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Biological Imaging for Optimising CTV and GTV Contouring in Prostate Cancer to Improve the Possibilities for IMRT Dose Escalation

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Trial Information

Biological Imaging for Optimising CTV and GTV Contouring in Prostate Cancer to Improve the Possibilities for IMRT Dose Escalation


To investigate the possibilities to improve Clinical Target Volume (CTV) and Gross Tumour
Volume (GTV) delineation by using the latest biological imaging modalities on 15 patients
with prostate cancer. Our ultimate goal is to set new GTV and CTV definitions and redefine
the choice of irradiation margins in Intensity Modulated RadioTherapy (IMRT) for prostate
cancer. Furthermore, try to translate the functional imaging data into a Tomotherapy IMRT


Treatment results after standard dose external beam irradiation of locally advanced prostate
cancer are insufficient. According to RTOG-8531, RTOG-8610 and EORTC series on T1 to T4
tumours, 5-year overall survival ranges 60 - 73% and 5-year disease free survival ranges 15
- 67%.

Local control can be enhanced by adjuvant androgen suppression, the 5-year disease free
survival increases significantly to 36 - 89%. Unfortunately, androgen suppression
significantly deteriorates quality of life.

Increasing the irradiation dose also improves local control. However, local toxicity,
especially rectal and bladder complications, restrict the dose which can be given with
conformal external beam irradiation with population based uncertainty margins. Setup
inaccuracy and organ movement determine the irradiation margins needed. Modern position
verification techniques, e.g. using fiducial markers in the prostate in combination with
megavoltage imaging techniques, allow a reduction of the margins and offer the possibility
for dose escalation in the prostate. Studies of IMRT have utilised these sophisticated
position verification techniques and this approach appears feasible. A further reduction of
the margins, and thus a possible further increasing of the irradiation dose, can be expected
from improving the delineation of the prostate contour. Imaging can be performed to
delineate anatomic structures or biological processes within the intraprostatic malignant

CT is commonly used for anatomy delineation, based on early studies. Although the image
quality has improved gradually, unfortunately, CT still severely overestimates the prostate
volume. Furthermore, Teh et al found in 712 prostatectomy patients large mean differences
between CT-based estimates of the GTV and PTV and Pathological Prostate Volume (PPV). Rasch
et al found an average ratio between CT and MRI volumes of 1.4. Also the MRI technique
improved and now produces a much better imaging quality, e.g. by increasing Tesla, by using
the present phased array coils and by using thinner slice thickness. The accuracy of
detecting extracapsular extension in prostate carcinoma with endorectal and phased-array
coil MR imaging reaches 77% for experienced readers. Concluding, MRI is superior to CT in
GTV contouring, but MRI alone (using combined T1 SE and T2 TSE) may not be sufficient for
visualisation of the GTV. It is expected that biological imaging will improve GTV
delineation further. Within the GTV a Biological Target Volume (BTV) will become visible,
which may further improve the efficacy of cancer radiotherapy.

In biological imaging the use of the different imaging techniques have yet to be explored.
Currently, there are two topics of importance. The first topic is perfusion. In prostate
cancer, the degree of vascularisation appears to correlate with aggressive behaviour and
risk of metastasis. In prostate cancer approximately two times as many microvessels exist in
the malignant tissue compared to normal tissues. Furthermore, in benign tissues the
capillaries are restricted for the most part to the periglandular stroma immediately
adjacent to the epithelium, whereas the distribution in carcinoma appears to be more random.
Differences in perfusion have been shown to correlate with active prostate cancer areas.
Dynamic contrast-enhanced MRI is able to show the microvessel density (MVD) in the prostate.
Second is the metabolic activity in prostate cancer. The ratios of choline and creatine
(normal value 0.22 +/- 0.13 ppm) reveals metabolic active prostate cancer tissue. Increased
choline and/or a reduced citrate indicate prostate cancer. The ratio of choline and
creatine-to citrate is related to the Gleason score of the tumour. Concluding, MRI and MRS
allow combined structural and metabolic evaluation of prostate cancer location,
aggressiveness and stage. The same could be performed using combined CT and PET. Sutinen et
al found a clear evidence for detecting areas with [11C] choline in prostate cancer using
PET. To our knowledge no data exist comparing [11C] choline PET and MRS in prostate cancer.
The technology for biological imaging remains in evolution, and continued advances in
accuracy and can be expected.

