BT has been used for more than a century to successfully treat various cancers, and numerous studies have investigated its dosimetric characteristics compared to new emerging EBRT techniques. Table 1 presents the 53 publications that include comparative data from at least 5 patients. The table indicates the number of patients included in the study and the reference CT image set used for comparison. The CTV–PTV margins used in the EBRT studies are also shown in the table. We found one study for brain and head and neck, two for lung, three for liver, six for skin and eight for breast tumours. Most studies were published for gynaecological and prostate cancer (16 for both).
Six articles with very few patients were found that examined technical considerations and/or the feasibility of using EBRT as an alternative to BT. Three studies, using only one patient, investigated whether 3D-CRT and IMRT can achieve a brachy-like dose distribution for cervical cancer [68,69,70]. BT irradiation of the vaginal cuff of patients with endometrial cancer has also been simulated with advanced EBRT using two and four patients, respectively [71, 72]. A treatment planning study compared BT dosimetry with 3D-CRT and IMRT in a patient with squamous cell carcinoma of the scalp .
As there are no generally accepted and commonly used dose–volume parameters for evaluation of the plans, different quantifiers have been used in the studies, making comparisons difficult. The most commonly used parameters in the reviewed studies are shown in Table 2.
In a study by Milickovic et al. , treatment plans of five patients with recurrent glioblastoma multiforme treated with stereotactic radiosurgery were re-planned as a simulation of HDR-BT. They used identical structure sets and dose prescriptions. The dose gradient at the target volume surface was steeper with BT, resulting in less intermediate doses. With BT, the target coverage and conformity were slightly better, the maximum dose to the brainstem was lower, but the lenses received higher doses with no statistical difference.
BT has been used for partial breast irradiation for decades, initially only in clinical trials, but it is now a standard treatment method in selected patient groups due to its good clinical results . Boost doses following whole-breast irradiation can also be effectively delivered with BT [19, 75]. Charagvandi et al.  have dosimetrically compared single-fraction ablative RT with interstitial BT and VMAT in early-stage breast cancer. The PD was 15 Gy to the PTV and 20 Gy integrated boost to the GTV. The CTV was created from the GTV by a 2-cm extension (this corresponds to the PTV in BT), and an additional 3‑mm margin was added around the CTV to obtain the PTV for the VMAT plans. For both treatment techniques, the same preoperative CT scans of 20 patients with identical contours were used. Two partial arcs were used in VMAT planning and BT plans were calculated with inverse planning simulated annealing (IPSA) optimization using a median of 16 catheters. The target coverage for GTV and PTV was excellent for both techniques (100% and 99%, respectively). The median of mean ipsilateral lung doses was smaller with BT (0.8 Gy vs. 1.3 Gy, p < 0.05). The same was true for the heart, with values of 0.4 Gy and 0.7 Gy, respectively (p < 0.05). The median V2.8 Gy was also less with BT (0 Gy vs. 0.3 Gy, p < 0.05), and its maximum value was only 0.2 Gy in BT compared to 5.9 Gy in VMAT. There was no difference in doses to skin represented by D1cm3, (15.9 Gy vs. 15.2 Gy), but the contralateral breast received less dose with BT (median Dmean: 0 Gy vs. 0.2 Gy, p < 0.05). The authors concluded that both techniques are feasible for this two-dose level, single-fraction ablative radiotherapy for early-stage breast cancer, but the PTV is overdosed with BT. We note that this is a natural consequence of an inhomogeneous dose distribution with hotspots around the sources. A detailed dosimetric comparison of multicatheter interstitial BT (MIBT) and IMRT plans for partial breast irradiation was performed by Major et al. . For 34 patients with early-stage breast cancer treated with interstitial HDR-BT, additional IMRT plans were created using identical CT data and contours. In IMRT plans, the PTV was created from the CTV using a 5-mm isotropic margin. The dose prescription was the same for both techniques, i.e., 7 × 4.3 Gy (total 30.1 Gy). In the BT plans, the mean catheter number was 15 (range 7–28), and geometrical and graphical optimization was used. The IMRT plans were generated with 4–5 fixed-gantry coplanar fields with 6‑MV energy photon beams using a sliding-window technique. Although the V100 for the ipsilateral non-target breast was higher with BT (2.4% vs. 0.4%), the medium isodose lines more closely surrounded the PTV in BT plans, resulting in less dose to the breast (V75: 6.1% vs. 11.7%, p < 0.05, V50: 13.7% vs. 25.5%, p < 0.05). The ipsilateral lung was better protected with BT, all parameters were significantly smaller (e.g., mean lung dose: 5.1% vs. 7.1%, D2cm3: 36.5% vs. 50.2%, p < 0.05). The heart dosimetry was generally better for IMRT. The mean heart dose for left-sided lesions (n = 21) was 2.0% for IMRT and 4.5% for BT (p < 0.05), but the D2cm3 was lower with BT (18.3% vs. 19.7%, p = 0.0129). For skin the D1cm3 was 60.2% for BT and 87.8% for IMRT (p < 0.05), and regarding the ribs, all parameters were significantly lower with BT. Dose to contralateral breast and lung was also smaller with BT, with a significant difference for D0.1 cm3 and D1cm3.
