Radiotherapy Plan and Chart Review Guide
Radiotherapy Plan and Chart Review Guide
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1
14
15 Contents
16 I. Introduction ................................................................................................................................................ 3
17 1. Scope.................................................................................................................................................. 4
18 2. The charges of this MPPG .................................................................................................................. 5
19 II. Definition ................................................................................................................................................... 6
20 III. Expectations and Responsibilities............................................................................................................. 9
21 1. External Beam Radiation Therapy ..................................................................................................... 9
22 (a) Initial plan/chart check ...................................................................................................................12
23 (b) Weekly chart check ........................................................................................................................13
24 (c) Final chart check .............................................................................................................................14
25 2. Brachytherapy ......................................................................................................................................14
26 IV. Essential Content of a Treatment Plan Document .................................................................................15
27 1. External Beam Plan Document ........................................................................................................16
28 2. Brachytherapy Plan Document ........................................................................................................17
29 V: Recommended Checklist During Plan and Chart Review ........................................................................17
30 1. External Beam Plans and Charts ......................................................................................................17
31 a. Checklist for Planners ..................................................................................................................17
32 b. Initial Plan/Chart Checklist for Physicists....................................................................................18
33 c. Initial Plan/Chart Checklist for Therapists ...................................................................................20
34 d. Weekly Chart Review Checklist ...................................................................................................20
35 e. Final Chart Review Checklist ........................................................................................................20
36 2. Brachytherapy Plans/ Charts ...........................................................................................................21
37 a. Initial Plan/Chart Checklist for Physicists ...................................................................................21
38 b. Initial Plan/Chart Checklist for Therapists .................................................................................21
39 c. Weekly Chart Review Checklist ..................................................................................................22
40 f. Final Chart Review Checklist ......................................................................................................22
41 VI: Computer-aided Plan/Check and Automation .......................................................................................22
42 VII: Discussion ..............................................................................................................................................24
43 VIII: Summary ...............................................................................................................................................26
44 References: ..................................................................................................................................................28
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46 I. Introduction
47
48 Task group (TG) 40 report [1], published in 1994, established the foundation of comprehensive
49 quality assurance (QA) for radiation therapy. Most current medical physics practices in radiation
50 therapy stem from this report. With the advancement of radiation therapy in the past two
51 decades, several additional QA reports have been published [2-4], each addressing one specific
52 aspect of QA topics covered in TG 40. A recently published TG 275 [5] provided evidence-
53 based recommendations on physics plan and chart review for radiation therapy based on a survey
54 of AAPM members and failure mode and effect analyses (FMEA). In parallel with TG 275, the
55 purpose of this report is to provide specific checklist during plan/chart review for dosimetrists,
56 medical physicists, and therapists based on minimum practice standards. Since radiation therapy
57 is a coordinated team effort, this report also clarifies the responsibilities of each team member
58 (radiation oncologists, medical physicists, dosimetrists, and therapists). The differences between
59 this MPPG and TG 275 are elaborated the last section of this report.
60
61 A patient chart typically consists of many types of documents, including diagnostic reports,
62 consultation reports, simulation documents, treatment plan reports, daily treatment records, and
63 on-treatment visit reports. With the advent of electronic medical records (EMR), many clinical
64 reports reside in a general hospital EMR system, while other radiation-related technical reports
65 may reside in a radiation specific EMR system. One integrated EMR system is ideal; but
66 currently not feasible because hospital EMR systems are generally incapable of sending radiation
67 treatment plans to the treatment equipment and recording radiation treatment parameters
68 automatically, both of which are critical for radiation therapy. The purpose of having a patient
69 chart reviewed by different team members at multiple time points throughout the course of
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70 treatment (e.g. prior to treatment (initial), during treatment (weekly), and at the end-of-treatment
71 (final) is to ensure accurate and precise radiation treatment planning and delivery. To
72 accomplish these tasks, one of the most important documents of a radiation therapy-related
73 patient chart is the treatment plan report, along with other supporting documents for treatment
74 delivery.
