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Introducing Proton Beam Therapy
into the NHS
Richard A. Amos, MSc, CPhys, CSci, FIPEM
Operational Lead for Proton Beam Therapy Physics
Dept. of Radiotherapy Physics, UCLH
Honorary Senior Lecturer
Dept. of Medical Physics & Biomedical Engineering, UCL
#HCS15 Healthcare Science: Making it Happen
The Grand Connaught Rooms, London
March 17th, 2015
Brief history of proton radiotherapy
1946: Therapeutic use of proton beams first proposed by Robert Wilson1
1. Wilson RR. Radiological use of fast protons. Radiology. 1946;47:487-491
1954: First patient treated at the UC Lawrence Berkeley Laboratory (LBL)
– Treated the pituitary gland with beams passing entirely through the brain.
1957: Proton radiosurgical techniques for brain tumors developed at the Gustaf-Werner
Institute, Uppsala, Sweden
– First to use range modulation
1961: Radiosurgery of small intercranial targets at the Harvard Cyclotron Laboratory
70’s – 80’s: Physics facilities worldwide – notably, the Paul Scherrer Institute (PSI) in Switzerland
1989: The world’s first hospital-based low-energy ocular proton beam therapy facility opened at
Clatterbridge Cencer Centre, UK
1990: The world’s first hospital-based high-energy proton beam therapy facility opened at
Loma Linda University Medical Center, California
2000 -: Rapid growth in number of proton facilities internationally
Why Proton Beam Radiotherapy?
3
Personal experience in proton beam radiotherapy
2002 – 2005: 2005 – 2013:
•First hospital-based proton therapy facility in
the world.
•First patient treated in 1990
•17,829 patients treated by end of 2013*
•World-leading cancer treatment and
research center.
•Proton Therapy Center opened in 2006
•First in the USA to treat with PBS in 2008
•4,746 patients treated by end of 2013*
*http://www.ptcog.ch/
•250 MeV synchrotron developed in collaboration with Fermi National Accelerator Laboratory
•3 gantries (passive scattering)
•1 fixed clinical beamline (passive scattering)
•1 fixed ocular beamline (passive scattering)
•1 fixed experimental beamline (passive scattering)
•250 MeV synchrotron (Hitachi PROBEAT system)
•3 gantries (2 passive scattering + 1 pencil beam scanning)
•1 fixed clinical beamline (passive scattering)
•1 fixed ocular beamline (passive scattering)
•1 fixed experimental beamline (passive scattering)
Accelerator
Using magnetic fields, the hydrogen protons
are accelerated to two thirds the speed of
light.
Nozzle
A 21,000-pound magnet guides the beam to
the patient through a nozzle.
Electromagnets
The magnets focus the
proton beams toward
the gantry.
Gantry
The gantry can rotate 360° around the
patient to position the nozzle.
Beam delivery system: Passive scattered beam
Beam delivery system: Pencil beam scanning
• 94 Energies: 72.5 - 221.8 MeV
• Range: 4.0 – 30.6 cm
• Adjustability: 0.1 cm
• Max field size: 30x30 cm2
• Beam size: 5 - 14 mm (air)
• Energy absorber (range shifter)
Current Indications for NHS Patients
Travelling Abroad for PBT
• Adult
• Base of Skull & Spinal Chordoma
• Base of Skull Chondrosarcoma
• Spinal & Paraspinal Bone and Soft Tissue Sarcomas (Non
Ewing’s)
• Paediatric
• Base of Skull & Spinal Chordoma
• Base of Skull Chondrosarcoma
• Spinal & Paraspinal ‘adult type’ Bone and Soft Tissue
Sarcomas
• Rhabdomyosarcoma
• Orbit
• Parameningeal & Head & Neck
• Pelvis
• Ependymoma
• Ewing’s Sarcoma
• Retinoblastoma
• Pelvic Sarcoma
• Optic Pathway and other selected Low Grade Glioma
• Craniopharyngioma
• Pineal Parenchymal Tumours (not Pineoblastoma)
• Esthesioneuroblastoma
08/09 09/10 10/11 11/12 12/13 13/14
0
20
40
60
80
100
120
140
160
Paediatric Adult
Indication 2009
Framework
assumption
2012
Updated
assumption
Indication 2009 Framework
assumption
2012 Updated
assumption
Chordoma/ Chondrosacoma 15 Ocular/Orbital 2 25
Rhabdomyosarcoma (Orbit) 5 Chordoma 60 60
Rhabdomyosarcoma (Parameningeal and H&N) 15 Chondrosarcoma 30 30
Rhabdomyosarcoma( Pelvis) 10 Para- Spinal / Spinal Sarcoma 180 180
Osteosarcoma 3 Meningioma 100 100
Ewings 9 Acoustic Neuroma 100 100
PPNET 5 Craniospinal NOS (Pineal) 10 10
Ependymoma 25 Head & Neck & Paranasal Sinuses 300 300
Low Grade Glioma 5 PNET(medulloblastoma ) 30 30
Optic Pathway Glioma 12 Difficult cases 300 123
Craniopharyngioma 15 TYA 200
Medulloblastoma (PNET) 70
Hodgkins 5
Retinoblastoma 5
Meningioma 3
Intracranial germinoma 10
Nasopharynx (H&N) 15
Difficult Cases-Esthe/Neuro/Liver 5
Very Young Age 20
Total 252 330 Total 1,110 1157
What will UK Service look like?
