Dose Escalation Using Fiducial Markers in Image Guided Volumetric Modulated Arc Therapy to the Focal Lesion Micro Boost of Localized Prostate Cancer

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.

Study Overview

• Status: Completed
• Conditions: Prostatic Adenocarcinoma
• Intervention / Treatment: Radiation: Dose escalation to prostate focal lesion

Detailed Description

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.

• Study Type: Interventional
• Enrollment (Actual): 30
• Phase: Phase 2

Contacts and Locations

Study Locations

• Egypt
  • Maadi
    • Cairo, Maadi, Egypt, 11728
      • Radwa Fawzy Saleh Ahmed

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 36 years to 76 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Performance status ECOG: 0-2
2. Pathologically proven prostatic adenocarcinoma.
3. Localized prostate cancer (Gleason's score: 2-10, Baseline serum prostatic antigen: >4 ng/dl, T1a-T3b).
4. No extra prostatic invading adjacent structures.
5. Adequate hematological, renal & hepatic profile.
6. Insertion of more than one fiducial marker in the prostate.
7. Patient did verbal & written consent and adherence to treatment.

Exclusion Criteria:

1. Patient weight >130 kg.
2. Performance status EGOG: 3-4.
3. Distant metastasis.
4. Previous pelvic radiotherapy.
5. Previous prostatectomy.
6. Urinary bladder stones.
7. General contraindications for MRI (i.e. cardiac pacemaker, metal implants or history of severe allergic reaction after administration of contrast agent).
8. Concomitant neoplastic disease or previous anti neoplastic therapy.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Health Services Research
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm

Intervention / Treatment

Experimental: Dose escaltion; insertion of 3 fiducial markers, prostate will receive 78 Gy with dose escalation to prostate focal lesion up to 87 Gy

Radiation: Dose escalation to prostate focal lesion; For each patient the radio-opaque marker (used for treatment verification) will be inserted by ultrasound guidance & local anaesthetic with an 17ga x 30cm brachytherapy needle that has 1.2mm x 3mm one gold marker. The ultrasound probe (as used for transrectal 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Measurement of systemic error in mm and random error in cm in the different three direction X-Y-Z	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 by mm for 35 fraction. The off-line portal pre-correction images will be verified daily to detect average shifts in the three diresctions. 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 fractioned 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.	12 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Biochemical relapse of PSA above normal level 4 ng/dl	Follow up of the patients will be done every 3 months up to 12 months to detect biochemical control by PSA measuring. PSA & pelvic ultrasound.	12 months
subjective toxicity assessment	Genito-urinary & gastro-intestinal will be assessed using RTOG toxicity score weekly during radiotherapy sessions.	12 months
Objective toxicity assessment	Patient reported out coming will be assessed using FACIT questionnaire (validated Arabic translation) every 3 months up to 12 months.	12 months

Collaborators and Investigators

• Sponsor: Kasr El Aini Hospital

Study record dates

Study Major Dates

• Study Start: May 1, 2016
• Primary Completion (Actual): December 1, 2017
• Study Completion (Actual): April 1, 2018

Study Registration Dates

• First Submitted: August 21, 2016
• First Submitted That Met QC Criteria: December 23, 2017
• First Posted (Actual): December 27, 2017

Study Record Updates

• Last Update Posted (Actual): August 14, 2019
• Last Update Submitted That Met QC Criteria: August 12, 2019
• Last Verified: August 1, 2019

More Information

Terms related to this study

• Keywords: Dose escalation; VMAT; Fiducial marker; Localized Prostate; Focal Lesion; Random error during dose escalation radiotherapy; fiducial marker image guided technique
• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Carcinoma; Neoplasms, Glandular and Epithelial; Adenocarcinoma
• Other Study ID Numbers: Prostate

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: Yes
• IPD Plan Description: Abstract and paper publication