75
76 Treatment plans for radiation oncology consist of two major components: a clinical element and
77 a technical element. The clinical component of a treatment plan includes the intent of radiation
78 treatment (definitive, adjuvant, or salvage), radiation dosage, fractionation scheme, and anatomic
79 contours that are delineated either to receive the prescribed treatment doses or to be protected
80 from a specific tolerance dose. The technical component of a treatment plan includes the details
81 of patient positioning along with the immobilization devices, placement of radiation beams, and
82 the aperture shapes of radiation beams (designed either manually or by computer optimization)
83 to achieve highly conformal radiation dose distributions to the treatment target volumes while
85 1. Scope
86
87 This MPPG report is focused on the technical component of a treatment plan, referred to as the
88 treatment plan in subsequent sections. The goal of this MPPG is to provide essential checklist
89 items for medical physicists who conduct plan/chart reviews according to the minimum
91
92 The purpose of a new (initial) plan/chart review is to ensure compliance with the prescription,
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93 no clinically significant deviations are present, and that all information necessary for the
94 therapists to deliver the treatment has been provided. Significant deviations in the plan/chart
95 include errors, inconsistencies, or ambiguities, which may cause confusion for the team and
96 potentially resulting in treatment errors. A recent publication [6] from the Radiation Oncology
97 Incident Learning System (RO-ILS) reported that 33% of reported events occur during the
99 hazards is best accomplished by catching errors as far upstream as possible and including
100 multiple layers of plan check/review. The possibility of an error propagating through to the
101 patient can further be minimized by using a standardized treatment plan document, a consistency
102 check from the planners, and a pretreatment check by radiation therapists.
103
104 The purpose of weekly on-treatment (weekly) chart review is to verify that the prescription is
105 being fulfilled. If for clinical reasons, the prescription is altered, medical physicists are
106 responsible for ensuring that the modified prescription is followed accordingly. At the end-of-
107 treatment (final) chart check, medical physicists are responsible for ensuring that all technical
108 documents for that patient are signed/approved and that the treatment course is completed. If for
109 clinical reasons or patients’ decisions, the treatment course is not completed, a radiation
110 oncologist should document the specific reason in the chart. This MPPG provides essential
111 checklists for medical physicists to utilize while carrying out the responsibilities of initial,
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115 (1) To define roles of a dosimetrist, therapists, a physicist in training, and a qualified
116 medical physicist as they pertain to the treatment plan/chart review process for external
118 (2) To define essential checklist items for initial, weekly and final plan/chart review.
119 (3) To make recommendations on the timing of the initial, weekly, and final
120 plan/chart review, especially for special procedures (e.g. TBI, stereotactic body
122
123 This MPPG considers typical treatment plans in radiotherapy, including the most frequently used
124 external beam radiotherapy (C-arm linear accelerators) using photons and electrons (excluding
125 proton plans) and the most frequently practiced brachytherapy procedures, such as high dose rate
126 (HDR) brachytherapy for gynecological treatments. It is not feasible for this MPPG to cover
127 every procedure or situation, and as such, the medical physicist should collaborate with other
128 members of the department to establish and document appropriate procedures for those falling
129 outside of this work. Working with radiation oncologists, medical physicists are responsible for
130 confirming a patient-specific high-quality plan is developed; however, the quality of a treatment
131 plan is ultimately the radiation oncologist’s responsibility. This MPPG does not expound on the
133
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136 The following terms will be used throughout this report. Their definitions are generally
137 understood by the radiation oncology community. For others who are not familiar with these
139 QMP: For the purpose of providing radiation oncology therapy clinical professional services, a
140 Qualified Medical Physicist is an individual who is competent to practice independently in the
141 subfield of therapeutic medical physics. The ACR strongly recommends that the individual be
142 board certified. Individual who is not board certified but is licensed by the state, or documented
143 by home institution as passing the institution's competency requirement are also considered as
144 QMP. This definition is more aligned with the ACR definition [7] to be more encompassing
146 AU: Authorized Users are radiation oncologists who are authorized to utilize a high dose rate
147 (HDR) brachytherapy unit and are required by the Nuclear Regulatory Commission (NRC) and
148 agreement states to be present at the treatment console during high dose rate (HDR)
150 AMP: Authorized Medical Physicists are individuals who are listed on the HDR license of
151 brachytherapy and are required by the NRC and the agreement States to be present at the
152 treatment console during brachytherapy treatments. For States that require a license to practice
154 Prescription: Following the guideline of American Society of Radiation Oncology (ASTRO) on
155 the prescription [9], a Radiation Oncologist should provide the following minimum information
156 in the written prescription for external beam radiation: anatomic site, delivery technique
157 including photon/electron, energy, total dose, number of fractions, and the percent isodose line
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158 that is used for normalization to a specific point or to a specific volume. If IGRT is applicable,
159 the prescription should specify the alignment method (e.g. bone or soft tissue) and the frequency
161 Written directive: Used for brachytherapy plans, similar to the prescription in EBRT plans
162 defined above, a Radiation Oncologist should provide the following minimum information in the
163 written prescription: anatomic site, isotope, activities, total dose, number of fractions, and the
164 percent isodose line that is used for normalization to a specific point or to a specific volume.
