7/30/2011 Summarize some basic strategies that you already know Jerry Soen Talk through these strategies and how they were applied in two real life projects MS, Senior Medical Physicist, Advocate Christ Medical Ctr., Oak Lawn, Il. Mark Pankuch Director and Medical Physics and Dosimetry – CDH CDH--Proton Center, Warrenville, Il. Acceptance and commissioning TPS Implementation of 44-D CT into the proton environment The field of Radiation Oncology is rapidly advancing New technologies Advances Ad / upgrade d tto currentt equipment i t Think back to your training and the basic skills you acquired and strengthened in school. Mentally M t ll switch it h gears from f the th fast f t pace off the th clinic li i to the thoughtful processes of research New process and uses for new and current equipment Much of the burden for planning and implementation falls on the Medical Physics Staff If you hire a consulting physicist, you still need to know the process, the results and the limitations of the system. What does this new system accomplish? “ When an we start using ____” Ability to perform new treatment techniques Rapid Arc, VMAT, IGRT I Improved d on older ld ttechniques h i Frameless SRS What are the expectations for use in your clinic 4-D CT Prospective, Retrospective, Gating 1 7/30/2011 Take the time to study the Background How was it created? Understand the basic physics involved Background and White Papers produced by manufacturer Who created it? Vendor, Universityy Group p Journal articles referenced by manufacturer Why was it necessary? Where we not so good in the past (IGRT) How will this help my clinic? What do your Doctors, Administration, Therapists expect Get to know your colleges that have approached the paradigm before Read manual, actively participate in training Learn what you new system can and cannot do. Understand limitations. Gather data obtained by others Don’t reinvent the wheel Through journal articles they’ve written Through the Manufacturer University Physicists that have already developed it Look at other’s work and appreciate trends in data Identify outliers of data and explain them AAPM Chapter physicists Obtain the appropriate equipment Special phantoms or chambers to gather information QA equipment necessary for ongoing quality assurance of the particular paradigm. Include all that you need in the purchase of the new paradigm. DON’T CHEAT YOURSELF. Play the safety card if necessary. Show your administrator swollen, twisted pain ridden bodies if necessary – GET WHAT YOU NEED. 2 7/30/2011 Outline a plan of attack Work from a simple model that is intuitive but can be easily verified to a high degree of accuracy.. accuracy Make you model more complex and test Stress the paradigm – Find out what are its limitations, NOTHING IS PERFECT, There is no such thing as 100% right. Understand the error bars. Plan for enough time Do not work alone Attend meetings Use vendor contacts Local AAPM Chapters Initiate outside contacts Go home and sleep at night. Equipment fails Unexpected results Remain flexible There will never be enough time Lets discuss this theory in practical clinical examples Commissioning of the CMS Monaco Treatment planning System Accelerator and Treatment planning Commissioning Implementation of 44-D CT into the proton therapy environment Jerry Soen, MS, DABR, FACR Senior Medical Physicist Advocate Christ Hospital, Oak Lawn, Il. 3 7/30/2011 What were the Goals to be accomplished Our goal here Not to explain the whole process but to 3. Help you to not see these caveats as brick walls but opportunities to learn and to either bust through, leap, or walk around them Breakdown of tasks Data acquisition phase 1. Photon data for each accelerator – both algorithms • 2. Electron data for each accelerator – Pencil beam Acceptance of New Elekta Accelerator Data input to Xio TPS and commissioning both photon and electron algorithms Send data to CMS for Monaco commissioning Calibrate new