- Open Access
MRI and CT imaging for preoperative target volume delineation in breast-conserving therapy
Radiation Oncologyvolume 9, Article number: 63 (2014)
Accurate tumor bed delineation after breast-conserving surgery is important. However, consistency among observers on standard postoperative radiotherapy planning CT is low and volumes can be large due to seroma formation. A preoperative delineation of the tumor might be more consistent. Therefore, the purpose of this study was to determine the consistency of preoperative target volume delineation on CT and MRI for breast-conserving radiotherapy.
Tumors were delineated on preoperative contrast-enhanced (CE) CT and newly developed 3D CE-MR images, by four breast radiation oncologists. Clinical target volumes (CTVs) were created by addition of a 1.5 cm margin around the tumor, excluding skin and chest wall. Consistency in target volume delineation was expressed by the interobserver variability. Therefore, the conformity index (CI), center of mass distance (dCOM) and volumes were calculated. Tumor characteristics on CT and MRI were scored by an experienced breast radiologist.
Preoperative tumor delineation resulted in a high interobserver agreement with a high median CI for the CTV, for both CT (0.80) and MRI (0.84). The tumor was missed on CT in 2/14 patients (14%). Leaving these 2 patients out of the analysis, CI was higher on MRI compared to CT for the GTV (p < 0.001) while not for the CTV (CT (0.82) versus MRI (0.84), p = 0.123). The dCOM did not differ between CT and MRI. The median CTV was 48 cm3 (range 28–137 cm3) on CT and 59 cm3 (range 30–153 cm3) on MRI (p < 0.001). Tumor shapes and margins were rated as more irregular and spiculated on CE-MRI.
This study showed that preoperative target volume delineation resulted in small target volumes with a high consistency among observers. MRI appeared to be necessary for tumor detection and the visualization of irregularities and spiculations. Regarding the tumor delineation itself, no clinically relevant differences in interobserver variability were observed. These results will be used to study the potential for future MRI-guided and neoadjuvant radiotherapy.
International Clinical Trials Registry Platform NTR3198.
The standard treatment of early-stage breast cancer is lumpectomy, or wide local excision, followed by whole breast irradiation with an additional boost dose to the tumor bed (TB) in patients with a higher risk of local recurrence [1, 2]. Since most local recurrences occur in or nearby the TB, several accelerated partial breast irradiation (APBI) studies are ongoing in early-stage breast cancer patients. APBI targets the breast tissue immediately surrounding the TB. The advantages of APBI are a shorter overall treatment time and a potential dose reduction in the normal tissues (i.e. breast, heart and lung) compared to whole breast irradiation . Accurate TB delineation on the radiotherapy planning CT scan after lumpectomy is important for both TB boost irradiation and APBI. However, in radiotherapy practice, there is no gold standard to validate the accuracy of our target volume delineation after lumpectomy. As an alternative, consensus among observers is often used to assess the precision of our target volume delineation. The degree of consensus is generally called the interobserver variability (IOV), and quantified by a conformity index (CI) which is the volume of agreement among observers divided by the total encompassing volume. The current CT guided delineation after lumpectomy is prone to a high IOV. Several studies showed a low CI and a large distance between the centers of mass (dCOM) among observers [4–13].
Besides the high IOV in the current postoperative radiotherapy setting, there is also the concern of large postoperative treatment volumes due to seroma and hematoma formation. Irradiation of these disproportionally large target volumes can lead to extended subcutaneous fibrosis, poor cosmetic results and even missing the target [14–17]. Furthermore, these large volumes can cause low-risk patients aiming for APBI to be ineligible for this treatment due to the inability to meet the dose-volume constraints [18, 19].
The poor consistency in target volume definition and large volumes after lumpectomy might be avoided by irradiating the tumor preoperatively. Since the tumor is still in situ without any seroma formation, this would probably lead to a high delineation precision and small treatment volumes. Several groups are studying the potential for neoadjuvant irradiation in early stage breast cancer patients [18, 20, 21]. In these studies, IOV and normal tissue dose were reduced, which shows that neoadjuvant irradiation could result in more precise target volume definition and localization and smaller volumes [20–22]. Furthermore, Bondiau et al. reported the feasibility of a neoadjuvant stereotactic body irradiation in combination with neoadjuvant chemotherapy in locally advanced breast cancer patients .
