Table of Contents Table of Contents
Previous Page  606 / 1082 Next Page
Information
Show Menu
Previous Page 606 / 1082 Next Page
Page Background

S590

ESTRO 36 2017

_______________________________________________________________________________________________

Results

Fifty patients (36 male and 14 female, mean age 61, range

14-82 years) were included. RT was post-operative in 22

patients (44.0%) and 25 (50.0%) patients received

concurrent CT.

At T0 evaluation, 32/50 patients (64.0%) were emotionally

distressed (cut off value DT score≥4) and 12/50 patients

(24%) showed anxiety/depression (cut off value HADS

score≥14). No difference was observed according to

previous surgery.

During RT, patients who were distressed (32/50) or

anxious and depressed (12/50) at the beginning of

treatment did not show any significant variation of their

DT score, while HADS score significantly improved at T2

evaluation (median HADS score 19 and 15, at T0 and T2

respectively, p=0.03). Patients who were not distressed

(18/50) or anxious and depressed (38/50) at baseline,

showed a worsening of DT score at both T1 (p=0.02) and

T2 (p=0.01) as compared to baseline; HADS score remained

substantially stable at T1 while worsened at T2 (p=0.03).

At T1, 9/40 (22.5%) evaluable patients had G≥3 acute

toxicity. Twenty seven/40 (67.5%) patients had significant

emotional distress and 9/40 (22.5%) patients had

significant anxiety and depression. Emotional distress was

more frequently observed among patients who were also

experiencing severe toxicity (77.7 versus 22.5%

respectively, p<0.01). These patients were also more

frequently anxious and depressed (55.5 versus 24.0%

respectively, p=0.08).

At T2, 10/34 (29.4%) evaluable patients had G≥3 acute

toxicity. Twenty five/34 (73.5%) patients had significant

emotional distress and 12/34 (35.3%) patients had

significant anxiety and depression. No significant

difference was observed according to severe toxicity

occurrence.

Conclusion

Patients with H&N cancer frequently experience

emotional distress and side effects of radiotherapy are

stressful and anxiety provoking events. Beside adequate

medical support, these patients also require focused

psychological interventions.

EP-1081 Tumor response after palliative radiotherapy

in head and neck cancer and its influence on survival

M. Cruz

1

, C. Sousa

1

, D. Branco

1

, L. Khouri

1

, J. Brandão

1

, G.

Melo

1

1

Instituto Português de Oncologia de Coimbra, Radiation

Oncology, Coimbra, Portugal

Purpose or Objective

The aim of this study is to evaluate tumor response in Head

and Neck (H&N) cancer patients who underwent different

fractionation schemes of palliative radiotherapy (RT) and

its influence on overall survival.

Material and Methods

This is a retrospective unicentre study including patients

diagnosed with H&N cancer not suitable for curative

treatment. Those patients completed palliative

radiotherapy to primary local-regional sites in our

department between January 2013 and December 2015.

Radiation therapy was delivered using a mega-voltage

linear accelerator with 6 MV photons. Target volumes

generally included the gross tumor volume with 1 to 2 cm

margins. Tumor response patterns were evaluated

following a cervical and chest Computed Tomography (CT)

performed 4-6 weeks after RT.

Results

53 patients were included in this study (73.4% male). Mean

age was 71.3 years (±1.2). Primary tumor was localized in

oropharynx in 34% of the patients, oral cavity in 20.7% and

larynx in 18.9% of the patients. 92.4% of the tumors were

histologically classified as squamous cells carcinoma. At

the time of the diagnosis, 86.8% of the patients had stage

IV

disease.

Mean Karnofksy Performance Status (KPS) was 68%.

RT palliative schemes chosen were 50Gy delivered in 20

fractions during 4 weeks (50Gy/20fr/4w) in 35% of our

patients, 30Gy/10fr/2w in 32%, 37.5Gy/15fr/3w in 18.9%

and 40Gy/20fr/4w in 13.2% of our patients.

After the analysis of cervical and chest CT, 61.2% of the

patients had partial response while 10.2% had complete

imagiologic response, 18.4% had imagiologic progression

and 8.2% had stabilised disease.

After a mean follow-up period of 27.2 months (±8,3),

overall

survival

was

9.55

months

(±9,3).

The group with better tumor response on CT was the group

that underwent for the 50Gy/20fr/4w scheme (in which

89.4% had partial/complete response) with no need for

interruption of the treatment due to toxicity. The group

with longer overall survival was the group that underwent

for the 30Gy/10fr/2w (11.8 months) and the shortest

overall survival was verified after the 37.5Gy/15fr/3w

scheme (5.2 months). Despite these results, there were no

statistically significant differences between the four RT

schemes delivered to our patients and overall survival

(p=0.41).

Patients who had better tumor response on CT (partial or

complete response) had longer overall survival comparing

to patients who had stabilised disease or progression (11.6

months

vs.

6.65

months;

p=0,011).

Conclusion

There is no consensus regarding the choice of the optimal

RT fractionation scheme used in palliative care of H&N

cancer patients and careful patient selection. Patients

with advanced incurable H&N cancer have a poor

prognosis but the addition of palliative RT provides better

local-regional control of the disease with the possibility of

longer survival rates. More studies should be carried out in

order to evaluate predictive factors of tumor response as

a mean of improving patient’s outcomes and quality of

life.

EP-1082 Primary surgery vs. radiotherapy in early-

stage oropharyngeal cancer: a single centre experience

C. Pedro

1

, B. Mira

2

, P. Silva

1

, E. Netto

3

, R. Pocinho

1

, A.

Mota

1

, P. Pereira

1

, M. Ferreira

2

, T. Alexandre

2

, I.

Sargento

2

, P. Montalvão

4

, M. Magalhães

4

, S. Esteves

5

, F.

Santos

1

1

Instituto Português de Oncologia de Lisboa Francisco

Gentil- EPE, Radiotherapy Department, Lisboa, Portugal

2

Instituto Português de Oncologia de Lisboa Francisco

Gentil- EPE, Oncology Department, Lisboa, Portugal

3

NOVA Medical School UNL, Radiation Oncology, Lisboa,

Portugal

4

Instituto Português de Oncologia de Lisboa Francisco

Gentil- EPE, Otorhinolaryngology Department, Lisboa,

Portugal

5

Instituto Português de Oncologia de Lisboa Francisco

Gentil- EPE, Clinical Research Unit, Lisboa, Portugal

Purpose or Objective