Interstitial BT was also compared with 3D-CRT for breast cancer [19, 21, 76]. Using a relatively large patient cohort with 136 patients, Terheyden et al.  found significant dose reductions to organs at risk using an HDR-BT boost compared to 3D-CRT. In a study with 15 patients, boost doses to deep-seated tumour beds were calculated for interstitial BT and EBRT (3D-CRT photon or electron) . The target coverage was similar for BT and EBRT, but the conformity was best with BT. The COIN was 0.67 for BT and less than 0.3 for EBRT. The volume of the ipsilateral breast exposed to medium to high doses (>50%) was smaller with BT, and the skin, ribs and lung were better protected with BT in this dose range. The EBRT was more favourable for low doses. The mean heart dose was higher with BT (1.69 Gy vs. 0.33 Gy, biologically equivalent doses, p < 0.05). In another study, treatment plans of 30 patients treated with interstitial BT and another 30 with 3D-CRT were compared . Doses to OARs were significantly lower with BT. For example, for ipsilateral breast the mean V100 was 13% vs. 15% (p = 0.05) and the V50 was 25% vs. 50% (p < 0.05). For ipsilateral lung the V30 was 1% vs. 8% (p < 0.05), and for heart the Dmax was 25% vs. 49% (p < 0.05), respectively.
Following the previous study with IMRT, the same group investigated the dosimetric characteristics of stereotactic irradiation with CyberKnife (CK) (Accuray Inc., Sunnyvale, CA, USA) in treatment of the partial breast. First, virtual MIBT plans were created on CT images used for CK treatments . In the more conformal CK plans, the doses to skin, ipsilateral lung and ribs were higher compared to BT: skin D1cm3 was 86.1% vs. 46.1% (p = 0.0018), ipsilateral lung D1cm3 45.0% vs. 38.4% (p = 0.0272) and ribs D1cm3 73.6% vs. 49.0% (p = 0.0013), but the heart was slightly better protected with CK (D1cm3 10.5% vs. 11.2%, p = 0.0534). Then, in another study, MIBT and CK were dosimetrically compared using two separate patient cohorts : 32 APBI patients received their treatments with MIBT and another 32 with CK. The protocol for target volume definition and the fractionation were identical in the two groups. CK plans were more conformal, but the skin and ribs were better protected with MIBT. The mean D1cm3 for skin was 58.4% vs. 79.0% (p = 0.0007), and for ribs 43.1% vs. 69.0% (p = 0.0004) in the MIBT and CK plans, respectively. The mean doses to the ipsilateral lung were the same (4.9%), but doses to most exposed small volumes were significantly smaller for MIBT. The heart parameters were smaller with CK, but the differences were not significant. Doses to contralateral breast and lung were small with both techniques, but CK resulted in smaller values. We note that in both studies [22, 23], CK treatments were performed with tracking and an MLC-based step-and-shoot IMRT technique, and an isotropic margin of 2 mm around the CTV was used to create the PTV.