Alternatively, preoperative imaging in radiotherapy supine position might also have potential value to improve the standard post-lumpectomy TB delineation, since it provides additional information about the original tumor location .
To correctly delineate the tumor, imaging quality is of great importance. Since it is unknown what the optimal imaging modality for preoperative target volume delineation is, delineation was studied on both contrast-enhanced (CE) CT and MRI. In daily clinical practice, CT is the standard imaging modality for target volume delineation in breast cancer patients. However, MRI has a superior soft tissue contrast which can be explored with different sequences to show endogenous contrast or the distribution of an administered contrast agent. This enables differentiation between the tumor and benign lesions like post-biopsy hematomas or cysts. Furthermore, MRI has a high sensitivity for detection of invasive breast cancer and a good correlation with histopathology findings [24, 25]. However, standard diagnostic MRI is performed in prone position, while patients in most departments are irradiated in supine position. Acquiring images in supine radiotherapy position is generally limited by narrow bore sizes of standard MRI scanners. Therefore a new MRI protocol was designed in a wide bore MRI scanner.
The purpose of this study was to quantify the consistency of preoperative target volume delineation for breast-conserving radiotherapy. To identify the best imaging modality for preoperative target volume delineation, preoperative delineation was performed on both CE-CT and a newly developed 3D CE-MRI in supine radiotherapy position.
Patients and selection
The study was approved by our institutional review board and registered in the International Clinical Trials Registry Platform (NTR3198). Fourteen early-staged breast cancer patients, scheduled for lumpectomy at the University Medical Center Utrecht or St. Antonius hospital, were included in this study. All patients gave written informed consent. Patients eligible for inclusion had a clinical T1-T2, N0 staged adenocarcinoma of the breast and were scheduled for lumpectomy and sentinel node procedure. Patients with lobular carcinoma, a history of ipsilateral breast surgery, contra-indications for 1.5 Tesla MRI, iodine allergy, and patients who received neoadjuvant treatment were not eligible. In case of additional suspected findings on study MRI or CT imaging, patients were referred to their physician for additional diagnostic work-up.
Patient positioning and image acquisition
Patients underwent both CT and MRI in radiotherapy supine position prior to surgery. On CT, they were positioned with arms in abduction and hands above the head at 10° inclination and with the use of a knee support (C-Qual, CIVCO medical solutions, Reeuwijk, The Netherlands). If palpable, the tumor was marked on the skin with a CT/MRI compatible wire. CE-CT images were obtained at 3 mm slice thickness and a minimal in-plane resolution of 1 × 1 mm2 (Brilliance, Philips Medical Systems, Best, The Netherlands), with a delay time of 120 s after intravenous contrast agent injection (Ultravist, 80 ml, 3 ml/s) . Delay time was shortened to 80s after the 6th patient according to Kuroki-Suzuki et al. in attempt to improve tumor enhancement .
