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S288

ESTRO 36 2017

_______________________________________________________________________________________________

A. Vestergaard

1

, L. Muren

1

, H. Lindberg

2

, L. Dysager

3

, K.

Jakobsen

2

, H. Jensen

3

, J. Petersen

1

, U. Elstrøm

1

, A. Als

4

,

M. Høyer

4

1

Aarhus University Hospital, Department of Medical

Physics, Aarhus C, Denmark

2

Copenhagen University Hospital- Herlev, Department of

Oncology, Herlev, Denmark

3

Odense University Hospital, Department of Oncology,

Odense, Denmark

4

Aarhus University Hospital, Department of Oncology,

Aarhus C, Denmark

Purpose or Objective

Large changes in bladder shape and size during a course of

radiotherapy (RT) make adaptive RT (ART) appealing in

the treatment of this tumour site. Patients with bladder

cancer unfit for surgery and chemotherapy were treated

in a multicentre phase II trial of daily plan selection with

the primary aim of reducing gastro-intestinal (GI)

morbidity. Acute and late morbidity is reported from the

trial and the frequency of acute diarrhoea is compared to

a previous cohort of similar patients treated with non-

adaptive RT (non-ART).

Material and Methods

All 54 patients (median age 80 years) received 60 Gy in 30

fractions to the bladder; in 41 of the patients the pelvic

lymph nodes were simultaneously treated to 48 Gy. Cone-

beam CT (CBCT) image guidance was used for daily set-up

and treatment was delivered by volumetric modulated arc

therapy (VMAT). The first five fractions were delivered

using large, population-based margins(non-ART: 20 mm

sup and ant; 15 mm post; 10 mm lat and inf); the bladder

contours from the CBCTs acquired during the first four

daily treatment sessions were used to create a library of

three plans, corresponding to a small, medium and large

size bladder. From fraction six all patients were treated

using daily online plan selection, where the smallest plan

covering the bladder was selected prior to each treatment

delivery. Morbidity scoring was performed at baseline,

every second week during RT and two weeks as well as 3,

12 and 24 month after RT using CTCAE v. 4.0. The

frequency of any grade 2 or higher GI morbidity was

evaluated at treatment completion. Peak acute morbidity

was assessed using the scorings until 3 months after RT

and peak late morbidity was evaluated after 12 months of

follow up. The frequency of peak acute diarrhoea was

compared to the cohort treated with non-ART. Acute and

late genito-urinary (GU) morbidity was also recorded.

Median follow-up was 12 months.

Results

Frequency of use of small size plans was 46%, medium 25%

and large 31%. The median volume ratio of PTV-ART vs.

non-ART across the treatment course was 0.68 (range:

0.46-0.93 for individual patients). Any GI morbidity grade

2 or higher was reported by 11 patients (20%) at treatment

completion and returned to baseline level at the 3 months

follow-up. Peak acute grade 2 or higher diarrhoea was

reported by 12 patients (22%). In the previous cohort of

patients treated with non-ART, 15 (30%) reported grade 2

or higher diarrhoea. An expected increase in acute GU

morbidity during RT was observed compared to baseline

scoring, but primarily grade 1. Late GU morbidity was

comparable to baseline.

Conclusion

Daily adaptive plan selection in RT of bladder cancer

results in a considerable dose sparing of normal tissue.

This phase II trial indicates that adaptive RT can be

delivered with low risk of morbidity.

Poster Viewing : Session 12: Gynaecology and prostate

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M.X. Qu

1

, V. Velker

2

, E. Leung

3

, J. Kwon

4

, M.A. Elshaikh

5

,

I. Kong

6

, N. Logie

7

, L.C. Mendez

3

, L. Van der Putten

4

, E.

Donovan

6

, A.R. Munkarah

8

, E.M. Wiebe

7

, A.V. Louie

2

, D.P.

D'Souza

2

1

Queen's University, Oncology, Kingston, Canada

2

Western University, Radiation Oncology, London,

Canada

3

University of Toronto, Radiation Oncology, Toronto,

Canada

4

University of British Columbia, Obstetrics &

Gynaecology, Vancouver, Canada

5

Henry Ford Hospital, Radiation Oncology, Detroit, USA

6

McMaster University, Oncology, Hamilton, Canada

7

University of Alberta, Oncology, Edmonton, Canada

8

Henry Ford Hospital, Gynecology/Oncology, Detroit,

USA