Analysis of the pooled data from the three studies [20, 22, 23] shows that the mean V50 values for the non-target breast are 10.0% vs. 15.3%, D1cm3 values for the ipsilateral lung are 37.8% vs. 48.2%, D1cm3 values for the skin are 54.9% vs. 84.3%, and D1cm3 values for the ribs are 45.9% vs. 70.6% in favour of BT.
Gynaecological cancers are the most common treatment sites for BT. For the first time, Schefter et al.  simulated how IMRT can mimic the dose distribution of a BT treatment for cervical cancer. For a single case, they contoured the reference isodose curve of a standard BT treatment as the target volume for IMRT and optimized the dose distribution of IMRT on this. Without detailed dosimetric analysis, IMRT was found to be able to reproduce the BT dose distribution to a large extent. In a similar study, the dose distribution of a tandem and ovoids was duplicated by IMRT, resulting in a good agreement in the 100% isodose envelope, with a steeper dose falloff for BT . Using data of 9 patients with locally advanced cervical cancer, Georg et al.  compared high-tech EBRT with high-tech BT. For BT treatments, intracavitary applicators and interstitial needles were used. In addition to the BT plans, photon IMRT and intensity-modulated proton therapy (IMPT) plans were also prepared and compared. Due to optimization constraints in the EBRT plans, the D1cm3 and D2cm3 for rectum, bladder and sigmoid were very similar for all plans, but at the cost of lower D90 of the PTV in EBRT plans compared to BT. The total volumes irradiated with doses higher than 3 Gy, 5 Gy and 7 Gy were about twice as large for EBRT as for BT. From their study, the authors conclude that both IMRT and IMPT appear to be inferior to BT. In another study, for 10 cervical cancer patients, Shwetha et al.  generated a pear-shaped dose distribution of HDR-BT using sliding-window IMRT. Both D1cm3 and D1cm3 for the rectum were significantly lower with BT (77.4% vs. 87.7%, p = 0.0021 and 69.1% vs. 81.4%, p = 0.0006, respectively), and the bladder also received less dose with BT (D1cm3: 81.0% vs. 88.7%, p = 0.162). There was also a significant difference in the volume of normal tissue receiving 10% of the PD (33.1% vs. 38.8%, p = 0.0006). It was concluded that IMRT may be the treatment of choice for cervical cancer when HDR-BT is not available or when a noninvasive treatment technique is preferred. IMRT was compared to interstitial BT for cervical cancer by Sharma et al. . Twelve patients who were not suitable for intracavitary BT were treated with interstitial BT, with a mean of 18 needles (range 14–26). Then, parallel IMRT plans were prepared and compared with the BT plans. Due to the large number of needles used in BT, the dose distributions were more conformal (conformity index defined as volume covered by the referenced isodose/volume of the PTV: 0.94 vs. 0.90, p = 0.034), the coverage was better, and the doses to bladder and maximal dose to rectum were significantly lower in BT plans. The authors conclude that interstitial BT provides better dosimetry compared to IMRT and recommend it as a standard treatment for cervical cancer patients who are not suitable for intracavitary BT. SBRT with CK was also compared to BT. In a feasibility study, Cengiz et al.  generated SBRT plans on CT scans of 11 patients treated with tandem and two ovoids. The BT dose distributions were prescribed to point A. In the SBRT plans, they found better dose distributions in the PTV and lower maximum doses to critical organs at the expense of higher doses to the bone marrow. Neumann et al.  investigated CK robotic radiosurgery as an alternative to BT for cervical cancer. They calculated BT and CK treatment plans simulating BT-like dose distributions with different homogeneity for 11 patients and compared the plans with each other and with 38 other patients treated with BT. In CK plans with BT-like inhomogeneity, OAR constraints could not be met, but when the maximum dose was limited to 143% for CK, OAR protection was similar to BT, with better target coverage and conformity. They concluded that CK with a moderately inhomogeneous dose distribution is an equivalent option for boost irradiation of cervical cancer patients.
