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S314

ESTRO 36 2017

_______________________________________________________________________________________________

than men (p< 0.001) and patients presenting nasal cavity

tumors scored higher that all other tumoral sites (p=0.08).

Conclusion

HNC patients undergoing radiation therapy have high

levels of emotional distress, anxiety and claustrophobia.

Given the high percentage of psychological distress,

awareness and management of these issues are primordial

as they may have significant impact on treatment

acceptance and tolerability as well QOL during and after

treatment.

PO-0609 18F-FDG-PET in Guiding Dose-painting with

IMRT in Oropharyngeal Tumours (FiGaRO) – Early Results

A. Michaelidou

1

, L. Pike

2

, C. Thomas

3

, L. Penketh

4

, Y.

Suh

5

, S. Barrington

2

, M. Evans

4

, M. Lei

1

, T. Guerrero

Urbano

1

1

Guy's and St Thomas' NHS Foundation Trust, Clinical

Oncology, London, United Kingdom

2

The PET Centre at St Thomas' Hospital, Nuclear

Medicine, London, United Kingdom

3

Guy's and St Thomas' NHS Foundation Trust,

Radiotherapy Physics, London, United Kingdom

4

Velindre Cancer Centre, Clinical Oncology, Cardiff,

United Kingdom

5

Royal Marsden NHS Foundation Trust, Clinical Oncology,

London, United Kingdom

Purpose or Objective

IMRT ± chemotherapy is an effective treatment for stage

III/IVa oropharyngeal squamous cell carcinoma (SCC).

Treatment failures occur mostly at the primary site and

are difficult to salvage. Dose escalation strategies are

being explored, with target volume definition and toxicity

considered the main challenges. IMRT can boost doses to

selected areas (dose painting) without exceeding normal

tissue tolerances.

18

F-FDG-PET/CT can mediate this, by

defining areas of metabolic activity for dose escalation.

This Phase 1 multicentre study aims to test the feasibility

and safety of

18

F-FDG-PET/CT dose-painted IMRT in locally

advanced oropharyngeal SCC. We present toxicity results

in the first 15 patients.

Material and Methods

Patients with ≥T2, HPV-negative or high-risk HPV-positive

disease, suitable for radical treatment with neo-adjuvant

chemotherapy and chemo-IMRT, are eligible.

PET/CT is acquired after one chemotherapy cycle, in the

radiotherapy position, in the immobilization shell. The

FDG-avid gross tumour volume (GTV-T

18

F-FDG-PET) is

manually delineated by a nuclear medicine physician then

copied onto the fused CT for direct planning. Thirty daily

fractions are delivered in 6 weeks, at 3 dose levels. The

radical volume (PTV1) receives 65Gy, the prophylactic

volume (PTV2) 54Gy and the GTV-T

18

F-FDG-PET receives

71.5Gy.

Results

Fifteen patients (14 male, 1 female; mean age-61, range

49-71) were treated April’14-March’16, at two centres

(median follow-up 10 months, range 4-26 months. Eight

(53.3%) are HPV-negative, 7(46.7%) are HPV-positive.

Average GTV-T

18

F-FDG-PET volume was 11.9cc (range 1.6-

67.7cc). Target volume objectives were met in all (median

D

95

98.1%, range 96.1-98.9%; Median D

5

102.9%, range

101.1-103.6%), whilst respecting normal tissue tolerances

and

PTV1

hotspot constraints.

On the CTCAEv.4.0 scale, end of treatment toxicities

were: Grade 4–none; Grade 3 - dysphagia-46.7%(n=7),

mucositis-26.7%(n=4), pain-13.3%(n=2), salivary gland-

6.7% (n=1); Grade 2- dysphagia-53.3%(n=8), mucositis-

73.3%(n=11),

pain-73.3%(n=11),

salivary

gland-

86.7%(n=13),

dermatitis-73.3%(n=11),

xerostomia-

66.7%(n=10), fatigue-46.7%(n=7). Three month post-

treatment toxicities were: Grade 4–none; Grade 3 -

dysphagia-20.0%(n=3); Grade 2- dysphagia-20.0%(n=3),

mucositis-13.3%(n=2), pain-20.0%(n=3), xerostomia-

53.3%(n=8).

On the RTOG/EORTC scale 3-month post treatment

toxicities were: Grade 4-none; Grade 3-salivary gland-

6.7%(n=1), oesophagus-6.7%(n=1); Grade 2–salivary gland-

46.7%(n=7), oesophagus-13.3%(n=2), mucosa-13.3%(n=2),

joint(TMJ)-6.7%(n=1). On LENTSOMA categories one

patient had a grade 4 toxicity - oropharyngeal dysphagia

(gastrostomy dependent). Six (40.0%) had grade 3

toxicities and 13 (86.7%) had grade 2 toxicities.

There were 2 local recurrences within 1 year, both

underwent salvage surgery with clear margins.

Conclusion

18

F-FDG-PET-guided selective dose escalation is feasible,

with acceptable acute toxicity. Late toxicity assessment

(3, 6 and 12-months post-treatment) is ongoing.

PO-0610 Effects of an oral health promotion program

in head and neck cancer patients receiving radiotherapy

E. Kim

1

, H.G. Wu

1

, J.H. Kim

1

, K.S. Kim

1

, T. Yu

1

, C.W.

Wee

1

, N. Choi

1

, B.S. Jang

1

, S.H. Jeon

1

, H.J. Lee

2

, D.H.

Han

2

1

Seoul National University College of Medicine, Radiation

Oncology, Seoul, Korea Republic of

2

Seoul National University College of Dentistry,

Preventive and Social Dentistry, Seoul, Korea Republic of

Purpose or Objective

To develop oral health promotion program and evaluate

its effectiveness in head and neck cancer (HNC) patients

receiving radiotherapy (RT).

Material and Methods

This was an open-label, non-randomized, prospective

study in 84 HNC patients treated with RT. Dental health

promotion program consisted of oral exam, oral health

education, fluoride varnish and mouthwash. Forty-seven

patients were assigned to an experimental group with the

dental health care program and 37 to a control group.

Clinical benefit was measured by the European

Organization for Research and Treatment of Cancer

(EORTC) Quality of Life Questionnaire head and neck

module (QLQ-H&N35) and the oral examination before and

up to 6 months after RT.

Results

Compared with the control group, the experimental group

showed significant improvement in sexuality, use of pain

killers, and worried about future (p = 0.045, p = 0.049, and

p < 0.001, respectively). Oral health promotion program

did not affect the development of xerostomia. Subgroups

of patients with old age (≥ 60 years), stage IV HNC, and

radical RT reported significant improvement in quality of

life by oral health promotion protocol. Although caries

experience significantly increased in a control group (p =

0.002), there was no significant change in an experimental

group. The experimental group showed significantly

decreased plaque score and bleeding on probe (p < 0.001

and p = 0.004).

Conclusion

Administration of our oral health promotion program

decreased dental problems and slightly improved patients’

quality of life. We recommend the dental care program

for HNC patients receiving RT to reduce treatment related

oral toxicities.

PO-0611 Long-term prognostic impacts of pretreatment

plasma EBV DNA status in nasopharyngeal carcinoma

J.C. Lin

1

, W.Y. Wang

2

, J.W. Huang

1

1

Taichung Veterans General Hospital, Department of

Radiation Oncology, Taichung, Taiwan

2

Hung Kuang University, Department of Nursing,

Taichung, Taiwan

Purpose or Objective

To investigate the prognostic impacts of pretreatment

plasma EBV (pEBV) DNA in patients with nasopharyngeal

carcinoma.

Material and Methods