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S508

ESTRO 36

_______________________________________________________________________________________________

Conclusion

It is feasible to generate conventionally fractionated

treatment plans for LA NSCLC patients on a 1.5 T MR-linac

with minor differences in dose-volume metrics, which are

unlikely to be clinically meaningful. When using standard

PTV margins, isotoxic dose escalation was limited on the

MR-linac. However, reducing margins alleviates these

observed effects. This study only represents an early

indicator of the treatment implications of MRI-guided

radiotherapy. It is conceivable that the availability of MRI-

guidance will result in further benefits through inter- and

intrafractional treatment adaptation.

PO-0917 Nationwide audit of small fields output

calculations in Poland

W. Bulski

1

, K. Chelminski

1

1

The Maria Sklodowska-Curie Memorial Cancer Center,

Medical Physics Department, Warsaw, Poland

Purpose or Objective

The delivery of accurate intensity-modulated radiation

therapy (IMRT) or stereotactic radiotherapy depends on a

multitude of steps in the treatment delivery process.

Within the treatment planning system’s (TPS) dose

calculation algorithm, various unique small field

dosimetry parameters are essential, such as multileaf

collimator modeling and field size dependence of the

output. One of the most considerable challenges in this

process is to determine accurate small field size output

factors. Modern radiotherapy routinely involve s the use

of small radiation fields as components of IMRT. Because

of the difficulties in commissioning small field data, a set

of field size dependent output factors could prove to be

an invaluable tool to confirm the validity of an individual

institution’s dosimetry parameters. Such a set of data has

been prepared by the Radiological Physics Center (RPC),

M. D. Anderson Cancer Center, Houston. The RPC has

gathered multiple small field size output factor datasets

for X-ray beam qualities, ranging from 6 to 18 MV, from

Varian, Siemens and Elekta linear accelerators. These

datasets were measured at 10 cm depth and ranged from

10×10 cm

2

to 2×2 cm

2

. Within the framework of the IAEA

CRP E2.40.16 project "Development of Quality Audits for

Radiotherapy Dosimetry for Complex Treatment

Techniques, a methodology of the audit of small field

output performance was established.

Material and Methods

The participants had to calculate t he output factors for

the beams formed by the multi-leaf collim ator (MLC).

The results of their calculations were compared with the

reference RPC data. 32 Polish radiotherapy departments

took part in the audit. In total, 65 beams were audited.

The participants of the audit were asked to calculate the

number of monitor units (MU) for the delivery of a

prescribed dose to water with square fields of different

sizes. A dose of 10 Gy was prescribed to a reference point

at 10 cm depth on the central axis, at 100 cm source-to-

phantom distance (SFD). The output factors for five field

sizes, 10×10, 6×6, 4×4, 3×3 and 2×2 cm

2

, shaped by a

multileaf collimator (MLC), were calculated.

Results

For Elekta accelerators, all the calculation results show a

deviation from the reference values lower than 3%. For

Siemens and Varian accelerators, the resulting

calculations for fields larger than 2×2 cm

2

differ less than

4%. For 2×2 cm

2

large fields formed by Siemens and Varian

MLC, the differences between the calculated and

measured output factors often exceed 5%, but still are

below 10%.

Conclusion

The RPC measured values provide a consistent dataset for

small field output factors that can be used as a redundant

QA check of a treatment planning system dosimetry data

for small-field treatments. The results of the audit are

very useful for the participants who should carefully

investigate any detected discrepancies between the

standard dataset and calculated values, with attention to

the specific beam model.

PO-0918 Radiotherapy and Her2 targeting agents:

synergism and antagonism in clonogenic and confluence

assays

N. Suchowerska

1

, J. Toohey

2

, S. Carroll

2

, L. Rogers

2

, G.

Lyons

3

, J. Beith

4

, A. Dos Santos Esteves

2

, D.R. McKenzie

5

1

Chris O'Brien Lifehouse, Radiation Oncology,

Camperdown- Sydney, Australia

2

Chris O'Brien Lifehouse, Radiation Oncology,

Camperdown Sydney, Australia

3

Royal Prince Alfred Hospital, Dermatology Cancer,

Sydney, Australia

4

Chris O'Brien Lifehouse, Medical Oncology, Camperdown

Sydney, Australia

5

University of Sydney, School of Physics, Sydney,

Australia

Purpose or Objective

Her2 amplified cancers, comprising 15-20% of patients

presenting with breast cancer, are now routinely

prescribed Trastuzumab (Herceptin), a monoclonal

antibody targeting Her2 receptors, leading to a significant

improvement in outcomes in this previously high risk

breast cancer subtype. Such targeting agents are rapidly

being introduced into the clinic, based on trials showing a

survival advantage. Now combination therapies with drug

conjugates have emerged. The biological interactions of

combined targeting agents, when given concurrently with

radiation, are not well described. Our aim is to identify

whether there is a synergistic or antagonistic interaction

between targeting agents and ionising radiation for two

distinct Her2+ subtypes.

Material and Methods

Two molecular subtypes of HER2+ breast cancer cell lines

were used: HCC-1954, which is ER and PR hormone

negative and BT-474, a luminal B which is ER negative and

PR positive. Both cell lines were treated to Her2 targeting

agents (Trastuzumab and T-DM1) and radiation (6MV

photons, 0 to 4Gy), individually and in combination to

identify whether the response was synergistic, additive or

antagonistic. The alpha/beta ratio was experimentally

determined for each cell line. Synergy (

S

) is defined as the

fractional difference between the observed (

S

o

) and the

predicted survival for each treatment given alone (

S

1

x

S

2

):

The observed response was determined using two assays:

the clonogenic assay and the confluence assay.

Results

The alpha/beta ratio for HCC-1954 (ER-/PR-/Her2+) and

BT474 (Luminal B ER-/PR+/Her2+) are found to be 35 Gy

and 5 Gy respectively, highlighting a heterogeneous

treatment response. The survival of HCC-1954 was not

affected by Trastuzumab alone, but when combined with

radiation, a synergistic interaction was observed. BT-474