For MRI, patients were positioned on an MRI compatible 10° wedge board (Thorawedge, CIVCO medical solutions, Reeuwijk, The Netherlands). To acquire MR images, an anterior receive coil was used. To prevent breast deformation by the anterior receive coil, a polymethyl methacrylate (PMMA) support was designed, which is adjustable to patient habitus and breast size. MRI patient setup is shown in Figure 1. The bore of a standard MRI scanner is too narrow to acquire images in this position. Therefore, we used a wide bore (70 cm) MRI scanner (Ingenia 1.5 T, Philips Medical Systems, Best, The Netherlands). The following 3D high resolution images were acquired: T1 weighted (T1w) fast field echo (FFE) ± fat suppression (Dixon), T2 weighted (T2w) turbo spin echo (TSE) + fat suppression, and a dynamic series of contrast-enhanced T1w images ± fat suppression after contrast agent administration. For T1w Dixon FFE MRI, acquired 3D resolution was 0.99 × 1.05 × 2.19 mm3 reconstructed to 0.95 × 0.95 × 1.1 mm3 using overcontiguous slices and for T2w TSE MRI, the voxels measured 0.78 × 0.78 × 1.2 mm3 acquired with a resolution of 1.25 × 1.32 × 2.41 mm3. In the dynamic T1w series, the first 3D image was acquired before and 6 images after intravenous contrast injection (Gadobutrol (Gadovist, Bayer), 0.1 mmol/kg, 1 ml/s), at 60s intervals with an acquired resolution of 1.20 × 1.21 × 2.41 mm3 reconstructed to 1.16 × 1.16 × 1.2 mm3 using overcontiguous slices. The total acquisition time of this protocol was 21 minutes. Small displacements between sequences during image acquisition caused by patient motion were corrected for by using a rigid mutual information registration on a box around the tumor. No breast deformation by the anterior receive coil was observed.
To quantify differences in tumor visualization on CT and MRI, the shape (1–round, 2–oval, 3–lobular, 4–irregular) and margin (1–smooth, 2–irregular, or 3–spiculated) of the tumor were rated by an experienced breast radiologist .
Target volume delineation
Four experienced breast radiation oncologists independently delineated the GTV on both CT and MRI data, with at least a 4-week interval between delineation sessions, using an in-house developed software tool (Volumetool) . Written delineation instructions were formulated in a consensus meeting with all observers, supervised by an experienced breast radiologist. MRI delineations were performed on preoperative 3D CE T1w images with an individually prescribed fixed window and level as determined by an experienced breast radiologist. Observers were allowed to consult other sequences, which were registered to the CE-MRI series to differentiate between structures, i.e. tumor (gadolinium uptake causes a high signal on CE T1w images), post-biopsy hematoma (blood causes a high signal on both CE and non-CE T1w images), and cysts (fluid causes a high signal on T2w images). Clinical target volumes (CTVs) were created by adding a 1.5 cm margin around the GTV, restricted by the chest wall and a 5 mm margin beneath the skin surface. Delineation of a preoperative GTV different from the tumor location as confirmed during histopathological examination of the lumpectomy specimen (gold standard) was considered as ‘misdelineation’.
The conformity index (CI) and distance between the centers of mass (dCOM) for both the GTV and CTV contours as delineated by the 4 observers were calculated for all possible observer pairs. The CI per observer pair was calculated by using the following formula: . Consequently, CI = 1 implies a perfect agreement among observers, while CI = 0 means there is no overlap. For dCOM, a value of 0 means that two delineations are centered at the same position.
Median values and accompanying ranges were used to describe the data since not all variables were normally distributed. A Wilcoxon signed-rank test was performed to compare paired variables using IBM SPSS Statistics 20 (Chicago, IL, USA) with a significance level of α = 0.05.
Patient and tumor characteristics are shown in Table 1. Median age was 61 years (range 48–70). Median clinical tumor diameter (as measured on diagnostic ultrasound/MRI) was 15 mm (range 7–30 mm), and median microscopic tumor diameter (as measured by histopathological examination) was 12 mm (range 6–29 mm). On CE-MRI, tumor margins were scored more spiculated compared to CE-CT (Table 1, Figure 2). Tumor shape was mainly scored as an irregular mass on CE-MRI and as a lobular mass on CE-CT.
Interobserver variability and volumes
In Figure 3a and 3b, GTV delineations of the 4 observers are shown on both preoperative CE-CT and CE-MRI in one patient. To illustrate the comparison with the current standard CT delineations after lumpectomy, postoperative delineations of this patient are shown in Figure 3c as a clinical example.
