Literature DB >> 35729505

Incidental irradiation of the regional lymph nodes during deep inspiration breath-hold radiation therapy in left-sided breast cancer patients: a dosimetric analysis.

Jule Wolf1,2, Steffen Kurz1,2, Thomas Rothe1,2, Marco Serpa1,2, Jutta Scholber1,2, Thalia Erbes3, Eleni Gkika1,2, Dimos Baltas1,2, Vivek Verma4, David Krug5, Ingolf Juhasz-Böss3, Anca-Ligia Grosu1,2, Nils H Nicolay1,2,6, Tanja Sprave7,8.   

Abstract

BACKGROUND: Radiotherapy using the deep inspiration breath-hold (DIBH) technique compared with free breathing (FB) can achieve substantial reduction of heart and lung doses in left-sided breast cancer cases. The anatomical organ movement in deep inspiration also cause unintended exposure of locoregional lymph nodes to the irradiation field.
METHODS: From 2017-2020, 148 patients with left-sided breast cancer underwent breast conserving surgery (BCS) or mastectomy (ME) with axillary lymph node staging, followed by adjuvant irradiation in DIBH technique. Neoadjuvant or adjuvant systemic therapy was administered depending on hormone receptor and HER2-status. CT scans in FB and DIBH position with individual coaching and determination of the breathing amplitude during the radiation planning CT were performed for all patients. Intrafractional 3D position monitoring of the patient surface in deep inspiration and gating was performed using Sentinel and Catalyst HD 3D surface scanning systems (C-RAD, Catalyst, C-RAD AB, Uppsala, Sweden). Three-dimensional treatment planning was performed using standard tangential treatment portals (6 or 18 MV). The delineation of ipsilateral locoregional lymph nodes was done on the FB and the DIBH CT-scan according to the RTOG recommendations.
RESULTS: The mean doses (Dmean) in axillary lymph node (AL) level I, II and III in DIBH were 32.28 Gy (range 2.87-51.7), 20.1 Gy (range 0.44-53.84) and 3.84 Gy (range 0.25-39.23) vs. 34.93 Gy (range 10.52-50.40), 16.40 Gy (range 0.38-52.40) and 3.06 Gy (range 0.21-40.48) in FB (p < 0.0001). Accordingly, in DIBH the Dmean for AL level I were reduced by 7.59%, whereas for AL level II and III increased by 22.56% and 25.49%, respectively. The Dmean for the supraclavicular lymph nodes (SC) in DIBH was 0.82 Gy (range 0.23-4.11), as compared to 0.84 Gy (range 0.22-10.80) with FB (p = 0.002). This results in a mean dose reduction of 2.38% in DIBH. The Dmean for internal mammary lymph nodes (IM) was 12.77 Gy (range 1.45-39.09) in DIBH vs. 11.17 Gy (range 1.34-44.24) in FB (p = 0.005). This yields a mean dose increase of 14.32% in DIBH.
CONCLUSIONS: The DIBH technique may result in changes in the incidental dose exposure of regional lymph node areas.
© 2022. The Author(s).

Entities:  

Keywords:  Breast cancer; Deep inspiration breath-hold radiation therapy; Incidental irradiation; Lymph nodes

Mesh:

Year:  2022        PMID: 35729505      PMCID: PMC9210647          DOI: 10.1186/s12885-022-09784-x

Source DB:  PubMed          Journal:  BMC Cancer        ISSN: 1471-2407            Impact factor:   4.638