accelerator Verify accuracy of Xio data for TPS • • • • Things I needed to know • • • • • • • • • • Acceptance p and Commissioning g of new Elekta Infinity y accelerator • Commissioning of CMS Xio for Convolution / Superposition algorithms • Verification with CMS of complete and proper acquisition of Monte Carlo data for CMS / Monaco 2. Talk about caveats that may appear along the way • • Data acquisition for Varian 2121-ex and Elekta Infinity accelerators for both CMS Xio and Monaco TPS 1. Help you think through the whole process • • What will be the end results of my work New techniques New ways of doing established techniques New algorithms What helps me get there from here Equipment that I need Software products that I need to use What is my time frame for accomplishment What is the quality that I need to achieve Some Caveats going in All scanning had to be performed with the facilities’ PTW scanner All scan and nonnon-scan data had to conform to CMS guidelines for each algorithm All Monaco scan data had to be sent to CMS for verification prior to acceptance for commissioning by CMS What will be the end results of the Work • VMAT utilizing MONACO (Monte Carlo) Algorithm • Moving from Clarkson to Conv/Super Conv/Super for 3D planning • Fit of Conv/Super Conv/Super for CMS Xio IMRT planning for Varian Varian--21ex and Elekta Infinity • New Accelerator – Elekta Infinity 4 7/30/2011 What should I know How can I know • Do some research • As much as possible about the history and the background of these algorithms and accelerators • Understand the strengths and weaknesses of the algorithms • How do these algorithms deal with heterogeneities, curved surfaces, various densities, target volume sizes, etc. • • • • • Websites – Elekta.com, Varian.com Technical Reports and ‘White Papers” from the company – they explain the history and reasoning behind their choice of algorithm Talk to physicists that are very familiar with the productproduct- NEVER ACT ALONE Research papers that discuss the implementation of these products Web--ex training sessions Web Why do I need to know What else do I need to know • YOU ARE THE PHYSICIST! • You have to be able to troubleshoot problems • Good quality assurance necessitates and understanding of all components • The weaknesses of the systems will eventually show themselves, you need to be able to explain them • The data I need to take for each algorithm and the format of the data • How the data is to be taken on the phantom • How H it may h have tto b be reformatted f tt d for f exportt to t either the TPS or the TPS company • Read, study, memorize and other wise thoroughly digest TGTG-106 • Accelerator beam data commissioning equipment and procedures, Indra J Das, et al, Med Phys 35(9), 9/2008 Beam Data Collection Sheets Beam Data Collection Sheets •They tell you: • • • • • What data to collect The extent of data to be collected Format Chamber sizes to use Non-scan data 5 7/30/2011 What else do I need to know • • • • • Your scanning phantom and your dosimetry equipment You should be well schooled in the phantom you will use – Take time to practice how to take data Know what you can change and how to setup the phantom Know the manual – Most manuals are hard to understand often because they are translated Establish a preflight check of your equipment Know what is ‘good’ data and ‘bad’ data Non--scan Data Non Think while you scan • Put all nonnon-scan data into spreadsheets • Plot and fit nonnon-scan data where possible while taking it • Output factors – Sp, Sp Sc Sc, OF OF, etc. etc • Use spreadsheets to accurately calculate output and wedge factors and virtual source distances, etc. • Take this data when you are fresh • Compare it against other published data for comparison • • • • Recheck your setup constantly Does this data make sense? Follow a checklist After each set of scans review what you have to make sure you have it all • Make electronic copies of all that you do