Prostatic Adenocarcinoma Clinical Trial
Official title:
The Impact of Dose Escalation Using Gold Markers in Image Guided Volumetric Modulated Arc Radiotherapy to the Focal Lesion Micro Boost of Localized Prostate Cancer
Gold markers implanted in the prostate are used frequently for position verification of the
prostate during external-beam radiotherapy. By using the markers as a surrogate for the
prostate itself, not only set-up errors, but also the internal motion of the prostate
relative to the bony anatomy can be identified.
It is thus believed that escalated dose marker guided radiotherapy should result in better
biochemical control compared to conventional external beam radiotherapy, with a similar or
lower incidence of toxicity. However, clinical data to support this is still limited. The
purpose of this study is to directly compare late toxicity as well as biochemical control
between patients treated with dose escalated marker guided radiotherapy versus conventional
dose non-marker guided radiotherapy who has otherwise been treated with similar radiotherapy
planning techniques and equipment.
Prostate magnetic resonance imaging has undergone several technical improvements and shows
promises for prostate tumor detection and localization. In addition to morphological
information, magnetic resonance imaging allows an estimation of physiological properties of
tissues. Diffusion-weighted magnetic resonance imaging is sensitive to restriction of
diffusion of water molecules, and dynamic contrast enhanced magnetic resonance imaging can
analyze tissue micro vascular properties. Multi para metric magnetic resonance imaging
combining Diffusion-weighted and Dynamic contrast enhanced has demonstrated its value in
distinguishing malignant from benign prostate tissue.
Higher radiation dose levels were consistently associated with improved biochemical control
outcomes and reduction in distant metastases. Radiation dose was one of the important
predictors of long-term biochemical tumor control. Dose levels < 70.2 Grey and 70.2-79.2 Grey
were associated with 2.3 and 1.3-fold increased risks of pro static specific antigen relapse
compared with higher doses. However, further dose escalation to the whole gland is limited
due to an unacceptable high risk of acute and late toxicity. Moreover, local recurrences
often originate at the location of the macroscopic tumor, so boosting the radiation dose at
the macroscopic tumor within the prostate might increase local control. A reduction of
distant metastases and improved survival can be expected by reducing local failure. Treating
the dominant focus or boosting the dose to this area while reducing the dose to as much
healthy tissue as possible has significant potential for improving treatment.
Thirty consecuative loclized prostate cancer patients will be recruited according to
inclusion & exclusion criteria. Once the patient meets the selection criteria stratification
will be done according to the following risk group classification:
Stage Gleason score PSA Low risk T1-T2a 2-6 < 10 ng/mL Intermediate risk T2b-T2c 7 10-20
ng/mL High risk T3a 8-10 > 20 ng/mL
The patient will receive 2-6 months of neo adjuvant hormonal treatment, followed with
concomitant hormonal treatment during the radiation course for intermediate and high risk
groups then adjuvant hormonal for 2-3 years in the high risk group.
For each patient the radio-opaque marker (used for treatment verification) will be inserted
by ultrasound guidance & local anesthetic with an 17 GA x 30 cm brachy therapy needle that
has 1.2 mm x 3 mm one gold marker. The ultrasound probe (as used for trans rectal biopsy)
will be introduced rectally with the patient in the left lateral position. After measuring
the volume of the prostate and determining the desired position (preferably in the corpus of
prostate), three gold markers will be inserted as follows: one into right side, one into left
side of the base and the third in the apex of the prostate. All patients will receive a
course of preventive antibiotic treatment that consists of ciprofloxacine 500 mg BID, 1 day
before implantation and 4 consecutive days. Patients under anti-platelet therapy will be told
to stop the medication 5 days before implantation.
CT images will be done within 5 days of markers insertion in the same treatment supine
position with Knee & ankle support. CT images will be taken in 1.25 mm slice thickness from
the top of the 4th lumbar vertebrae to ischial tuberosities. Patients will be asked to
evacuate bowels prior to scanning, and bladder will be kept comfortably full by drinking two
glasses of water (250-500 ml) 30 min prior to the scan.
The reference marks, one mid line and two lateral, will be placed at the level of the upper
border of the symphysis pubis or iliac crest. No contrast will be used so as to avoid the
dose artifact by it during treatment planning and dose calculation.
Multi parametric magnetic resonance imaging combing Diffusion-weighted & Dynamic contrast
enhanced with intravenous contrast will be done prior to Marker insertion with the sequence
of: axial T1 & T2, coronal T2 & spare, post contrast dynamic axial & sagittal and diffusion
with ADC. The views of MRI images will be in 1.25 mm thickness with 0 gap. Fusion of both CT
images & MRI images will be done using manual registration guided by bony landmarks.
Delineation of clinical target volumes & risk organs will be done on CT images guided with
MRI fused images according to Radiation therapy oncology group criteria. MRI T2 weighted
images will guide the pro static delineation from base to apex, with more accurate
identification of the apex compared to CT. Also Diffusion-weighted with Dynamic contrast
enhanced magnetic resonant imaging will be of value for identification of dominant focal
lesion of the prostate.
The patient will be treated with radical radiotherapy to prostate 78 Gray/35# (2.2 Gray/#)
with simultaneous integrated boost to focal lesion 87.5 Grey/35# (2.5 Gray/#). Lymph node 60
Grey if positively involved. Seminal vesicle will receive 78 Gray if involved & 54 Gray if
not. Roche formula will be used to estimate lymph node & seminal vesicle involvement if more
than 15%:
- Seminal vesicle involvement (%) = PSA + [10× (Gleason-6)]
- Pelvic lymph node involvement = 2/3 × PSA + [10× (Gleason score -6)]
Constrains for organs at risk will be followed according to QUANTEC. Plan acceptance for
Planning target volume of the targets will be done as follows:
- D 95(95% of the prescribed dose) must be received by at least 95% of the planning target
volume.
- D max (dose received by 2% of the volume) should not exceed 107% and should be inside
the clinical target volume.
- D min (dose received by 98% of the volume) should not be less than 90% and should be
outside the clinical target volume.
In addition to the standard quality assurance procedures carried out for any radiation
technique, such as dose output calibration, ISO-center and Multi-leaf collimator
verification, V MAT patients will undergo specific pretreatment quality assurance measures to
check ISO-center absolute dose (using ionization chamber and slap phantom) and dose (using
portal image and portal dosimeter module on the planning system).
Position verification will be done guided with implanted gold markers with daily portal
imaging (AP & lateral) correction protocol in mediolateral, superior-inferior &
inward-outward directions. The portal correction images will be verified daily to detect
average shifts in the three directions using 2D-2D match & Marker Match. Random or
inter-fraction errors which are deviations between different fractions will be taken weekly
during a treatment series. Systematic errors Which are deviations between the planned patient
position and the average patient position of a course of fractional therapy will be taken in
the first three settings. The mean and standard deviation (SD) of the systematic error and SD
of random errors will be analyzed. To represent true magnitude of errors, the absolute value
of the deviations will be also considered. These means will be used in calculations of the
off-line treated Dose-Volume Histogram versus Planned Dose-Volume Histogram and in
measurement of systemic & random error to define reasonable planning target volume.
Follow up of the patients will be done with mean of 12 months to detect biochemical control &
disease free survival. PSA & pelvic ultrasound will be done every 3 months for first 2 years
then every 6 months for 3-5 years. Genito-urinary, gastro-intestinal & hematological toxicity
will be assessed using Radiation Therapy Oncology Group toxicity score & patient reported out
coming will be assessed using questionnaire (validated Arabic translation) every 3 months.
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