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6th ICHNO

page 55

6

th

ICHNO Conference

International Conference on innovative approaches in Head and Neck Oncology

16 – 18 March 2017

Barcelona, Spain

__________________________________________________________________________________________

markers in bioimaging may allow individualization of

treatment by dose painting and adaptive radiotherapy.

PO-114 Alterations in tumour hypoxia in serial F-

MISO/PET-CT during chemoradiation in HNSCC

H. Bunea

1

, A. Bunea

1

, L. Majerus

1

, C. Stoykow

2

, M. Mix

2

,

A.L. Grosu

1

1

Universitatsklinik Freiburg, Klinik für

Strahlenheilkunde, Freiburg, Germany

2

Universitatsklinik Freiburg, Klinik für Nuklearmedizin,

Freiburg, Germany

Purpose or Objective

Tumor hypoxia, a common feature of locally advanced

head and neck cancer (HNSCC), is associated with higher

malignancy and increased radioresistance. The decrease

of tumor hypoxia during fractionated radiation treatment

is assumed to be decisive for treatment success. [18F]-

Fluoro-Misonidazole PET (F-MISO-PET) allows noninvasive

assessment of hypoxia during treatment. The purpose of

the present study was to noninvasively assess the time

course of tumor hypoxia.

Material and Methods

A prospective serial imaging study was conducted in

patients undergoing definitive chemoradiation (dRCTx,

total dose 70Gy) for locally advanced HNSCC,

accompanied by cisplatin in weeks 1, 4 and 7. Tumor

hypoxia was assessed by F-MISO-PET by static scans

acquired 2.5 h p.i. Tumor volumes were determined for

FDG PET/CT scans and the coregistered F-MISO/CT scans.

At baseline MRI, FDG-PET/CT and F-MISO-PET were

acquired (week 0). Additional F-MISO-PET/CT scans were

acquired in treatment weeks 2 and 5. Normal sample

distribution was confirmed with Shapiro-Wilk test.

Unpaired

t-test

analysis

of

the

mean

SUVmax(tumor)/SUVmean(muscle) ratios of F-MISO-PET in

weeks 0, 2 and 5 were performed. Significance-level was

defined as p<0.005.

Results

Between 2012 and 2014 18 patients (16 men, two women,

mean age 60 years), treated for HNSCC with dRCTx were

included. All received a total dose of 70 Gy in 35 fractions.

Concomitant cisplatin chemotherapy was administered in

weeks 1, 4 and 7. 14 patients had all F-MISO-PET scans,

while 4 had two F-MISO-PET scans (week 0, 5). The mean

follow-up time was 14.6 months (range: 4 - 28 months).

Mean SUVmax(tumor)/SUVmean(muscle) in weeks 0, 2 and

5 were 1.9 (n=18, SD ± 0.1), 1.5 (n=14, SD ± 0.1) and 1.2

(n=18, SD ± 0.1), respectively. Unpaired t-test for

SUVmax(tumor)/SUVmean(muscle) between week 0 and 5

was performed, showing a singnificant decrease

(p<0.0001). Between weeks 0 and 2 (p=0.0346) and

between weeks 2 and 5 the decrease again was highly

significant (p=0.0113). In two patients no residual hypoxia

was measured in week two, resulting in

SUVmax(tumor)/SUVmean(muscle) =1.0. In week 5 this

was found in seven patients. In two patients hypoxia had

increased in week 2 but decreased in week 5 compared to

pre-treatment measurements. In one patient hypoxia had

increased by the end of treatment.

Conclusion

Differences in hypoxia between weeks 0-2, 2-5 and 0- 5,

respectively, show statistical significance. This is crucial

in the process of re-oxygenation. As concluded in previous

works, change of treatment strategy, e.g. by means of

dose escalation might be most efficient early during

treatment. However further analysis, with more patients

and correlation to disease-free and overall-survival are

needed.

PO-115

A [18F] FDG-PET adaptive thresholding

algorithm delineation of RT tumour volumes of head

and neck cancer

L. Deantonio

1

, M. Paolini

1

, L. Vigna

2

, G. Loi

2

, L. Masini

1

,

G. Sacchetti

3

, R. Matheoud

2

, M. Brambilla

2

, M. Krengli

1

1

University Hospital Maggiore della Carità,

Radiotherapy, Novara, Italy

2

University Hospital Maggiore della Carità, Medical

Physics, Novara, Italy

3

University Hospital Maggiore della Carità, Nuclear

Medicine, Novara, Italy

Purpose or Objective

The aim of this study was to evaluate a [18F] FDG-PET

adaptive thresholding algorithm (ATA) for the delineation

of the biological tumour volume for the radiotherapy (RT)

treatment planning of head and neck cancer patients.

Material and Methods

Thirty-eight patients, who underwent exclusive intensity

modulated RT with simultaneous integrated boost (IMRT-

SIB) for head-and-neck squamous cell carcinoma (3 oral

cavity, 9 nasopharynx, 19 oropharynx, 6 hypopharynx, and

1 larynx cancer) were included in the present study.

Thirty-five/38 patients presented a locally advanced

disease, and 33/38 received a concomitant

chemoradiotherapy treatment. For all patients [18F] FDG-

PET/CT was performed in treatment position with the

customized thermoplastic mask. Two radiation oncologists

defined the primary gross tumour volumes (GTV) using the

ATA implemented on the iTaRT workstation (Tecnologie

Avanzate, Italy). The algorithm used specific calibration

curves that depended on the lesion-to-background ratio

(LB ratio) and on the amplitude of reconstruction

smoothing filter (FWH). The reproducibility of ATA in

volume estimation was determined evaluating the volume

overlap of multiple segmentation of the same lesions by

different operators. Each primary tumour volume

segmented by the ATA (GTV

ATA

) was compared to the GTVs

contoured on two different sets. In the first, the two

radiation oncologist manually draw the standard GTV

(GTV

ST

) based on clinical information, CT simulation, and

magnetic resonance imaging (MRI); in the second, a fixed

image intensity threshold method (40% of maximum

intensity) of [18F] FDG-PET standardized uptake value was

used to define the GTV

40%SUV

.

Results

The ATA previously performed only in a phantom study

generate a GTV in all head and neck patients. The mean

value of volumes based on the three different methods are

reported in Table 1.

The GTV

ATA

was smaller than the GTV

ST

(17 vs 21 cc); the

similarity coefficient (DICE) was 0.7 (Sensibility 66%,

specificity 85%). GTV

ATA

is a part of the GTV

ST

.

The GTV

ATA

was bigger than the GTV

40%SUV

(17 vs 15 cc), the

DICE was 0.2.

Conclusion

The proposed ATA resulted robust and reproducible in a

clinical context. The ATA used in the present study allows

the delineation of a BTV for dose escalation. A IMRT-SIB

with a boost based on GTV

ATA

is feasible.

PO-116 Potential applications of spectral CT imaging in

patients with head and neck squamous cell carcinoma

B. Peltenburg

1

, J.W. Dankbaar

2

, M.J. Willemink

2

, R. De

Bree

3

, T. Leiner

2

1

UMC Utrecht, Radiation Oncology, Utrecht, The

Netherlands

2

UMC Utrecht, Radiology, Utrecht, The Netherlands

3

UMC Utrecht, Head and Neck Surgical Oncology,

Utrecht, The Netherlands