Preoperative tumor delineation resulted in a high median CI of the CTV, for both CT (0.80) and MRI (0.84)). However, the tumor was missed on CT in 2/14 patients (14%). This resulted in wide ranges in CI on CT (range 0.00-0.93 for the CTV) compared to MRI (range 0.47-0.93). The first patient in which misdelineation occurred was a patient with multiple macrocalcifications in the breast, as seen on mammography. On CE-MRI all 4 observers contoured the tumor. On CE-CT a benign lesion was contoured by 3 observers, resulting in a CI ranging from 0.00 to 0.52. The second patient had a tumor centrally located in the breast. On CE-MRI all observers contoured the tumor, while on CE-CT one observer contoured dense fibroglandular tissue resulting in a range in CI of 0.00-0.59. Outcomes of the analysis including misdelineations are provided as Additional file 1.
To only focus on differences in contouring the actual tumor, and not on tumor detection, the 2 misdelineations were excluded from further IOV and volume analysis. Results of this analysis are shown in Table 2. The CI for the GTV was significantly higher on MRI (p < 0.001) compared to CT. No difference in CI for the CTV was found (p = 0.123). Delineated volumes were significantly larger on MRI for both the GTV and CTV (both p < 0.001). There was no difference in dCOM between CT and MRI for both the GTV and CTV.
To our knowledge, this is the first study in which the feasibility of 3D CE-MRI of patients in radiotherapy supine position using a wide bore MRI scanner has been demonstrated. Different sequences of high resolution 3D CE and non-CE images were acquired with isotropic voxel sizes ≤ 1.2 mm.
In the present study, target volume delineation before lumpectomy resulted in a high agreement and small treatment volumes among observers compared to standard postoperative TB delineation as reported in literature (Table 3).
Since the optimal imaging modality for preoperative target volume delineation was unknown, delineation was studied on both CT and MRI. MRI appeared to be essential for tumor detection. For tumor delineation itself, the CI of the GTV was significantly higher on MRI and ranges on CT were wider. However, median differences were small (0.05) and may not be considered clinically relevant. For the CTV, no significant difference was found, since interobserver differences are blurred when expanding structures while uniformly excluding the skin and chest wall. However, more tumor spiculations and irregularities were observed on MRI due to its high spatial resolution (Table 1, Figure 2). This did not appear to result in a decreased GTV conformity on MRI compared to CT.
The more irregular and spiculated tumor visualization on CE-MRI might have caused the significantly larger target volumes on MRI. Thin branches in the cranio-caudal or medio-lateral direction caused a relatively large volume expansion when applying a CTV margin. Even though large volumes can lead to increased toxicity and worse cosmesis, these effects do not outweigh the chances of not including peripheral tumor branches in the target volume, especially in APBI. However, despite the high level of consensus among observers, we acknowledge that no definitive statements can be made about the accuracy of the delineations, with the lack of pathologic validation of these branches as the gold standard. A pathology study must validate whether these branches are actual tumoral extensions or rather fibrotic strands or interstitial reactions, before standard inclusion of these branches in the preoperative GTV. With the implementation of high resolution imaging, the strict boundary between the GTV and the CTV with its microscopic spread might be fading. The appropriate preoperative CTV margin on MRI is therefore subject to debate and will also be further refined according to the future information about the appearance of local recurrences in the breast in the APBI studies .
In the last decade, several other attempts have been made to improve the current postoperative target volume delineation (Table 3b and c). Delineation on postoperative MRI resulted in contradicting results [8, 9]. Jolicoeur et al. found an improved IOV and smaller volumes, while Giezen et al. found similar volumes with a degraded IOV. In two other studies, IOV was assessed on postoperative CT while preoperative CE-CT images in the same treatment position were provided [11, 12]. This resulted in an improved IOV in one of these studies. Preoperative delineation was studied on CE-CT by Boersma et al., resulting in a low IOV, which was in line with our study findings (Table 3d) .
Our reported findings on preoperative MRI-guided delineation resulted in high and stable conformity among observers (Table 3e). Furthermore, our preoperatively delineated GTVs were considerably smaller compared to postoperative volumes reported in literature (Table 3a). CTVs were larger, although preoperative volumes would have less outliers since there is no seroma formation. The larger CTVs in our study were caused by a uniform 1.5 cm volume expansion, while the postoperative results in Table 3a reflect ‘boost’ volumes, in which the microscopic resection margin is often subtracted from this margin. PTVs were not compared in this study, since PTV margins are institution-dependent due to the method of position verification being practiced. These PTV margins might even be changed or improved in a preoperative setting, due to less volume distortions. Overall, the high CI in combination with the small and stable volumes in this study, imply that a future neoadjuvant irradiation would be more accurate and lead to less toxicity.