In a recent paper, a dosimetric and radiobiological comparison of IMRT and intracavitary (IC) BT boost following 3D-CRT whole-pelvis irradiation for gynaecological cancer was performed . IMRT boost plans were prepared for 15 patients to mimic IC BT. In terms of conformity and homogeneity, IMRT performed better, but the small volume of OARs received a lower dose using BT. The D2cm3 for rectum, bowel and bladder were 47.9%, 39.1% and 30.9% for BT and 89.5%, 91.1% and 78.6% for IMRT, respectively. The NTCP (normal tissue complication probability) values were higher for 3D-CRT plus BT than for 3D-CRT plus IMRT, but it should be noted that BT included three different fractionation schemes with both HDR and PDR treatments.
Jones et al.  evaluated the feasibility of SBRT dosimetry for early-stage endometrial cancer and compared the dosimetry with HDR-BT. SBRT treatment plans for helical tomotherapy (HT) were generated on CT scans of 10 patients previously treated with IC HDR-BT. Identical OAR contours were used, and PTV in SBRT plans was created by a 2-mm extension of the primary CTV (uterus plus cervix). SBRT achieved significantly higher target volume coverage than BT, but the volume of the uterus irradiated with the 150% isodose was higher with BT (22.7% vs. 16.7%, p = 0.05). The dose to the bladder was slightly lower for SBRT but higher to rectum and sigmoid. For bowels and femoral heads, BT resulted in significantly lower doses compared to SBRT. Based on these results, the authors conclude that SBRT with HT is a feasible treatment option and is regarded as a reasonable potential back-up alternative to IC BT for endometrial cancer. In another comparison of HDR-BT and SBRT for inoperable endometrial cancer, doses to normal tissues were higher for SBRT plans .
Dosimetric comparisons for vaginal irradiation have also been published [37,38,39,40, 71, 72]. Aydogan et al.  analysed the dose distributions of IMRT versus HDR-BT in the vagina during postoperative irradiation of patients with early endometrial cancer. Ten patients treated with BT were selected and IMRT plans were generated on the same CT scans. When the dose was prescribed at a 0.5-cm distance from the surface of the cylinder, IMRT resulted in a lower dose to rectum (Dmean: 19.6% vs. 33.5%) and bladder (Dmean: 25.9% vs. 32.5%), with similar target coverage and less inhomogeneity. However, the integral dose was 7.2% higher for IMRT. For most parameters, Yildrim et al.  found very similar results with comparative dosimetry between BT, VMAT and HT for 12 patients, except for bladder D2cm3, which was significantly lower for BT. Recently, a study on irradiation of the vaginal cuff with VMAT and BT in postoperative endometrial cancer was published . Using BT CT scans of 8 patients, two different VMAT plans were generated, and equivalent uniform doses (EUD) were calculated to account for different dose heterogeneities. Dose distributions were more heterogeneous for BT, with a mean EUD for CTV of 136.9% vs. 130% and 111.0% for BT and the two types of VMAT, respectively. Near-maximal doses for rectum and bladder were significantly higher in the BT plans (D0.1 cm3: 131% vs. 112% for rectum and 129% vs. 108% for bladder). However, BT was superior in terms of dose falloff outside the CTV, dose to femoral heads and integral body dose. These results are in very good agreement with the findings of Pedicini et al. . In contrast, Grelewicz et al.  obtained results different from those published before. In their study, using data of only 4 patients, BT plans showed better OAR (bladder, rectum, sigmoid) sparing compared to IMRT and VMAT plans. However, EBRT plans were normalized to achieve the same mean dose for the target volume as in the BT plans.
