Table of Contents Table of Contents
Previous Page  743 / 1082 Next Page
Information
Show Menu
Previous Page 743 / 1082 Next Page
Page Background

S727

ESTRO 36 2017

_______________________________________________________________________________________________

mean PTV

Boost

(SD, range) HI was 0.08 (0.02; 0.05-0.11)

and 0.07 (0.03; 0.05-0.12) (p=0.31) respectively.

No statistically significant difference in target volume

coverage or dose to rectum, other bowel or bladder

outside PTV

Boost

was seen between the two plans. Table

below summaries the dosimteric outcomes.

Conclusion

SIB delivery was achieved with comparable target and

normal tissue constraints for both techniques. VMAT

faster delivery times are likely to mean it is favoured for

this group of patients both because of reduction in intra-

fraction organ filling opportunity and departmental

throughput.

References

1.

Huddart RA, Hall E, Hussain SA, Jenkins P, Rawlings C,

Tremlett J, Crundwell M, Adab FA, Sheehan D, Syndikus I

et al

: Randomized noninferiority trial of reduced high-

dose volume versus standard volume radiation therapy for

muscle-invasive bladder cancer: results of the BC2001 trial

(CRUK/01/004).

Int J Radiat Oncol Biol Phys

2013,

87(2):261-269

2. Cowan RA, McBain CA, Ryder WD, Wylie JP, Logue JP,

Turner SL, Van der Voet J, Collins CD, Khoo VS, Read GR:

Radiotherapy for muscle-invasive carcinoma of the

bladder: results of a randomized trial comparing

conventional whole bladder with dose-escalated partial

bladder radiotherapy.

Int J Radiat Oncol Biol Phys

2004,

59(1):197-207.

Acknowledgments

We acknowledge NHS funding to the

NIHR Biomedical Research Centre for Cancer and to Cancer

Research UK (CRUK).

Electronic Poster: Clinical track: Skin cancer / malignant

melanoma

EP-1371 Primary oesophageal melanoma responds to

hypofractionated radiotherapy

K. Griffin

1

, A. Scarsbrook

2

, W. Merchant

1

, G.

Radhakrishna

3

, O. Donnelly

3

1

St James' Institute of Oncology, Pathology, Leeds,

United Kingdom

2

St James' Institute of Oncology, Radiology, Leeds,

United Kingdom

3

St James' Institute of Oncology, Oncology, Leeds, United

Kingdom

Purpose or Objective

Oesophageal melanoma is rare; current practice would be

to consider surgical treatment first, with radiotherapy

reserved for unresectable or patients not suitable for

oesophagectomy. We report our experience of three

consecutive patients who responded to high-dose

hypofractionated radiotherapy to localised oesophageal

melanoma primaries.

Material and Methods

Each patient had endoscopic biopsy confirming primary

oesophageal melanoma. Prior to treatment whole-body

PET scans were performed to aid tumour localisation and

exclude nodal or distant metastases. PET scans were

repeated after completion of radiotherapy and patients

were followed-up clinically thereafter. Each patient gave

written consent for publication.

Two patients (A&B) received 50 Gy in 16 daily fractions

using a 3D conformal technique. The third patient (C)

received 30 Gy in 10 daily fractions followed by

intraluminal brachytherapy (16 Gy in 2 treatments, one

week apart).

Results

In all three cases tumours were Braf wildtype, PET-avid on

pre-treatment scans and no distant or nodal metastases

were

identified.

All three patients developed odynophagia requiring

analgesia during and for several weeks following

treatment and lost weight, though no patient required

admission or enteral feeding support.

On post-treatment PET scans all patients had a response

in the oesophageal primary;

Patient A had a complete response. She remained disease-

free, with normal swallowing, until she died due to

myocardial infarction, 30 months after diagnosis (26

months since completion of treatment).

B had a good partial response; pretreatment 6 cm tumour

with SUVmax 20.8 - following treatment 2.8 cm,SUVmax

9.7. His swallowing remained normal without further

intervention until 24 months after diagnosis (22 months

after treatment) - at which point he reported mild

dysphagia and a further endoscopy identified residual

melanoma. He remains

stent-free.

C had complete response of the primary oesophageal

melanoma but the post-treatment PET identified

metastatic disease in both lungs and peritoneal cavity. She

died 12 months after diagnosis (9 months after

treatment).

Conclusion

Oesophageal primaries are a rare site for non-cutaneous

melanomas with little evidence to guide management.

Based on our series tumours are FDG-avid and PET-CT is

likely to be useful in planning treatment.

Hypofractionated radiotherapy appears to be effective in

achieving local control and should be considered an

alternative to surgery for melanoma arising in the

oesophagus.

EP-1372 Preliminar results of fractionated cyberknife

stereotactic radiotherapy for uveal melanoma.

I. Bossi Zanetti

1

, M. Pellegrini

2

, G. Beltramo

1

, V. Ravera

2

,

A. Bergantin

1

, A.S. Martinotti

1

, I. Redaelli

1

, P. Bonfanti

1

,