165 Clinical Plan: A radiation oncologist should provide the following in a clinical component of a
166 treatment plan: instructions to the planners on how to create the planning target volume (PTV), if
167 desired, total dose, fractionation scheme, and dose limits to the organs at risk (OARs), if they are
168 different from the institutional established standard tolerances, as indicated in ACR guidelines
170 Chart: All of the documents that accompany a patient-specific radiation treatment, including:
171 treatment prescription, treatment plan (clinical and technical plans), treatment delivery
172 parameters, recorded treatment deliveries, and image guided radiotherapy (IGRT) images.
173 Plan: The technical component of a treatment plan, consists of the total dose, fractionation
174 scheme, energy, treatment method, treatment parameters, and the isodose line that is used for
177 CT: Computed Tomography, which is acquired during simulation and used for treatment
178 planning.
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179 IGRT: Image-Guided Radiation Therapy, utilizing imaging, including Cone Beam CT (CBCT),
180 kilo-voltage (KV) or mega-voltage (MV) image pairs, for accurate patient alignment during
182 4D-CT: Multiple sets of CT scans obtained during regular respiration cycles, to obtain image
183 datasets that can be used to determine tumor/normal organ motions, and to create a better
184 representation of the tumor/normal organs by creating an internal target volume (ITV) or an
186 Initial Plan/Chart Check: The same as the new plan/chart check, applied to any plan that is
188 Weekly Chart Review: The same as the on-treatment chart check.
189 Final Chart Review: The same as the end-of-treatment chart check.
190
195 In compliance with the American College of Radiology (ACR) practice guideline [10], radiation
196 oncologists are responsible for the delineation of the tumor volumes, including the gross tumor
197 volume (GTV) and clinical target volume (CTV). For the internal target volume (ITV) and
198 planning target volume (PTV), radiation oncologists can either create these target volumes, or
199 provide a written instruction to the planners on how to create ITV and PTV volumes from the
200 contoured GTV and CTV volumes. Radiation oncologists are responsible for reviewing and
201 approving contours of all target volumes and OARs. Any OARs that are not clearly discernible
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202 on the planning images should be delineated by radiation oncologists. Upon approval of all
203 targeted volumes and OARs, radiation oncologists should provide detailed written instructions to
204 the planner about the desired dose-volume coverage to the targeted volumes and dose limits to
205 clinically relevant OARs (sometimes referred to as dose constraints) [8, 9]. The primary
206 responsibility of a planner is to create a treatment plan in accordance to these dose constraints
208
209 In the event that the prescription must be changed during planning, the radiation oncologist
210 should document the change in writing [12]. Some institutions may require a physicist to check
211 the plan quality (which, as mentioned previously, is not in the scope of this MPPG) before the
212 radiation oncologist’s approval. Before plan approval, some institutions may have a physicist
213 check important planning parameters such as the removal of the CT couch (or insertion of a
214 couch model), isocenter coordinates, normalization methods, and calculation point placements,
215 in an attempt to catch errors early in the planning process. Other institutions use a quality
216 checklist for the planner to perform a self-check or use a computer program to perform a plan
217 consistency check to eliminate obvious errors, which will be further discussed in Section V.