Head and neck
A comparative dosimetric analysis of target volume and OARs between interstitial HDR-BT and VMAT for localised head and neck cancer was performed at our institute . Thirty-eight patients with tongue, floor of mouth and base of tongue cancer treated with interstitial BT were selected for the analysis. For each patient, a VMAT plan was generated using identical CT data and contours (Fig. 1). The CTV was defined as GTV +5 mm margin limited to mandible. A median of seven catheters (range 3–12) were used in the BT plans and geometrical/graphical optimization was applied without inverse optimization. There was no difference in the target coverage represented by V98 between the two techniques (90.2% vs. 90.4%). In terms of dose to the mandible and spinal cord, BT was the better technique (D0.1 cm3: 77.0% vs. 85.4%, p < 0.05; D2cm3: 48.4% vs. 68.4%, p < 0.05 for mandible; D0.1 cm3: 9.7% vs. 12.3%, p < 0.05 and D2cm3: 9% vs. 10.0%, p < 0.05 for spinal cord for BT and VMAT, respectively). Doses to the parotid salivary glands were generally lower for BT. Six out of ten parameters were significantly lower with BT for both ipsilateral and contralateral glands, for example, D0.1 cm3 (11.2% vs. 18.0%, p < 0.05) and D2cm3 (7.0% vs. 10.5%, p < 0.05) for ipsilateral glands. All parameters for the ipsilateral submandibular glands were lower with BT, but the differences were not significant, whereas for contralateral submandibular glands, all but one parameter was significantly lower with BT. Note that the volumes of the PTVs in this study were exactly the same for both treatment modalities, as there was no additional margin around the CTVs for VMAT planning. However, with EBRT, the target volume is usually larger due to setup errors and patient movement. It follows that if larger PTVs had been used in VMAT plans, the dose to OARs would have been higher, which would have further highlighted the superiority of BT.
In one study, virtual BT plans were created on CT images taken for stereotactic ablative radiotherapy (SABR) of liver metastasis, and the BT and SABR plans were compared dosimetrically . PTV was the same for both planning techniques and the comparison was based on the same target volume coverage (V100 = 94%). The mean dose to the small bowel and right kidney was higher for BT (10.8% vs. 7.1% and 6.7% vs. 4.2%), but mean dose to the stomach was similar. For BT, the mean V150 was 63.6%, indicating a significant dose escalation within the PTV. The dose falloff was steeper for BT, but the difference was not significant. It should be noted that only nine comparative plans were analysed, but the authors concluded that BT could result in a dose escalation to the PTV at similar doses to OARs compared to SABR. Another study by Hass et al.  included 85 patients with primary or secondary liver malignancy. All patients were treated with interstitial BT using an HDR afterloading technique with an Ir-192 source. A virtual SBRT plan was then calculated for each patient using the original BT planning CTs with catheter placement. To create the SBRT PTV, a margin of 5–10 mm was added to the target volume used in BT, resulting in an increase in the mean PTV volume from 34.7 cm3 (BT) to 73.2 cm3 (SBRT). The PD was the same (15 Gy or 20 Gy depending on histology), and the same OAR dose constraints were used for both techniques. With BT, the target coverage was better, especially in the 20-Gy PD group. The mean D99.9, which is effectively the minimum dose in the PTV, was 19.9 Gy in BT and 17.5 Gy in SBRT plans (p < 0.001). D90 was significantly higher in the BT plans (24.3 Gy vs. 16.5 Gy for 15-Gy PD and 29.2 Gy vs. 20.6 Gy for 20-Gy PD) due to a more heterogeneous dose distribution of BT. For BT, the dose to the liver was lower. In the 20-Gy PD group, the mean V5Gy was 611 cm3 in the BT and 694 cm3 in the SBRT plans (p = 0.001). These volumes correspond to 41.8% and 45.9% of the liver volume (p = 0.007), respectively. In the 15-Gy PD group, the same volume parameter was lower in the BT plans, with no statistical difference, but for the whole patient cohort, BT was significantly more favourable. In a recent study, Walter et al.  compared 46 HDR-BT treatment plans with virtually planned SBRT plans. Using EQD2 (equivalent dose in 2-Gy fractions) and clinically relevant doses, BT was found to be superior in sparing normal liver tissues. Target coverage was better, but conformity was worse for BT.
