ACCELERATORS AND MEDICAL PHYSICS 4 - physique.cuso.ch · EPFL 4- 4.11.10 - U. Amaldi 1 ACCELERATORS...

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EPFL 4- 4.11.10 - U. Amaldi 1 ACCELERATORS AND MEDICAL PHYSICS 4 Ugo Amaldi University of Milano Bicocca and TERA Foundation

Transcript of ACCELERATORS AND MEDICAL PHYSICS 4 - physique.cuso.ch · EPFL 4- 4.11.10 - U. Amaldi 1 ACCELERATORS...

Page 1: ACCELERATORS AND MEDICAL PHYSICS 4 - physique.cuso.ch · EPFL 4- 4.11.10 - U. Amaldi 1 ACCELERATORS AND MEDICAL PHYSICS 4 Ugo Amaldi University of Milano Bicocca and TERA Foundation.

EPFL 4- 4.11.10 - U. Amaldi 1

ACCELERATORS AND MEDICAL PHYSICS

4

Ugo Amaldi

University of Milano Bicocca and TERA Foundation

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The distribution of the dose in hadrontherapy

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The narrow peak has to

be enlarged longitudinally

3

Spread Out Bragg Peak

SOBP

General laws:

R = Ro (E/Eo)1.82

ΔR/R = 1.8 ΔE/ E

For Δd<1.5 mm at d=150 mm

ΔE/ E < 0.5%

tail

cobalt 60

linac

light ion

(carbon)

proton

Longitudinally and transversally

the carbon peak is 3 times

narrower than the proton peak.

The widths are prop. to 1/√M

3

Distal

fall-off

Δd/d=1%

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Carbon ions have less multiple scattering than

protons : higher lateral precision

carbon beam

proton beam

Depth in tissue

12 cm

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Protons and ions spare healthy tissues

charged hadron beam

that loses energy in matter

27 cm

tumour

target200 MeV - 1 nA

protons

4800 MeV – 0.1 nAcarbon ions

VERY LOW

CURRENTS !

Photons ProtonsPhotons ProtonsX raysprotons or

carbon ions

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Two methods for imparting the dose:

“passive” system

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Respiratory gating with a synchrotron

Cyclotrons are better because the beam is always present

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1A. Standard procedure: Passive beam spreading

with respiratory gating

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Collimator

Double scatterer

Bolus: has to be

machined for each case.

PSI

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1A. Standard procedure: Passive beam spreading

with respiratory gating

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Collimator

Double scatterer

Bolus: has to be

machined for each case.

PSI

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1B. Advanced procedure: layer stacking

with respiratory gating

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2A. Active “spot scanning” technique by PSI

(Villigen)

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1

2

3

1

2

3

‘spot’ position

During the displacement

the cyclotron beam is

switched off for 5 ms

Distance between the centers

is 75% of the FWHM

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Gantry 2

Gantry 1

ACCEL

SC cyclotron

250 MeV protons

ExperimentOPTIS

PROSCAN

TERA

2A. Active “spot scanning” technique by PSI

with respiratory gating (Villigen)

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PROSCAN at PSI (Villigen):

with Gantry 1 and Gantry 2

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2A. Active “spot scanning” technique by PSI

with respiratory gating (Villigen)

PROTONS

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Next: Spot scanning compensated by correcting the

spot position and multipainting

PROTONS

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Feedback from a

device which detects

the position of the

tumour

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2B. Active “raster scanning” technique by GSI

with respiratory gating (Darmstadt)

Distance between the centers of the

mini-voxels is 30% of the FWHM.

The beam is always on.

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The GSI pilot project : 1997-2008

Gerhard Kraft

J. Debus

450 patients treated

with carbon ions

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GSI: procedure to cover uniformly a spherical target

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More dose at the periphery

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Conformity of the irradiation with protons and ions

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IMPT = Intensity Modulated Particle Therapy with protons

4 NON-UNIFORM FIELDS

PSI

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To be compared with IMRT with photons

9 NON-UNIFORM FIELDS

PSI

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Protons are quantitatively different from X-rays

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Carbon ions are qualitatively different from X-rays

Carbon ions deposit in a cell 22 times more energy than a proton

producing not reparable multiple close-by double strand breaks

Carbon ions can control radio-resistant tumours

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Biological effects of protons and carbon ions

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Electrons put in motion by X rays: “sparsely ionizing”

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d=200 nm

X beam

30 cm

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d=200 nm

30 cm

Beam of 200 MeV proton

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d=50 nm

d= 15 nm

d=90 nm

Protons1: more favorable dose- 2. same „indirect effects‟

X ray beam

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d=200 nm

30 cm

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d=50 nm

d= 15 nm

d=90 nm

Protons1: more favorable dose- 2. same „indirect effects‟

Also protons are „sparsely ionizing

Beam of 200 MeV proton

X ray beam

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Microscopic distribution of the X ray dose