Introduction

Incidental irradiation of cardiac structures in left-sided breast cancer increases the risk of subsequent ischaemic cardiac events [1]. Notably, any Gy increase in mean cardiac dose correlates linearly with a 7.4% increase in non-threshold cardiac events [2]. Different absorbed doses and irradiated volumes result in a variety of pathophysiologic events: macrovascular damage to the coronary vessels such as atherosclerosis and myocardial infarction, or microvascular damage with valvular heart disease and heart failure [3, 4]. Disturbingly, breast cancer patients who developed cardiac disease after initial cancer diagnosis have a higher risk of recurrence and cancer-specific death [5]. In particular, dose-dependent vulnerability of the left ventricle and all coronary segments justifies more rigorous dose reduction [6-9]. Currently, deep inspiration breath hold technique (DIBH) in the supine position allows reproducible cardiac shift from the irradiation field. Therefore, it is a widely used protective heart approach [10]. DIBH can be performed by tangential 3D-conformal radiotherapy (3DRT) or rotational/multiangle intensity-modulated radiotherapy (IMRT/VMAT) [11]. Tangential 3DRT of the mammary gland tissue often unintentionally includes the locoregional lymph nodes in the radiation fields with therapeutic dose. This dose may be sufficient for the eradication of microscopic tumor residues. This hypothesis is supported by the results of the ACOSOG Z0011 study, where patients with 1–2 involved sentinel lymph nodes upon sentinel lymph node dissection had similar axillary recurrence rates whether they received secondary axillary lymph node dissection or not [12]. However, a retrospective review revealed that high tangents and supraclavicular irradiation were used in a significant proportion of patients [13]. We propose that DIBH may lead to differences in the incidental radiation dose of the axillary, supraclavicular and internal mammary lymph nodes due to changes in their position [14, 15] in relation to the tangential radiation portals. In the absence of published data in this regard from randomized trials of DIBH vs free breathing (FB) RT in the supine position, reporting institutional experiences is necessary. The goal of this single-institutional retrospective study was to investigate dosimetric differences of incidental locoregional lymph nodes irradiation between DIBH and FB for left-sided breast cancer patients.

Materials and methods

Patient selection and treatment planning

From December 2017 to July 2020, 148 out of 247 patients with left-sided or bilateral breast cancer which were screened for irradiation in DIBH technique were included in this analysis. The majority of patients (131 patients, 88.5%) received 3DRT in DIBH. The remaining 17 (11.5%) patients received RT in FB either due to suboptimal compliance or lack of dosimetric benefits of DIBH. BCS or mastectomy with axillary lymph node staging was performed according to institutional protocols. Systemic therapy was administered according to current guidelines [16] and individual recommendations of the multidisciplinary tumor board. A tumor bed boost was administered for all premenopausal patients or for postmenopausal patients with additional risk factors (tumor stage ≥ T2, extensive intraductal component, grade 3, HER2-positive or triple-negative tumors). All patients received coaching for DIBH in the CT room using a Surface Image Guided RT (SGRT) system (C-RAD, Catalyst, C-RAD AB, Uppsala, Sweden). The patients were asked to take a deep breath and hold it for a duration of 20 s. The width of the gating window was set to 5 mm. All patients received two CT scans with a slice thickness of 2 mm (Brilliance, CT Big Bore, Philips, Cleveland, OH) in FB and DIBH. Treatment planning (Oncentra MasterPlan, Nucletron, Veenendaal, The Netherlands and/or Eclipse™ planning systems (Varian Medical Systems)) was carried out using standard tangential treatment portals (6 or 18 MV; Synergy; Elekta, Crawley, United Kingdom). Adjuvant WBI or thoracic wall RT was delivered using either moderate hypofractionation (40.05 Gy in 15 fractions) or conventional fractionation (50.00–50.40 Gy in 25–28 fractions). Boost irradiation was delivered sequentially (10–16 Gy in 5–8 fractions), with simultaneous integrated boost (58.80–61.60 Gy in 25–28 fractions) or IORT (single dose of 20 Gy with 50-kV photons [17]). During follow up, all patients were examined every three to six months for the first two years in the radiation oncology department, followed by annual visits thereafter. Breast ultrasound was performed every 6 months for the first three years. Mammograms were obtained six months after WBI, and yearly after the first mammography. Suspected recurrences were biopsy confirmed.