and put them somewhere else • Don’t keep your scanning chamber in water longer than 8 hours Real time analysis avoids mistakes Real time analysis avoids mistakes 23IX 6X Photons Output Factors Measured @ dmax OF 6X OF measured @ dMax Field Field Size nC Size OF 2 3.29 2 0.873 3 3.41 3 0.905 4 3.48 4 0.923 5 3.55 5 0.942 6 3.61 6 0.958 7 3.65 7 0.968 8 3.69 8 0.979 10 3.77 10 1.000 12 3.38 12 0.897 15 3.89 15 1.032 20 3.97 20 1.053 25 4.03 25 1.069 30 4.09 30 1.085 35 4.13 35 1.095 40 4.16 40 1.103 1.200 1.200 1.000 1.000 0.800 0.800 0.600 OF Output Factors • ‘Good’ Data vs ‘Bad’ Data Series1 Poly. (Series1) 0.600 y = -0.00000042x4 + 0.00004303x3 - 0.00162797x2 + 0.03009878x + 0.82423954 0.400 0.400 0.200 0.200 0.000 -5 0.000 0 10 20 30 40 0 5 10 15 20 25 Field Size (sq cm) 30 35 40 45 50 6 7/30/2011 Once scanning is complete • Data sent back to TPS company Prepare it for either return to the company or consultant or local beam fitting Local beam fitting can be difficult. • Some p portions are intuitive • Others are nonnon-intuitive and do not seem to make sense – Don’t be afraid “If man can make it and break it, you can fix it” • Don’t stall out – start asking questions • Utilize tools that are given to you, try different things to see the effects, learn the limits • Keep pressing buttons • • Two sets of data were reviewed by two different physicists • 1. One showed comparative data from other facilities and requested a retake of some data 2. The other did not understand the process well and as a result there were major portions that had to be reacquired in formats different from what was specified • Local Commissioning Local Commissioning • Remember • Utilize helps given to you by the company • • Elekta-CMS provides commissioning Elektaguides on their website website.. It provides • • • • Accelerator specific information Steps of action Documentation Warnings (Do not avoid these) Help desk • • • • Varian provides • • •Photons – Preconfigured beam data, technical guides •Electron (PB) & (MC) have technical guides and ‘cookbooks’ •Excellent help desk • Verification • • • • • • Start from the intuitive and simple Have the right equipment – today’s new paradigms require the latest quality assurance equipment q p Administrators are now attuned to safety concerns Learn to trust your equipment Establish a plan of verification before you start Do not try to be exhaustive – TPS are no longer table lookup they are calculation engines Not everything will fit perfectly – there are reasonable limits Tighten your fits where most of your plans will be used – 4x4 to treatment p 20x20 IMRT planning – 1x1 to 10x10 Wedges – 5x5 to 15x15 Find someone who can review what you are doing Your verification will find any errors that need to be corrected Verification Read, memorize and otherwise digest the following Task Groups and subcommittees – 53,114, 142, and IMRT Subcommittee Quality Assurance for clinical radiotherapy treatment planning –TG 53, B. Frass,, et.al, Med Phys 25, 10/1998 Frass Verification of monitor unit calculations for nonnon-IMRT clinical radiotherapy –Report of AAPM Task Group 114, Robin Stern, et.al. Med Phys 38, 01/2011 Quality assurance of medical accelerators – TG 142, E. Klein, et.al. Med Phys, 10/2009 Guidance document on delivery, treatment planning, and clinical implementation of IMRT: Report of the IMRT subcommittee, G. Ezzell Ezzell,, et.al, Med Phys, 30, 08/2003 7 7/30/2011 This is not intuitive Simple Verification tools Eclipse Monitor Units to deliver 100 cGy Field Size Depth 1.5 5 10 5 105 115 143 10 99 107 128 15 96 103 120 20 94 100 116 15 178 155 144 136 20 224 193 174 163 5 10 15 20 Monitor Unit difference Eclipse vs RadCalc 5 10 15 20 5 10 15 20 1.5 -2 -1 -1 -2 5 -2 -1 -1 -1 10 0 1 0 1 Enhanced Dynamic Wedge Check 23IX Depth of 5 cm 10x10 6 MV @dmax wedge Mu to Del. 100cgy Open 10 x 10 Degree Reading 1.75 10 1.53 114 1.75 15 1.49 117 1.75 20 1.45 121 1.75 25 1.41 124 30 1.36 129 45 1 