When comparing our results to published data in Table 3, we have to be aware of the different methods used in the other studies. For instance, the method of CI calculation, observer backgrounds and multi-centricity of a study can influence the observed results regarding IOV . Interobserver studies often use small patient groups due to the high workload (Table 3). Furthermore, it has to be noted that the CI is volume dependent. The smaller the volume being studied, the more the CI is influenced by small interobserver differences. This especially accounts for our small preoperative GTVs, but also emphasizes that when comparing different studies, the studied volume (i.e. GTV, TB, CTV or PTV) must be taken into account.
Can we, from the results of this study, conclude that MRI superior to CT for preoperative tumor delineation? In this study, MRI was essential for tumor detection. However, alternatives for tumor detection can be considered, e.g. optimizing CT parameters like contrast-enhancement of the tumor, or clearly marking the tumor by fiducials. This might be easier to implement, less time consuming and less expensive. When using preoperative imaging for a preoperative irradiation or ablative interventional technique, treating another area but the GTV would be unacceptable. Furthermore, more detail could be visualized by MRI, which could contribute to an accurate target definition. Therefore, in our future studies, CE-MRI in radiotherapy supine position will be used in addition to CT, as CT is required for treatment planning. In our institute, an MRI linear accelerator is being developed in collaboration with Philips Medical Systems (Best, The Netherlands) and Elekta (Stockholm, Sweden) . This system can provide online tumor tracking using MRI during radiotherapy, which makes it possible to adapt the plan to the actual tumor position. The results of our study show that a preoperative irradiation of breast tumors could be beneficial in terms of delineation consistency and treatment volumes. There would be more certainty that the correct target is delineated when the tumor is in situ. Moreover, preoperative target volumes would probably be more stable in the absence of seroma formation, and not being subject to seroma shrinkage [17, 31]. The advantages of preoperative CE-MRI for treatment planning will be further studied with respect to the dosimetric consequences . CE-MRI in supine position could also be used for other purposes. For instance, it might provide additional information to improve the consistency in target volume definition in standard postoperative CT-guided delineation . Furthermore, it might aid tumor localization for breast conserving surgery or interventional procedures .
In conclusion, preoperative target volume delineation resulted in small treatment volumes with a high consistency among observers. MRI appeared to be necessary for tumor detection and the visualization of irregularities and spiculations. Regarding delineation of the tumor itself, no clinically relevant differences in interobserver variability among imaging modalities were observed. These results will be used to study the potential for a future MRI-guided and neoadjuvant radiotherapy.
Clinical target volume
Distance between centers of mass
Fast field echo
Gross tumor volume
Magnetic resonance imaging
Planning target volume
T1 weighted MRI sequence
T2 weighted MRI sequence
Turbo spin echo.
Darby S, McGale P, Correa C, Taylor C, Arriagada R, Clarke M, Cutter D, Davies C, Ewertz M, Godwin J, Gray R, Pierce L, Whelan T, Wang Y, Peto R, Early Breast Cancer Trialists’ Collaborative Group (EBCTCG): Effect of radiotherapy after breast-conserving surgery on 10-year recurrence and 15-year breast cancer death: meta-analysis of individual patient data for 10,801 women in 17 randomised trials. Lancet 2011, 378: 1707-1716.