Statistical analysis

For the planned dosimetric evaluation, lymph nodes levels of interest (axillary lymph node levels I, II, III, supraclavicular (SC) and internal mammary (IM) lymph nodes) as well as the contralateral breast were retrospectively delineated (Fig. 1). The delineation was done on both the FB and the DIBH scan according to the RTOG recommendations [18]. DVH parameters were then extracted for all delineated structures (volume, Dmean, D50%, Dmax, Dmin, V30, V40).
Fig. 1

Delineation of locoregional lymph nodes and isodose distribution. a-c: Delineation of the supraclavicular (green), axillary lymph levels I (yellow) and II (light blue axillary lymph nodes in level III (blue), internal mammary (orange). a + c: CT scan in DIBH; b + d: CT scan in FB; a-d: Visualization of isodose distribution in DIBH and FB

Delineation of locoregional lymph nodes and isodose distribution. a-c: Delineation of the supraclavicular (green), axillary lymph levels I (yellow) and II (light blue axillary lymph nodes in level III (blue), internal mammary (orange). a + c: CT scan in DIBH; b + d: CT scan in FB; a-d: Visualization of isodose distribution in DIBH and FB Data are reported as a mean, median (range), and frequencies. For all dosimetric parameters, mean values and their corresponding ranges as well as the relative dose reduction were determined. DVH parameters of the FB vs. DIBH plans were compared using a Wilcoxon signed-rank test. P-values < 0.05 were considered statistically significant. Effect size was assessed according to Cohen (1988) [19]. Analysis was performed using SPSS version 27 (IBM, Armonk, NY, USA).

Results

Altogether, 148 patients with 296 CT scans were analyzed. Baseline characteristics are shown in Table 1. Most patients had T1 (67.6%, n = 100) and N0 stage (87.8%, n = 130) with positive estrogen and progesterone receptor status. Poor differentiation (G3) and Ki-67 > 20% were present in 25.7% and 41.9 of patients, respectively. A minority of patients required re-resection to achieve clear margins (12.8%). Only four patients received mastectomy (2.7%). About 23% of patients received hypofractionated radiotherapy.
Table 1

Patient, tumor and treatment characteristics for patients treated using deep inspiration breath hold technique for whole breast or thoracic wall irradiation in our institution between 2017 and 2019 (n = 148). Staging of breast cancer was based on the 7th Edition of the UICC TNM classification

Total patients: n = 148n%
BCS14396.6
ME42.7
no surgery10.7
TNM classification
 PTis1711.5
 pT110067.6
 pT22919.6
 pT310.7
 pT410.7
 N013087.8
 N1a1812.2
 M014799.3
 M110.7
Resection status
 R012886.5
 initially R1, after second resection R01912.8
 no resection10.7
Grading
 G12617.6
 G28054.1
 G33825.7
 not specified42.7
Hormone receptor status
ER
 positive13188.5
 negative1711.5
 not specified00
PR
 positive12181.8
 negative2718.2
 not specified00
Ki-67 Score
 low (< 10%)138.8
 intermediate (10–25%)5839.2
 high (> 25%)6241.9
 not specified1510.1
HER2 status
 04731.8
 1 + 5235.1
 2 + 2013.5
 3 + 138.8
 not specified1610.8
TNBC106.8
Radiotherapy
 Conventional fractionation11477
 Moderate hypofractionation3423
 SIB4631.1
 IORT5335.8
 3DRT148100
 DIBH13188.5
 FB1711.5
SLND
 Yes12282.4
 No1812.2
 ALND85.4
Chemotherapy
 Neoadjuvant2416.2
 Adjuvant3221.6
Endocrine therapy11678.4

Abbreviation: ALND Axillary lymph node dissection, BCS Breast conserving surgery, 3DRT 3D-conformal radiotherapy, ER Estrogen receptor, IORT Intraoperative radiotherapy, ME Mastectomy, PR Progesterone receptor, SIB Simultaneous integrated boost, SLND Sentinel lymph node dissection, TNBC Triple negative breast cancer, p Pathological

