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S511

ESTRO 36 2017

_______________________________________________________________________________________________

17/19 procedures from MRI1 to MRI2 and in 13/18

procedures from MRI1 to MRI3. Concordance between

scoring by photo and MRI was found in 24/37procedures.

Average needle migration was 2.9 ± 1.6 mm for anterior

needles and 3.6 ± 1.5 mm for posterior needles (students

t-test, p=0.08)

Conclusion

Needle migration was of acceptable magnitude measured

from MRI1 to MRI2, but of considerable magnitude from

MRI1 to MRI3. Insufficient concordance between scoring by

photo and MRI indicates that visual inspection is

inadequate for evaluating implant stability. A likely

explanation for the lack of concordance between for

photos and MRI is the developing oedema following needle

insertion.

PO-0930 CT to TRUS based Prostate HDR: what is the

optimal dosimetric margin to use?

F. Lacroix

1

, M. Lavallée

1

, E. Vigneault

1

, W. Foster

1

, A.G.

Martin

1

1

Centre Hospitalier Universitaire de Québec- L'Hôtel-

Dieu de Québec, Department of radio-oncology, Quebec,

Canada

Purpose or Objective

The contouring volume variability resulting from

delineating the target with Computed Tomography (CT) or

Transrectal Ultrasound (TRUS) results in a 30 to 50%

increase in volume when contouring a prostate on CT

versus TRUS due to the poor soft tissue contrast of CT. This

may have a significant dosimetric impact when moving

from a CT to a TRUS based prostate high-dose rate (HDR)

brachytherapy planning as the treated volumes are

susceptible to differ significantly. This study aims at

determining the proper dosimetric margin to apply when

going from CT to TRUS based planning in order to

compensate for this volume difference. By doing so, we

aim to treat the same volume of prostatic tissue in CT or

TRUS and insure a constancy in quality of care for prostate

cancer patients treated with HDR.

Material and Methods

Twenty-seven prostate cancer patients were given a 15Gy

HDR boost using a TRUS-based catheter insertion and

planning approach. A 2 mm isotropic dosimetric margin

was used for the TRUS planning. An average of 17

catheters were implanted. Without moving patients still

under general anesthesia, a CT on rails located inside the

operating room was used to image the pelvis. Three

experienced radiation oncologists specialized in

brachytherapy delineated the prostate on the resulting CT

images and an offline, independent CT based planning was

performed. A 1 mm isotropic dosimetric margin was used

in CT planning. The prostate volume, 15Gy volume and

V100 of the prostate were then collected and compared

for the US and CT based plans.

Results

The average prostate, 15Gy volumes and V100 are

presented in table 1.

Table 1: Average prostate volume, 15Gy volume and

V100 for TRUS and CT based planning

Modality

Average prostate

volume (CC)

Average 15 Gy

volume (CC)

V100

(100%)

TRUS

38.0

50.2

96.3

CT

44.3

54.2

96.0

The average TRUS volume is 16.5% smaller than the

average CT volume. When using a 2 mm dosimetric

margin, the volume receiving 15Gy is smaller by 8% in

TRUS compared to CT based planning. The V100 are almost

identical with both modalities. The standard deviation on

the TRUS prostate volume is slightly lower (10.6) than on

CT (11.2).

Conclusion

Our study shows an average systematic 16% smaller

prostate volume on TRUS compared to CT. This differs

from the 30 to 50% smaller volumes on TRUS reported in

the literature. This discrepancy is probably due to the

presence of catheters implanted under TRUS guidance in

CT based planning which means that catheters are

inserted under TRUS guidance in both planning modalities.

These catheters act as fiducial markers to delimit the

prostate capsule transversely on CT. The residual 16%

volume variation is largely due to the uncertainty in

identifying the prostate apex. A 2.8 mm isotropic

dosimetric margin should be used in order to treat

comparable volumes in TRUS compared to CT based

planning.

PO-0931 Clinical outcome and quality of life after MRI-

guided HDR boost for prostate cancer.

F. Lakosi

1

, A. Miovecz

1

, G. Antal

1

, J. Pall

2

, D. Nagy

3

, M.

Csima

4

, J. Hadjiev

1

, I. Rep a

1

, G. Toller

1

1

Kaposvar University, Radiotherapy, Kaposva r, Hungary

2

Csolnoky Ferenc Hospital, Radiotherapy, Veszprem,

Hungary

3

Kaposi Mor Teaching Hospital, Urology, Kaposvar,

Hungary

4

Kaposvar University, Faculty of Pedagogy, Kaposvar,

Hungary

Purpose or Objective

To analyze 5-year clinical outcome and quality of life

(QoL) after MR-guided high-dose-rate brachytherapy

(HDR-BT) combined with 3D conformal external beam

radiotherapy (3D-EBRT).

Material and Methods

Fifty-two patients with intermediate (IR) (n=22) to high-

risk (HR) (n=30, 18 T3 diseases) localized prostate cancer

were treated with 46-60 Gy of 3D EBRT preceded and/or

followed by a single dose of 8-10 Gy MR-guided HDR-BT.

Template reconstruction, trajectory planning, image

guidance, contouring and treatment planning were

exclusively based on MR images. Ninety-six percent of the

patients received androgen deprivation. Biochemical

relapse–free survival (bRFS, Phoenix definition), local

relapse-free survival (LRFS), distant metastasis-free

survival (DMFS), cancer-specific survival (CCS) and overall

survival (OS) were analyzed actuarially. Morbidity were

scored using CTCAEv4.0, while patients self-reported

urinary and bowel QoL was measured with the Expanded

Prostate Cancer Index Composite (EPIC) instrument and

International Prostate Symptom Score (IPSS) at baseline

and at regular intervals up to 6 years.

Results

Median follow-up time was 73 (range:13-103) months. The

crude/5-year actuarial rates of bRFS, LRFS, DMFS, CSS and

OS were 94/97.4 %, 98/100 %, 96/97 %, 100/100 % and

92/91 %, respectively. Two distant failures occurred in HR

group, while one local recurrence in IR group. The main

urinary toxicity was dysuria, which were Gr. 2 in 24/52

cases, including 9 patients with alfa blocker use at

baseline. There were 3 urinary strictures including one Gr.

3 event. Late GI morbidity was mild, representing Gr. 1

diarrhea (10/51), Gr. 1 urgency (9/51), Gr. 2 proctitis

(1/52) and Gr. 2 fecal incontinence (1/52), respectively.

A significant decline in urinary domain was observed

within the first 3 months, which mostly recovered by 6

months, thereafter declined progressively (p>0.05) and

remained stable from 4th years follow up (p>0.05)

(Figure). A similar trend was seen for bowel QoL, where a

significant decline occured within the first 3 months that

subsequently returned to nearly baseline level within 6

months, however, in contrast to urinary functions

remained stable over time (p>0.05). The evolution of IPPS

scores showed the same pattern as EPIC urinary scores.