Critical Appraisal of the Treatment Planning Performance of Volumetric Modulated Arc Therapy by Means of a Dual Layer Stacked Multileaf Collimator for Head and Neck, Breast, and Prostate
Abstract:Purpose:To ascertain whether a new delivery system (the Halcyon system) equipped with
dual-layer stacked multileaf collimator operating in a mode, which allows
independent, fully interdigitating motion of both layers and 6 flattening
filter free energy, could generate plans of high clinical quality compared
to a well-established delivery system with single layer multileaf
collimator.Methods:Twenty patients in each of the 3 groups (advanced head and neck, breast, and
high-risk prostate) were selected for an in … Show more
“…The unique features of Halcyon (mainly the double layer MLC) justify the need for pre-clinical dosimetric investigations to define the field of applicability or the deficiencies of the platform. As a comparison technique, as a novelty factor compared to [13], the Helical Tomotherapy was chosen. The role of HT for cervix uteri was appraised in several studies showing how complex dose distributions with a high degree of conformal avoidance (simultaneous achievement of target coverage and healthy tissue sparing) could be achieved [7][8][9].…”
Section: Discussionmentioning
confidence: 99%
“…Halcyon plans: The Halcyon is a ring-based delivery system [13,[22][23][24]. It consists of a linear accelerator capable of producing a 6MV flattening filter-free (FFF) photon beam delivering (when calibrated to deliver 1.0Gy per 100 monitor units (MU) at the reference conditions of source-surface distance (SSD) 100 cm at d max depth of 1.3 cm) a maximum dose rate of 800MU/min.…”
Section: The Treatment Planning Techniques and Featuresmentioning
confidence: 99%
“…After its clinical introduction in 2017, the performance of the new radiotherapy delivery platform Halcyon (H, Varian Medical Systems, Palo Alto, USA) was investigated for a variety of different treatment indications [10][11][12][13][14][15][16][17][18][19][20]. In general, the potential performance equivalence between H and other carm delivery systems was proven for head and neck, breast, prostate [13] and brain tumours [15]. Some studies focused on cervix uteri cancer planning.…”
Purpose: To ascertain the dosimetric performance of a new delivery system (the Halcyon system, H) equipped with dual-layer stacked multi-leaf collimator (MLC) for risk-adapted targets in cervix uteri cancer patients compared to another ring-based system in clinical operation (Helical Tomotherapy, HT). Methods: Twenty patients were retrospectively included in a treatment planning study (10 with positive lymph nodes and 10 without). The dose prescription (45Gy to the primary tumour volume and a simultaneously integrated boost up to 55Gy for the positive patients) and the clinical planning objectives were defined consistently as recommended by an ongoing multicentric clinical trial. Halcyon plans were optimised for the volumetric modulated arc therapy. The plan comparison was performed employing the quantitative analysis of the dose-volume histograms.Results: The coverage of the primary and nodal target volumes was comparable for both techniques and both subsets of patients. The primary planning target volume (PTV) receiving at least 95% of the prescription isodose ranged from 97.2 ± 1.1% (node-negative) to 99.1 ± 1.2% (node-positive) for H and from 96.5 ± 1.9% (node-negative) to 98.3 ± 0.9% (node-positive) for HT. The uncertainty is expressed at one standard deviation from the cohort of patient per each group. For the nodal clinical target volumes, the dose received by 98% of the planning target volume ranged 55.5 ± 0.1 to 56.0 ± 0.8Gy for H and HT, respectively. The only significant and potentially relevant differences were observed for the bowels. In this case, V 40Gy resulted 226.3 ± 35.9 and 186.9 ± 115.9 cm 3 for the node-positive and node-negative patients respectively for Halcyon. The corresponding findings for HT were: 258.9 ± 60.5 and 224.9 ± 102.2 cm 3 . On the contrary, V 15Gy resulted 1279.7 ± 296.5 and 1557.2 ± 359.9 cm 3 for HT and H respectively for node-positive and 1010.8 ± 320.9 versus 1203.8 ± 332.8 cm 3 for node-negative. Conclusion: This retrospective treatment planning study, based on the dose constraints derived from the Embrace II study protocol, suggested the essential equivalence between Halcyon based and Helical Tomotherapy based plans for the intensity-modulated rotational treatment of cervix uteri cancer. Different levels of sparing were observed for the bowels with H better protecting in the high-dose region and HT in the mid-low dose regions. The clinical impact of these differences should be further addressed.
