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6th ICHNO

6

th

ICHNO Conference

International Conference on innovative approaches in Head and Neck Oncology

16 – 18 March 2017

Barcelona, Spain

__________________________________________________________________________________________

Conclusion

With proper case selection reRT can be delivered with

acceptable toxicities and is associated with improved

outcomes.

OC-044 ART DECO (CRUK/10/018): dose escalated vs

standard dose IMRT in locally advanced head and neck

cancer

C. Nutting

1

, J. Morden

2

, D. Bernstein

3

, M. Beasley

4

, V.

Cosgrove

5

, S. Fisher

6

, B. Foran

7

, T. Guerrero-Urbano

8

, D.

Gujral

9

, K. Harrington

1

, E. Junor

10

, H. Mehanna

11

, A.

Miah

12

, N. Palaniappan

13

, S. Ramkumar

14

, P. Sanghera

15

, M.

Sen

16

, A. Sibtain

17

, W. Soe

18

, C. West

19

, D. Piercey

2

, S.

Witts

2

, M. Emson

2

, E. Hall

2

1

The Institute of Cancer Research and The Royal Marsden

NHS Foundation Trust, Head and Neck Unit, Sutton,

United Kingdom

2

The Institute of Cancer Research, ICR-Clinical Trials and

Statistics Unit, Sutton, United Kingdom

3

The Royal Marsden NHS Foundation Trust, Radiotherapy

Physics, Sutton, United Kingdom

4

Bristol Haematology and Oncology Centre, Oncology,

Bristol, United Kingdom

5

St James's University Hospital, Radiotherapy Physics,

Leeds, United Kingdom

6

University of Leeds, LICAP, Leeds, United Kingdom

7

Weston Park Hospital, Oncology, Sheffield, United

Kingdom

8

Guy's and St Thomas' Hospitals NHS Trust, Oncology,

London, United Kingdom

9

Imperial College Healthcare NHS Trust, Oncology,

London, United Kingdom

10

Western General Hospital, Oncology, Edinburgh, United

Kingdom

11

University of Birmingham, INHANSE, Birmingham,

United Kingdom

12

The Royal Marsden NHS Foundation Trust, Sarcoma

Unit, Sutton, United Kingdom

13

Velindre Hospital, Oncology, Cardiff, United Kingdom

14

Southampton General Hospital, Oncology,

Southampton, United Kingdom

15

Queen Elizabeth Hospital, Oncology, Birmingham,

United Kingdom

16

St James's University Hospital, Oncology, Leeds, United

Kingdom

17

St Bartholomew's Hospital, Oncology, London, United

Kingdom

18

Glan Clwyd Hospital, Oncology, Rhyl, United Kingdom

19

University of Manchester, Radiation Biology,

Manchester, United Kingdom

Purpose or Objective

Radical (chemo)radiotherapy offers curative treatment for

patients with locally advanced laryngeal or

hypopharyngeal cancer. IMRT permits safe dose-escalation

and hence potential improved locoregional control given

reduction in volume of normal tissue receiving high dose

radiation.

Material and Methods

Patients with histologically squamous cell laryngeal or

hypopharyngeal cancer (AJCC III-IVa/b) were randomised

to dose-escalated (DE-IMRT) (primary tumour:

67.2Gray(Gy)/28 fractions(f), at risk nodes: 56Gy/28f) or

standard dose (ST-IMRT) (primary tumour: 65Gy/30f, at

risk nodes: 54Gy/30f) IMRT. Patients received 2 cycles

concomitant cisplatin, and up to 3 cycles platinum-based

induction chemotherapy. Treatment allocation (1:1) used

minimisation, balancing for centre, tumour site, nodal

status and planned chemotherapy. Primary endpoint was

locoregional failure- free rate (LRFFR) i.e. time to

locoregional relapse or completion of radiotherapy in

patients with persistent disease 3 months after treatment

(clinical assessment). Target recruitment was 354

patients; 100 events required to detect improvement in 2-

year LRFFR from 60% to 77.5% (two-sided α=0.05, 90%

power). LRFFR was analysed using competing risks

methodology (with death as competing event), compared

between groups by Gray’s test. Secondary endpoints

(α=0.01) included toxicity (CTCAEv4.0, LENT SOMA),

patient-reported quality of life and overall survival.

Results

276 patients (138 ST-IMRT; 138 DE-IMRT) were randomised

(2011-2015) from 32 UK centres. 84% were male, 66% had

laryngeal tumours, 98% were N0-2, mean age was 62 years.

Planned chemotherapy was 40% induction and

concomitant,

48%

concomitant

only,

13%

none. Recruitment stopped early due to planned interim

futility analysis (subhazard ratio (SHR)>1 after 50%

required events). 32/138 (23%) ST-IMRT and 37/138 (27%)

DE-IMRT patients reported LRFFR events, SHR for DE-IMRT

1.22 (95%CI 0.76–1.94), p=0.42. Grade≥2 acute pharyngeal

mucositis and 3 month post-RT pharyngeal dysphagia was

higher with DE-IMRT (p=0.008, p=0.01 respectively).

Conclusion

There was no evidence for a statistically significant

improvement in locoregional control with DE-IMRT

compared with ST-IMRT. DE-IMRT was associated with a

worse toxicity profile.

OC-045 Recurrence patterns after 40 Gy to the elective

treated neck in head and neck cancer.

D. Nevens

1

, F. Duprez

2

, J. Daisne

3

, J. Schatteman

4

, W. De

Neve

2

, S. Nuyts

1

1

University Hospital Gasthuisberg, Radiation Oncology

Department, Leuven, Belgium

2

Ghent University Hospital, Department of Radiation

Oncology, Ghent, Belgium

3

MaternitéUniversité Catholique de Louvain- CHU-UCL-

Namur- site Sainte-Elisabeth, Radiation Oncolgy

Department, Namur, Belgium

4

Ghent University Hospital, Nuclear Medicine, Ghent,

Belgium

Purpose or Objective

To investigate the patterns of regional recurrences with

emphasis on recurrences in the electively irradiated lymph

node regions after dose de-escalation to 40 Gy (EQD2Gy)

in head and neck cancer.

Material and Methods

Two hundred thirty-three patients treated with

radio(chemo)therapy using

40 Gy (EQD2Gy) to the

elective lymph node regions were included. All regional

recurrences were reconstructed and projected on the