219
220 After plan approval, a planner will assemble all necessary information pertinent to the delivery
221 of the plan, such as the creation of digitally reconstructed radiographs (DRRs), setup beams,
222 source to skin surface distance (SSD) parameters, and the key treatment table parameters, when
223 appropriate. Furthermore, a comprehensive treatment plan report is generated. This plan report
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224 is the basis for all levels of plan review by both physicists and therapists. This report can also be
225 used for peer review, billing purposes, and even for patients, who may request this document
226 when transferring care or for re-treatment considerations. The recommended documentation for
227 this plan report is detailed in Section IV. In addition to the plan report, a planner is responsible
228 for transferring the treatment delivery parameters to a Record and Verify (R&V) system, if the
229 R&V system has a separate database from the treatment planning system. The information that is
230 transferred may include additional shifts from the initial isocenter (or reference point) set during
231 simulation, modification of patient external contours (e.g. add bolus on specific region), all
232 essential treatment parameters for each field, and images (DRRs, reference images) associated
233 with the treatment isocenter. This information is essential for radiation therapists to perform
235 Therapists are responsible for positioning the patient for treatment, according to the simulation
236 report, setup instruction, and treatment plan document. To ensure precise patient positioning,
237 radiation therapists must confirm all essential information is available, approved, and consistent.
238 Prior to each treatment, therapists must set up patients with patient-specific devices or patient-
239 specific settings of a reusable immobilization device. A recommended checklist for therapists is
241
242 Plan/chart review consists of reviewing the treatment plan and/or report, relevant documentation
243 such as setup instructions, and daily treatment records to ensure accuracy, consistency, and
244 clarity. Reviews should occur at multiple time points during the treatment process: initially,
245 weekly, and at the conclusion of treatment (final) during the course of treatments.
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246
247 (a) Initial Plan/Chart Check
248
249 A QMP is responsible for an initial plan/chart check. It is a good practice to perform the initial
250 check prior to the first treatment. The essential checklist for the initial check is discussed in
251 Section V.1b and listed in Table 4. The majority of the DICOM data are transferred via network;
252 however, some information may need to be entered manually. During the initial check, it is
253 important to focus on these elements due to the higher risk of human error. Certain treatment
254 parameters may be automatically checked (see Section VI). We recommend all radiation dose
255 relevant components and critical verification imaging parameters in treatment fields be approved
256 and locked after the initial check to avoid any accidental alterations during the treatment course.
257 Treatments should not be allowed to proceed if the approval status is revoked.
258
259 If the initial check is completed by a QMP-designated physicist, then a QMP must complete an
260 initial check prior to the delivery of 10% of the prescribed dose or prior to the third treatment,
261 whichever comes first. The QMP-designated physicists must be someone who is a trained
262 medical physics resident, or other physicist who is supervised by a QMP. The QMP must
263 document the competency the designated physicists on plan and chart review of each specific
264 EBRT treatment modality (i.e. conventional EBRT, SBRT, and SRS). For emergency treatments
265 occurring after hours, an on-call QMP may be contacted to review the treatment plan remotely.
266 For institutions that do not have an on-call QMP, a radiation oncologist may conduct the
267 secondary initial check and a QMP shall check the plan on the next business day, or prior to the
268 treatment on the next business day if additional fractions are prescribed.
269
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270 (b) Weekly Chart Review
271
272 The purpose of weekly chart review is to conduct a systematic review of recorded treatment
273 delivery data, including any overrides, incomplete treatments, any unusual isocenter shifts after
274 the initial image verification, the status of verification image approval, and documentation of
275 SSDs. If daily image guidance is indicated in the prescription, weekly chart reviews should
276 check whether the frequency of image guidance is followed and that the shifts after IGRT are
277 within a reasonable range. A specific weekly chart checklist is discussed in Section V. 1d and
278 listed in Table 8. Any dosimetric changes in a treatment plan should be considered as a new
279 plan, and a new report of the modified plan should be created. For example, a change in daily
280 fraction dose requires a new report to document on the changes of monitor units (MUs). The
281 modified plan should undergo an initial plan/chart check. Weekly chart reviews should be
282 completed within a window of every five treatment fractions. If a treatment course is five
283 fractions or less, the institution should consider developing a process to ensure at least one
284 weekly chart review is conducted during the course of treatment, ideally near the beginning of
285 the course. For single fraction treatment, a weekly chart check can be omitted, but the chart
286 should be reviewed by a QMP within one business day of treatment completion.
287
288 Weekly chart reviews should be completed by a QMP or their trained designees, which may
289 include dosimetrists, medical physics residents, and other physicists. When a designee completes
290 the weekly chart review, the QMP must co-sign the document, indicating that the designees are
291 under the supervision of the QMP. It is recommended, when possible, that QMPs and/or their
292 designees conduct the weekly chart reviews on an alternating basis, so that the same person does
293 not check the chart for the entire treatment course.