“…The unique features of Halcyon (mainly the double layer MLC) justify the need for pre-clinical dosimetric investigations to define the field of applicability or the deficiencies of the platform. As a comparison technique, as a novelty factor compared to [13], the Helical Tomotherapy was chosen. The role of HT for cervix uteri was appraised in several studies showing how complex dose distributions with a high degree of conformal avoidance (simultaneous achievement of target coverage and healthy tissue sparing) could be achieved [7][8][9].…”
Section: Discussionmentioning
confidence: 99%
“…Halcyon plans: The Halcyon is a ring-based delivery system [13,[22][23][24]. It consists of a linear accelerator capable of producing a 6MV flattening filter-free (FFF) photon beam delivering (when calibrated to deliver 1.0Gy per 100 monitor units (MU) at the reference conditions of source-surface distance (SSD) 100 cm at d max depth of 1.3 cm) a maximum dose rate of 800MU/min.…”
Section: The Treatment Planning Techniques and Featuresmentioning
confidence: 99%
“…After its clinical introduction in 2017, the performance of the new radiotherapy delivery platform Halcyon (H, Varian Medical Systems, Palo Alto, USA) was investigated for a variety of different treatment indications [10][11][12][13][14][15][16][17][18][19][20]. In general, the potential performance equivalence between H and other carm delivery systems was proven for head and neck, breast, prostate [13] and brain tumours [15]. Some studies focused on cervix uteri cancer planning.…”
Purpose: To ascertain the dosimetric performance of a new delivery system (the Halcyon system, H) equipped with dual-layer stacked multi-leaf collimator (MLC) for risk-adapted targets in cervix uteri cancer patients compared to another ring-based system in clinical operation (Helical Tomotherapy, HT). Methods: Twenty patients were retrospectively included in a treatment planning study (10 with positive lymph nodes and 10 without). The dose prescription (45Gy to the primary tumour volume and a simultaneously integrated boost up to 55Gy for the positive patients) and the clinical planning objectives were defined consistently as recommended by an ongoing multicentric clinical trial. Halcyon plans were optimised for the volumetric modulated arc therapy. The plan comparison was performed employing the quantitative analysis of the dose-volume histograms.Results: The coverage of the primary and nodal target volumes was comparable for both techniques and both subsets of patients. The primary planning target volume (PTV) receiving at least 95% of the prescription isodose ranged from 97.2 ± 1.1% (node-negative) to 99.1 ± 1.2% (node-positive) for H and from 96.5 ± 1.9% (node-negative) to 98.3 ± 0.9% (node-positive) for HT. The uncertainty is expressed at one standard deviation from the cohort of patient per each group. For the nodal clinical target volumes, the dose received by 98% of the planning target volume ranged 55.5 ± 0.1 to 56.0 ± 0.8Gy for H and HT, respectively. The only significant and potentially relevant differences were observed for the bowels. In this case, V 40Gy resulted 226.3 ± 35.9 and 186.9 ± 115.9 cm 3 for the node-positive and node-negative patients respectively for Halcyon. The corresponding findings for HT were: 258.9 ± 60.5 and 224.9 ± 102.2 cm 3 . On the contrary, V 15Gy resulted 1279.7 ± 296.5 and 1557.2 ± 359.9 cm 3 for HT and H respectively for node-positive and 1010.8 ± 320.9 versus 1203.8 ± 332.8 cm 3 for node-negative. Conclusion: This retrospective treatment planning study, based on the dose constraints derived from the Embrace II study protocol, suggested the essential equivalence between Halcyon based and Helical Tomotherapy based plans for the intensity-modulated rotational treatment of cervix uteri cancer. Different levels of sparing were observed for the bowels with H better protecting in the high-dose region and HT in the mid-low dose regions. The clinical impact of these differences should be further addressed.