23 1.23 142 60 1.04 168 20x20 wedge Degree Reading 10 1.5 15 1.4 20 1.32 25 1.24 30 1.16 45 0.94 60 0.71 Mu to Del. 100cgy 117 125 133 141 151 186 246 Oct-08 Eclipse AAA-MU 113 116 119 122 126 139 163 Average error -1.21 -1.23 -1.40 -1.70 -2.08 -2.30 2 30 -3.13 -1.87 Eclipse AAA-MU 115 122 130 138 147 181 240 Average Error -1.43 -2.40 -1.94 -2.22 -2.56 -2.78 -2.63 -2.28 IMRT or Complex Paradigm Verification 20 4 5 2 2 Potential % Differences in Dose Delievered RadCalc vs Measured 1.5 5 10 15 20 0.94 0.86 0.00 -0.56 -1.79 0.00 0.93 -0.78 -1.28 -1.57 0.00 0.97 0.00 0.00 -0.58 1.05 0.00 -0.86 0.00 -1.23 Oveall average error -0.1943 Simple Verification tools 15 1 1 1 1 5 10 15 20 5 10 15 20 5 10 15 20 RadCalc Calculated Monitor Units Normalized to 10 cm 1.5 5 10 15 107 117 143 177 100 108 127 154 97 104 120 143 96 101 115 135 20 220 188 172 161 Measured vs. Eclipse calculated MU Open Fields 1.5 5 10 15 20 3.57 3.25 2.64 2.12 1.69 3.78 3.52 2.96 2.43 1.98 3.91 3.66 3.15 2.64 2.18 3.99 3.76 3.27 2.79 2.32 1.5 5 10 15 20 106 116 143 178 224 100 107 128 156 191 97 103 120 143 173 95 101 116 135 163 1.5 5 10 15 20 0.95 0.87 0.00 0.00 0.00 1.01 0.00 0.00 0.65 -1.04 1.04 0.00 0.00 -0.69 -0.57 1.06 1.00 0.00 -0.74 0.00 OAE 0.18 -0.03 Simple Verification tools 6 MV % Diff. Measured vs CMS Calculated Upper 15deg 30deg 45deg 60deg 23IX 5*5 0.50 1.14 0.69 0.85 10*10 0.56 0.43 0.39 0.00 15*15 0.60 0.93 0.00 0.34 20*20 0.63 0.98 0.43 30*30 0.00 -1.61 OAE 0.40 20 MV % Diff. Measured vs CMS Calculated Upper 15deg 30deg 45deg 60deg 5*5 -1.97 0.00 -0.86 -0.35 10*10 0.00 0.00 0.00 0.00 15*15 0.74 0.61 0.00 0.00 20*20 0.00 0.00 -0.51 30*30 -0.80 -0.67 OAE -0.22 IMRT or Complex Paradigm Verification •Start with a simple plan •Utilize your simple Solid Water QA phantom as your patient •Move to an anthropomorphic phantom if available •Transfer plans to electronic quality assurance devices and perform quality assurance •These quality assurance measurements should have very good results •If simple plans do not have good verification results, begin to check the items which can most influence the plan first •Dosimetric leaf gap •Radiation output specification •MLC transmission •If all else fails, begin to ask questions •Step back for a period of time •Remember it is intended to work correctly •If they do, move to more complicated plans 8 7/30/2011 In Conclusion •Take time to discover what you need to know •Try to have someone work with you •Utilize spreadsheets and graphs to help you look at data published data to compare p •Utilize other p •Have someone who has done this before help to review your data •Do not try and force error bars to something unachievable •Document, Document, Document Implementation of 4 4--D CT into the proton therapy environment Why 44-D CT for Protons? In Proton Therapy, there is a sharp fall off at the distal edge of the treatment field g is moving, g, the equivalent q If the target path--length of the protons can vary path Incorrect calculations of the path path--length can lead to extreme under dosing of targets or extreme overdosing of critical structures. What are we trying to achieve with 4 4--D CT? Target have the potential to move as a result of the respiratory cycle Current imaging methods were obtained on static target or a blurred moving target Blurring of a moving target would not yield correct depth measurements Gather Information Task Group 76 : The management of respiratory motion in radiation oncology Med. Phys. 33 (10), 2006. Knopf et al. Workshop on 4D4D-treatment planning in actively scanned therapy therapy. Med Med. Phys Phys. 37 (9) (9), 2010 2010. Europe Y Kang et al. 4D Proton Tretment Planning Strategy For Mobile Lung Tumors. Int. J Rad Onc Biol Phys 67 (3) 2007 - MD Anderson 9 7/30/2011 Talk to those with experience “Active 44-D Lung Treatment Gating and Tumor Tracking” Anil Sethi Sethi,, Iris Rusu – Loyola University University, Chicago Chicago, IL Thoracic Workshop Program ProCure