Bartelink H, Horiot JC, Poortmans PM, Struikmans H, Van den Bogaert W, Fourquet A, Jager JJ, Hoogenraad WJ, Oei SB, Warlam-Rodenhuis CC, Pierart M, Collette L: Impact of a higher radiation dose on local control and survival in breast-conserving therapy of early breast cancer: 10-year results of the randomized boost versus no boost EORTC 22881–10882 trial. J Clin Oncol 2007, 25: 3259-3265. 10.1200/JCO.2007.11.4991
Theberge V, Whelan T, Shaitelman SF, Vicini FA: Altered fractionation: rationale and justification for whole and partial breast hypofractionated radiotherapy. Semin Radiat Oncol 2011, 21: 55-65. 10.1016/j.semradonc.2010.08.007
Struikmans H, Warlam-Rodenhuis C, Stam T, Stapper G, Tersteeg RJ, Bol GH, Raaijmakers CP: Interobserver variability of clinical target volume delineation of glandular breast tissue and of boost volume in tangential breast irradiation. Radiother Oncol 2005, 76: 293-299. 10.1016/j.radonc.2005.03.029
Petersen RP, Truong PT, Kader HA, Berthelet E, Lee JC, Hilts ML, Kader AS, Beckham WA, Olivotto IA: Target volume delineation for partial breast radiotherapy planning: clinical characteristics associated with low interobserver concordance. Int J Radiat Oncol Biol Phys 2007, 69: 41-48. 10.1016/j.ijrobp.2007.01.070
Hurkmans C, Admiraal M, van der Sangen M, Dijkmans I: Significance of breast boost volume changes during radiotherapy in relation to current clinical interobserver variations. Radiother Oncol 2009, 90: 60-65. 10.1016/j.radonc.2007.12.001
Coles CE, Wilson CB, Cumming J, Benson JR, Forouhi P, Wilkinson JS, Jena R, Wishart GC: Titanium clip placement to allow accurate tumour bed localisation following breast conserving surgery: audit on behalf of the IMPORT Trial Management Group. Eur J Surg Oncol 2009, 35: 578-582. 10.1016/j.ejso.2008.09.005
Jolicoeur M, Racine ML, Trop I, Hathout L, Nguyen D, Derashodian T, David S: Localization of the surgical bed using supine magnetic resonance and computed tomography scan fusion for planification of breast interstitial brachytherapy. Radiother Oncol 2011, 100: 480-484. 10.1016/j.radonc.2011.08.024
Giezen M, Kouwenhoven E, Scholten AN, Coerkamp EG, Heijenbrok M, Jansen WP, Mast ME, Petoukhova AL, Struikmans H: MRI- versus CT-based volume delineation of lumpectomy cavity in supine position in breast-conserving therapy: an exploratory study. Int J Radiat Oncol Biol Phys 2012, 82: 1332-1340. 10.1016/j.ijrobp.2011.05.008
van Mourik AM, Elkhuizen PH, Minkema D, Duppen JC, van Vliet-Vroegindeweij C, Dutch Young Boost Study Group: Multiinstitutional study on target volume delineation variation in breast radiotherapy in the presence of guidelines. Radiother Oncol 2010, 94: 286-291. 10.1016/j.radonc.2010.01.009
Boersma LJ, Janssen T, Elkhuizen PH, Poortmans P, van der Sangen M, Scholten AN, Hanbeukers B, Duppen JC, Hurkmans C, van Vliet C: Reducing interobserver variation of boost-CTV delineation in breast conserving radiation therapy using a pre-operative CT and delineation guidelines. Radiother Oncol 2012, 103: 178-182. 10.1016/j.radonc.2011.12.021
van den Assem MB, Visser J, Zonderland HM, van Tienhoven G, Crama KF, Bijker N: 459 pre-operative CT scan in breast conserving therapy for determination of the boost volume for radiotherapy. Eur J Cancer 2012,48(Supplement 1):S180-S181.
