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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

__________________________________________________________________________________________

was performed in general anaesthesia using systemic

bleomycin (15.000 IU/m

2

) prior to electroporation with

sequences of 8 pulses of 100µs and 1000 V/cm applied

voltage to electrode distance ratio. Evaluation of tumour

response was assessed from PET/CT-, MRI- scans and

biopsies. Primary objective was tumour response

measured using RECIST criteria. Secondary objectives

included tumour response in the treatment area from MRI

and multiple time point FDG PET scans as well as patient

evaluation of treatment using pain score and quality-of-

life questionnaires (EORTC QLQ-C30 and QLQ-H&N35).

Results

Nineteen patients were included in this ongoing trial and

treated for a recurrent carcinoma in the head and neck

area. Due to large tumours, treatment could in most cases

only be applied to parts of the tumour thereby leading to

a debulking. Thirteen patients were evaluable according

to RECIST criteria at evaluation 8 weeks after treatment.

One patient died before evaluation. Five patients had

cystic tumours at evaluation and therefore not evaluable

according to RECIST criteria. Overall response in the 13

patients evaluable by REICST was 62% (8 of 13 pts): of

these 2 (15%) had complete remission (CR), 6 (46%) had

partial remission (PR), while progression (PD) was

observed in 5 (39%). The MRI and PET results from the

treatment area are currently being assessed.

There was no change in pain score from baseline to

evaluation.

Quality-of-life

questionnaires

only

demonstrated a change in dysphagia.

Conclusion

Electrochemotherapy was feasible in patients with

recurrent head and neck cancer without further standard

treatment options. Overall response rate was 62% with

limited side effects, warranting continuation of the study.

PO-096 Dosimetric evalutation of volumetric modulated

arc therapy (VMAT) in sinonasal cancer raiotherapy

E. Donini

1

, S. Magi

2

, S. Ricci

2

, E. Pasquini

3

, G. Frezza

1

1

Ospedale Bellaria - AUSL Bologna, Radiotherapy,

Bologna, Italy

2

Ospedale Bellaria - AUSL Bologna, Medical Physics,

Bologna, Italy

3

AUSL Bologna, Ear- Nose and Throat Metropolitan Unit,

Bologna, Italy

Purpose or Objective

To assess dosimetric parameters of volumetric modulated

arc therapy (VMAT) for nasosinusal malignancies with

regard to the coverage of planning target volume (PTV)

and the sparing of organs at risk (OAR).

Material and Methods

Nine patients with naso sinusal malignancies were treated

with postoperative radiotherapy (VMAT, 2-3 non coplanar

arcs) between 2015 and 2016. Seven patients were

treated on primary target volume only (tumor bed), two

patients required also nodal irradiation. Planning goals

were the following: PTV: > 98% volume covered by >95%

of prescribed dose; >107% of prescribed dose to < 2% PTV

volume; for organs at risk (OARs): maximum doses

(D(max)) < 60 Gy to the brainstem, < 54 to the optic

chiasm, < 50 to the optic nerves, <40 Gy to the eyes and <

5 Gy to the lenses. Dose was prescribed to the median dose

according to ICRU 83. Dose-volume histogram, the

maximum, minimum, and mean doses to the target

volumes and organs at risk, and monitor units (MUs) were

evaluated.

Results

VMAT offered a good tumor volume coverage and provided

a good sparing of OARs (mean Dmax ipsilateral optic

nerve:45,8 Gy, mean Dmax contralateral optic nerve:

43,3; mean Dmax optic chiasm: 46,4 Gy; mean Dmax

brainstem: 37,9 Gy; mean Dmax ipsilateral eye: 47,6 Gy;

mean Dmax contralateral eye: 33,3 Gy). VMAT showed low

MUs (mean MUtot: 583,7) and low treatment delivery.

Conclusion

VMAT's plans further reduce doses to critical structures

that are in close proximity to the target volume, and

reducing treatment delivery time, decrease the effects of

intrafractional uncertainties that can occur because of

patient movement during treatment delivery.

Poster: Biology, HPV and molecular targeting

PO-097 Droplet Digital PCR for detection of circulating

tumour DNA in blood of head and neck cancer patients

J.H. Van Ginkel

1

, M.M.H. Huibers

1

, R.J.J. Van Es

2

, R. De

Bree

3

, S.M. Willems

1

1

UMC Utrecht, Pathology, Utrecht, The Netherlands

2

UMC Utrecht, Oral and Maxillofacial Surgery and Head

and Neck Surgical Oncology, Utrecht, The Netherlands

3

UMC Utrecht, Head and Neck Surgical Oncology, Utrecht,

The Netherlands

Purpose or Objective

During posttreatment surveillance of head and neck

cancer patients, imaging is insufficiently accurate for the

early detection of relapsing disease. Free circulating

tumor DNA (ctDNA) may serve as a novel biomarker for

monitoring tumor burden during posttreatment

surveillance of these patients. In this exploratory study,

we investigated whether low level ctDNA in plasma of

head and neck cancer patients can be detected using

droplet digital PCR (ddPCR).

Material and Methods

TP53

Mutations were determined in surgically resected

primary tumor samples from 6 patients with high stage (II-

IV), moderate to poorly differentiated head and neck

squamous cell carcinoma (HNSCC). Subsequently,

mutation specific ddPCR assays were designed.

Pretreatment plasma samples from these patients were

examined on the presence of ctDNA by ddPCR using the

mutation-specific assays. The ddPCR results were

evaluated alongside clinicopathological data.

Results

In all cases, plasma samples were found positive for

targeted

TP53

mutations in varying degrees (absolute

quantification of 4.2 – 422 mutational copies/ml).

Mutations were detected in wild-type

TP53

background

templates of 7,667 – 156,667 copies/ml, yielding

fractional abundances of down to 0.03%.

Conclusion

Our results show that detection of tumor specific

TP53

mutations in low level ctDNA from HNSCC patients using

ddPCR is technically feasible and provide ground for future

research on ctDNA quantification for the use of diagnostic

biomarkers in the posttreatment surveillance of HNSCC

patients.