Table of Contents Table of Contents
Previous Page  601 / 1096 Next Page
Information
Show Menu
Previous Page 601 / 1096 Next Page
Page Background

S585

ESTRO 36

_______________________________________________________________________________________________

Other = 23) were tested for HPV infection. Furthermore,

the clinical outcome for all tumor sides was examined with

uni and multivariate analysis. We analyzed p16 in all

tumor tissues as a surrogate marker for HPV infection with

immunohistochemistry. Moreover, risk factors such as

nicotine, alcohol abuse, location of the tumour, resection

margin of the tumour tissue, histology, lymph nodes

involvement, extracapsular spread, tumour stage, and the

treatment of the tumour (surgery, chemo and radiation

therapy) were examined for local tumour control and

overall survival for all patients.

Results

The prevalence of HPV infection in oropharynx-carcinoma

patients in Dusseldorf was 33%. Patients with HPV-positive

oropharyngeal carcinomas showed a tendency towards

longer survival time, (p = 0.76, HR: 2.42, 95% CI 0.91 -

6.44) compared to HPV-negative tumours. This association

was independent from alcohol and nicotine abuse. Other

tumour locations like larynx or hypopharynx carcinoma

showed no association between HPV infection and clinical

outcome. As expected the tumour stage in all tumour

locations was significant in the uni and multivariate

analysis for local control and overall survival.

Conclusion

The HPV infection in Dusseldorf was lower than

anticipated. Furthermore, in our study it seems that p 16

positive oropharyngeal carcinoma patients have a better

clinical outcome than p 16 negative patients. In this

patient group p 16 can be used as a prognostic biomarker.

This was independent from alcohol and nicotine abuse.

But for other tumor localizations we could not find a

better clinical

outcome.

EP-1064 Does parotid sparing adaptive radiotherapy

(PSART) benefit patients? Interim results of PARITY

study

M. Arunsingh

1

, C. Nallathambi

1

, S. Prasath

1

, A.

Balakrishnan

1

, R.K. Shrimali

1

, R. Achari

1

, I. Mallick

1

, S.

Chatterjee

1

1

Tata Medical Center, Department of Radiation

Oncology, Kolkata, India

Purpose or Objective

Intensity Modulated Radiotherapy (IMRT) to the head and

neck cancer has been proven to reduce the incidence of

long-term xerostomia and thereby improve quality of life

(QOL) of survivors. However, it is also well known that

there are ongoing changes in the dose intended to the

parotids during radiotherapy often resulting in higher

parotid doses. Parotid sparing adaptive radiotherapy

(PSART) provides dosimetric corrections for such

unintended higher doses. Our study evaluates the clinical

benefits of PSART and also calculates the resource

intensiveness.

Material and Methods

Thirty-nine of the planned 90 patients of head and neck

cancer were screened if to at least one or both parotid

(index parotid/s) were receiving a mean dose (MD) of

between 25 to 30Gy and were recruited. The index parotid

was delineated on the verification images acquired on 14

th

and 19

th

day and the MD was determined by overlaying the

fused verification image on the planned CT. Dosimetric

comparison was done using adaptive planning. If the MD

had increased by 2% of the initial intended dose, an

adaptive plan (AP) was attempted with an aim to reduce

MD by 2% without compromising PTV coverage; this plan

was then used to deliver the remaining treatment. The

time required and number of personnel involved during

each step was recorded and person hours (PH) were

calculated using the formula: (Minutes x Personnel

involved)/60. Xerostomia was assessed by a questionnaire

(XeQOLS) at baseline, at 3 and 9 months after completion

of treatment.

Results

Eighteen patients underwent radical radiotherapy with

remaining receiving adjuvant treatment. Thirty were

treated on Tomotherapy whilst others were treated on

Novalis Tx. The median increase in parotid dose was 1.1Gy

corresponding to a median reduction in the parotid volume

of 1.1cc. Twenty-three patients required an AP with

fifteen requiring it after the 14

th

day. An acceptable

adaptive plan, which met the criteria as described above,

was achieved for 19 of these 23 patients. A median of 7.5

fractions were delivered with the adaptive plans. Median

PH required for normal RT of a patient was 26PH while an

additional 14.34PH was required in those undergoing

PSART. All components of the XeQOLS (physical, pain,

social and personal) were worse at 3 months compared to

baseline and improved over time at 9 months in all

patients irrespective of whether they underwent PSART or

not (Figure 1). However, early data does not reveal any

significant difference in QOL for those who underwent

PSART. (Table 1)

XeQOLS

Score at 9

months

No

PSART

Patients(Medi

an Score)

PSART

Patients(Medi

an Score)

Significanc

e, p(Mann-

Whitney)

Physical

Domain

1.00

2.00

0.64

Pain

Domain

1.00

2.00

0.64

Physiologic

al Domain

1.00

2.13

0.92

Social

Domain

0.67

2.17

0.64

Total Score

0.93

2.07

0.77

Conclusion

The results confirm that PSART, which is resource

intensive procedure, definitely reduces dose to the

parotid. However, it is still unclear if such plans improve

clinical QOL parameters further to the planned IMRT

plans. Completion of this study could give us further

confirmation on the clinical benefits of PSART.

EP-1065 Prediction of Dysphagia and Xerostomia

based on CT imaging features of HNSCC Patients

K. Pilz

1,2

, S. Leger

1

, A. Zwanenburg

1

, C. Richter

1,2,3,4

, M.

Krause

1,2,3,4,5

, M. Baumann

1,2,3,4,5

, S. Löck

1,2,4

, E.G.C.

Troost

1,2,3,4,5

1

OncoRay - National Center for Radiation Research in

Oncology, Faculty of Medicine and University Hospital

Carl Gustav Carus- Technische Universität Dresden-

Helmholtz-Zentrum Dresden – Rossendorf, Dresden,

Germany

2

Department of Radiation Oncology, Faculty of Medicine

and University Hospital Carl Gustav Carus- Technische

Universität Dresden, Dresden, Germany

3

German Cancer Research Center DKFZ, Germany and

German Cancer Consortium DKTK partner site Dresden,

Dresden, Germany

4

Helmholtz-Zentrum Dresden – Rossendorf, Institute of

Radiooncology, Dresden, Germany