7

μm

e- range = 15

mm

X ray = 3 MeV γ

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150 ionizations/cell

Microscopic distribution of the X ray dose

7

μm

e- range = 15

mm

X ray = 4 MeV γ

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X ray = 4 MeV γ

150 ionizations/cell

Microscopic distribution of the X ray dose

7

μm

e- range = 15

mm

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Microscopic distribution of the proton dose

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Microscopic distribution of the proton dose

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Microscopic distribution of the proton dose

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Microscopic distribution of the proton dose

Protons are “sparsely ionizing”

as photons/electrons

SAME CLINICAL EFFECTS BUT

MUCH BETTER “CONFORMITY”

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30 cm

d= 4 nm

d= 2 nm

4 cm

Carbon ions: 1. more favorable dose- 2. „direct effects”

d= 0.3 nm

d=200 nm

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Beam of 200 MeV protons

X ray beam

Beam of 4800 MeV carbon ions

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30 cm

d= 4 nm

d= 2 nm

4 cm

Ioni carbonio: 1. dose più favorevole - 2. effetti „diretti‟ sulle

cellule tumorali

d= 0.3 nm

d=200 nm

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Carbon ins are „densely ionizing

Beam of 200 MeV protons

X ray beam

Beam of 4800 MeV carbon ions

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Effect of ΔE/Δx = LET

Mauro Belli et al

ISS

Sparsely ionizing radiation

with respect to the dimensions

of the double helix (2 nm)

Densely ionizing radiation

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Two qualitatively different microscopic dose distributions

densely ionizing radiation sparsely ionizing radiation

Visualization

of repair

proteins

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Definition of Radio-Biological Effectiveness

RBE is defined with respect

to standard X rays:

RBE = = = 5

For a given effect on a given cell

the RBE value is a function of LET

Dγ 5

D 1

C+6

no repair

X rayswith repair

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Response of different cells to high-LET radiations

Survival of V79 aerated and anoxic cells versus LET of carbon-12 ions

with oxygen without oxygen

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Response of different cells to high-LET radiations

Survival of V79 aerated and anoxic cells versus LET of carbon-12 ions

with oxygen without oxygen

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Effect of LET on RBEs of many cells for many „end-points‟„

LET > 20 keV/μm and RBE > 1.5 in the last 40 mm

so that carbon can control radioresistant tumours

i.e. tumours which need 2-3 times larger doses to be controlled with either X rays or protons

4800 MeV stop

RB

E

200 MeV stopp

C

LET (keV/μm)1 MeV/cm

X rays

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The “effective dose” in Gye is defined as Gy x RBE „

At GSI the values of RBE are computed with X-ray cell survival data

by using the Local Effect Model (LEM) by G. Kraft el al.

To obtain a „flat‟ dose in Gye the “physical dose” is not „flat‟

GSI

Spread Out Bragg Peak

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The GSI Local Effect Model (LEM)

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Survival =

Different for

tumour and

healthy tissues

RBE computed from Survivals

M. Scholz, GSI

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Elective indications of carbon ions

calculated with LEM

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NO

YES

YES

YES

M. Scholz, GSI

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Elective indications of carbon ions

calculated with LEM

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NO

YES

YES

YES

M. Scholz, GSI About 80% of all solid tumours

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Numbers of potential patients (*)

X-ray therapy

every 10 million inhabitants: 20'000 pts/year

Protontherapy

12% of X-ray patients 2'400 pts/year

Therapy with Carbon ions for radio-resistant tumour

3% of X-ray patients 600 pts/year

TOTAL every 10 M about 3'000 pts/year

______

(*) Combining studies made in Austria, Germany, France and Italy in the framework

of ENLIGHT - Coordinator: Manjit Dosanjh –

Projects in FP7: ULICE, PARTNER, ENVISION , ENTERVISION for a total of 22 MEuro

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52 -83 %31 – 75 %5 year

survival

Soft-tissue

carcinoma

77 %61 %24-28 %local control

rate

Salivary gland

tumours

100 %23 %5 year

survival

Liver tumours

7.8 months6.5 monthsav. survival

time

Pancreatic

carcinoma

63 %21 %local control

rate

Paranasal sinuses

tumours

96 % (*)95 %local control

rate

Choroid

melanoma

16 months12 monthsav. survival

time

Glioblastoma

63 %40 -50 %5 year

survival

Nasopharynx

carcinoma

89 %88 %33 %local control

rate

Chondrosarcoma

70 %65 %30 – 50 %local control

rate

Chordoma

Results carbon

GSI

Results carbon

HIMAC-NIRSResults photonsEnd pointIndication

Table by G. Kraft

2007

Results of

carbon ions

Similar to protons

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THE END

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