Patient, tumor and treatment characteristics for patients treated using deep inspiration breath hold technique for whole breast or thoracic wall irradiation in our institution between 2017 and 2019 (n = 148). Staging of breast cancer was based on the 7th Edition of the UICC TNM classification Abbreviation: ALND Axillary lymph node dissection, BCS Breast conserving surgery, 3DRT 3D-conformal radiotherapy, ER Estrogen receptor, IORT Intraoperative radiotherapy, ME Mastectomy, PR Progesterone receptor, SIB Simultaneous integrated boost, SLND Sentinel lymph node dissection, TNBC Triple negative breast cancer, p Pathological

Axillary lymph node levels I, II and III

The DVH parameters for levels I-III, SC and IM are summarized in Table 2.
Table 2

Comparison of selected DVH parameters for locoregional lymph node levels in axillary levels I-III, supraclavicular and internal mammary region and contralateral breast in DIBH and FB technique

DVH parameterFBDIBHChange [%]p-valueEffect size r
Mean valueRangeMean valueRange
Axillary level I
 Volume [ccm]62.6217.90–126.9062.8316.70–119.400.340.2100.103
 Dmean [Gy]34.9310.52–50.4032.282.87–51.7-7.59 < 0.00010.375
 D50% [Gy]39.022.75–52.0535.421.64–53.35-9.23 < 0.00010.388
 Dmax [Gy]51.439.71–64.1251.2739.10–63.95-0.250.9970
 Dmin [Gy]3.180.00–44.212.750.00–43.88-13.520.0090.213
 V30 Gy [%]68.5514.54–10062.220.5–100-9.23 < 0.00010.384
 V40 Gy [%]52.990.00–10047.090.00–100-11.13 < 0.00010.321
Axillary level II
 Volume [ccm]17.988.10–40.4018.217.55–40.601.280.0620.153
 Dmean [Gy]16.400.38–52.4020.100.44–53.8422.56 < 0.00010.453
 D50% [Gy]15.290.38–52.3719.650.44–52.3228.52 < 0.00010.423
 Dmax [Gy]34.540.58–57.9438.800.69–60.1112.33 < 0.00010.376
 Dmin [Gy]2.800.22–42.772.960.00–46.805.710.0020.253
 V30 Gy [%]28.410.00–10036.330.00–10027.88 < 0.00010.415
 V40 Gy [%]17.740.00–10022.940.00–10029.31 < 0.00010.439
Axillary level III
 Volume [ccm]8.614.00–19.408.283.80–20.10-3.83 < 0.00010.445
 Dmean [Gy]3.060.21–40.483.840.25–39.2325.49 < 0.00010.466
 D50% [Gy]2.380.21–47.193.230.25–44.9735.71 < 0.00010.463
 Dmax [Gy]10.550.27–52.9413.090.30–52.3224.08 < 0.00010.492
 Dmin [Gy]0.800.13–3.580.870.16–3.248.75 < 0.00010.45
 V30 Gy [%]2.410.00–80.843.600.00–81.4449.380.1170.129
 V40 Gy [%]1.350.00–70.922.160.00–67.69600.2120.103
Supraclavicular
 Volume [ccm]27.1615.16–38.5025.9713.02–37.30-4.38 < 0.00010.723
 Dmean [Gy]0.840.22–10.800.820.23–4.11-2.380.0020.26
 D50% [Gy]0.750.20–4.380.760.21–2.681.330.0010.275
 Dmax [Gy]1.910.54–23.892.060.46–39.437.850.0190.192
 Dmin [Gy]0.370–1.380.400–1.508.11 < 0.00010.375
 V30 Gy [%]0.000.00–0.000.000.00–0.0001.0000
 V40 Gy [%]0.000.00–0.000.000.00–0.0001.0000
Internal mammary
 Volume [ccm]7.643.80–9.527.543.70–9.45-1.31 < 0.00010.522
 Dmean [Gy]11.171.34–44.2412.771.45–39.0914.320.0050.231
 D50% [Gy]9.901.25–49.9311.971.47–47.5720.910.0010.273
 Dmax [Gy]35.211.74–64.5836.021.99–59.482.30.1440.12
 Dmin [Gy]1.840.55–3.651.870.60–3.891.630.1270.126
 V30 Gy [%]11.030.00–86.5514.280.00–78.7429.470.0190.193
 V40 Gy [%]4.830.00–82.666.450.00–67.6133.540.0200.192
Breast right
 Volume [ccm]795.47128.00–2762.68801.19121.80–2759.060.720.0230.187
 Dmean [Gy]0.620.12–1.810.630.12–1.691.610.2340.098
 D50% [Gy]0.530.00–1.0200.540.00–1.701.890.6610.036
 Dmax [Gy]5.340.38–45.775.120.55–40.31-4.120.0460.164
 Dmin [Gy]0.000.00–0.220.010.00–0.5900.0190.193
 V30 Gy [%]0.010.00–0.860.000.00–0.00-10.3170.082
 V40 Gy [%]0.000.00–0.280.000.00–0.0000.3170.082