In one study, Milickovic et al.  selected 5 patients with intrathoracic malignancies and compared BT and SBRT treatment plans using identical sets of structures. In the BT plans, the number of catheters ranged between 6 and 10 and an inverse optimization technique was used. In terms of target coverage by the PD, V100 was higher for BT (93% vs. 89%, p = 0.03), but there was no difference between the two modalities for V95 and V90. Conformity was better (COIN: 0.84 vs. 0.79, p = 0,134) and the dose gradient was significantly higher (R50 : 2.47 vs. 4.03, p = 0.002) for BT. The maximum spinal cord dose was 12.8% in BT and 21.1% in SBRT plans (p = 0.022). Differences in the other dosimetric parameters were not significant for OARs, but BT resulted in lower values for three out of five parameters. Chan et al.  performed a dosimetric analysis between HDR-BT and SBRT for primary and metastatic lung lesions. Virtual BT plans were created for 9 patients treated with SBRT using a single catheter. For both techniques, the target volume included the GTV with a 3-mm margin to account for tumour deformation. The mean GTV was 7.2 cm3. Since the most advanced technology of real-time tumour tracking was used for SBRT, there was no difference in PTV volumes (no CTV–PTV margin). Two VMAT planning approaches were used, a margin-based and a robust optimization method. Dose distributions were calculated using the same category of dose calculation algorithms (collapsed cone convolution), with tissue heterogeneity corrections also in BT planning . The PD was 34 Gy and the dose constraints for OARs were based on the RTOG protocol 0915 . In the BT plans, the mean GTV and PTV doses were significantly higher (GTV: 122.2 Gy vs. 50.4 Gy and PTV: 65.1 Gy vs. 43.4 Gy, p < 0.05, respectively) and the R50 dose gradient (volume ratio of 17 Gy to 34 Gy) was better (2.9 vs. 4.3, p < 0.05). The results from the margin-based method for SBRT plans are given below. In the low dose range, the whole lung received a higher dose with BT (V5Gy: 239 cm3 vs. 237.7 cm3), but the trend was reversed at higher doses (V7Gy: 153 cm3 vs. 156 cm3 and V20Gy: 34.7 cm3 vs. 36 cm3). Dose constraints per the RTOG 0915 protocol were achieved for all critical organs except in some cases for the chest wall in BT. However, the overall mean Dmax and D1cm3 were lower in the BT plans (22.6 Gy vs. 25.0 Gy and 15.2 Gy vs. 18.4 Gy, respectively). All other DVH metrics showed no statistical difference between BT and SBRT. Based on their results, the authors conclude that SBRT using an advanced MLC tracking technique and non-coplanar VMAT can achieve dosimetric quality comparable to HDR-BT, and that the high GTV dose in BT may be beneficial for enhanced killing of radioresistant tumour cells.
For localized prostate cancer, BT has been the treatment of choice for decades, including LDR seed implantation and HDR monotherapy, as well as for a boost following or during teletherapy. But various EBRT techniques are also available and have excellent results in clinical applications. In an early study, HDR-BT dose distributions for prostate cancer were approximated by CK with very similar dosimetry but using identical PTVs for both techniques . HDR-BT plans were also compared with step-and-shoot IMRT and HT . At the same target coverage (V95 = 100%), the rectum received the lowest dose with BT (Dmean: 3.9 Gy vs. 6.6 Gy in IMRT and 5.6 Gy in HT). The bladder was also better spared by BT, and V10% for normal tissue was more than eight times lower with BT than with IMRT or HT. In another early study, treatment plans of HDR-BT and IMRT for localised prostate cancer were compared using two separate patient cohorts . In the BT plans, rectum and bladder received lower doses with very similar target coverage. Sudahar et al.  investigated the similarity between the dose distributions of CK and HDR-BT. Using equivalent doses, they found similar peripheral target doses between the two treatment techniques, but higher doses within the PTV and a steeper dose gradient in BT plans. Spratt et al.  performed a dosimetric analysis with 5 patients, creating virtual SBRT plans and attempting to reproduce the HDR dose distributions. In the SBRT plans, PTVs were created from 100% isodose lines of the BT plans. This resulted in very similar target coverage, but BT was better in most rectal and bladder parameters. Intraprostatic doses were much higher in the BT plans, and these could not be achieved with SBRT even when direct violations of OAR dose constraints were allowed. A group in Vienna performed a dosimetric comparison between BT (LDR, HDR) and EBRT (VMAT, proton, carbon ion) techniques with particular emphasis on the dose to OARs . For each of 10 patients with localized prostate cancer, five individually optimized treatment plans were generated using the