A Retrospective Analysis of Dose Distribution and Toxicity in Patients with Left Breast Cancer Treated with Adjuvant Intensity-Modulated Radiotherapy: Comparison with Three-Dimensional Conformal Radiotherapy.

BACKGROUND: A better understanding of the organs-at-risk (OAR) dose metrics and the related toxicity induced by radiotherapy (RT) for left breast cancer (BC) will improve the quality of life. This study addressed the issue for left-BC patients treated with intensity-modulated radiotherapy (IMRT) compared to three-dimensional conformal radiotherapy (3D-CRT). PATIENTS AND METHODS: Between 2012 and 2018, 308 left-BC patients underwent adjuvant RT at our hospital. Before June 2015, 134 patients were treated with 3D-CRT. Thereafter, 174 patients underwent IMRT. The patient's characteristics in the IMRT group did not significantly different compared to those in the 3D-CRT group.
RESULTS: Among the total study population, the incidence of ≥grade 2 radiation dermatitis (RID) was 17.3%. Higher volumes receiving 105% (≥5.7%) and 107% (≥1%) of prescribed dose and 3D-CRT technique were associated with a higher risk of RID. Regarding lung toxicity, the mean lung dose (≥10.2Gy) and V20 (≥20%) of ipsilateral lung were significantly associated with the incidence of RT-induced pulmonary changes. By dosimetry analysis, IMRT achieved better dose conformity and delivered lower mean doses to heart and ipsilateral lung compared to 3D-CRT. Furthermore, propensity sore and multivariate analysis showed that IMRT technique helped to reduce RT-induced dermatitis and lung toxicity.
CONCLUSION: Our data suggest that the volume of OAR exposed to higher doses is a predictor of RT-induced toxicity. Adjuvant RT with IMRT technique offered better dose conformity and spared high-dose levels to OARs to reduce radiation-related morbidity for BC patients.

Introduction

Adjuvant radiotherapy (RT) substantially reduces recurrence rates of breast cancer (BC), and improves overall survival.1,2 However, RT-induced toxicities have been noted, including skin, lung and heart toxicity.1,3–5 Radiation dermatitis is the common clinical problem for BC patients receiving adjuvant RT.6–8 Various RT techniques, such as intensity-modulated RT (IMRT), have been developed to improve dose conformity within the irradiated compared to conventional RT.9 IMRT delivers a more homogenous dose and may result in a lower rate of moist desquamation than conventional RT technique.10,11 We previously reported that an incidence of 23% for moist desquamation induced by three-dimensional conformal radiotherapy (3D-CRT) and the volume of hotspots was a predictor for the risk of moist desquamation.12 In the present study, we analyzed the RT dosimetry and the related dermatitis in Left-BC patients underwent IMRT compared to 3D-CRT.

In addition, RT-induced cardiopulmonary disease is correlated with the absorbed dose and irradiated volume.5,13 The higher the volume or the higher the dose of irradiated heart, the higher risk of developing ischemic heart disease.14 A linear relationship between the mean heart dose (MHD) and the rate of cardiac events was identified.15 Regarding lung toxicity, the irradiated volume exceeding a defined dose (Vdose), ipsilateral mean lung dose (MLD) and dose per fraction influenced the RT-induced lung morbidity.16–19 A better understanding of dosimetric parameters and its relationship with the incidence of RT-induced toxicity will help to improve the quality of life. Therefore, this study analyzed the exposures of organs-at-risk (OAR) dose metrics for left-BC patients underwent IMRT compared to those by 3D-CRT at our institution.