Comparison of mean values (ranges) of DVH parameters for levels I-III, supraclavicular and internal mammary region and contralateral breast and relative changes in percent between DIBH and FB technique using two-sided Wilcoxon signed-rank test and effect size

Abbreviation: DIBH Deep inspiration breath hold, DVH Dose-volume histogram, FB Free breathing

Comparison of selected DVH parameters for locoregional lymph node levels in axillary levels I-III, supraclavicular and internal mammary region and contralateral breast in DIBH and FB technique Comparison of mean values (ranges) of DVH parameters for levels I-III, supraclavicular and internal mammary region and contralateral breast and relative changes in percent between DIBH and FB technique using two-sided Wilcoxon signed-rank test and effect size Abbreviation: DIBH Deep inspiration breath hold, DVH Dose-volume histogram, FB Free breathing The mean dose (Dmean) in level I, II and III in DIBH were 32.28 Gy (range 2.87–51.7), 20.10 Gy (range 0.44–53.84) and 3.84 Gy (range 0.25–39.23) vs. 34.93 Gy (range 10.52–50.40), 16.40 Gy (range 0.38–52.40) and 3.06 Gy (range 0.21–40.48) in the FB group (p < 0.0001 for all) (Fig. 2). In comparison to FB, Dmean for level I was reduced by 7.59% (effect size, r = 0.38) and increased for level II and III by 22.56% (r = 0.45), and 25.49% (r = 0.47).
Fig. 2

Ratio of Dmean for axillary level I-III in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing

Ratio of Dmean for axillary level I-III in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing The D50% in level I, II, and III in DIBH were 35.42 Gy (range 1.64–53.35), 19.65 Gy (range 0.44–52.32) and 3.23 Gy (range 0.25–44.97) vs. 39.02 Gy (range 2.75–52.05), 15.29 Gy (range 0.38–52.37) and 2.38 Gy (range 0.21–47.19) in the FB group (p < 0.0001 for all) (Table 2). Thus, in comparison to FB D50% for level I was reduced by 9.23% (r = 0.39), whereas it was increased for level II and III D50% by 28.52% (r = 0.42), and 35.71% (r = 0.46) (Table 2). The mean values of V30Gy, and V40Gy for level I in the DIBH cohort were decreased by 9.23% and 11.13% (p < 0.0001 for both, r = 0.38 and r = 0.32), respectively. There was an increase in the mean values of V30, and V40 for level II in DIBH 27.88% (p < 0.0001, r = 0.41) and 29.31% (p < 0.0001, r = 0.44) respectively. There was a non-significant increase in the mean values of V30Gy and V40Gy for level III with DIBH (Table 2). The mean volumes of the lymph node levels were assessed in FB and DIBH. There were small, but significant volume decreases in DIBH for level III by 3.83% (p < 0.0001) but not for level II by 1.28% (p = 0.062).

