Outcomes of
treatment with
stereotactic
radiosurgery or proton
beam therapy for
choroidal melanoma
MJ Sikuade
1
, S Salvi
1
, PA Rundle
1
, DG Errington
2
,
A Kacperek
2
and IG Rennie
1
Abstract
Aim To present our experience of the use of
stereotactic radiosurgery and proton beam
therapy to treat posterior uveal melanoma
over a 10 year period.
Methods and materials Case notes of
patients treated with stereotactic radiosurgery
(SRS), or Proton beam therapy (PBT) for
posterior uveal melanoma were reviewed.
Data collected included visual acuity at
presentation and final review, local control
rates, globe retention and complications. We
analysed post-operative visual outcomes and
if visual outcomes varied with proximity to
the optic nerve or fovea.
Results 191 patients were included in the
study; 85 and 106 patients received
Stereotactic radiosurgery and Proton beam
therapy, respectively. Mean follow up period
was 39 months in the SRS group and
34 months in the PBT group. Both treatments
achieved excellent local control rates with eye
retention in 98% of the SRS group and 95%
in the PBT group. The stereotactic
radiosurgery group showed a poorer visual
prognosis with 65% losing more than 3 lines
of Snellen acuity compared to 45% in the PBT
group. 33% of the SRS group and 54% of
proton beam patients had a visual acuity of
6/60 or better.
Conclusions Stereotactic radiosurgery and
proton beam therapy are effective treatments
for larger choroidal melanomas or tumours
unsuitable for plaque radiotherapy. Our
results suggest that patients treated with
proton beam therapy retain better vision post-
operatively; however, possible confounding
factors include age, tumour location and
systemic co-morbidities. These factors as well
as the patient’s preference should be
considered when deciding between these two
therapies.
Eye (2015) 29, 1194–1198; doi:10.1038/eye.2015.109;
published online, 10 July 2015
Introduction
The primary aim of treatment for uveal
melanoma is tumour destruction. Secondary to
this is preservation of the eye and retention or
restoration of visual function. To this end,
a number of treatment options exist including
plaque brachytherapy,
1,2
proton beam
irradiation
3,4
stereotactic radiosurgery,
5
local
resection
6
and to a lesser extent transpupillary
thermotherapy
7
or photodynamic therapy
8
as
well as of course primary enucleation. The
treatment modality used is dependent on several
factors including size and location of the
tumour, proximity to the optic disc or fovea,
suitability for surgery and patient choice.
Since the results of the COMS study which
suggested no difference in mortality for patients
with medium-sized melanomas treated with
either brachytherapy or enucleation,
2
eye-
conserving therapies have been used in the
majority of patients. Treatment of larger
tumours as well as tumours in close proximity to
the optic nerve is more challenging as accurate
placement of a plaque to cover the entire tumour
can be technically difficult. Other eye sparing
radiation treatments such as proton beam
therapy (PBT) and stereotactic radiosurgery
(SRS) do not suffer from these limitations and
have been used for many years to treat these
more challenging melanomas. As both of these
treatments options are available at our national
ocular oncology centre (in conjunction with the
Douglas Cyclotron Unit at the Clatterbridge
Oncology Centre), this study was designed to
compare outcomes in our patient cohort over a
10-year period.
1
Sheffield Ocular Oncology
Service, Royal Hallamshire
Hospital, Sheffield, UK
2
Department of Oncology,
Douglas Cyclotron,
Clatterbridge Cancer
Centre, Wirral, UK
Correspondence:
MJ Sikuade, Department of
Ophthalmology, Royal
Hallamshire Hospital,
Glossop Road, Sheffield,
South Yorkshire S10 2JF,
UK
Tel: 0114 27 13619;
Fax: 0114 271 2902.
E-mail: mjsikuade@
doctors.net.uk
Received: 5 March 2015
Accepted in revised form:
30 April 2015
Published online:
10 July 2015
Presented as a poster at the
North of England
Ophthalmological Society
Centenary Conference.
CLINICAL STUDY
Eye (2015) 29, 1194–1198
© 2015 Macmillan Publishers Limited All rights reserved 0950-222X/15
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