Landis DM, Luo W, Song J, Bellon JR, Punglia RS, Wong JS, Killoran JH, Gelman R, Harris JR: Variability among breast radiation oncologists in delineation of the postsurgical lumpectomy cavity. Int J Radiat Oncol Biol Phys 2007, 67: 1299-1308. 10.1016/j.ijrobp.2006.11.026
Vrieling C, Collette L, Fourquet A, Hoogenraad WJ, Horiot JH, Jager JJ, Pierart M, Poortmans PM, Struikmans H, Maat B, Van Limbergen E, Bartelink H: The influence of patient, tumor and treatment factors on the cosmetic results after breast-conserving therapy in the EORTC ‘boost vs. no boost’ trial. EORTC Radiotherapy and Breast Cancer Cooperative Groups. Radiother Oncol 2000, 55: 219-232. 10.1016/S0167-8140(00)00210-3
Collette S, Collette L, Budiharto T, Horiot JC, Poortmans PM, Struikmans H, Van den Bogaert W, Fourquet A, Jager JJ, Hoogenraad W, Mueller RP, Kurtz J, Morgan DA, Dubois JB, Salamon E, Mirimanoff R, Bolla M, Van der Hulst M, Warlam-Rodenhuis CC, Bartelink H, EORTC Radiation Oncology Group: Predictors of the risk of fibrosis at 10 years after breast conserving therapy for early breast cancer: a study based on the EORTC Trial 22881–10882 ‘boost versus no boost’. Eur J Cancer 2008, 44: 2587-2599. 10.1016/j.ejca.2008.07.032
Benda RK, Yasuda G, Sethi A, Gabram SG, Hinerman RW, Mendenhall NP: Breast boost: are we missing the target? Cancer 2003, 97: 905-909. 10.1002/cncr.11142
den Hartogh MD, van Asselen B, Monninkhof EM, van den Bosch MA, van Vulpen M, van Diest PJ, Gilhuijs KG, Witkamp AJ, van de Bunt L, Mali WP, van den Bongard HJ: Excised and irradiated volumes in relation to the tumor size in breast-conserving therapy. Breast Cancer Res Treat 2011, 129: 857-865. 10.1007/s10549-011-1696-7
Nichols EM, Feigenberg SJ, Marter K, Cheston SB, Lasio G, Tkaczuk K, Kesmodel S, Buras R, Regine WF: Preoperative radiation therapy significantly increases patient eligibility for accelerated partial breast irradiation using 3D-conformal radiotherapy. Am J Clin Oncol 2012, 36: 232-238.
Pignol JP, Rakovitch E, Keller BM, Sankreacha R, Chartier C: Tolerance and acceptance results of a palladium-103 permanent breast seed implant phase I/II study. Int J Radiat Oncol Biol Phys 2009, 73: 1482-1488. 10.1016/j.ijrobp.2008.06.1945
van der Leij F, Elkhuizen PHM, Janssen TM, Poortmans P, van der Sangen M, Scholten AN, van Vliet-Vroegindeweij C, Boersma LJ: External beam partial breast irradiation: difference in pre- and postoperative target volume delineation. Radiother Oncol 2012,103(Supplement 1):S246.
Palta M, Yoo S, Adamson JD, Prosnitz LR, Horton JK: Preoperative single fraction partial breast radiotherapy for early-stage breast cancer. Int J Radiat Oncol Biol Phys 2012, 82: 37-42. 10.1016/j.ijrobp.2010.09.041
Kim L, Shaitelman S: What is the target volume for preoperative accelerated partial breast irradiation (APBI)? In regards to Nichols et al. (Int J Radiat Oncol Biol Phys 2010;77:197–202) and Palta et al. (Int J Radiat Oncol Biol Phys 2010, in Press). Int J Radiat Oncol Biol Phys 2011, 80: 314-315. author reply 315–316
Bondiau PY, Courdi A, Bahadoran P, Chamorey E, Queille-Roussel C, Lallement M, Birtwisle-Peyrottes I, Chapellier C, Pacquelet-Cheli S, Ferrero JM: Phase 1 clinical trial of stereotactic body radiation therapy concomitant with neoadjuvant chemotherapy for breast cancer. Int J Radiat Oncol Biol Phys 2013, 85: 1193-1199. 10.1016/j.ijrobp.2012.10.034
Schmitz AC, van den Bosch MA, Loo CE, Mali WP, Bartelink H, Gertenbach M, Holland R, Peterse JL, Rutgers EJ, Gilhuijs KG: Precise correlation between MRI and histopathology - exploring treatment margins for MRI-guided localized breast cancer therapy. Radiother Oncol 2010, 97: 225-232. 10.1016/j.radonc.2010.07.025