Supraclavicular and internal mammary region and contralateral breast

The Dmean for the SC in DIBH was 0.82 Gy (range 0.23–4.11), as compared to 0.84 Gy (range 0.22–10.80) with FB (p = 0.002). This results in a Dmean reduction of 2.38% (r = 0.26) in DIBH (Fig. 3). The mean volumes of the SC in FB were 27.2 cm3 (range 15.2–38.5) vs. DIBH: 26 cm3 (range 13–37.3). This resulted with moderate volume decrease in DIBH for SC by 2.4% (p < 0.0001).
Fig. 3

Ratio of Dmean for the supraclavicular region in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing

Ratio of Dmean for the supraclavicular region in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing The Dmean for IM was 12.77 Gy (range 1.45–39.09) in DIBH vs. 11.17 Gy (range 1.34–44.24) in FB (p = 0.005). This yields a Dmean increase of 14.32% (r = 0.23) in DIBH (Fig. 4). The mean of V30Gy, and V40Gy for IM in DIBH were by 29.47% (p = 0.019, r = 0.19) and 33.54% (p = 0.02, r = 0.19) (Table 2). The mean volume of the IM in FB was 7.6 cm3 (range 3.80–9.5) compared to 7.5 cm3 (range 3.7–9.5) in DIBH. This corresponded to a small, but significant decrease in volume in DIBH for IM by 1.3% (p < 0.0001).
Fig. 4

Ratio of Dmean for the internal mammary region in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing

Ratio of Dmean for the internal mammary region in DIBH to FB position (Y-axis) in the entire cohort (X-axis, n = 148). Abbreviation: DIBH: deep inspiration breath hold; FB: free breathing Mean values for right (contralateral) breast were 795.5 cm3 (range 128–2762.7) for FB and 801.2 cm3 (range 121.80–2759.1) for DIBH. The mean relative difference between DIBH and FB was small (relative increase of 0.72%), but statistically significant (p = 0.023).