• 2 sites selected
– The Christie (Manchester)
– UCLH (London)
• 2 Sites, 1 Service
– Integrated clinically within the hospital
setting
– Integrated with existing conventional
photon facilities
– Collaboration across all areas
• Referral
• Protocol Development
• Technology
• Research
– Due to open in 2018
• Geographical access
• Viable centre size
• Integrated radiotherapy department
– Some cases may require proton and conventional radiotherapy
• High quality and recognised complex case mix
– Paediatric practice
Why UCLH?
Brain/CNS
Breast
Endocrine
Gynae
Haematology
Operational Expectations
Facility opening times:
 24Hour/day
 Clinical time:
 5 days per week
 14 Hours per day
 Quality Assurance Checks
 Maintenance Requirements
PBT patient mix (2012)
FY'12 Proton NTS Through May
142, 22%
242, 36%
95, 30%
47, 7%
32, 5%
PED/CNS
22%
GU
36%
THORACIC
30%
HN
7%
Other
5%
FY’12
Annualized
PEDI/CNS 191
GU 311
THORACIC 261
HN 63
OTHER 32
TOTAL 857
Low-risk prostate cancer
Proton therapy IMRT
a. b.
a.
b.
c.
d.
Head & Neck
IMPT H&N - Example
• Simultaneous spot optimization
• Spot spacing = 1 cm
• Distal & prox. margins = 0 cm
• Lateral margin = 0.8 cm
Field 1 Field 2
Field 3
Field 1 Field 2
Post-irradiation photography!
proton 3D-CRT
(a) tangential beams, (b) en face beam
Howell R, Amos R, Kanke J, et al. Predicted risk of cardiac effects with modern
cardiac-sparing radiation therapy techniques.
Proceedings to PTCOG 53. International Journal of Particle Therapy: Fall 2014, Vol. 1, No. 2, pp 617 - 618
Proton Physics Research & Implementation Group
http://www.pprig.co.uk/pprig/
5,000 mile commute!
Thank you!

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Richard Amos (UCLH) - Introducing proton beam therapy into the NHS #HCS15

  • 1. Introducing Proton Beam Therapy into the NHS Richard A. Amos, MSc, CPhys, CSci, FIPEM Operational Lead for Proton Beam Therapy Physics Dept. of Radiotherapy Physics, UCLH Honorary Senior Lecturer Dept. of Medical Physics & Biomedical Engineering, UCL #HCS15 Healthcare Science: Making it Happen The Grand Connaught Rooms, London March 17th, 2015
  • 2. Brief history of proton radiotherapy 1946: Therapeutic use of proton beams first proposed by Robert Wilson1 1. Wilson RR. Radiological use of fast protons. Radiology. 1946;47:487-491 1954: First patient treated at the UC Lawrence Berkeley Laboratory (LBL) – Treated the pituitary gland with beams passing entirely through the brain. 1957: Proton radiosurgical techniques for brain tumors developed at the Gustaf-Werner Institute, Uppsala, Sweden – First to use range modulation 1961: Radiosurgery of small intercranial targets at the Harvard Cyclotron Laboratory 70’s – 80’s: Physics facilities worldwide – notably, the Paul Scherrer Institute (PSI) in Switzerland 1989: The world’s first hospital-based low-energy ocular proton beam therapy facility opened at Clatterbridge Cencer Centre, UK 1990: The world’s first hospital-based high-energy proton beam therapy facility opened at Loma Linda University Medical Center, California 2000 -: Rapid growth in number of proton facilities internationally
  • 3. Why Proton Beam Radiotherapy? 3
  • 4.
  • 5.
  • 6. Personal experience in proton beam radiotherapy 2002 – 2005: 2005 – 2013: •First hospital-based proton therapy facility in the world. •First patient treated in 1990 •17,829 patients treated by end of 2013* •World-leading cancer treatment and research center. •Proton Therapy Center opened in 2006 •First in the USA to treat with PBS in 2008 •4,746 patients treated by end of 2013* *http://www.ptcog.ch/
  • 7. •250 MeV synchrotron developed in collaboration with Fermi National Accelerator Laboratory •3 gantries (passive scattering) •1 fixed clinical beamline (passive scattering) •1 fixed ocular beamline (passive scattering) •1 fixed experimental beamline (passive scattering)
  • 8. •250 MeV synchrotron (Hitachi PROBEAT system) •3 gantries (2 passive scattering + 1 pencil beam scanning) •1 fixed clinical beamline (passive scattering) •1 fixed ocular beamline (passive scattering) •1 fixed experimental beamline (passive scattering)
  • 9.