Peters NH, Borel Rinkes IH, Zuithoff NP, Mali WP, Moons KG, Peeters PH: Meta-analysis of MR imaging in the diagnosis of breast lesions. Radiology 2008, 246: 116-124. 10.1148/radiol.2461061298
Kuroki-Suzuki S, Kuroki Y, Ishikawa T, Takeo H, Moriyama N: Diagnosis of breast cancer with multidetector computed tomography: analysis of optimal delay time after contrast media injection. Clin Imaging 2010, 34: 14-19. 10.1016/j.clinimag.2009.03.004
Ikeda DM, Hylton NM, Kinkel K, Hochman MG, Kuhl CK, Kaiser WA, Weinreb JC, Smazal SF, Degani H, Viehweg P, Barclay J, Schnall MD: Development, standardization, and testing of a lexicon for reporting contrast-enhanced breast magnetic resonance imaging studies. J Magn Reson Imaging 2001, 13: 889-895. 10.1002/jmri.1127
Bol GH, Kotte AN, van der Heide UA, Lagendijk JJ: Simultaneous multi-modality ROI delineation in clinical practice. Comput Methods Programs Biomed 2009, 96: 133-140. 10.1016/j.cmpb.2009.04.008
Kouwenhoven E, Giezen M, Struikmans H: Measuring the similarity of target volume delineations independent of the number of observers. Phys Med Biol 2009, 54: 2863-2873. 10.1088/0031-9155/54/9/018
Lagendijk JJ, Raaymakers BW, Raaijmakers AJ, Overweg J, Brown KJ, Kerkhof EM, van der Put RW, Hardemark B, van Vulpen M, van der Heide UA: MRI/linac integration. Radiother Oncol 2008, 86: 25-29. 10.1016/j.radonc.2007.10.034
Tersteeg RJ, Roesink JM, Albregts M, Warlam-Rodenhuis CC, van Asselen B: Changes in excision cavity volume: prediction of the reduction in absolute volume during breast irradiation. Int J Radiat Oncol Biol Phys 2009, 74: 1181-1185. 10.1016/j.ijrobp.2008.09.056
van Heijst TC, den Hartogh MD, Lagendijk JJ, van den Bongard HJ, van Asselen B: MR-guided breast radiotherapy: feasibility and magnetic-field impact on skin dose. Phys Med Biol 2013, 58: 5917-5930. 10.1088/0031-9155/58/17/5917
Alderliesten T, Loo C, Paape A, Muller S, Rutgers E, Peeters MJ, Gilhuijs K: On the feasibility of MRI-guided navigation to demarcate breast cancer for breast-conserving surgery. Med Phys 2010, 37: 2617-2626. 10.1118/1.3429048
The author thanks surgeons and trial nurses of the UMCU and St. Antonius Hospital for recruiting patients. Furthermore, we would like to acknowledge L. vd Bunt, C.C. Rodenhuis, M.A.S. Albregts.
The authors declare that they have no competing interests.
All authors read and approved the final manuscript. MD participated in the design of the study, study coordination, data acquisition, data analysis, drafting the manuscript. MP participated in the design of the study, acquisition of the data, revised the manuscript critically for intellectual content. ID participated in acquisition of the data and revised the manuscript critically for intellectual content. CK participated in acquisition of the data and revised the manuscript critically for intellectual content. RT participated in acquisition of the data and revised the manuscript critically for intellectual content. AK participated in data analysis and interpretation, revised the manuscript critically for intellectual content. HV participated in the design of the study, interpretation of the data and revised the manuscript critically for intellectual content. MB participated in the design of the study and revised the manuscript critically for intellectual content. MV participated in the design of the study and revised the manuscript critically for intellectual content. BA participated in the design of the study, acquisition of the data, helped to draft the manuscript and revised it critically for intellectual content. DVB participated in the design of the study, acquisition and interpretation of the data, helped to draft the manuscript and revised it critically for intellectual content.