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S263

ESTRO 36 2017

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difference in overall survival (OS), Quality of Life or use of

dexamethasone. These unexpected results were criticized

because OS was poorer (2 months) than the alleged

survival in common radiotherapy practice, suggesting

selection bias. Indeed, only 6% of included patients had a

favorable RPA class 1. Furthermore, patients with a more

favorable primary tumor such as breast cancer, could

perhaps benefit more from WBRT. Therefore, we

compared the QUARTZ data with survival after WBRT in

‘common radiotherapy practice’ from a large multicenter

retrospective cohort in the Netherlands.

Material and Methods

Survival data from

all patients with brain metastases from

NSCLC or any type of breast cancer treated with WBRT

between 2000 and 2014 were analyzed. Patients were

treated in seven different institutes (both academic and

non-academic covering 33% of Dutch radiotherapy

practices). All patients were treated with 5 fractions of 4

Gy. Survival was calculated from the first day of

radiotherapy until the day of death or last follow-up. Date

of death was retrieved from the Dutch Municipal Personal

Records Database.

Results

Between 2000 and 2014, 3270 patients were identified,

2384 with brain metastases from NSCLC (73%) and 886

from primary breast cancer (27%). The median OS was 2.7

months for the NSCLC group and 3.8 months for the breast

cancer group (p<0.001). At time of analysis, 97% of all

patients was deceased. There was no difference between

academic and non-academic centres. No correlation

between the year of treatment and OS was found.

Conclusion

The survival of patients after WBRT for brain metastases

from NSCLC treated in Dutch ‘common radiotherapy

practice’ is practically the same as in patients treated in

the British QUARTZ study. Survival for patients with brain

metastases from breast cancer is only marginally better.

Our analysis supports the conclusion from the QUARTZ

study that there is insufficient evidence to consider WBRT

the standard of care for patients with multiple brain

metastases. We advocate more studies in this patient

population and recommend a more restrictive use of WBRT

in daily radiotherapy practice.

PV-0505 Association between the diagnosis-to-

treatment interval and overall survival in Taiwan OSCC

C.T. Liao

1

, Y.W. Wen

2

, S.H. Ng

3

, L.Y. Lee

4

, C.Y. Lin

5

,

H.M. Wang

6

, C.H. Lin

7

, T.C. Yen

8

1

Chang Gung Memorial Hospital, Otorhinolaryngology-

Head and Neck Surgery, Taoyuan, Taiwan

2

Chang Gung University, Clinical Informatics and Medical

Statistics Research Center, Taoyuan, Taiwan

3

Chang Gung Memorial Hospital, Diagnostic Radiology,

Taoyuan, Taiwan

4

Chang Gung Memorial Hospital, Pathology, Taoyuan,

Taiwan

5

Chang Gung Memorial Hospital, Radiation Oncology,

Taoyuan, Taiwan

6

Chang Gung Memorial Hospital, Medical Oncology,

Taoyuan, Taiwan

7

Chang Gung Memorial Hospital, Plastic and

Reconstructive Surgery, Taoyuan, Taiwan

8

Chang Gung Memorial Hospital, Nuclear Medicine,

Taoyuan, Taiwan

Purpose or Objective

To investigate the association between the diagnosis-to-

treatment interval (DTI) and overall survival (OS) in

patients with oral cavity squamous cell carcinoma (OSCC).

Material and Methods

A total of 18,677 patients with first primary OSCC

identified in the Taiwanese Cancer Registry Database

between 2004 and 2010 were examined. The effect of DTI

on 5-year OS rates was investigated with multivariate Cox

regression analysis. After the identification of the optimal

cutoff for DTI based on the 5-year OS rates, DTI was

classified in the following 20-day groups: ≤20 days (57% of

the study patients), 21−45 days (34%), 46−90 days (6%),

and ≥91 days (3%). In additional exploratory analyses, DTI

was reclassified in the following 30-day interval groups:

≤30 days (81% of the study patients), 31−60 days (14%),

61−90

days

(2%),

and

≥91

days

(3%).

Results

Multivariate analyses identified DTI (≤20 days

vs.

other

subgroups), sex (female

vs.

male), age (<65 vs. ≥65 years),

clinical stage (p-Stage I

vs.

p-Stage II, III, IV), and

treatment modality (initial surgery

vs.

initial non-surgery)

as independent prognostic factors for 5-year OS.

Compared with a DTI ≤20 days, the DTI categories ≥91 days

(hazard ratio [HR]: 1.28,

P

<0.001), 46−90 days (HR: 1.25,

P

<0.001), and 21−45 days (HR: 1.07,

P

=0.007) were

independently associated with a higher risk of 5-year

mortality. Similar results were obtained for DTI ≤30 days

groups.

Conclusion

DTI is independently associated with 5-year OS in OSCC

patients. A DTI longer than 30 days or even 20 days may

potentially decrease survival.

PV-0506 Comparison of Clinical Behavior of Viral

Related Oropharyngeal and Nasopharyngeal Carcinoma

S.H. Huang

1

, J. Waldron

2

, J. Su

3

, S. Bratman

2

, J. Kim

2

, A.

Bayley

2

, J. Ringash

2

, M. Giuliani

2

, A. Hope

2

, J. Cho

2

, A.

Hansen

4

, R. Jang

4

, J. De Almeida

5

, B. Perez-Ordonez

6

, I.

Weinreb

6

, L. Tong

2

, W. Xu

3

, B. O'Sullivan

2

1

Princess Margaret Cancer Centre University Health

Network, 2B-Radiation Therapy, Toronto, Canada

2

Princess Margaret Cancer Centre / University of

Toronto, Radiation Oncology, Toronto, Canada

3

Princess Margaret Cancer Centre / University of

Toronto, Biostatistics, Toronto, Canada

4

Princess Margaret Cancer Centre / University of

Toronto, Division of Medical Oncology, Toronto, Canada

5

Princess Margaret Cancer Centre / University of

Toronto, Otolaryngology - Head & Neck Surgery,

Toronto, Canada

6

Princess Margaret Cancer Centre / University of

Toronto, Pathology, Toronto, Canada

Purpose or Objective

To compare clinical behavior between viral related

oropharyngeal (OPC) and nasopharyngeal carcinoma (NPC)

at a western institution.

Material and Methods

We reviewed all newly diagnosed viral related OPC and

NPC treated with IMRT from 2005-2014. Viral etiology was

confirmed by p16 immunohistochemistry staining for HPV

and EBER in situ hybridization for EBV. Demographics, the

new HPV+ OPC specific UICC/AJCC TNM (ICON-S) and