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S151

ESTRO 36 2017

_______________________________________________________________________________________________

prognosis significantly superior than HPV negative

tumor.Although their survival is excellent, standard RT-CT

regimens produce substantial

toxicity.In

that scenario

strategies for de-intensification have been

developed.De

-

intensification is to modify the standard treatment in

order to reduce the long-termtoxicities associated with

radiation / chemotherapy while maintaining the high cure

rates.Prognostic factors allow us to select patients with

excellent outcomes that can benefits from de-

intensification strategies. This factors are: Oropharyngeal

cancer, P16 +, minimalsmoking history, non bulky primary

and non-extensive nodal spread (not N2c-N3).Strategies

for de-intensification are: Select chemo responders and

reduce RT dose or thevolume, reduce RT dose and

cisplatin, replace cisplatin with cetuximab, use

TORSresection and reduce adjuvant RT dosePublished de-

escalation clinical trial will be presented and discussed as

well as the mostimportant ongoing

trials.As

conclusions:

radiation de-escalation is experimental and should be

conducted in clinicaltrials, appropriate candidates for de-

escalation are well defined, there are differentstrategies

for de-intensification, preliminary data show efficacy but

the effect on long-termtoxicity reduction need to be

proved.

Symposium with Proffered Papers: Costs and value of

radiotherapy innovations: how to assess

SP-0294 Health Technology Assessment: what’s in a

word?

A. Aggarwal

1

1

London School of Hygiene and Tropical Medicine, Health

Services Research and Policy, London, United Kingdom

Health Technology Assessments (HTA) aim to ensure

rational and fair decisions are made on resource allocation

for new health interventions. The advantage of HTAs are

their universality when making decisions regarding which

treatments across all medical specialities represent the

best value to society. However, few if any countries

internationally use HTA in the evaluation of radiation

technologies. Instead these processes have largely

focussed on new cancer drugs, informing reimbursement

policy for public health systems.

In the absence of HTA processes, low regulatory barriers

have resulted in the relentless diffusion of increasingly

expensive radiotherapy innovations which offer ever-

marginal gains in the therapeutic ratio. Without a rational

and evidence based approach to evaluation the costs of

delivering cancer care will continue to rise exponentially.

I will discuss how a commitment to HTA processes is

imperative in order to avoid many of the entrenched

interests and inefficient practices that have manifest in

high income countries due to differences in cancer care

delivery, and health system financing. I will also highlight

the challenges in establishing HTA for radiotherapy

interventions, given the diversity in innovation, and

limitations within the evidence base to enable

comparative effectiveness research.

In addition I will offer insights into the challenges of

implementing HTA decisions in practice, using the

experiences of the UK National Institute for Health and

Clinical Excellence (NICE) as an example. Specifically, the

impact of political, public and media pressure on HTA

assessments of cancer therapies as well as the negative

consequences of bypassing these value driven approaches

to reimbursement policy.

SP-0295 Radiotherapy costs: the good, the bad and the

ugly

L.Perrier

5

Cancer Centre Léon Bérard, Clinical Research and

Innovation Direction, Lyon, France

Abstract not received

OC-0296 A critical quality appraisal of studies

estimating the cost of radiotherapy

N. Defourny

1

, P. Dunscombe

2

, C. Grau

3

, Y. Lievens

4

, L.

Perrier

5

1

ESTRO A.I.S.B.L., HERO, Brussels, Belgium

2

University of Calgary, Department of Oncology, Calgary,

Canada

3

Aarhus University, Department of Clinical Medicine,

Aarhus, Denmark

4

University Hospital Ghent, Radiation Oncologist, Ghent,

Belgium

5

Cancer Centre Léon Bérard, Clinical Research and

Innovation Direction, Lyon, France

Purpose or Objective

In the context of growing healthcare expenses combined

with reduced economic growth, health economics (HE)

studies are becoming paramount. Considerable interest in

the domain is apparent when looking at the number of

articles indexed with HE keywords. Nevertheless, a recent

literature review has revealed very few articles

calculating the cost of radiotherapy, and a large

heterogeneity in the methodologies used. The aim of this

complementary review is to report on existing guidance in

HE and to critically assess guideline compliance in the

radiotherapy literature.

Material and Methods

A systematic literature review of cost computation studies

in external photon beam radiation therapy (EBRT) from

1981-2015 was recently conducted by us. Building on this

earlier work, existing HE guidelines have been reviewed

and a list of relevant items for cost estimations has been

compiled. The guidelines searched were ISPOR’s Good

Practices For Outcome Research guidelines, HE evaluation

quality appraisal instruments and National guidelines

(EUnetHTA). A standardised framework focusing on

recommendations on cost assessment was designed with

the help of these guidelines. Fifty-two HE studies meeting

criteria established in our earlier literature review were

studied in-depth: cost assessment methods, descriptions

of methodologies (e.g. sample size, time horizon, or

discounting clearly mentioned), and relevant statistical

analyses performed (e.g. selection bias treated,

sensitivity analyses done) were all critically appraised

within the framework.

Results

Guidance on HE analyses is often provided in the form of

a checklist of items to be addressed. Direction on the cost

type to estimate, the analysis to conduct, and methods for

tackling uncertainty of data are outlined, e.g. ‘’identify

relevant cost for each alternative and value the cost

appropriately’’. Evaluation of the 52 studies against

published HE recommendations revealed shortcomings in

the cost assessment methodologies, the implications of

that choice, and the calculation methods used.

Among selected studies, heterogeneity was observed in

the quantity and quality of the information disclosed.

While documentation of cost items and sample size was

found in 67% of the 52 articles, and the reference year of

cost data was present in 85%, only 37% of the articles

specified data sources used by the authors, 35% stated

their discounting methods and just 8% mentioned the

study’s time horizon. Descriptive statistics analyses were

present in 35% of the studies and uncertainty treatment in

48%.

Conclusion

Existing guidance on formulating the cost part of HE

evaluation studies establishes an outline framework while

giving researchers a high degree of freedom. The limited

number of studies investigating the cost of EBRT do not

systematically follow these published HE guidance leaving