Proton Therapy Center, Oklahmoma City; August 20 - 21, 2010 Date: August 20 – Friday 16:00 ‐ 17:00 pm: 17:00 – 17:15 pm: 17:15 – 17:45 pm: 17:45 – 18:30 pm: 18:30 – 19:15 pm: 19:15 – 19:45 am: 19:45 – 20:45 pm: 20:45 – 21:00 pm: 21:00 – 21:15 pm: 21:15 pm ProCure Thoracic Workshop, OKC, Ok. What are the limitations of the systems? Reconstruction Pattern Prospective Retrospective Breath Hold, Hold Gating What limits capability? CT scanner Treatment delivery system Active scattered vs. passive Understand the process Vendor Training Arrival + Tour of ProCure Center + ICIO Sameer Keole + Niek Schreuder The OKC facility The OKC patient population and the need to treat lung tumors Sameer Keole + Kiran Prabhu Avril The MDA way of treating lung cancers – Case mix and protocols Richard Amos + Joe Chang Dinner Break Larry Kestin Lung treatments in a general perspective What’s done in photon world and the role of protons in lung treatments The technical challenges of treating lung tumors with protons Using Passive scattering – 4D CT + Margins etc Richard Amos Using Uniform Scanning Omar Zeidan + Anthony Mascia Some clinical cases from the first Chicago CDH treatments Mark Pankuch The initial results on Ridge filter based US for lung treatments Niek Schreuder Using respiration management Jerry Jesseph Short summary + Wrap‐up for the day Niek + Sameer Date: August 21 – Saturday morning 8:30 – 9:15 am: The UFPTI way of treating lung cancers – Case mix and protocols 9:15 – 10:15 am: What shall ProCure treat in OKC: general discussions 1. The Short term focus 2. The long term focus 10:15 – 10:30 am: Break 10:30 – 11:30 am: What lung protocols shall PCG open or Join 11:30 – 12:30 am: Next steps and action items Zuofeng Li + Brad Hoppe Sameer + Niek + others Larry Kestin + Sameer Niek Get the equipment you need CT Phantoms Acrylic Head Phantom Home made 4 4--D Phantom Number, Location and Space for 44-D Work Stations System to review proton doses in different phases of the cycle \ Auto contouring tool Address any Regulatory Considerations Additional Shielding needed in CT room due to higher usage factors Calibration Phantom / 44-D Home Phantom Patient Dose measurements D Documentation t ti off MSAD ffor St State t regulations Experiment with techniques/parameters to better understand the system Evaluation of larger CT dose from Radiation Safety / ALARA 10 7/30/2011 Work--out Work Work Work--Flow Organize the implementation 4-D would be used for Lung patients Contour using MIP and Mean Due to clinical limitations at the start, lung treatment would be considered lower priority Develop a method to produce dose calculations on all ten phases Contouring Tools Goal was to Begin Simple First cases were not Lung Colleges from ProCure Thoratic symposium i h d shared had h d th their i concerns with ith prone treatments of spine target Had unexpected needs for 44-D Imaging Simple 4 4--D Opportunity Prone Spine Prone CSI Adapt as you learn more 4-D Scan would give us information on the magnitude of movement of spine MIP vs Ave Test movie loops to verify dose Have a physicist and dosimetrist present att the th time ti off simulation i l ti Imaging dose would be higher than without 44 -D Physicians agreed risk worth the benefit After contouring on MIP, preferred to review contours on movie loop before planning Excellent Candidates 11 7/30/2011 Work--Flow Modifications Work Where are we now? All Prone spine fields use 44 -D Lung cases have begun Limited to <1.0cm of motion Abdominal cases being reviewed Dose optimization and adaptive planning In Conclusion In Conclusion Your Centers will ask you to implement new technology. Reiterated what your advisors taught you on proper scientific technique It will be your responsibility to ensure it is done correctly and is determined safe for the patients Medical Physics is a community with a unified goal to provide better, safer care. Embody the “team” approach, even if you are alone. 12