External dosimetry Dosimetry in new radiotherapeutic techniques



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External dosimetry Dosimetry in new radiotherapeutic techniques Albert Lisbona Medical Physics Department CLCC René Gauducheau 44805 Saint-Herblain France a-lisbona@nantes.fnclcc.fr

Objective : To describe external dosimetric methods used in new radiotherapeutic techniques.

Course objectives What are "new "radiotherapy techniques those using xray beams for : «Standard» - IMRT, helical tomotherapy, Linac based stereotactic radiotherapy (radiosurgery, ).

Radiotherapy objective Centre de Lutte Contre le Cancer To deliver the absorbed dose prescribed in the totality of the target volume at better than ± 5% while limiting to the maximum the irradiation of surrounding healthy tissues, organs Delivered dose =>Prescribed dose ±5%

External Radiotherapy Medical prescription : Dose variations from 5 to 10% to the target volume can lead to a significant change in the local tumor control and in the toxicity Random errors Human factor Systematic errors Network, TPS, beam calibration,...

Objective ( ) Imply : A precise knowledge of the physical and dosimetric properties of the beams used for radiotherapy (in house calibration, relative dose distributions, ). Perticular attention to pay during the different steps : Treatment preparation (anatomic patient data acquisition, choice of the radiotherapy technique, medical prescription ), Treatment delivery (patient positionning, in vivo dosimetry, controls).

Detectors

To know the detectors used in radiotherapy beams (limitations eg : detector size vs field size) To use in connection with radiotherapy technique.

Some air cavity ionisation chambers chambres used in radiotherapy beams Ionisation chambers 0,1cm 3 < Vair < 1cm 3 7 mm < internal diameter < 25 mm - low Z for thin wall thickness - wall material air or water equivalent RX or γ Co 60 E- HE Capuchon d équilibre électronique d épaisseur adaptée au Co 60 dans l air

Reference detector for radiotherapy = ionisation chamber calibrated in a Second Standard Dosimetry Lab Centre de Lutte Contre le Cancer application = «absolute dosimetry» and relative dosimetry Main advantages and characteristics of the ionisation chamber - well known geometric and physics properties - good response reproducibility - low response dependance with energy, dose, dose rate - calibration in a SSDL every 3 ans (France) "Absolute" Dosimétry : Reference dose rate measurement

Relative dosimetry : Check of symetry and homogeneity beam 1D, 2D ou 3D measurements

DIODES : PRINCIPLE Centre de Lutte Contre le Cancer irradiation electron-hole creation current absorbed dose

MOSFET : Metal Oxyde Semiconductor Field Effect Transistor Centre de Lutte Contre le Cancer Characteristics : Si small transistor (2 p zones inserted in n zone) isolant métallique Principle : A polarization voltage is applied during irradiation Th irradiation induces an increase of the transistor threshold voltage The measurement of the threshold voltage is a linear function of absorbed dose

RADIOTHERMOLUMINESCENCE DOSIMETRY PRINCIPE

Photographic film Films Kodak Dose sensitivity Conversion curve OD vs dose depending on film characteristics Dose rate sensitivity Film response is independant versus dose rate (for the dose rate range used for radiotherapy)

Radiochromic Film Characteristics New type of film for dosimetry in radiotherapy - one of the more used : Gafchromic film Gafchromic film composition - 9,0 % H - 60,6 % C -11,2 % Zn -19,2 % O > composition closed to human tissue, better tissue equivalent (Z between 6 et 6.5, closer than radiographic film) Non irradied Gafchromic film is incolore > blue coloration when irradiated

Principle Centre de Lutte Contre le Cancer Under irradiation radiochromic film polymerises due to a special included colourant Self-processsing : Definitive film coloration < 24 h after irradiation The polymer on the support absorbes the light so transmission light through the film can be measured with a flat scanner (or a bed scanner) Optical density measured for a narrow wavelength (choice of a light source adapted to the film in order to get the best sensitivity, response) OD vs dose linear relation can be established under calibration

IMRT

IMRT Today several technical solutions to deliver IMRT treatments : «Standard» IMRT (static mlc beams), Rotational IMRT (VMAT, IMAT), Helical radiotherapy (Tomotherapy).