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294
295 (c) Final Chart Review
296
297 The purpose of final chart review is to review all treatment delivery parameters and documents
298 to ensure that the treatment prescriptions have been fulfilled accurately and all pertinent
299 technical documents are signed and approved. The final chart review should be completed by a
300 QMP within five business days of the patient’s last delivered fraction [7]. For single fraction
301 treatment course, we recommend completing the final chart review on the same day of the
302 treatment or no later than the next business day, if the weekly chart review is omitted.
303
304 2. Brachytherapy - HDR
305
306 There is a broad scope of procedures encompassed within the brachytherapy realm. As an
307 example, this MPPG examines a common high dose rate (HDR) brachytherapy for gynecology
308 cancer. The plan/chart check procedure developed for this procedure may be extended to other
310
311 The initial check for HDR should be performed by an AMP. In situations where an AMP is in a
312 solo practice, an AMP designated team member (either a therapist, a dosimetrit, or an AU) who
313 is trained for the HDR procedure may complete the initial plan/chart check if the HDR plan was
315
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316 This MPPG suggests an essential brachytherapy checklist for a new plan/chart checks in Section
317 V.2. In practice, some institutions generate a new plan for every fraction. The new plan is
318 checked again, which can be considered as the weekly chart review. In institutions where the
319 same brachytherapy plan is delivered over multiple fractions, the AMP should complete a
320 weekly chart review within a window of every 5 fractions, similar to those conducted for EBRT.
321 If an institution decides not complete weekly chart reviews on a brachytherapy procedure
322 because a new plan is created each fraction, a QMP should review a treatment procedure
323 document after each treatment to ensure the treatment record, pre- and post-radiation surveys,
324 and documentation of the presence of appropriate clinical personnel (an AU) is completed.
325
326 The final chart review should be performed at the end of the treatment course. The guidelines
327 are the same as for EBRT. The AMP should check the accuracy of all treatment delivery
328 parameters and documents to ensure the AUs’ directives have been fulfilled accurately and that
329 all pertinent technical documents are signed and approved. It is recommended the final chart
330 review be completed by an AMP at the day of final treatment, or no later than the next business
331 day.
332
335 A treatment plan report should be generated after the radiation oncologist (or AMP)’s review and
336 approval of the treatment plan. This report allows careful preservation of the treatment plan
337 stored in a central location, either in the hospital EMR system or radiation oncology specific
338 medical record system (Record and Verify System) along with other treatment-related
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339 documents. For purpose of patient care, the treatment plan report can be easily readable by all
340 caretakers as well as the patients themselves, who are not familiar with (or do not have access to)
342
345 The treatment plan report is often in a file format, such as PDF, where modification is restricted.
346 A treatment plan report should display information in a consistent manner from patient to patient
347 by standardizing the components, order, and the specific displays (i.e. isodose lines appearing at
348 standard levels and colors). For the prescription, it is recommended to include the anatomic site
349 name and laterality, total dose, number of fraction, and the percent isodose line that is used for
350 normalizing to a specific point or to a specific volume (see Table 3) according to the prescription
351 guideline from American Society of Radiation Oncology (ASTRO) [9]. Nomenclature such as
352 beam names should be standardized and designed to reduce confusion and improve safety. For
353 organ names and tumor volume names, it is recommended to use the established nomenclature
354 standard described by TG 263 [13]. We recommend including at least one isodose image for
355 each of the three orthogonal planes at isocenter or in the middle of the target(s) with isodose
356 lines shown in absolute dose and including the prescription dose level(s).
357
358 The second column in Table 1 shows the various components of a treatment plan report for
359 external beam and brachytherapy plans. Optional elements should be considered depending on
360 specific institutional workflow, clinical practice, or billing requirements. The components of the
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361 treatment plan report should be reconsidered when implementing new technology, e.g. proton
362 therapy. A treatment plan report must demonstrate that the prescription is being fulfilled. The
363 documentation should clearly convey how the plan fulfills the specific radiation oncologist
364 intent. Setup information including documentation of immobilization devices is important for
365 reproducible treatments. If setup information is not documented elsewhere, it should be included
369 A brachytherapy (HDR) plan document should follow the same order as the EBRT plan
370 document. The Third column in Table 1 shows the various components of a HDR plan report.
