGRT, performed for first fractions,<br />

may be helpful for eliminating gross systematic errors,<br />

especially after virtual simulation.<br />

114<br />

TOTAL INTRAVENOUS ANES<strong>THE</strong>SIA (TIVA),<br />

TARGET-CONTROLLED INFUSION AND DA<br />

VINCI ROBOT-ASSISTED PROSTATECTOMY<br />

Ciro Visconti1 , Albertina Mastroluca2 , Giovanna Pavone2 ,<br />

Giuseppe Melchionda2 , Latiano Costanzo3 and Antonio Cisternino3 1Urology, 2Department of Anesthesiology and Intensive<br />

Care, 3Department of Urology, IRCCS, Casa Sollievo della<br />

Sofferenza, Opera Padre Pio, San Giovanni Rotondo, Foggia,<br />

Italy<br />

Background: Robotic prostatectomy provides a prolonged<br />

Trendelenburg position of about 40˚ and CO 2<br />

pneumoperitoneum for surgical exposure with potential<br />

significant changes in hemodynamic and respiratory<br />

parameters for the patient, such as the rising of central venous<br />

pressure (CVP) and pulmonary capillary wedge pressures.<br />

CVP measures the filling pressure of the right ventricular<br />

volume and gives an estimate of the intravascular volume<br />

status and the interplay of the circulating blood volume<br />

venous tone. Measuring CVP is widely considered a useful<br />

aid in the management of a patient’s fluid status during<br />

surgery. Target-controlled infusion (TCI) is a total intravenous<br />

anesthesia (TIVA) technique that maintains constant plasma<br />

and effect-site concentrations of anesthetic agents due to the<br />

pharmacokinetic models incorporated in the TCI pump. The<br />

precise dosing of the anesthetic drugs leads to superior<br />

hemodynamic stability and fast recovery after surgery for<br />

patients. The use of propofol/remifentanil TIVA-TCI in<br />

combination tends to have a synergistic action and the rate of<br />

equilibration between blood and effect-site depends on<br />

cardiac output, central blood volume, cerebral blood flow,<br />

lipid solubility and degree of ionization of drug. We evaluated<br />

TIVA-TCI of propofol and remifentanil and hemodynamic<br />

and respiratory parameters during Da Vinci robot-assisted<br />

prostatectomy. Patients and Methods: In our retrospective<br />

study, we evaluated 15 consecutive patients scheduled for<br />

robot-assisted endoscopic radical prostatectomy in TIVA-TCI<br />

with non-invasive monitoring of arterial blood pressure, heart<br />

rate, pulse oximetry, end-tidal (ET) CO 2, peak and plateau<br />

airway pressure and state entropy (SE), assessing anesthetic<br />

depth and continuous invasive CVP on a S/5 Datex-Ohmeda<br />

monitor. Accurate measurement of CVP was obtained with<br />

cannulation of the internal jugular vein. The depth of<br />

anesthesia was obtained with TIVA-TCI in propofol/<br />

1867

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