3D CRT To increase target dose with sparing of healthy tissue. Use of adapted equipments : 3D dose calculation software (convolutionsuperposition algorithms), Linac, MLC, Real-time imaging devices. IMRT To increase target dose with sparing of healthy tissue by 3D CRT optimization. Same equipments + : Inverse planning software using doses-volumes constraints (knowledge data bases).

The linac

The multi leaves collimator (from 3 mm to 10 mm width size at isocenter)

Treatment Planning System A 3D software application using : A calculation software supporting convolution superposition algorithms, An inverse planning software planification for IMRT. SV PTV = Σ i=1 N [ IW i PTV ( Di PTV -GD PTV )2 ] SV OAR = Σ j=1 M [ IW j OAR ( D j OAR -GD OAR )2 ]

Example : Head & Neck and IMRT

Ballistic 4 MV X-ray 5 beams with following gantry angulations : 0, 72, 144, 216, 288

Example of doses-volumes Centre de Lutte Contre le Cancer constraints in H&N Target volumes objectives 70 Gy to the therapeutic volume at least 95 % of the dose delivered to 95 % of the target volume. 50 Gy to the prophylactic volumes (delineation as Amsterdam-Brusells medical consensus) at least 95 % of the dose delivered to 95 % of the target volumes. Organs At Risk (OAR) constraints Spinal cord : 100 % vol < 46 Gy Larynx : 50 % vol < 40 Gy Left and Right parotids : 50 % vol < 30 Gy

Patient setup

Centre de Lutte Contre le Cancer MLC Segmentation

Qualitative evaluation 3D CRT IMRT

Qualitative evaluation 3D CRT IMRT

Qualitative evaluation 3D CRT IMRT

Qualitative evaluation 3D CRT IMRT

Quantitative evaluation 3D CRT IMRT

IMRT Pre treatment verification

Objectives To validate the calculation by a measurement To "treat" one fraction of a phantom (anthropomorphic shape, plastic slabs) with the fluences defined and validated by the physician and the physicist for the patient treatment. In the phantom we can introduce different detectors : Ionization chambers, Radiographic, radiochromic films, 2D arrays detectors

Equipment pre-treatment verification Centre de Lutte Contre le Cancer Parallelepipedic Phantom (RW3) DSP 95 cm Each treatment beam in a simple, reproducible geometry 5 cm An ionisation chamber can be inserted and/or a radiographic film between 2 slabs of tissue equivalent material Beam per beam Verification

H&N rao IMRT Field A dosimetric film (photographic or radiochromic) is calibrated (OD vs dose) and directly compared to the calculated TPS dose distribution.

H&N rao IMRT Field

H&N ant IMRT Field

H&N ant IMRT Field Comparison of two dose matrices (calculated, measured).here the criterions are dose difference (3 %) and distance to agreement (3 mm). Values exceding 1 fail the criteria.

Patient specific QA - Equipment Centre de Lutte Contre le Cancer H&N phantom from PTW (RW3 water equivalent material) insertion of a small volume detection ionisation chamber insertion of a radiographic film between 2 slabs Global verification using the patient treatment ballistic validated

Contrôle qualité Plan de traitement Analyse qualitative Centre de Lutte Contre le Cancer Dose profiles comparison Calculated and measured isodoses

External audits or comparisons between delivered and calculated Centre de Lutte Contre le Cancer doses Results from studies of the accuracy of dose determinations of IMRT treatments. (GUIDELINES FOR THE VERIFICATION OF IMRT- ESTRO Booklet 9)

Linac based Stereotactic Radiosurgery Stereotactic Radiotherapy

Stereotactic RadioSurgery - SRS BrainLab frame

Stereotactic RadioTherapy - SRT intracranial fractionné Bivalb mask BrainLab with mouth support

Dedicated Linac - NOVALIS Centre de Lutte Contre le Cancer Novalis Technical Data Integrated M3 micro-mlc 10x10 cm² 26 pairs of tungsten leaves 60mm thickness 14 pairs 3mm width at isocenter (42x42mm²) 6 pairs 4.5mm width at isocenter 6 pairs 5.5mm width at isocenter Leaves Transmission < 4% Leaves speed : 1.5 cm/s

Radiosurgical circular cones Centre de Lutte Contre le Cancer Radiosurgical circular cones ranging from Ø 4 mm to 15 mm Patient frame (or mask) support with 5 degrees of freedom

Acoustic neuroma : 1 single fraction 14 Gy @ 80 % Centre de Lutte Contre le Cancer