Patients and Methods

Patients Characteristics of and Treatment Techniques

This retrospective study was approved by the institutional review board of Chang Gung Memorial hospital (N0. 201900936B0), and a waiver of informed consent was obtained. This study adhered to strict confidentiality guidelines and in compliance with regulations regarding personal electronic data protection and the Declaration of Helsinki. There were 308 left-BC patients who completed the planned RT course from 2012 to 2018 enrolled into the study. Among these patients, 218 patients undergone breast-conserving surgery (BCS), and 90 patients received total mastectomy, then followed by adjuvant RT. Before June 2015, 134 patients received 3D-CRT. Thereafter, 174 patients underwent IMRT. In all, 282 patients had prophylactic skincare with moisture ointment every day from the beginning of RT. If required, adjuvant chemotherapy was performed sequentially rather than concurrently with radiotherapy in these patients (200 patients). Patients were observed at 3 weeks after the completion of RT, then 3-month intervals for the first 2 years and every 6 months thereafter. The Radiation Therapy Oncology Group (RTOG) scale was used to evaluate acute skin toxicity during the radiation treatment at weekly clinical examinations, and continued for 3 weeks after the end of radiotherapy. Grade 2 skin toxicity is described in the RTOG Acute Morbidity Scale as “tender or bright erythema, patchy moist desquamation/moderate edema”, and Grade 3 “confluent moist desquamation other than skin folds, pitting edema”. The correlation between acute radiation dermatitis (RID) and the examined risk factors were calculated as the percentage of patients with ≥ grade2 skin toxicity. In addition, the radiation-induced lung injury was evaluated during and after radiation therapy. Clinically symptom was defined according to the modified Common Toxicity Criteria of the National Cancer Institute of Canada (CTC-NCIC).20 Chest computed tomography (CT) was evaluated 1–3 months after completion of radiation therapy. Density changes on chest CT were evaluated by comparing with the CT image prior to radiation therapy. Then chest X-ray films were performed annually during follow-up. If there were new abnormal findings found on Chest X-ray films, the patients would receive chest CT scan. An increase in density was graded according to a CT adapted modification of Arriagada’s classification (0 = no change; 1 = low opacity in linear streaks; 2 = moderate opacity; 3 = complete opacity).19,21 The correlation between RT-induced pulmonary changes and the examined risk factors was calculated as the percentage of patients with ≥ grade 1 density change in CT scan.

CT-Simulation and Radiotherapy Planning

At the time of simulation, these left BC-patients underwent CT scans with free-breathing (FB), and the corresponding CT plans for adjuvant RT. In general, adjuvant RT was prescribed according to the planning target volume (PTV), which was 50 Gy in 25 fractions (268 patients) or 42.56 Gy in 16 fractions (40 patients). Of the 308 patients, 125 received simultaneous nodal irradiation. The skin, heart and ipsilateral lung were defined as OARs. The targets were delineated according to the Radiation Therapy Oncology Group (RTOG) breast cancer consensus definitions.22 The CTV was expanded by 10 mm, but within 2 mm of the skin surface, to create the planned target volume (PTV) generated on the free-breathing CT scans.12,23,24 For patients who required simultaneous nodal irradiation, the supraclavicular lymph nodes were included into the CTV. The goal was to deliver 95% of the prescribed dose to at least 95% of the PTV while minimizing the dose delivered to the lung, heart, and contralateral breast. The dose constraint (in 2 Gy per fraction) of the volume of treatment volume (TV) receiving 110% of prescribed dose (V110%) was <5%, of the heart was V25 Gy <10%, and the criteria for the ipsilateral lung was V20 ≤25%; V5 Gy ≤50%, for the whole lung was V20 <20%; V5 Gy <30%, and a minimized dose to the contralateral lung and breast. For patients treated with hypofractionation regimen, the dose to OARs was corrected.25 The 3D-CRT plans consisted of two major opposed open tangential half beams. Multileaf collimators (MLCs) were used to shield the heart, left lung and achieve the optimized dose distribution of the 3-dimensional plan. We usually used 1~2 additional segment (“field-in-field” technique) to further improve dose homogeneity and minimize the volume of radiation hotspots. Approximately 10% of the prescription dose was delivered with this shrunken field. The IMRT was a multi-beam (6–8 beams) step and shoot technique with a dose rate of 600 MU/min. The gantry separation between ipsilateral fields ranged from 5° to 10°. The multi-leaf collimator moving speed for beam delivery was set at 2.5 cm per second. The plans were generated from a full inverse planning system (Philips Pinnacle3 treatment planning system, Fitchburg, WI, USA) for optimization to generate the IMRT plan. We analyzed several parameters including PTV, the volume enclosed within the prescribed dose (TV), and the areas receiving an excessive dose such as V105% and V107% (percent volume receiving 105% and 107% of the prescribed dose, respectively). Figure 1A shows the isodose distribution of a representative patient, illustrating the radiation hotspots (V105% and V107%) related to the location of acute radiation dermatitis.