371 Optional elements should be considered depending on specific institutional workflow, clinical
372 practice, or billing requirements. The major differences in documents between EBRT and
373 brachytherapy plans are on the sections of plan summary and beam eye views. For
374 brachytherapy plans, it is of utmost importance to examine the reconstruction view of each
375 catheter and/or source position(s), including orientation (for example, tip verses catheter end). It
376 should be noted that the verification of the reconstruction may not be fully possible with a
377 printout alone but likely requires a review with the TPS.
378
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385 As mentioned in Section III, the primary responsibility of a planner is to create a treatment
386 plan in accordance with the treatment prescription and other written instructions provided by
387 a radiation oncologist. In addition, a planner must assemble necessary information for the
388 therapists to deliver the plan, including isocenter shifts, IGRT reference images, and cross-
389 verification parameters (e.g. SSDs, table positions, etc.). To assist a planner, it is
390 recommended that a planer conducts a self-check during planning or after the plan is
391 completed. The self-check items are listed in Table 2. Once the plan is approved by a
392 radiation oncologist, it is recommended that a planner creates a plan report following a
393 standard format established by each local institution. The recommended components of a
394 treatment plan report are listed in Table 1. The final section in Table 2 lists checklist items
395 that are essential for therapists to deliver the plan. The optional items listed in Table 2 can be
396 added to the planner’s checklist, depending on the preference of the local institution and
397 practice.
398
401 A treatment prescription (and/or written directive) from a radiation oncologist is the
402 foundation for any new treatment, and thus it is recommended that the treatment prescription
403 be standardized, clear and concise, and follows the prescription guideline from American
404 Society of Radiation Oncology (ASTRO) [7]. The essential items to be included in the
405 prescription are listed in Table 3. During new plan/chart review, a QMP should ensure that
406 these items are documented in the prescription and are consistent with the corresponding
407 treatment plan report. Upon reviewing the plan report, it is recommended that a QMP
408 follows checklist in Table 4. In the treatment plan, the isocenter or the initial reference point
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409 that was marked during CT simulation must agree with the skin marks on the patient since
410 this is the starting point of treatment plan and delivery including any additional shifts
411 required during the planning process. A recent publication [5] from Radiation Oncology
412 Incident Learning System (RO-ILS) reported that a potential systematic error in 15% of
413 reported events was a wrong isocenter, which could have originated from the initial isocenter
414 marked on the patient skin mismatching the isocenter that was sent for treatment planning.
415 Therefore, this MPPG recommended that a photo documenting the initial alignment point
416 marked on the patient skin be added in the R&V system, which can assist therapists to
417 identify the alignment point ( sometimes, it referred to as the laser alignment point).
418 Furthermore, this MPPG also recommend documenting the agreement between the
419 coordinates or location of the initial isocenter sent to the treatment planning system and the
420 initial alignment on the patient skin markers. For example, for institutions that implement the
421 virtual simulation (identify the iso-center after completion of planning CT acquisition) one
422 can acquire an additional single slice axial CT scan after acquisition of the planning CT. This
423 single slice image should contain three radio-opaque markers that are placed on the skin
424 where three laser points intersected. A planner should then verify the initial isocenter (or
425 reference point) matched with points marked on the patient skin.
426
427 Optional items included in Table 4 can be added to the checklist depending on the specific
428 practice of each institution. A QMP should ensure that essential information from the
429 treatment plan report are correctly transferred into the R&V system and approved by
430 assigned responsible teams. The last section in Table 4 lists the essential checklist items. The
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431 optional items in this section of Table 4 can be added to the checklist depending on the
433
436 Prior to any new treatment, therapists should conduct a new plan/chart review to confirm all
437 essential information is available, approved, and consistent. The importance of therapists
438 conducting an initial check is well demonstrated [14]. A recommended checklist for
439 therapists is listed in Table 5. Optional items in Table 5 can be added to the checklist
441
444 A recommended checklist for weekly chart check is listed in Table 8. The optional items
445 listed in Table 8 can be added to the checklist depending on the specific practice of each
446 institution. After completion of the weekly chart review, we recommend that a formal report
447 to be generated to document the date of the weekly chart review, the treatment site,
448 accumulated dose, number of fractions delivered to date, and other checklist items listed in
449 Table 8. For a new plan or a modified plan that has dosimetric impact, the first on-treatment
450 chart check should also include a quick check on plan quality, which serves as another level
451 of assessment to ensure that there are no gross errors in the plan.
