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S203

ESTRO 36 2017

_______________________________________________________________________________________________

MONDAY, 8 MAY 2017

Teaching Lecture: State of the art multimodality

treatment of rectal cancer

SP-0378 State of the art multimodality treatment of

rectal cancer

C. Rödel

1

1

Klinikum der Johann Wolfgang Goethe Univ Frankfurt

univ hospital, Academic Department of Radiation

Oncology, Frankfurt, Germany

The monolithic approach to apply the same schedule of

preoperative 5-fluorouracil (5-FU)- or capecitabine-based

chemoradiotherapy (CRT), or short-course preoperative

radiotherapy, to all patients with clinically staged TNM

stage II/III rectal cancer need to be questioned. Five

randomized trials have been completed to determine if

the addition of oxaliplatin to preoperative 5-

FU/capecitabine-based CRT offers an advantage

compared with single-agent CRT. In contrast to the

German CAO/ARO/AIO-04 trial, results from the ACCORD

12, STAR-01, PETACC-6 and NSAPB R-04 trials failed to

demonstrate a significant improvement of early or late

efficacy endpoints with the addition of oxaliplatin. Most

of the phase II trials incorporating cetuximab into CRT

reported disappointingly low rates of pCR; the

combination of CRT with VEGF inhibition showed

encouraging pCR rates but at the cost of increased surgical

complications. Novel clinical trials currently address (1)

the role of induction and consolidation chemotherapy

before or after CRT, (2) minimal or omitted surgery

following complete response to CRT, or (3) the omission of

radiotherapy for selected patients with response to

neoadjuvant chemotherapy. The notion of different

multimodal treatment concepts according to tumor stage,

location, mesorectal fascia margin status, molecular

profiles, tumor response, and patients’ preferences

becomes increasingly popularand will render the

multimodal treatment approach of rectal cancer more

risk-adapted.

Teaching Lecture: SBRT for spine and non-spine bone

metastases: what role in routine practice?

SP-0379 SBRT for spine and non-spine bone

metastases: what role in routine practice?

M. Dahele

1

1

VU University Medical Center, Amsterdam, The

Netherlands

Not all bone metastases, tumours and patients are equal -

the underlying theme of this session is a practical, more

personalized approach to the treatment of patients with

bone metastases.

Topics will include:

What is SBRT for bone metastases?

Do current clinical guidelines for the treatment of bone

metastases mention SBRT?

Why consider SBRT for bone metastases?

What data is there for spine and non-spine bone SBRT?

What are the options if there is no “high-level” data to

support using SBRT?

Is SBRT the only way to deliver high doses to bone

metastases?

What are some of the reasons for being cautious with SBRT

and high-dose radiotherapy for bone metastases?

What are some of the clinical challenges of bone SBRT?

What resources are needed to provide SBRT for bone

metastases?

Teaching Lecture: Challenges in proton radiotherapy

SP-0380 How to reduce range uncertainties

A. Knopf

1

1

Knopf Antje, Groningen, The Netherlands

Sources of range uncertainties

[1]

- Imaging (CT imaging and calibration / CT conversion)

- patient setup

- intra-fractional changes

- beam delivery (measurement uncertainty during

commissioning)

- dose calculation (biology, mean excitation energy,

range degradation)

Monitor range uncertainties

- PET [2]

- Prompt gamma [3]

Correct for range uncertainties

-Range probe + adaptation

Range probe can be done in different ways

-Shoot through [4]

-CBCT [5]

-Implanted detectors [6]

Reduce range uncertainties

-Dual

energy

CT [7]

-Proton radiography [8]

-MC dose calculations [1]

References:

[1] Paganetti H (2012) Range uncertainties in proton

therapy and the role of Monte Carlo simulations. Phys

Med Biol. 57(11):R99-117

https://www.ncbi.nlm.nih.gov/pubmed/22571913

[2] Paganetti H and Fakhri G El (2015) Monitoring proton

therapy with PET. Br J Radiol. 88(1051): 20150173

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC462854

1/

[3] Verburg J and Seco J (2014) Proton range verification

through prompt gamma-ray spectroscopy. PMB 59(23)

7089-7106

http://iopscience.iop.org/article/10.1088/0031-

9155/59/23/7089/meta

[4] Mumot at al. (2010) Proton range verification using a

range probe: definition of concept and initial analysis.

PMB 55(16):4771-82

https://www.ncbi.nlm.nih.gov/pubmed/20679697

[5]

Bentefour el H (2015) Using CBCT for pretreatment range

check in proton therapy: a phantom study for prostate

treatment by anterior-posterior beam. J Appl Clin Med

Phys. 16(6):5212

https://www.ncbi.nlm.nih.gov/pubmed/26699545

[6] Bentefour el H (2015) Validation of an in-vivo proton

beam range check method in an anthropomorphic pelvic

phantom using dose measurements. Med Phys.

42(4):1936-47

https://www.ncbi.nlm.nih.gov/pubmed/25832084

[7] Moehler C et al. (2016) Range prediction for tissue

mixtures based on dual-energy CT. PMB 61(11):N268-75.

https://www.ncbi.nlm.nih.gov/pubmed/27182757

[8] Farace P et al. (2016) Pencil beam proton radiography

using a multilayer ionization chamber. PMB 61(11):4078-

87

https://www.ncbi.nlm.nih.gov/pubmed/27164479

Review articles:

Kraan AC (2015) Range Verification Methods in Particle

Therapy: Underlying Physics and Monte Carlo Modeling.

Front Oncol. 5:150

https://www.ncbi.nlm.nih.gov/pubmed/26217586

Knopf AC and Lomax A (2013) In vivo proton range

verification: a review. PMB 58(15):R131-60

https://www.ncbi.nlm.nih.gov/pubmed/23863203