Radiosurgery Trigeminal Neuralgia : 1 single fraction 80 Gy Centre de Lutte Contre le Cancer

Cerebral ArterioVenous Malformations Centre de Lutte Contre le Cancer AVM 22 Gy @ 80% - 1 fraction 6 DCA

Dedicated Linac - NOVALIS Centre de Lutte Contre le Cancer Caractéristiques techniques : Novalis Integrated BrainLab M3 micro-mlc 10x10 cm²

Dosimetry measurements Centre de Lutte Contre le Cancer Percentage Depth Dose (PDD) C McKerracher and D I Thwaites - Phys. Med. Biol. 44 (1999) 2143 2160 Ø 40 mm Ø 12.5 mm

Dosimetry measurements Centre de Lutte Contre le Cancer Off Axis Ratio - OAR C McKerracher and D I Thwaites - Phys. Med. Biol. 44 (1999) 2143 2160 Ø40 mm Ø12.5 mm

Off Axis Ratio - OAR Dosimetry measurements George X Ding - Phys. Med. Biol. 51 (2006) 2549 2566 6MV Various detectors Field size 6x6 mm²

Off Axis Ratio - OAR Dosimetry measurements Detector choice spatial resolution Diode - diamond for very narrow beams Pin Point ionisation chamber for other field sizes Alternative : photographic or radiochromic film Jaws settings (Primary collimation) influence minimlc and circular cones Jaws settings values too small (vs mlc or cone size) can lead to a large degradation of the small field size OAR

Dosimetry measurements Centre de Lutte Contre le Cancer Off Axis Ratio - OAR George X Ding - Phys. Med. Biol. 51 (2006) 2549 2566 6MV Field size 6x6 mm² Jaws settings leaves

Output Factor (Scatter Factor) As for PDD and OAR this measurement becomes more difficult to perform as field size decreases The delivered dose to the patient is directly proportionnal to the OF measured value. Drawbacks : Dosimetry measurements Size detector vs field size Lateral Electronic Equilibrium Problem Detectors Ionization chamber Pin Point type 0.015 cm³ Diamond detector Diode Radiographic or radiochromic film

Dosimetry measurements Centre de Lutte Contre le Cancer Output Factor George X Ding - Phys. Med. Biol. 51 (2006) 2549 2566 For a minimlc BrainLab m3

Output Factor (Scatter Factor) MiniMLC : SFD Diode vs PinPoint 0.015cm³ Dosimetry measurements Novalis 6MV Xray beam 1,30 1,20 1,10 Output Factor Diode/Pin Point Normalized to 100x100 1,00 0,90 0,80 0,70 0,60 Pin Point 0,015cm3 Diode SFD Ratio Diode/PP Dose difference = 25 % 0,50 0,40 0 10 20 30 40 50 60 70 80 90 100 MLC Field Size [mm] Most important differences below 12x12mm², for clinical situations this difference is reduced by field size shaped X-jaws and Y-jaws settings 2mm more than leaves settings An under response is reported for diode (2%) between 18x18 et 60x60 mm²

Dosimetry measurements Centre de Lutte Contre le Cancer Output Factor (Scatter Factor) Circular cones : measurement comparisons between differents detectors Novalis 6MV Xray beam Scatter Factors circular cones - CRG Diamant Nantes PinPoint Nantes Solberg Diode SFD Nantes Film EDR2 1 0,9 Dimensions 4 to 15 mm Dode relative 0,8 0,7 0,6 0,5 0,4 0 5 10 15 20 Jaws settings 50x50mm² Important differences below 10mm Diametre des collimateurs en mm

There is no international dosimetry code of practice (IAEA 2010?) for the narrow beams in radiotherapy (IMRT, radiosurgery, )

End to End checks

End to End checks Jaws settings X mm 16 22 28 37 Y mm 17 22 28 38 Mes/Cal 0,918 0,979 0,995 0,984

Conclusion Centre de Lutte Contre le Cancer Mesures dans les minifaisceaux sont délicates Instruments de mesures spécifiques adaptés aux mesures à réaliser investissements Moyens humains et temps machine Minutie Contraintes techniques liées aux mesures Connaître les limites : matériel, détecteurs

Conclusion Adequate staff, and sufficient training for all the members of the team involved in new techniques. Guidance, recommendation on quality assurance for new techniques (using new concepts based on risk analysis). Dosimetric audits for comparison and validation.

Gracias Thank you