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S588

ESTRO 36 2017

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(Rs>0.75) were not included in the multivariate analysis.

A two-variable model was suggested as the optimal order

by bootstrap method. The optimal model (Rs=0.452,

p<0.001) includes V45 of the cervical esophagus

(OR=1.016) and Dmean of the cricopharyngeal muscle

(OR=1.057). The model AUC (Fig1a) was 0.82 (95% CI 0.69-

0.95). The comparison of the predicted incidence of acute

radiation-related toxcity and the actuarial incidence in

the

population

is

shown

in

Figure

1b.

Conclusion

We propose a 2-variable predictive NTCP model including

both cervical esophagus and cricopharyngeal muscle

dosimetric parameters with a good prediction

performance for acute radiation-related toxicity in H&N

cancer pts

EP-1078 Transient xerostomia in head and neck

cancers with significant parotid inclusion in target

volume

A. Datta

1

, A. Mukherji

1

, E. Thiraviyam

1

1

Jawaharlal institute of post graduate medical education

and research, radiation oncology, Puducherry, India

Purpose or Objective

To assess xerostomia patterns in patients requiring

significant parotid inclusion in target volumes for

treatment of locally advanced head and neck cancers.

Material and Methods

30 patients (male = 20, female = 10) with head and neck

cancers (oral cavity = 6, oropharynx = 8, nasopharynx = 3,

larynx = 7) of AJCC stage II = 4, III = 12, and IV = 14 who

were treated with radical chemo radiation from August

2013 – September 2015 and received significant parotid

dose (more than 22 Gy Dmean) were analyzed

retrospectively at 3, 6 and 12 months post completion of

treatment. They received an external radiotherapy dose

of 69.34 Gy EQD2 (to HR-CTV, mean HI – 0.13, mean CI –

0.99) using SIB-IMRT by VMAT technique. Their xerostomia

patterns were recorded based on subjective complaints

(Grade 1 = slight dryness, Grade 2 = moderate dryness,

Grade 3 = complete dryness, Grade 4 = fibrosis).

Results

1 patient died during treatment due to aspiration and 1

patient developed a second primary in lung at 10 months.

The mean of Dmean to right parotid was 43.95 Gy (23-

51.2) to a mean volume of 16.71 cc (9-30.2) while for the

left parotid it was 43.6 Gy (23.1-58.2) to a mean volume

of 16.9 cc (7.7-26.3). The mean spared right parotid

(outside PTV) Dmean was 23.1 Gy (30.2-69.2% of whole

parotid volume, mean volume 42.5%) while for the left

parotid it was 26.3 Gy (22-65% of whole parotid volume,

mean volume 48.7%). At 3 months of completion of

treatment Grade 2 and 3 xerostomia were seen in 2 (6.9%)

and 27 (93.1%) patients respectively. At 6 months Grade 2

and 3 xerostomia were seen in 12 (41.3%) and 17 (58.7%)

patients respectively. While at 12 months Grade 1, 2 and

3 xerostomia were seen in 7 (24.1%), 16 (55.2%) and 6

(20.7%) respectively. 1 patient had a stable residual

disease.

Conclusion

Significant parotid inclusion in target volumes for locally

advanced cases had a reversible loss of parotid function at

12 months of completion of treatment. However, loss of

function was irreversible when the Dmean was greater

than or equal to 50 Gy.

EP-1079 Carotid blowout syndrome after reirradiation

with particle therapy in the head and neck region

J.E. Dale

1

, S. Molinelli

2

, E. Ciurlia

2

, O. Dahl

1,3

, P.

Fossati

2,4

1

Haukeland University Hospital, Department of oncology,

Bergen, Norway

2

CNAO Foundation, Pavia, Italy

3

University of Bergen, Department of clinical science,

Bergen, Norway

4

European Institute of Oncology IEO, Milano, Italy

Purpose or Objective

Carotid blowout syndrome (CBS) is a serious complication

to treatment of neoplasms in the head and neck (H&N)

region. Surgery, infection, necrosis and tumor properties

are the most significant risk factors, but the rate of CBS is

also affected by properties of radiotherapy (RT). Rates

seem to increase in hypofractionated or accelerated

hyperfractionated regimens. We here investigate the

cumulative doses received by the carotid artery (CA) and

CBS-rate in a cohort of patients reirradiated with particle

therapy in the H&N region.

Material and Methods