452
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455 A QMP should conduct a final chart checks to ensure the treatment prescriptions and/or
456 written directive have been fulfilled accurately and all pertinent documents are signed and
457 approved. A recommended checklist for final review is listed in Table 9. It is recommended
458 to generate a formal document to report the date of the final chart check, the treatment site,
459 total dose, and total number of fractions delivered in accordance to the prescription. This
460 recommendation is compliant with ACR practice guideline[7]. If the prescribed treatment
461 course was not completed, a comment should be added in the existing prescription, or a
462 separate note or document. This document and the existing prescription should be stated on
464
467
469 As discussed in Section III 2, during HDR planning, the accuracy of image co-
470 registration, applicator specification and placement, catheter reconstruction, and catheter
471 channel parameters (such as indexing/ length and the appropriate identification of the first
472 dwell positions) are important parameters to verify before transferring the treatment data
473 to the treatment console. We recommend each new plan be checked by an AMP listed on
475
477 Prior to each treatment, we recommend that therapists (or an AMP if a therapist is not
478 involved in the procedure) conduct a pre-treatment check following Table 7. The
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479 checklist can serve as a part of the treatment procedure document and be signed by an
480 AMP and an authorized radiation oncologist, who are present during the treatment.
481
483 Weekly chart review for brachytherapy plans is only required when the same
484 brachytherapy plan is delivered over multiple fractions. The applicable items are listed in
487 Similar to external beam, an AMP should conduct the final chart reviews to ensure the
488 treatment prescriptions and/or written directive have been fulfilled accurately and all
489 pertinent documents are signed and approved. A recommended checklist for final review
490 for brachytherapy plans is the same as the EBRT plans as listed in Table 9. If the
491 prescribed treatment course was not completed, a comment (or a note) should be added in
493
496 Some vendors and individual institutions have developed computer programs to
497 automatically check various parts of a patient plan or chart [15-20]. These programs are
498 effective in checking simple logistic requirements and numerical consistency. For example, a
499 computer program can check whether prescriptions or portal images are approved by radiation
500 oncologists[21], and whether radiation treatment parameters are in agreement with the planned
501 parameters [20] . A comprehensive literature review about computer-aided plan/chart check can
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502 be found in TG275 [5]. Due to significant variations in workflows among different clinical
503 practices, these programs cannot completely replace the function of a physicist in the process of
504 the plan and chart review. Computer programs, however, can assist in certain areas of plan/chart
505 review. For example, vendor-provided programs [22, 23] can assist with checking whether plan
506 DVHs meet clinical requirements, but these programs cannot substitute careful examinations of
508 With automation, plan document components recommended in Table 1 can be easily
509 standardized and implemented. Most items listed in Table 2 can be checked automatically to
510 avoid errors in the upstream during treatment planning, but items such as whether bolus is
511 applied appropriately and whether contours of normal/critical structures are completed and
512 accurate will still rely on human judgment and experiences. Some items in Table 3 can be
513 extracted from treatment plan documents, but items such as CBCT frequency, IGRT alignment
514 structures, and special motion management techniques vary from patient to patient, requiring
515 human judgment and discretion. While a majority of the items listed in Table 4 can be checked
516 by computer programs, items such as whether the isocenter of a plan (if no isocenter shift)
517 matches with isocenter markers on the patient’s skin, beam clearance, and anatomy structure
518 density override, still need human attention. Computer-aided programs can provide an alert list
519 for initial and weekly plan/chart review, calling for special attention to certain missing or
520 mismatched items, therefore can help streamline the whole process.
522 rigorously validate them to avoid potential systematic errors. With increasing use of artificial
523 intelligence and sophisticated statistical machine learning tools in the medical physics field,
524 more commercial computer-aided plan/chart review programs are expected to be available
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525 clinically in the near future. The combination of computer-aided and human plan/chart review
526 will significantly improve the effectiveness of this vital process while improving safety and
528
531 The primary goal of this MPPG is to provide essential checklist items for medical physicists who
532 conduct plan/chart reviews according to the minimum practice standards. The plan/chart review
533 process, particularly the initial plan review process, is critical to prevent errors and to ensure
534 smooth patient care. Thus this process should have multiple layers and take collective efforts of
535 the entire department, in addition to the physics check/review. This MPPG, therefore, also
536 recommends therapists conduct the initial plan/chart check prior to any new treatment. The
537 initial plan/chart checklist for the therapists overlapped with the checklist of initial plan/chart
538 check for the physicists on the important items, such as the prescriptions and location of the iso-
539 center. In addition to act as an additional layer of the safety check, another purpose of checklist
540 for therapists is to ensure the presence of important documents and the associated authorizations
541 and approval, according to the rules of ACR and other regulatory agencies, thus preventing
542 potential interruptions of patient care. This MPPG invited American Society of Radiologic
