Table of Contents Table of Contents
Previous Page  602 / 1096 Next Page
Information
Show Menu
Previous Page 602 / 1096 Next Page
Page Background

S586

ESTRO 36

_______________________________________________________________________________________________

5

National Center for Tumor Diseases partner site

Dresden, Dresden, Germany

Purpose or Objective

Radiochemotherapy (RCT) for patients with head and neck

squamous cell carcinoma (HNSCC) frequently causes

xerostomia and dysphagia, which may be alleviated by

treatment adaption, e.g., modulation of dose distribution

to the salivary glands. Current clinical models, which are

based on dosimetric parameters, mostly achieve moderate

prediction accuracy. Therefore, we aimed to improve the

prediction of xerostomia and dysphagia by using additional

imaging biomarkers based on computed tomography (CT)

scans.

Material and Methods

In this study 46 patients with UICC stage III/IV advanced

head and neck squamous cell carcinoma (HNSCC) were

considered (NCT00180180, [1]). All patients received

primary RCT and underwent a pre-treatment CT scan

without intravenous contrast agent. Patient-reported

xerostomia and dysphagia were evaluated at baseline,

every week during RCT, four weeks after treatment and

three monthly thereafter. 5040 imaging features were

extracted from the parotid and submandibular glands.

Feature reproducibility tests based on the RIDER re-test

data set [2] were performed leading to 1513 imaging

features in total. The most informative features were

selected by a univariate logistic regression analysis. The

developed radiomic signature was used to train and

validate multivariate logistic regression and random forest

models using repeated 5-fold cross validation. The

predication accuracy was assessed by the area under the

curve (AUC).

Results

The logistic regression and the random forest model

achieved similar performance in predicting xerostomia

(AUC=0.71). The developed signature consisted of one

dosimetric parameter and one imaging feature. For the

prediction of dysphagia both models achieved only a

moderate prediction accuracy (AUC=0.55).

Conclusion

For prediction of xerostomia, a signature was developed

and showed a good performance. For dysphagia only

moderately performing models could be obtained in this

cohort. Based on our results, subgroups of patients at a

high risk of xerostomia may be identified and offered

treatment adaption. However, further investigations are

currently ongoing, i.e., externally validating the

developed signature, which is an important step in

developing clinically relevant prediction models.

EP-1066 Hypofractionated accelerated SIB-VMAT

radiotherapy for H&N cancer: brachial plexus

constraint

M. Nuzzo

1

, L.P. De Vivo

1

, F. Deodato

1

, G. Macchia

1

, M.

Ferro

1

, M. Ferro

1

, L.G. Serino

1

, S. Cilla

2

, S. Cammelli

3

, A.

Farioli

4

, A. Arcelli

3,5

, A. Veraldi

3

, G.P. Frezza

5

, V.

Valentini

6

, A.G. Morganti

3

1

Fondazione di ricerca e cura "Giovanni Paolo II",

Radiotherapy Unit, Campobasso, Italy

2

Fondazione di ricerca e cura "Giovanni Paolo II", Medical

Physics Unit, Campobasso, Italy

3

University of Bologna, Radiation Oncology Center-

Department of Experimental- Diagnostic and Speciality

Medicine - DIMES, Bologna, Italy

4

University of Bologna, Department of Medical and

Surgical Sciences - DIMEC, Bologna, Italy

5

Ospedale Bellaria, Radiotherapy Department, Bologna,

Italy

6

Policlinico Universitario "A. Gemelli"- Universtà

Cattolica del Sacro Cuore, Department of Radiotherapy,

Rome, Italy

Purpose or Objective

To perform a dosimetric evaluation of the brachial plexus

(BP) dose in locally advanced H&N cancer patients

undergoing moderate hypofractionated-accelerated

chemoradiation performed by a SIB-VMAT technique.

Material and Methods

Patients with locally advanced H&N cancer receiving

induction chemotherapy (ICT) and subsequent platinum

based concurrent radiotherapy were included in this

retrospective analysis. Toxicity and outcomes data were

recorded during the routine follow-up. In all patients,

right (RBP) and left (LBP) BP were delineated according to

RTOG guidelines by the same radiation oncologist. RBP and

LBP mean doses, V50, V55 and V60 were recorded and

correlated with late neurological toxicity.

Results

From July 2010 to January 2015, 50 patients [M/F: 40/10;

median age: 57y, range 30-77; stage III: 11 (22%), stage IV:

39 (78%)] were treated and represent the object of the

analysis. ORL subsites were as follows: oropharynx (22;

44%), epipharynx (8;16%), oral cavity (9; 18%), larynx (4;

8%) and hypopharinx (7; 14%). Cisplatin plus 5-fluorouracil

chemotherapy schedule was administered as ICT in 72% of

cases, while 22% of patients received a 3-drugs protocol

(cisplatin, 5-fluorouracil and docetaxel). A moderate

accelerated hypofractionation was delivered by using a 2

arc SIB-VMAT technique. Doses to macroscopic disease (T

and N) ranged from 67.5/2.25 Gy (8 patients; 16%) to

70.5/2.35 Gy (42 patients; 84%), while the high and low

risk nodal areas received 60/2 Gy/die and 55.5/1.85 Gy in

30 fractions, respectively. As per DVH analysis, LBP and

RBP mean dose were 48.4 Gy and 48 Gy, V50 were 68.5%

and 68.9%, V55 were 56.1%and 58.9%, V60 were 28% and

32.6%, respectively. In 44% of cases part of the LBP was

included within the high dose PTV (67.5Gy in 12% and 70.5

Gy in 32% of patients). Conversely, in 46% of cases part of

the RBP was included within the high dose PTV (67.5Gy in

8% and 70.5 Gy in 38% of patients). With a median follow-

up of 19 months (range 3-53) no symptoms of brachial

plexopathy were reported, although in 87% of cases doses

to BP exceeded the suggested literature constraint of 60

Gy.

Conclusion

A SIB-VMAT moderate accelerated hypofractionation at

the doses reported in this analysis seems to be tolerable

and safe, without cases of neurological toxicity. Longer

follow-up and further prospective studies in larger series

are warranted to confirm these findings.

EP-1067 is adenoid cystic carcinoma (ACC)

radioresistant?: the effect of radiotherapy for ACC of

head and; neck

I. Jung

1

, J. Kim

1

, S. Ahn

1

, S. Song

1

, S. Yoon

1

, S. Kim

1

, J.

Park

1

, E. Choi

1

, S. Lee

1

1

Asan Medical Center- Univ of Ulsan, Radiation oncology,

Seoul, Korea Republic of

Purpose or Objective

The adenoid cystic carcinoma (ACC) of head and neck

showed insidious onset and usually advanced at initial

presentation. Because of limitation of anatomy of head

and neck, in some cases, wide excision may not be

possible. And even further, in other cases surgical excision

may not be

possible.

Therefore we evaluated efficacy and safety of definitive

radiation therapy in head and neck ACC. Also, we analyzed

prognostic factors in adjuvant radiation therapy of it.

Material and Methods

From January 1995 to December 2013, 94 patients

received radiotherapy for head and neck adenoid cystic

carcinoma in Asan medical center. Fourteen patients were

excluded because of systemic metastasis (n=7), other

primary cancer (n=3), incomplete RT (n=2), and previous