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S579

ESTRO 36 2017

_______________________________________________________________________________________________

The BTV

ATA

was bigger than the GTV

40%SUV

(17 vs. 15 cc) but

the difference was not statistically different (p> 0.05), the

CI was 0.8 and the DICE was 0.2.

Table 1. Tumour Volumes defined by the three different

methods.

GTV

Mean Volume

(cc)

Ranges

Standard

Deviation

GTV

ST

21.4

4.5 –

66.3

±16.0

GTV

40%SUV

14.7

1.3 – 58.5 ±13.7

GTV T

ATA

17.2

1.5 – 61.5 ± 12.8

Conclusion

The proposed adaptive thresholding algorithm resulted

robust and reproducible in the clinical context of head and

neck tumours. The tumour volumes obtained by the

algorithm were a part of the GTV

ST

and were similar to

GTV

40%SUV.

This tumour volume could allow the delineation

of a BTV for dose escalation in head and neck cancer

treated with

IMRT-SIB.

EP-1060 Analysis of failure patterns and prognostic

factors after postoperative IMRT for buccal cancer

Y.W. Lin

1

, L.C. Lin

1

1

Chi Mei Medical Center, Department of Radiation

Oncology, Tainan, Taiwan

Purpose or Objective

Squamous cell carcinoma (SCC) of buccal mucosa has a

high incidence of locoregional failure. Its aggressive

behavior and the change of lymphatic and vascular

drainage after surgery make the design of radiotherapy

difficult. The aim of this study is to analyze failure

patterns and prognostic factors in patients with locally

advanced buccal cancer after postoperative intensity

modulated radiotherapy (IMRT).

Material and Methods

Between January 2007 to October 2012, 84 patients with

histological confirmed SCC of buccal mucosa underwent

surgery followed by postoperative IMRT were

retrospectively analyzed.. All patients were stage III/IV

buccal cancer. The high-risk clinical target volume (CTV)

covered the surgical tumor bed and ipsilateral or bilateral

upper neck. The median dose to high-risk CTV was 60Gy.

Analyzed end-points were overall survival (OS), local

recurrence-free survival, loco-regional recurrence-free

survival, supra-mandibular notch recurrence-free survival,

distant metastasis-free survival, prognostic factors and

patterns of failure.

Results

The median follow up was 51 months (range, 2-112

months). The first recurrent sites were local tumor bed

(17 patients) with or without regional/distant recurrence.

The median time from treatment completion to first

locoregional recurrence was 7.3 months. Of the 17

patients with local recurrence, 11 exhibited the supra-

mandibular notch recurrence; most were classified as

marginal failure. The estimated 4-year local failure-free,

locoregional failure-free, distant metastasis-free and

overall survival rates were 72%, 63.3%, 85.9% and 68.8%.

In multivariate analysis, lymphovascular invasion (P =

0.002), N2 disease (P = 0.003), and ratio of tumor

thickness to tumor size larger than 1/3 (P = 0.014) were

independent prognostic factors for overall survival.

Patients received tumor excision with maxillectomy was a

predictive factor for the development of supra-mandibular

notch recurrence.

Conclusion

SCC of buccal mucosa is a highly aggressive form of oral

cavity cancer with a high locoregional failure rate and

most locoregional recurrences led to lethal events. Design

of postoperative IMRT for buccal cancer, especially CTV

delineation, based on failure patterns and

clinicopathological prognostic factors might transfer into

better disease control.

EP-1061 Towards a validated Decision Aid Tool for

advanced larynx cancer patients

A.J. Berlanga

1

, M. Petersen

2

, F. Hoebers

1

, S.

Delbressine

1

, M. Van den Breke

2,3,4

, P. Lambin

1

1

Maastro Clinic, GROW School for Oncology and

Developmental Biology- Maastricht University Medical

Centre, Maastricht, The Netherlands

2

The Netherlands Cancer Institute, Department of Head

and Neck Surgery and Oncology, Amsterdam, The

Netherlands

3

Academic Medical Center, Department of Oral and

Maxillofacial Surgery, Amsterdam, The Netherlands

4

University of Amsterdam, Institute of Phonetic Sciences,

Amsterdam, The Netherlands

Purpose or Objective

Advanced larynx cancer patients may be eligible for more

than one treatment: laryngectomy, radiotherapy,

chemoradiation, or combinations thereof. These

treatments have a distinct impact on quality of life (e.g.

disfigurement, speech, swallowing problems), and

outcomes depending on TNM-classification.

To empower these patients to participate in shared-

decision making, we are creating a web-based Patient

Decision Aid Tool (PDA,

www.treatmentchoice.info)

. The

goal is help patients to understand treatment options and

support clinicians to gain perspective of patients’

preferences.

Material and Methods

The PDA was validated following the International Patient

Decision Aid Standards (IPDAS). First, a prototype was

created considering literature and input from an

interdisciplinary group. A mixed-method (interview, 5-

Likert questionnaire) was used to identify patients’

decisional needs, and to evaluate if the tool was clear and

perceived as useful for shared-decision making.

Clinicians (N=8) and patients (N= 12) from two hospitals

were included.

Results

Patients and clinicians agreed on patient’s difficulty to

recall spoken information and understand risk

probabilities. They mentioned the need of information

about treatment options, side effects, and effectiveness.

Patients asked for information about procedures before

and

after

treatment.

Patients preferred information that is simple, visual, and

in small chunks. Clinicians preferred information adapted

to patient’s psychosocial level.

Patients were positive about the PDA. All criteria

(satisfaction, effectiveness, clarity, usability, usefulness,

intention use) had a median (IQR) of 4 ('agree”). Patients

asked for simpler terms, information on psychological

effects and the 'no treatment option”.

Considering these results, a new version was created

(Fig.1). It is a visual tool, containing video interviews with

clinicians and animations to explain the treatments.

This version will be validated by clinicians and patients for

comprehensibility and usability. Results will be considered

to create a final version. Thereafter, we will evaluate its

impact on shared decision-making in a multi-center

setting.