543 Technologists to review the report and obtained the endorsement from the society.
544
545 To catch errors upstream, this MPPG recommends a self-consistent checklist for planners and the
546 use of standard documentation of a plan. Since the planners are often dosimetrists, this MPPG
547 also reach out to the American Association of Medical Dosimetrists (AAMD) for their input and
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548 endorsement of self-consistent checklist and standard documentation. There are some debates
549 about whether a standard documentation is necessary if everyone has an access to the treatment
550 planning system to review the plan comprehensively. Given the complexity of a treatment
551 planning system, a planner typically accesses numerous treatment planning parameters through
552 many sub-windows and panels, therefore, we believe that not everyone has the skill and
553 confidence level as a planner in the use of a treatment planning system. A standard plan
554 document displays all key information of a plan in a consistent order and straightforward format,
555 facilitating those who are not familiar with the treatment planning system to grasp the content of
557
558 From the perspective of minimum practice standards, this MPPG is different from TG 275 [5]
559 although the underlining principles are the same. Within this task group, we included two
560 members from TG 275, who provided a valuable link between TG 275 and this MPPG. Based
561 on TG 275 and practice experiences of the task group members, which included academic and
562 community practices using different Record & Verify systems and treatment planning systems,
563 the recommended initial plan/chart checklist for physicists has about 50% - accordance of the
564 example checklist (Table 1c from TG 275). Some items in the example checklist of TG 275,
565 such as physician directives for simulation procedures, treatment prescriptions with respect to the
566 standard of care/clinical guideline, are not included in the recommended checklist of this MPPG
567 because we believe these items are beyond the training and responsibility of a medical physicist.
568 This view is supported by ACR guideline for 3D external beam radiation planning and conformal
569 therapy[10]. Furthermore, the accuracy of contours of tumor volumes and normal tissue volumes
570 is predominant in 3D and IMRT planning and is the responsibilities of radiation oncologists per
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571 ACR guideline[10]. To improve patient care workflow, it is a good practice for each planner to
572 conduct a sanity check of all contours to avoid replanning. This sanity check (included in Table 2
573 of planner checklist) is to detect gross errors such as skip slides, miss labels of contours, an
574 illogical relationship among GTV, CTV, ITV and PTV, stray voxels, to name a few. According
575 to the guideline of ATSRO [9], this MPPG recommends each local institution establishes its own
576 standard format of a treatment prescription for both EBRT and brachytherapy. Medical
577 physicists can provide supports to radiation oncologists to adhere to the ASTRO guideline. The
578 accuracy and completeness of a prescription are again beyond the clinical training and
579 responsibility of a medical physicist. Some items in the checklist of this MPPG are not in the
580 checklist of TG 275, including items such as the patient name and medical record numbers, and
581 item such as all beams associated with the same iso-center ( for single iso-center plans). The
582 weekly and final chart review checklists from this MPPG are mostly in agreement of
583 recommendation of TG 275. For institutions that desire to conduct more comprehensive and
584 thorough plan/chart review and have the required resources, they are encouraged to develop their
585 own checklists that combines checklists from TG 275 and this MPPG and more.
586 The scope of this MPPG is limited to most frequently used external beam radiotherapy (C-arm
587 linear accelerators) and most frequently used brachytherapy (for gynecological treatments). The
588 recommended checklists can be extended to other external beam modalities such as proton beam
589 radiotherapy, Cyberknife, and Tomotherapy while taking account for unique applications of
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593 This MPPG provides lists of the essential checklist items, according to the minimum practice
594 standards, for medical physicists, dosimetrists, and therapists to follow when conducting
595 plan/chart reviews. The report also provides essential components to include in a treatment plan
596 report, provides minimum personnel qualifications for those completing plan/chart review, and
597 provides appropriate timelines for when to complete plan / chart reviews.
598
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