Discussion

In this retrospective single-center analysis, we could demonstrate that the use of DIBH leads to significant changes in dose-volume parameters for patients with left-sided breast cancer treated with tangential 3DRT. For level I, DIBH lead to a decrease in incidental dose whereas DIBH was associated with increased doses for level II-III, supraclavicular and internal mammary lymph nodes. Since publication of the ACOSOG Z0011-trial, there has been a controversial discussion regarding the radiation dose required for control of subclinical disease in the axilla [20]. Although the trial protocol mandated standard tangential irradiation, a subsequent retrospective analysis of 228 patients showed that more than half of the patients were treated with high tangents and 15% received supraclavicular irradiation [13]. A meta-analysis of prospective partial breast irradiation-trials demonstrated an increased risk of axillary recurrences with an odds ratio of 1.75 (95%-confidence interval 1.07–2.88), further suggesting that incidental axillary irradiation might contribute to locoregional control [21]. A recent systematic review identified 13 retrospective studies with a total of 475 patients which analyzed dosimetric parameters of axillary lymph node levels for patients planned for adjuvant whole breast radiotherapy [22]. There was considerable variation in axillary doses depending on the use of high tangents and radiation technique. For patients treated with standard tangential 3DRT, median dose in axillary levels I-III ranged from 22 to 43.5 Gy, 3 to 35.6 Gy, and 1 to 20.5 Gy, respectively [22]. In addition to these retrospective studies, Hildebrandt et al. recently published prospective data from the quality assurance program of the INSEMA-trial [23]. Incidental axillary doses were analyzed for 234 patients who underwent central plan review. Axillary level I and II were treated with a median of 72.8% and 39.9% of the prescribed dose in the breast, respectively. Level III only received a median dose of 16.4% of the breast dose. More than 25% of patients were treated with a median dose ≥ 95% of the breast dose in level I. Patients with a body mass index (BMI) ≥ 30 kg/m2 had significantly higher median doses in level I-III. Most patients received 3DRT (76.1%), while DIBH was only used in 1 patient [23]. DIBH is a standard technique for patients with left sided breast cancer due to a significant dose reduction of cardiac structures [24-26]. In 2019, the breast cancer expert panel of the German Society for Radiation Oncology (DEGRO) recommended the use of DIBH for the treatment of patients with left sided breast cancer [10]. However, DIBH is not only associated with a change in the position of the heart and lungs but also with changes in the chest wall and surrounding soft tissue [14, 15]. This may affect the incidental dose to axillary lymph node levels as well as the supraclavicular and internal mammary lymph nodes. Borm et al. contoured axillary lymph node levels according to the RTOG atlas for 32 patients and compared incidental doses during DIBH and FB [15]. They demonstrated an overall three-dimensional movement of the axillary lymph node levels of 1.5 to 1.6 cm. The use of DIBH lead to a significant decrease in the incidental dose to level I and numerical, but mostly non-significant increases in the dose to level II and III [15]. Pazos et al. analyzed the influence of DIBH on doses to level I-III, supraclavicular and internal mammary nodes for 35 patients planned for radiotherapy of the breast or chest wall and the regional lymph nodes. Three-dimensional movement was between 0.79 cm for level I and 1.44 cm for internal mammary nodes. DIBH led to a significant decrease in the dose to level I and II compared to FB, however there were no significant differences for the other regions of interest [14]. In our analysis, the largest absolute changes were observed for level I with a decrease of 2.65 Gy (from 34.93 Gy to 32.28 Gy) and for level II with an increase of 3.7 Gy (from 16.40 Gy to 20.10 Gy). However, the clinical relevance may be more adequately addressed by comparing exposure to higher doses, such as V40Gy and V30Gy. While only small amounts of level II were exposed to these doses, DIBH led to an absolute decrease in the V40Gy and V30Gy of 6.3% and 5.9% for Level I, respectively. Level III as well as the supraclavicular and the internal mammary nodes were only minimally exposed to incidental irradiation. The observed changes, though in some cases statistically significant, may not be clinically relevant due to relatively small absolute differences. Compared to the analysis by Borm et al. [15], the changes in Dmean and V40Gy and V30Gy are somewhat smaller in magnitude. Contrary to their findings, we saw an increase in all dosimetric parameters for level II as well as Dmean to level III, but nor for V40Gy and V30Gy for level III. We observed considerably lower doses to level II and III, for example for Dmean of level II: 16.40 Gy (FB) and 20.10 Gy (DIBH) in our analysis compared to 23.7 Gy (FB) and 24.1 Gy (DIBH) for Borm et al. [15]. This may be related to differences in treatment planning and DIBH-technique. While we used a surface scanning-approach with a pre-defined gating window of 5 mm, the real-time position management system (RPM, Varian Medical Systems, Palo Alto, CA) was used by Borm et al. [15]. No details regarding the gating window were provided. Our analysis represents the largest cohort both in terms of dosimetric analysis in FB and in DIBH. We included intraindividual comparisons based on CT-scans in FB and DIBH for each patient. To exclude confounding by different radiotherapy techniques, only tangential 3DRT-plans were analyzed. It has been previously shown that IMRT or VMAT can also significantly impact incidental dose to the axilla [27-29]. Thus, our data cannot be extrapolated to patients receiving a combination of DIBH and IMRT/VMAT. Interindividual differences in anatomy may be responsible in part for dosimetric variability. Furthermore, compliance with breath hold as well as the quality of coaching for DIBH and the depth of inspiration may have an impact on anatomical changes and the position of lymph node areas in DIBH. Unfortunately, information on BMI was not available from the patient charts and could thus not be analyzed. The subgroup of patients with mastectomy was too small to provide reliable estimates for statistical comparisons. About 23% of patients in our analysis received hypofractionated radiotherapy, which in itself may lead to a decreased biologically effective dose to the unintentionally exposed axilla [30]. In conclusion, we could demonstrate a significant variability in incidental dose exposure to regional lymph node areas in patients with left-sided breast cancer by the use of DIBH. Further studies are needed to determine the clinical significance of these findings and to establish predictors of dosimetric changes based on patient-related factors.
  29 in total

