Table of Contents Table of Contents
Previous Page  600 / 1082 Next Page
Information
Show Menu
Previous Page 600 / 1082 Next Page
Page Background

S584

ESTRO 36 2017

_______________________________________________________________________________________________

October 1, 2013 and March 31, 2016. The LE of NPC

patients was obtained using linear extrapolation of a logit-

transformed curve and was adjusted by the corresponding

QOL function to calculate the QALE and SWPS.

Results

The mean age at diagnosis of the 875 non-metastatic NPC

patients was 50.7 years. The median duration from the

beginning of radiotherapy to the date of completing

questionnaires was 6.5 months (range, 0-154.9 months).

The average LE and QALE were estimated to be 15.7 years

and 14.5 quality-adjusted life years (QALYs) for NPC

patients and 29.5 years and 29.5 QALYs for the reference

population, respectively. On average, the lifelong

duration of pain and painkiller use were 5.7 years and 1.8

years. The lifelong duration of any impairment of

swallowing, smell and taste were 14.6 years, 8.5 years and

6.9 years, respectively. The life long duration of dry

mouth was 13.3 years. Furthermore, the lifelong duration

of tube-feeding was only 1.5 months.

Conclusion

This study offers more understandable information than

the 5 year survival outcomes when communicating with

patients or the general population regarding cancer risk

and the impact of treatments on the quality of life. In the

future, evaluating the robustness of comparative

assessments for the outcome of NPC patients undergoing

different treatment protocols will be possible.

EP-1070 Concurrent chemoradiation versus upfront

surgery for clinical T3-4 hypopharynx and larynx

cancer

G.S. Yoo

1

, D. Oh

1

, J.M. Noh

1

, Y.C. Ahn

1

, C.H. Baek

2

, Y.I.

Son

2

, H.S. Jeong

2

, J.M. Sun

3

, M.J. Ahn

3

, K. Park

3

1

Samsung Medical Center, Department of Radiation

Oncology, Seoul, Korea Republic of

2

Samsung Medical Center, Department of

Otorhinolaryngology-Head and Neck Surgery, Seoul,

Korea Republic of

3

Samsung Medical Center, Department of Medicine-

Division of Hematology-Oncology, Seoul, Korea Republic

of

Purpose or Objective

The optimal treatment regimen for advanced T stage

hypopharynx and larynx cancer is controversial. In this

study, we aimed to compare the oncologic outcomes and

functional larynx-preservation (FLP) rates for advanced

clinical T stage (T3-4) hypopharynx and larynx cancer

between definitive concurrent chemoradiotherapy (CCRT)

and upfront surgery with or without adjuvant therapy.

Material and Methods

We reviewed the medical records of 148 patients with

clinical T3-4 hypopharynx or larynx cancer who were

treated between January 2005 and May 2013. Primary

treatment was determined in the multidisciplinary team.

In the CCRT group (N=63), 7 (11.1%) patients received

induction chemotherapy, followed by definitive CCRT.

Fifty-five (87.3%) patients were treated with 3-

dimensional conformal radiation therapy (RT), and 8

(12.7%) patients with intensity-modulated RT. The median

RT dose in the CCRT group was 70 Gy (range, 15.4 to 72

Gy). In the surgery group (N=76), TL was performed in 47

patients (61.8%), partial laryngectomy in 28 patients

(36.8%), and partial pharyngectomy only in 1 (1.3%). Fifty-

nine (77.6%) patients received adjuvant RT and 5 (6.6%)

patients received adjuvant CCRT. Median RT dose in the

surgery group was 60 Gy (range, 52 to 70 Gy).

Results

Median follow-up duration was 46 months (range, 0 to 172

months). In total cohort, the 5-year locoregional control

(LRC), progression-free survival (PFS), and overall survival

(OS) rates were 68.7%, 56.5%, and 64.1%, respectively.

Between the CCRT and surgery group, there was

significant difference in LRC rate (CCRT vs. surgery, 57.5%

vs. 78.9% at 5 years, p=0.014). The ultimate LRC rate

including salvage treatment, however, was not different

significantly between the groups (73.2 vs. 81.7% at 5

years, p=0.209). There was no significant difference in

PFS (p=0.175), and OS rates (p=0.965) between the

groups. On the multivariate analysis, treatment modality

was not independent factor for oncologic outcomes.

The 5-year FLP rate was higher significantly in CCRT group

(75.4% vs. 35.5%, p<0.001). The laryngoesophageal

dysfunction-free survival rate in CCRT group was 56.9%.

On the multivariate analysis, treatment modality was

independent factor in FLP with hazard ratio of CCRT group

as 0.261 (95% confidential interval with 0.139-0.488,

p<0.001).

Conclusion

Under the multidisciplinary approach, there were no

significant differences in oncologic outcomes between the

CCRT and surgery groups, while CCRT gave more

opportunity to preserve the laryngeal function.

EP-1071 Organ-sparing SBRT in reirradiation of head

and neck cancer: efficacy, toxicity, and quality of life

I. Zhang

1

, G. Gill

1

, M. Marrero

1

, A. Sharma

1

, A. Riegel

1

, D.

Paul

2

, J. Knisely

1

, S. Teckie

1

, M. Ghaly

1

1

North Shore LIJ Health System, Radiation Medicine, New

Hyde Park, USA

2

North Shore LIJ Health System, Medical Oncology, New

Hyde Park, USA

Purpose or Objective

To present a retrospective analysis of the efficacy,

toxicity, and quality of life (QOL) of patients treated with

organ-at-risk (OAR)-sparing salvage stereotactic body

radiotherapy (SBRT) in previously-irradiated head and

neck cancer.

Material and Methods

From November 2012 to July 2015, 60 patients with in-

field recurrence of head and neck cancer underwent

reirradiation with OAR-sparing SBRT at our institution.

OARs were defined as critical structures that had

approached their radiation tolerances after prior

irradiation and had a high potential to impair QOL if

damaged with re-irradiation. Intact tumors were

prescribed 40 Gy while 35 Gy was prescribed for post-

operative treatments. Doses previously received by the

OARs were estimated by deformably registering the prior

treatment plan onto the new simulation CT to more

accurately delineate dose distributions (Figure 1: Prior

plan overlying the new planning CT without (top) and with

(bottom) deformable registration). Dose constraints for

SBRT were calculated with a biological equivalent dose

(BED) using an alpha/beta ratio of 3 to reduce the risk of