same contours. The dose distributions were converted to a radiobiologically identical fractionation. Although EBRT techniques represented the most advanced intensity-modulated treatment options with photons (VMAT), scanned protons (IMPT) and carbon ion (IMIT), BT techniques were clearly superior, especially in terms of dose to the bladder wall, rectal wall and normal tissues, with the lowest values. The Dmean for rectal wall was 10.5 Gy for HDR-BT and 28.2 Gy for VMAT, and in between for the other techniques. The V50 in cm3 was 1.5, 4.1, 7.2, 7.0 and 4.7 for HDR-BT, LDR-BT, VMAT, IMPT and IMIT, respectively. In the same order, the V50 for bladder wall was 0.6, 2.8, 5.5, 5.3 and 3.2 cm3, respectively. For the five techniques, the volumes of normal tissues that received 30% of the PD were 42, 120, 487, 198 and 253 cm3. The Dmean for urethra was lowest for HDR-BT (62.9 Gy) and highest with LDR-BT (106.6 Gy). The BT techniques resulted in negligible doses to femoral heads (Dmean < 2 Gy), while the EBRT techniques resulted in a Dmean of nearly 20 Gy on both sides. In another study by Fukuda et al. , when HDR-BT monotherapy plans were simulated with SBRT using common CT images and contour datasets (except PTV), SBRT was found to be significantly superior in almost all dosimetric parameters of the bladder and urethra. In the BT plans, however, rectum was significantly better spared.
Dosimetry of boosting of the dominant intraprostatic lesions (DIL) with VMAT, intensity-modulated proton therapy (IMPT) and HDR-BT was investigated by Andrzejewski et al. , and HDR-BT was found to be superior to VMAT and IMPT in terms of OAR sparing and DIL boosting. For example, the equivalent uniform dose (EUD) was 49.4 Gy, 47.9 Gy and 28.1 Gy for bladder, 53.3 Gy, 50.5 Gy and 35.1 Gy for rectum and 88.3 Gy, 86.6 Gy and 62.4 Gy for urethra in the order of VMAT, IMPT and HDR-BT, respectively. In a study by Eade et al. , stereotactic radiation therapy boost for prostate cancer was used to mimic the HDR-BT boost, and the SBRT dose distribution was found to be similar to BT. For the intraprostatic urethra, D10 was higher, but for bladder and rectum, the D1cm3 was lower with BT. Sannamed et al.  used single-fraction HDR-BT or integrated VMAT boost for tumour-targeted dose escalation in localized prostate cancer, treating 40 patients with both techniques. Dosimetry was compared using equivalent dose levels in 2‑Gy fractions (EQD2). Doses to OARs were comparable, but both rectal and bladder walls and urethra received lower doses with BT. Furthermore, mean and maximal target doses were higher with BT (p < 0.05). Due to its dosimetric characteristics, the authors consider HDR boost as the best technique to deliver boost dose to the GTV located near critical structures. In a recent study, Chatzikonstantinou et al.  compared CK SBRT plans with virtual HDR-BT plans based on the same 15 patients. The BT plans were ultrasound based and the PTV was equal to the prostate gland without margins. For a direct comparison of DVH values, a hypothetical single-fraction 35 Gy was used in the BT plans. In the SBRT plans, anisotropic margins of 3–5 mm around the GTV were used to create the PTV and a dose of 35 Gy was delivered in five fractions. Dose coverage of the GTV by the PD was higher in the SBRT plans (99.98% vs. 90.07%), but intraprostatic high-dose volumes were larger in BT the plans. The maximum rectal and bladder doses were significantly lower with BT (30.3 Gy vs. 36.4 Gy, p < 0.0001 and 32.7 Gy vs. 37.4 Gy, p = 0.0004, respectively). However, in terms of urethral dose, HDR-BT was worse, with a maximum dose of 45.6 Gy compared to 40.8 Gy (p < 0.0001) for SBRT. From these results, the authors conclude the superiority of HDR-BT for rectal and bladder dosimetry. Fröhlich et al.  performed a comparison of two BT (LDR and HDR) and two EBRT (VMAT, CK) techniques using the CT images sets of 10 patients treated with CK. EQD2 doses were calculated and compared. The EBRT plans were more conformal than the BT plans, with D2cm3 for the rectum and bladder being lowest in HDR-BT (36 Gy and 51.4 Gy), while D0.1 cm3 for the urethra was lowest (79.9 Gy) in VMAT. The hips and sigmoid were best protected by HDR-BT. In a feasibility study, Willigenburg et al.  created comparative SBRT treatment plans on an MR-linac system for 30 patients treated with focal salvage HDR-BT. Since intrafractional prostate motion detection and online replanning is available with the MR-linac, only a 1-mm CTV–PTV margin was used in the SBRT plans. The target coverage was very similar, but the urethra and rectum received a significantly lower dose with BT. At a PD of 19 Gy, the median D10% was 16.0 Gy vs. 17.5 Gy (p < 0.001) for the urethra, and D2cm3 was 8.6 Gy vs. 10.7 Gy (p < 0.001) for the rectum in the BT and SBRT plans, respectively.