“…There are a number of publications that either evaluate the operation of the Halcyon or provide recommendations on its clinical use . A recent publication provided a risk assessment of Halcyon acceptance testing and commissioning processes using the TGâ100 methodology .…”
Section: Introductionmentioning
confidence: 99%
“…There are a number of publications that either evaluate the operation of the Halcyon or provide recommendations on its clinical use. [1][2][3][4][5][6][7][8][9][10][11] A recent publication provided a risk assessment of Halcyon acceptance testing and commissioning processes using the TG-100 methodology. 12 In that work, 142 failure modes were identified with the top risk priority number (RPN) values ranging from 85.5 to 95.0 for the acceptance testing and commissioning, respectively.…”
Purpose
The Halcyon consists of precommissioned linear accelerator and treatment planning algorithms that were designed to simplify the acceptance, commissioning, and clinical workflow for imageâguided intensityâmodulated radiotherapy. The purpose of this work was to perform a comprehensive safety assessment for the clinical use of the Halcyon.
Methods
SystemsâTheoretic Process Analysis was used as the safety assessment tool. As part of the analysis, a number of control loops and control actions are created to describe system function. Safety is assessed by determining unsafe control actions and a corresponding list of causal scenarios that leads to accidents. The scope of the analysis was from the acceptance of the Halcyon to routine patient treatments. All aspects of treating patients were considered including the roles of physicians, physicists, dosimetrists, and therapists. The analysis was completed by four physicists with input from other members of the radiation therapy team. The causal scenarios were summarized using the causality categories from the consensus recommendations for incident learning database structures in radiation oncology (Med Phys, Vol. 39, No. 12, Dec 2012).
Results
Twentyâthree (23) control loops containing 52 control actions were created for the clinical use of the Halcyon. One hundred fortyâfour (144) unsafe control actions were identified with 385 associated causal scenarios. Twentyâseven percent (27%) of the causal scenarios were related to equipment technical issues, while 73% of the causal scenarios were predominantly related to procedural issues, human behavior, and organizational management.
Conclusions
For routine clinical use of closed or largely automated radiation therapy equipment, the majority of safety concerns is related to nontechnical issues. The Halcyon and other similar systems may present opportunities to streamline, reduce, or eliminate some traditional equipment commissioning and routine quality assurance activities in exchange for an increased focus on issues related to organizational management, procedures, and human behavior.
Purpose: Varian Halcyon linear accelerator version 2 (The Halcyon 2.0) was recently released with new upgraded features. The aim of this study was to report our clinical experience with Halcyon 2.0 for a dual-isocenter intensity-modulated radiation therapy (IMRT) planning and delivery for gynecological cancer patients and examine the feasibility of in vivo portal dosimetry. Methods: Twelve gynecological cancer patients were treated with extended-field IMRT technique using two isocenters on Halcyon 2.0 to treat pelvis and pelvic/or para-aortic nodes region. The prescription dose was 45 Gy in 25 fractions (fxs) with simultaneous integrated boost (SIB) dose of 55 or 57.5 Gy in 25 fxs to involved nodes. All treatment plans, pretreatment patient-specific QA and treatment delivery records including daily in vivo portal dosimetry were retrospectively reviewed. For in vivo daily portal dosimetry analysis, each fraction was compared to the reference baseline (1st fraction) using gamma analysis criteria of 4 %/4 mm with 90% of total pixels in the portal image planar dose.Results: All 12 extended-field IMRT plans met the planning criteria and delivered as planned (a total of 300 fractions). Conformity Index (CI) for the primary target was achieved with the range of 0.99-1.14. For organs at risks, most were well within the dose volume criteria. Treatment delivery time was from 5.0 to 6.5 min. Interfractional in vivo dose variation exceeded gamma analysis threshold for 8 fractions out of total 300 (2.7%). These eight fractions were found to have a relatively large difference in small bowel filling and SSD change at the isocenter compared to the baseline.Conclusion: Halcyon 2.0 is effective to create complex extended-field IMRT plans using two isocenters with efficient delivery. Also Halcyon in vivo dosimetry is feasible for daily treatment monitoring for organ motion, internal or external anatomy, and body weight which could further lead to adaptive radiation therapy.
K E Y W O R D Sdual-isocenter, extended-field IMRT, gynecological cancer, Halcyon 2.0, In vivo portal dosimetry ---
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