  • 10. Accelerator Using magnetic fields, the hydrogen protons are accelerated to two thirds the speed of light. Nozzle A 21,000-pound magnet guides the beam to the patient through a nozzle. Electromagnets The magnets focus the proton beams toward the gantry. Gantry The gantry can rotate 360° around the patient to position the nozzle.
  • 11. Beam delivery system: Passive scattered beam
  • 12. Beam delivery system: Pencil beam scanning • 94 Energies: 72.5 - 221.8 MeV • Range: 4.0 – 30.6 cm • Adjustability: 0.1 cm • Max field size: 30x30 cm2 • Beam size: 5 - 14 mm (air) • Energy absorber (range shifter)
  • 13. Current Indications for NHS Patients Travelling Abroad for PBT • Adult • Base of Skull & Spinal Chordoma • Base of Skull Chondrosarcoma • Spinal & Paraspinal Bone and Soft Tissue Sarcomas (Non Ewing’s) • Paediatric • Base of Skull & Spinal Chordoma • Base of Skull Chondrosarcoma • Spinal & Paraspinal ‘adult type’ Bone and Soft Tissue Sarcomas • Rhabdomyosarcoma • Orbit • Parameningeal & Head & Neck • Pelvis • Ependymoma • Ewing’s Sarcoma • Retinoblastoma • Pelvic Sarcoma • Optic Pathway and other selected Low Grade Glioma • Craniopharyngioma • Pineal Parenchymal Tumours (not Pineoblastoma) • Esthesioneuroblastoma 08/09 09/10 10/11 11/12 12/13 13/14 0 20 40 60 80 100 120 140 160
  • 14. Paediatric Adult Indication 2009 Framework assumption 2012 Updated assumption Indication 2009 Framework assumption 2012 Updated assumption Chordoma/ Chondrosacoma 15 Ocular/Orbital 2 25 Rhabdomyosarcoma (Orbit) 5 Chordoma 60 60 Rhabdomyosarcoma (Parameningeal and H&N) 15 Chondrosarcoma 30 30 Rhabdomyosarcoma( Pelvis) 10 Para- Spinal / Spinal Sarcoma 180 180 Osteosarcoma 3 Meningioma 100 100 Ewings 9 Acoustic Neuroma 100 100 PPNET 5 Craniospinal NOS (Pineal) 10 10 Ependymoma 25 Head & Neck & Paranasal Sinuses 300 300 Low Grade Glioma 5 PNET(medulloblastoma ) 30 30 Optic Pathway Glioma 12 Difficult cases 300 123 Craniopharyngioma 15 TYA 200 Medulloblastoma (PNET) 70 Hodgkins 5 Retinoblastoma 5 Meningioma 3 Intracranial germinoma 10 Nasopharynx (H&N) 15 Difficult Cases-Esthe/Neuro/Liver 5 Very Young Age 20 Total 252 330 Total 1,110 1157
  • 15. What will UK Service look like? • 2 sites selected – The Christie (Manchester) – UCLH (London) • 2 Sites, 1 Service – Integrated clinically within the hospital setting – Integrated with existing conventional photon facilities – Collaboration across all areas • Referral • Protocol Development • Technology • Research – Due to open in 2018
  • 16. • Geographical access • Viable centre size • Integrated radiotherapy department – Some cases may require proton and conventional radiotherapy • High quality and recognised complex case mix – Paediatric practice Why UCLH? Brain/CNS Breast Endocrine Gynae Haematology
  • 17. Operational Expectations Facility opening times:  24Hour/day  Clinical time:  5 days per week  14 Hours per day  Quality Assurance Checks  Maintenance Requirements
  • 18.
  • 19.
  • 20. PBT patient mix (2012) FY'12 Proton NTS Through May 142, 22% 242, 36% 95, 30% 47, 7% 32, 5% PED/CNS 22% GU 36% THORACIC 30% HN 7% Other 5% FY’12 Annualized PEDI/CNS 191 GU 311 THORACIC 261 HN 63 OTHER 32 TOTAL 857
  • 24. IMPT H&N - Example • Simultaneous spot optimization • Spot spacing = 1 cm • Distal & prox. margins = 0 cm • Lateral margin = 0.8 cm Field 1 Field 2 Field 3 Field 1 Field 2
  • 26.
  • 27. proton 3D-CRT (a) tangential beams, (b) en face beam
  • 28.
  • 29.
  • 30.
  • 31. Howell R, Amos R, Kanke J, et al. Predicted risk of cardiac effects with modern cardiac-sparing radiation therapy techniques. Proceedings to PTCOG 53. International Journal of Particle Therapy: Fall 2014, Vol. 1, No. 2, pp 617 - 618
  • 32.
  • 33. Proton Physics Research & Implementation Group http://www.pprig.co.uk/pprig/

Editor's Notes

  1. 21