Six studies have been published on the dosimetric comparison of surface mould HDR-BT and VMAT for the treatment of skin lesions on the scalp and the extremities [62,63,64,65,66,67]. Boman et al.  used four and three plans of patients treated with HDR-BT surface mould on the scalp and lower leg, respectively, and retrospectively created VMAT plans with the PTV created on the CTV of BT plans with an additional 3‑mm setup margin. For scalp cases, the conformity was always better for VMAT, D95 for CTV was similar and the mean CTV dose was higher for BT. The mean dose to brain was higher with BT and D0.1 cm3 was very similar. Similar observations were found for the leg cases, except for the D0.1 cm3 of normal tissue, which was lower for BT. In a recent study, Wills et al.  compared the plan quality of HDR-BT and VMAT for superficial treatment of skin on the scalp and lower limbs with significant curvature. BT plans were retrospectively re-planned for VMAT using identical CT data and CTV/OARs. The conformity index was significantly higher for VMAT. The CTV and PTV coverage by 95% of PD was similar in all cases. In scalp cases, the optic system and the lenses generally received a lower dose in VMAT, similarly to the brain. With BT, small volumes of normal tissue received high doses were similar to or higher than with VMAT, and the maximum dose to the skin surface was higher with BT. Using a relatively large cohort of 37 patients, Buzurovic et al.  dosimetrically compared HDR-BT and electron irradiation used for skin lesions of different sizes in various body sites. The quality of the plans was highly dependent on the geometry of the target, including size, curvature and topology. For the two techniques, target D2cm3 values were comparable, but doses to smaller volumes (0.5 cm3, 0.1 cm3) were higher with BT. For complex targets, BT provided excellent target coverage, as the dose could be adjusted to irregular surfaces using flexible flap applicators. There were complex cases where only BT provided clinically acceptable plans. For smaller, flat targets, electron beams provided plans similar to BT, with better dose homogeneity.
Dose calculation algorithms
The dose calculation algorithm is not always reported in publications. In most cases, only the name of the planning system is mentioned, especially for EBRT. In ten studies, neither the calculation algorithm nor the planning system was given. In nine cases the algorithm (collapsed cone, AAA, Monte Carlo) and in the other cases only the name of the planning system was given. As for BT, the TG-43 formalism was used in all but six studies. In four papers, no information on the method of dose calculation was provided and more advanced model-based dose calculation algorithms (MBDCA) were used only in two studies [45, 63]. Chan et al.  calculated BT dose distributions in the lung using the Advanced Collapsed Cone Engine (ACE; Elekta Brachytherapy, Veenendaal, the Netherlands). Boman et al.  used the Acuros BV (Varian, Palo Alto, CA, USA) and the TG-43 algorithm for dosimetric calculation in surface mould HDR-BT. They compared the dosimetric parameters calculated by both algorithms. CTV coverage (D95) was decreased by more than 13% for scalp cases and by at least 5.8% for lower leg cases when Acuros BV was compared with TG-43 plans. A 1-cm bolus (as a backscatter material) reduced the difference by 3% and 2% for the scalp and lower leg cases, respectively. Near maximum doses were higher for TG-43 (by 9.1% for scalp and by 4.8% for lower leg).