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S88

ESTRO 36

_______________________________________________________________________________________________

S. Ken

1

, F. Arnaud

1

, R. Aziza

2

, D. Portalez

2

, B. Malavaud

3

,

J. Bachaud

4

, P. Graff-Cailleaud

4

, S. Arnault

5

, A. Lusque

5

,

T. Brun

1

1

Institut Universitaire du Cancer - Oncopole - Institut

Claudius Regaud, Medical Physics and Engineering,

Toulouse, France

2

Institut Universitaire du Cancer - Oncopole - Institut

Claudius Regaud, Radiology, Toulouse, France

3

Institut Universitaire du Cancer - Oncopole - CHU de

Toulouse, Urology, Toulouse, France

4

Institut Universitaire du Cancer - Oncopole - Institut

Claudius Regaud, Radiotherapy, Toulouse, France

5

Institut Universitaire du Cancer - Oncopole - Institut

Claudius Regaud, Bureau des Essais Cliniques, Toulouse,

France

Purpose or Objective

Focal brachytherapy is proposed in our institute as an

alternative treatment to active surveillance for low-grade

prostate cancer (PCa). This study aims at characterizing

the tumor focus and its margin with multiparametric

Magnetic Resonance Imaging (mpMRI) in order to prepare

the clinical protocol of focal brachytherapy.

Material and Methods

Patients pre-qualified for this study were positive for PCa

(Gleason 3+3) on a previous standard biopsy series. New

series of mp-MRI-guided and ultrasound-targeted biopsies

were performed and in total, 17 patients with confirmed

tumor and diameter<20mm were included in this phase II

clinical trial (NCT01902680). mpMRI were acquired on a

1.5T Magnetom Aera Siemens scanner with 18-channel

surface body coil. Anatomic imaging consists in Fast Spin

Echo T2-weighted MRI (T2-MRI). In addition, same in-

plane acquisition of functional Diffusion Weighted MRI

(DWI-MRI) and Dynamic Contrast Enhanced MRI (DCE-MRI)

were performed.

After mpMRI registration, tumor volumes of interest (VOI)

were drawn on anatomic T2-MRI. VOI and VOI+2mm were

reported on functional DWI-MRI and DCE-MRI (Figure 1).

Extracted parameters were Apparent Diffusion Coefficient

(ADC) and KTrans. All parameters distributions were

analyzed with Olea Sphere v3.0 and compared to

contralateral normal appearing tissue.

Focal brachytherapy was then delivered to all patients

with linked

125

I seeds with a dose prescription of 152 Gy on

the Planning Target Volume (PTV=VOI+2mm).

Results

ADC parameters (mean, median, 25th and 75th

percentiles) are found to be significantly lower in tumor

volume (VOI) compared to contralateral normal tissue

(p<0.012 for all ADC parameters), confirming diffusion

tumor mass restriction. Different distributions of ADC and

Ktrans were observed among patients (Figure 2). Majority

(66.66%) of low ADC and abnormal Ktrans values were

included in the VOI. Interestingly, the 2mm margin allows

us to treat additional abnormal ADC and KTrans volumes

on 1/3 of the patients.

Conclusion

This study confirms that mpMRI is a non-invasive technique

able to characterize tumor margin in low-grade PCa.

Tumor characterization and delineation is a crucial step in

focal brachytherapy as only sub-volume of the prostate is

treated with high gradient dose levels. Target volume

margin definition is a hot topic when focal treatments

(e.g. cryotherapy or HIFU) are considered and mpMRI can

bring quantitative answers.

OC-0172 interstitial salvage HDR-brachytherapy for

recurrent prostate cancer after radiation therapy

P. Jiang

1

, C. Van der Horst

2

, B. Kimmig

1

, F. Zinsser

1

, B.

Poppe

3

, U. Luetzen

4

, K.P. Juenemann

5

, F.A. Siebert

1

, J.

Dunst

1

1

UKSH- Campus Kiel, Department of Radiation Oncology,

Kiel, Germany

2

Community Clinic Kiel, Department of Urology-, kiel,

Germany

3

Medical Campus Pius-Hospital- Carl von Ossietzky

University, University Clinic for Medical Radiation

Physics-, Oldenburg, Germany

4

UKSH- Campus Kiel, Department of Nuclear Medicine,

Kiel, Germany

5

UKSH- Campus Kiel, Department of Urology, Kiel,

Germany

Purpose or Objective

There is growing literature on local salvage treatments

following definitive radiation. However, data employing

interstitial high dose rate brachytherapy (HDR-BT) for

salvage treatment are rare, especially those with long-

term outcomes. This is a report of our results as a unique

published cohort with salvage HDR-BT after previous HDR-

BT treatment (Jiang et. al. 2016, brachytherapy, paper in

pressed). Emphasis was put on 5-year outcome and

toxicity.

Material and Methods

From 2009 to 2014, 29 patients with local failure after

previous radiotherapy for prostate cancer were treated

with salvage interstitial HDR-BT. Primary treatment was

combined external beam irradiation (EBRT) with 50Gy plus

HDR-BT-boost with 30 Gy in 27 patients. The primary

treatment carried the total dose to a combined biologic

equivalent dose in 2 Gy per fraction of about 178 Gy, by

assuming an α/β ratio of 1.5 for the tumor and about 146

Gy by an α/β ration of 3. 2 patients had undergone EBRT

with 66.6 Gy of the prostate bed as salvage treatment

after prostatectomy. The interval between primary

treatment and salvage treatment was 5.5 years (mean ±

SD: 5.5 ± 2.8 years).

All 29 patients had biochemical failure according to the

Phoenix definition. The diagnosis of local recurrence was

made on the basis of F-18 labeled cholin-PET. The

presence or co-existence of regional lymph node and/or

distant metastases was excluded by imaging methods.