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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

__________________________________________________________________________________________

SP-016 the value of proton therapy for head and neck

malignancies: reducing side effects and improving

outcomes

P. Blanchard

1

, S.J. Frank

1

1

The University of Texas MD Anderson Cancer Center,

Radiation Oncology, Houston, USA

Abstract text

Due to the close vicinity between target volumes and

several critical organ structures, head and neck cancer

radiotherapy is associated with multiple severe acute and

late toxicities. The improved survival in contemporary

patients has shed light over the potentially devastating

chronic complications that affect increasing numbers of

patients. Intensity modulated external-beam photon

radiation therapy (IMRT) allowed to spare some critical

structures, thereby reducing xerostomia and improving

patient reported outcomes (PRO) compared to traditional

2D/3D radiotherapy. However dose reduction to specified

structures during IMRT was associated with an increased

beam path dose to alternate non-target structures,

resulting in clinical toxicities that were uncommon with

previous approaches.

The physical advantage of proton beam therapy is its sharp

increase in dose deposited at the end of the particle

range, i.e. the Bragg peak, avoiding any exit dose beyond

the target and reducing the integral dose delivered.

Dosimetric comparisons between intensity-modulated

proton therapy (IMPT) and IMRT have consistently shown

that IMPT allowed a better sparing of normal tissues while

maintaining dose to target volumes. Clinical reports have

suggested improved swallowing and taste function,

reduced need for acute and long-term feeding tube

requirements, decreased rates of severe weight loss and

malnutrition or reduced rates of osteoradionecrosis, for

example. Some studies have even suggested that the

physical and biological properties of proton therapy could

result in improved survival in selected tumor types, such

as sinonasal malignancies. The magnitude of the expected

reduction in toxicity has been estimated using normal

tissue complication probability models (NTCP) and the use

of these models has been advocated to select the patients

that will benefit the most from proton therapy compared

to

IMRT.

The aim of this presentation is to demonstrate how proton

therapy could increase the therapeutic ratio in head and

neck cancer. We will 1) introduce basic physics and

dosimetry data; 2) discuss the clinical data published so

far; 3) address the issue of patient selection for IMPT; 4)

discuss the current limitations of proton therapy regarding

physical and biological uncertainties, as well as cost

effectiveness; and 5) discuss how to objectively evaluate

the value of proton therapy in the treatment of head and

neck cancers.

Keynote lecture

SP-017 New imaging techniques

R. Maroldi

1

1

University of Brescia, Radiology, Brescia, Italy

Abstract text

As chemo-radiation therapy is increasingly applied to head

and neck cancer, there is a growing need to develop non-

invasive surrogate-biomarkers to predict and assess the

response to a non-surgical treatment. Therefore, imaging

techniques exploring tumor properties other from CT

density, T2-T1 weighting or the single-phase "static"

enhancement pattern - have been devised. These

"functional techniques" aim at targeting tumor micro-

architecture (DWI), perfusion (DCE-MR) and heterogeneity

(texture analysis). Researches on DWI showed that a high

degree of restriction of water diffusion (low ADC)

correlates with increased cellular density and

extracellular space, a typical feature of neoplasms. DWI

researches points to high pre-treatment mean ADC and a

low increment in ADC early intra-treatment being

indicators of poor outcome. CT and MR perfusion

techniques have been developed to investigate the

changes induced by neo-angiogenesis in the

microcirculation of tumor. This has been accomplished by

analysis of the kinetics of the passage through the tissues

of a bolus of contrast agent (DCE-CT, DCE-MR) or of an

endogenous bolus (blood, ASL-MR perfusion). Presently,

most of the medical literature on perfusion analysis

encompasses pilot studies only. Nevertheless, one

emerging finding is that neoplasms showing great

heterogeneity of a parameter like Ktrans are associated to

a poorer prognosis. Probably related to the presence of

areas capable of surviving in conditions of hypoxia.

Overall, the availability of these imaging techniques has

resulted in the growth of multi-modality and multi-

parametric imaging. In addition, the analysis of the

quantitative data acquired by both standard and

functional imaging techniques has inspired the

development of novel approaches of analysis leading to

the extrapolation of textural, morphologic features with

the potential of providing metrics that can be used to

optimize the treatment.

Keynote lecture

SP-018 HNC Biomarkers - how do we translate biology

into useful assays for clinical care?

T. Seiwert

1

1

University of Chicago, Chicago, USA

Abstract text

With the advent of powerful new profiling technologies

(i.e.

next

generation

sequencing,

RNA

profiling/nanostring, liquid biopsy, multiplex immune

stains) our ability to query tumor biology and answer

clinically relevant questions in patient samples has

increased exponentially. However, understanding clinical

usefulness, technical limitations, and logistics of

implementing biomarker testing in clinical practice will

take significant, collaborative effort of the HNC

community. In this talk we will examine three examples

pertinent to HNC: 1) Emerging biomarkers for

Immunotherapy, 2) the usefulness and technical

limitations of liquid biopsy in curative intent and palliative

care, and 3) the hidden complexities of HPV testing, and

heterogeneity of HPV biology.

Proffered papers 2

OC-019 The phase III study INTERCEPTOR: preliminary

results

N. Denaro

1

, S. Vecchio

2

, A. Bagicalupo

3

, E. Russi

4

, M.

Rampino

5

, M. Benasso

6

, G. Numico

7

, L. Licitra

8

, O.

Ostellino

9

, M. D'amico

10

, P. Curcio

11

, M. Merlano

12

1

Azienda Ospedaliera S. Croce e Carle, oncology, Cuneo,

Italy

2

AOU San Martino IST Genova, Oncology, Genova, Italy

3

AOU S.Martino IST Genova, Radiotherapy, Genova, Italy

4

ASO Santa Croce e Carle, Radiotherapy, Cuneo, Italy

5

IRCCS Candiolo, Radiotherapy, Oncology, Italy

6

AO Savona, Oncology, Savona, Italy