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BackgroundAlthough re‐irradiation is increasingly used in clinical practice, almost no dedicated planning software exists.PurposeStandard dose‐based optimization functions were adjusted for re‐irradiation planning using accumulated equivalent dose in 2‐Gy fractions (EQD2) with rigid or deformable dose mapping, tissue‐specific α/β, treatment‐specific recovery coefficients, and voxelwise adjusted EQD2 penalization levels based on the estimated previously delivered EQD2 (EQD2deliv).MethodsTo demonstrate proof‐of‐concept, 35 Gy in 5 fractions was planned to a fictitious spherical relapse planning target volume (PTV) in three separate locations following previous prostate treatment on a virtual human phantom. The PTV locations represented one repeated irradiation scenario and two re‐irradiation scenarios. For each scenario, three re‐planning strategies with identical PTV dose‐functions but various organ at risk (OAR) EQD2‐functions was used: reRTregular: Regular functions with fixed EQD2 penalization levels larger than EQD2deliv for all OAR voxels. reRTreduce: As reRTregular, but with lower fixed EQD2 penalization levels aiming to reduce OAR EQD2. reRTvoxelwise: As reRTregular and reRTreduce, but with voxelwise adjusted EQD2 penalization levels based on EQD2deliv. PTV near‐minimum and near‐maximum dose (D98%/D2%), homogeneity index (HI), conformity index (CI) and accumulated OAR EQD2 (α/β = 3 Gy) were evaluated.ResultsFor the repeated irradiation scenario, all strategies resulted in similar dose distributions. For the re‐irradiation scenarios, reRTreduce and reRTvoxelwise reduced accumulated average and near‐maximum EQD2 by ˜1–10 Gy for all relevant OARs compared to reRTregular. The reduced OAR doses for reRTreduce came at the cost of distorted dose distributions with D98% = 92.3%, HI = 12.0%, CI = 73.7% and normal tissue hot spots ≥150% for the most complex scenario, while reRTregular (D98% = 98.1%, HI = 3.2%, CI = 94.2%) and reRTvoxelwise (D98% = 96.9%, HI = 6.1%, CI = 93.7%) fulfilled PTV coverage without hot spots.ConclusionsThe proposed re‐irradiation‐specific EQD2‐based optimization functions introduce novel planning possibilities with flexible options to guide the trade‐off between target coverage and OAR sparing with voxelwise adapted penalization levels based on EQD2deliv.
BackgroundAlthough re‐irradiation is increasingly used in clinical practice, almost no dedicated planning software exists.PurposeStandard dose‐based optimization functions were adjusted for re‐irradiation planning using accumulated equivalent dose in 2‐Gy fractions (EQD2) with rigid or deformable dose mapping, tissue‐specific α/β, treatment‐specific recovery coefficients, and voxelwise adjusted EQD2 penalization levels based on the estimated previously delivered EQD2 (EQD2deliv).MethodsTo demonstrate proof‐of‐concept, 35 Gy in 5 fractions was planned to a fictitious spherical relapse planning target volume (PTV) in three separate locations following previous prostate treatment on a virtual human phantom. The PTV locations represented one repeated irradiation scenario and two re‐irradiation scenarios. For each scenario, three re‐planning strategies with identical PTV dose‐functions but various organ at risk (OAR) EQD2‐functions was used: reRTregular: Regular functions with fixed EQD2 penalization levels larger than EQD2deliv for all OAR voxels. reRTreduce: As reRTregular, but with lower fixed EQD2 penalization levels aiming to reduce OAR EQD2. reRTvoxelwise: As reRTregular and reRTreduce, but with voxelwise adjusted EQD2 penalization levels based on EQD2deliv. PTV near‐minimum and near‐maximum dose (D98%/D2%), homogeneity index (HI), conformity index (CI) and accumulated OAR EQD2 (α/β = 3 Gy) were evaluated.ResultsFor the repeated irradiation scenario, all strategies resulted in similar dose distributions. For the re‐irradiation scenarios, reRTreduce and reRTvoxelwise reduced accumulated average and near‐maximum EQD2 by ˜1–10 Gy for all relevant OARs compared to reRTregular. The reduced OAR doses for reRTreduce came at the cost of distorted dose distributions with D98% = 92.3%, HI = 12.0%, CI = 73.7% and normal tissue hot spots ≥150% for the most complex scenario, while reRTregular (D98% = 98.1%, HI = 3.2%, CI = 94.2%) and reRTvoxelwise (D98% = 96.9%, HI = 6.1%, CI = 93.7%) fulfilled PTV coverage without hot spots.ConclusionsThe proposed re‐irradiation‐specific EQD2‐based optimization functions introduce novel planning possibilities with flexible options to guide the trade‐off between target coverage and OAR sparing with voxelwise adapted penalization levels based on EQD2deliv.
Purpose We aimed to evaluate the efficacy and safety of re-irradiation stereotactic body radiation therapy (SBRT) in patients with metastatic epidural spinal cord compression (MESCC) following high-dose conventional radiotherapy. Materials and methods Twenty-one patients met the following eligibility criteria: with an irradiation history of 50 Gy2 equivalent dose in 2-Gy fractions (EQD2) or more, diagnosed MESCC in the cervical or thoracic spines, and treated with re-irradiation SBRT of 24 Gy in 2 fractions between April 2018 and March 2023. Prior treatment was radiotherapy alone, not including surgery. The primary endpoint was a 1-year local failure rate. Overall survival (OS) and treatment-related adverse events were assessed as the secondary endpoints. Since our cohort includes one treatment-related death (TRD) of esophageal perforation, the cumulative esophageal dose was evaluated to find the dose constraints related to severe toxicities. Results The median age was 68, and 14 males were included. The primary tumor sites (esophagus/lung/head and neck/others) were 6/6/7/2, and the median initial radiotherapy dose was 60 Gy2 EQD2 (range: 50–105 Gy2, 60–70/ > 70 Gy2 were 11/4). Ten patients underwent surgery followed by SBRT and 11 SBRT alone. At the median follow-up time of 10.4 months, 17 patients died of systemic disease progression including one TRD. No radiation-induced myelopathy or nerve root injuries occurred. Local failure occurred in six patients, with a 1-year local failure rate of 29.3% and a 1-year OS of 55.0%. Other toxicities included five cases of vertebral compression fractures (23.8%) and one radiation pneumonitis. The cumulative esophageal dose was recommended as follows: Dmax < 203, D0.035 cc < 187, and D1cc < 167 (Gy3 in biological effective dose). Conclusion Re-irradiation spine SBRT may be effective for selected patients with cervical or thoracic MESCC, even with high-dose irradiation histories. The cumulative dose assessment across the original and re-irradiated esophagus was recommended to decrease the risk of severe esophageal toxicities.
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