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S697

ESTRO 36 2017

_______________________________________________________________________________________________

The outcomes of 42 completed NaF PET/CT studies are

outlined in Table 1. One patient underwent a NaF PET/CT

for staging of an unknown primary.

Conclusion

Accurate staging by way of adjunctive imaging is

important in the newly diagnosed patient cohort to aid

decisions regarding suitability for prostatectomy or radical

radiotherapy. Advanced staging beyond CT TAP and bone

scan is becoming more important in the metastatic setting

as more treatments become available. Determining the

burden of metastatic disease to direct treatment is also of

great importance.

Our figures showed that NaF PET CT changed the

management

of

60%

of

patients

overall.

A recurring theme, particularly in groups with first

suspected osseous metastases or suspected progression of

known osseous metastases, was that although NaF PET CT

was successful in finding more osseous metastases,

oftentimes patients were either not fit for, or refused,

further treatment. In addition a number of patients had

already commenced chemotherapy, ADT or hormonal

therapy prior to NaF PET CT, often based on rising PSA

level. In a significant number of cases also patients did not

have up to date standard staging i.e. bone scan and/or CT

thorax abdomen pelvis within three months of NaF PET,

which may have sufficed instead of advanced imaging in

certain cases.

NaF PET/CT is a useful additional imaging investigation in

clarifying the presence or absence of bone metastases in

scenarios of diagnostic uncertainty and it aided the

decision-making process regarding further therapeutic

strategies. However, care needs to be taken to use

advanced imaging in those where there is diagnostic

uncertainty and where treatment options still exist.

EP-1314 Changes in hormonal therapy during the first

24 months of treatment: a longitudinal cohort study

C. Hennequin

1

, D. Rossi

2

, M. Zerbib

3

, J.L. Moreau

4

, A.

Ruffion

5

, Y. Neuzillet

6

, T. Lebret

6

1

Hôpital Saint-Louis, Department of Radiation Oncolgy,

Paris, France

2

Hôpital Nord, Urology department, Marseille, France

3

Hopital Cochin, Urology Department, Paris, France

4

Centre d'Urology, Urology department, Nancy, France

5

Centre Hospitalier Lyon Sud, Urology Department, Lyon,

France

6

Hôpital Foch, Urology department, Suresnes, France

Purpose or Objective

Data are limited showing changes in patients’ use of

androgen deprivation therapy (ADT) in routine clinical

practice. The objective of the study was to describe the

number and type of modifications of ADT during the first

24 months of treatment.

Material and Methods

In this non-interventional, longitudinal cohort study, we

assessed the number and type of modifications of ADT

during the first 24 months of treatment in France. At

baseline and every 6 months, we collected clinical,

biological and therapeutic data and any changes of ADT

modality.

Results

Between July 2011 and January 2015, 891 pts were

evaluable at 24 months. Mean age was 74.1±8.7 years.

Indications for ADT were: biochemical relapse after local

treatment (21.4%), adjuvant to radiotherapy (RT) (31.6%),

metastases (24.2%) and locally advanced tumour without

local treatment (20.6%). Gleason score was >7, 7(4+3), 7

(3+4) and <7 in 33.6%, 23.1%, 26% and 17.3%, respectively.

For the subgroup treated with ADT adjuvant to RT (279

pts), mean age was 71.4±6.9 yrs, and 72.8% had at least

one comorbidity. Gleason score was >7, 7(4+3), 7 (3+4) et

<7 in 28.2%, 23.5%, 32.5% and 15.9% of pts respectively.

At 24 months, modification of ADT was reported by 43.8%

of the whole population and by 37.6% of the subgroup

treated with ADT adjuvant to RT. The main types of

modification (% of whole population) concerned the

formulation (molecule or duration of action) (61.3%),

duration of ADT (10.5%), switch to intermittent treatment

(10.0%), addition of chemotherapy (5.6%) or second line

hormonal manipulation (9.0%). Modifications of ADT

according to indications are summarized in table below.

Clear explanation for adaptations was given for only 110

patients (whole population): disease progression: 55.5% ;

patient request: 26.4%, tolerance: 12.7% and failure of

castration:

7.3%.

Conclusion

Change of initial modality of ADT is frequent in the first

24 months of treatment (43.8%) and numerically more

frequent in presence of metastases or biochemical relapse

than when ADT is added to RT. Surprisingly, the main type

of modification is formulation. The main reported reason

for modification is disease progression

.

EP-1315 Prostate cancer lymph nodal disease: SBRT

only or extensive prophylactic irradiation and boost?

A. Fodor

1

, C. Sini

2

, C.L. Deantoni

1

, C. Fiorino

2

, C.

Cozzarini

1

, B. Noris Chiorda

1

, I. Dell'Oca

1

, M. Picchio

3

, P.

Mangili

2

, E. Incerti

3

, R. Calandrino

2

, L. Gianolli

3

, N.G. Di

Muzio

1

1

San Raffaele Scientific Institute, Department of

Radiation Oncology, Milan, Italy

2

San Raffaele Scientific Institute, Medical Physics, Milan,

Italy

3

San Raffaele Scientific Institute, Department of Nuclear

Medicine, Milan, Italy

Purpose or Objective

Sensitivity and specificity of choline PET/CT is high on a

per patient basis, but not on a per lesion basis (positive

lymph nodes may be underdiagnosed). We report the

outcome of salvage radiotherapy, delivered with

TomoTherapy®(TT), in prostate cancer (PCa) patients

(pts) previously submitted to radical prostatectomy and

presenting persistent/ relapsing PSA and positive(+)

lymph-nodes(LN) at 11 C-choline PET/CT(PET), treated

with prophylactic TT on LN areas (pelvic/lombo-aortic,

LA) and simultaneous integrated boost(SIB) on PET+ LN.

Material and Methods

From March 2007-May 2013, 36 PCa pts treated with

radical prostatectomy (RP) +/- pelvic/LA LN

dissection(LND), and presenting +LN at PET, were treated

with TT. Analysis was restricted to oligometastatic

treatment-naïve PCa pts satisfying published selection

criteria for SBRT (Ost et al, Eur Urol 2016), including also