1.  Positive sentinel nodes without axillary dissection: implications for the radiation oncologist.

Authors:  Bruce G Haffty; Kelly K Hunt; Jay R Harris; Thomas A Buchholz
Journal:  J Clin Oncol       Date:  2011-10-31       Impact factor: 44.544

2.  Cardiac Structure Injury After Radiotherapy for Breast Cancer: Cross-Sectional Study With Individual Patient Data.

Authors:  Carolyn Taylor; Paul McGale; Dorthe Brønnum; Candace Correa; David Cutter; Frances K Duane; Bruna Gigante; Maj-Britt Jensen; Ebbe Lorenzen; Kazem Rahimi; Zhe Wang; Sarah C Darby; Per Hall; Marianne Ewertz
Journal:  J Clin Oncol       Date:  2018-05-23       Impact factor: 44.544

3.  Distribution of coronary artery stenosis after radiation for breast cancer.

Authors:  Greger Nilsson; Lars Holmberg; Hans Garmo; Olov Duvernoy; Iwar Sjögren; Bo Lagerqvist; Carl Blomqvist
Journal:  J Clin Oncol       Date:  2011-12-27       Impact factor: 44.544

4.  Deep-Inspiration Breath-Hold Radiation Therapy in Breast Cancer: A Word of Caution on the Dose to the Axillary Lymph Node Levels.

Authors:  Kai Joachim Borm; Markus Oechsner; Stephanie E Combs; Marciana-Nona Duma
Journal:  Int J Radiat Oncol Biol Phys       Date:  2017-09-20       Impact factor: 7.038

Review 5.  Heart-sparing radiotherapy techniques in breast cancer patients: a recommendation of the breast cancer expert panel of the German society of radiation oncology (DEGRO).

Authors:  Marciana-Nona Duma; René Baumann; Wilfried Budach; Jürgen Dunst; Petra Feyer; Rainer Fietkau; Wulf Haase; Wolfgang Harms; Thomas Hehr; David Krug; Marc D Piroth; Felix Sedlmayer; Rainer Souchon; Rolf Sauer
Journal:  Strahlenther Onkol       Date:  2019-07-18       Impact factor: 3.621

6.  Late cardiac mortality and morbidity in early-stage breast cancer patients after breast-conservation treatment.

Authors:  Eleanor E R Harris; Candace Correa; Wei-Ting Hwang; Jessica Liao; Harold I Litt; Victor A Ferrari; Lawrence J Solin
Journal:  J Clin Oncol       Date:  2006-08-14       Impact factor: 44.544

Review 7.  Radiation-Induced Vascular Disease-A State-of-the-Art Review.

Authors:  Eric H Yang; Konstantinos Marmagkiolis; Dinu V Balanescu; Abdul Hakeem; Teodora Donisan; William Finch; Renu Virmani; Joerg Herrman; Mehmet Cilingiroglu; Cindy L Grines; Konstantinos Toutouzas; Cezar Iliescu
Journal:  Front Cardiovasc Med       Date:  2021-03-30

Review 8.  Understanding radiation-induced cardiovascular damage and strategies for intervention.

Authors:  F A Stewart; I Seemann; S Hoving; N S Russell
Journal:  Clin Oncol (R Coll Radiol)       Date:  2013-07-20       Impact factor: 4.126

9.  The relationship between radiation doses to coronary arteries and location of coronary stenosis requiring intervention in breast cancer survivors.

Authors:  Anna-Karin Wennstig; Hans Garmo; Ulf Isacsson; Giovanna Gagliardi; Niina Rintelä; Bo Lagerqvist; Lars Holmberg; Carl Blomqvist; Malin Sund; Greger Nilsson
Journal:  Radiat Oncol       Date:  2019-03-07       Impact factor: 3.481

10.  Effect of hypofractionation on the incidental axilla dose during tangential field radiotherapy in breast cancer.

Authors:  Kai J Borm; Markus Oechsner; Mathias Düsberg; Gabriel Buschner; Weber Wolfgang; Stephanie E Combs; Marciana N Duma
Journal:  Strahlenther Onkol       Date:  2020-06-02       Impact factor: 3.621

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