Therefore, given the current inadequacies in the state of art of defining GTV and CTV in
prostate cancer, we propose a study on prostate visualisation using the latest anatomical
and biological (metabolic) imaging modalities. Combining the information of different
imaging techniques by introducing a BTV and through image fusion is likely to improve CTV
and GTV delineation. This will allow us to redefine the choice of margins. Finally, this
will result in an improved IMRT plan, where dose painting and dose escalation of the GTV is
the ultimate goal. This complies with the current opinion on radiation development. Progress
in functional imaging is likely to provide the tools required for individualised
risk-adapted radiotherapy.

By introducing a BTV within the GTV a non-uniform CTV delineation can be used and thus
margins can be minimised. This allows further escalation of the dose. Setup inaccuracy and
organ movement further determine the irradiation margins needed. Therefore, controlling day
to day position variability together with the delivery of optimised conformal irradiation
will be the next goals to set. Helical Tomotherapy is a novel approach to the delivery of
radiation for cancer treatment, which will be able to do both. It relies on a 6 MV linear
accelerator for treatment purposes and a 3.5 MV-CT scan for imaging purposes. Both are
mounted on a ring gantry that rotates around the patient as he advances through the ring. A
64-leaf collimator defines the radiation fan beam. In a theoretical study Helical
Tomotherapy plans required minimal operator interaction and resulted in excellent sparing of
normal structures in prostate IMRT. Therefore, in this study we also propose to fuse the
anatomic an biologic imaging data with a Tomotherapy MV-CT and make a inverse IMRT
Tomotherapy plan. This planning exercise will precede a feasibility study on functional
imaging and individualised day to day adapted radiotherapy by Tomotherapy.


- It will be possible, using biological (MRS) imaging data and anatomical (CT and MRI)
imaging data, to define a BTV within the GTV.

- By introducing a BTV within the GTV a non-uniform CTV delineation can be used and
margins can be minimised.

- It will be possible to translate the fused anatomic and biologic imaging data into a
clinically sufficient Tomotherapy IMRT plan.

Patients and methods:

Patients who are to receive external beam irradiation for prostate cancer (Stage T1-4 N0/x
M0), preferably not treated with anti-androgens and without metal hip prosthesis will be
approached to participate in this pilot study. The study will be performed on 15 patients
who will receive imaging additionally to the irradiation treatment.

Before start of treatment patients will receive a 3T MRI (T1 SE and T2 TSE), an MRS
determining the choline creatine levels in the prostate. Furthermore, an MV-CT will be made
as a prelude to future position verification studies. All images (CT, MRI and MRS) will be
matched. These combined data will be used to determine an optimal Tomotherapy IMRT plan.

Patients will be treated according to the current department protocol. This study is only an
imaging / treatment planning study. No changes in treatment will be made based on the
obtained imaging data set. The risk for the patients will be negligible. From the MV-CT
approximately 1 cGy. The MRI will be performed without contrast (so no dynamic gadolinium
enhanced MRI to evaluate perfusion distribution) to limit the patient burden and risk.
Regarding the total irradiation dose of 7200 till 8200 cGy to the patient this additional
risk is negligible. The current waiting time for the patient to start with radiotherapy is
approximately 5 to 6 weeks. In this waiting time the imaging studies will be performed, so
participation to the study will not result in any treatment delay for the patient. The MV-CT
scan will take approximately 30 minutes to perform and the combined MRI/MRS approximately 1

The Cross Cancer Institute in Edmonton facilitates all necessary imaging techniques: a 3T
MRI, MRS and a Helical Tomotherapy Unit (TomoTherapy Inc., Madison).

It is not necessary to determine specificity and accuracy of the imaging modalities. The
imaging here is only meant to assist in determining the metabolic and anatomic tumour areas
in the prostate. Missing a tumour part is not a problem yet because the whole prostate is
being treated to the minimal required dose. Overdosage on prostate tissue is not a clinical

Inclusion Criteria:

- Histologically proven prostate adenocarcinoma

Exclusion Criteria:

- Previous treatment for prostate cancer

- Contraindications to magnetic resonance imaging (MRI)

Type of Study:


Study Design:

Observational Model: Case-Only, Time Perspective: Prospective

Principal Investigator

Matthew Parliament, MD

Investigator Role:

Principal Investigator

Investigator Affiliation:

Cross Cancer Institute


Canada: Health Canada

Study ID:




Start Date:

May 2004

Completion Date:

February 2007

Related Keywords:

  • Prostate Cancer
  • prostate cancer
  • radiotherapy
  • biological imaging
  • Prostatic Neoplasms