Figure 1

Radiation hotspots related to acute skin toxicity. (A) Representative pictures of selected patients with grade 1 and 2 acute skin toxicity, and the isodose distribution are shown, respectively (% of prescribed dose: color curve; 95%: yellow curve; 105%: pink curve; 107%: light blue). (B) The volume of radiation hotspots in the groups of patients without and with radiation dermatitis.

Statistical Analyses

Student’s t-tests were utilized to analyze associations between RT-induced toxicity, dosimetric parameters and clinical characteristics, and to compare the dose distribution between the plans. Dose reduction to the OAR was compared between the 3D-CRT and IMRT plans. The p-value for a two-tailed test with a confidence interval of 95% was used. Linear regression analyses were also performed using SPSS version 17.0. In addition, the propensity score method, which simulates the effects of a randomized trial for observational data, was used to estimate study outcomes. Inverse probability of treatment weighting (IPTW) of the propensity scores was used to create a pseudo-population in which study groups were balanced across covariates using data blinded to outcomes. Covariate balance was assessed using the standardized difference, which is the difference between groups divided by the pooled standard deviation, with a goal-to-achieve value <0.1.

Results

Patients and Acute Skin Toxicity

All patients completed the planned course of treatment. The median age (±SD) of the overall study population was 54 ± 11 (range 24–88) years. The incidence of radiation dermatitis was 17.3% of the total study population. Among these 53 patients developed radiation dermatitis, 50 and 3 patients had grade 2 and 3 skin toxicity, respectively. Table 1 reveals that BMI > 24, total mastectomy, and simultaneous nodal irradiation were associated with a higher incidence of ≥ grade 2 RID. The incidence of RID was 24% (22/90) in patients with total mastectomy compared to 14% (31/218) in those with BCS (p=0.031), and 9% (16/183) in those without nodal irradiation compared to 30% (37/125) in those with nodal irradiation (p<0.001). We further analyzed the role of radiation hotspots in predicting acute skin toxicity. Figure 1B reveals that a higher volume of radiation hot spots were associated with a higher incidence of RID. To assess the predictive value of V105% and V107%, they were redefined as a binary variable by finding the value from a receiver-operating characteristic (ROC) curve that maximized the percentage correctly classified for acute radiation dermatitis. Accordingly, we divided the patients into two groups for TV-V105% with 5.7% (92% sensitivity and 79% specificity), and TV-V107% (98% sensitivity and 80% specificity) with 1%. As shown in Table 1, patients in the group with lower volumes of radiation hotspots had a significantly lower risk of developing radiation dermatitis compared to those with higher volumes of radiation hotspots.

Table 1

Factors Correlated with the RT-Induced Skin Toxicity

	Skin Toxicity		p value
	<Grade 2	≥Grade 2
Patients	255 (100%)	53 (100%)
Age
Range	24~88 y/o	30~80 y/o	0.81
Median	54y/o	53y/o
±SD	10.8	10.8
BMI			0.040*
≤24	126 (49.4%)	18 (34%)
>24	129 (50.6%)	35 (66%)
Surgery type			0.031*
BCS	187 (73.3%)	31 (58.5%)
Mastectomy	68 (26.7%)	22 (41.5%)
RT technique			<0.001*
3D-CRT	99 (38.8%)	35 (66.0%)
IMRT	156 (61.2%)	18 (34.0%)
Nodal irradiation			<0.001*
No	167 (65.5%)	16 (30.2%)
Yes	88 (34.5%)	37 (69.8%)
Prophylactic skin care			0.78
No	21 (8.2%)	5 (9.4%)
Yes	234 (91.8%)	48 (90.6%)
Dosimetry (mean±SD)
CTV-V95%	98.91±0.1%	98.6± 0.2%	0.137
PTV-V95%	95.9±0.1%	94.6± 0.3%	0.135
TV-V105%	3.7±0.2%	11.6±0.8%	<0.001*
<5.7%	200 (78.4%)	4 (7.5%)	<0.001*
≥5.7%	55 (21.6%)	49 (92.5%)
TV-V107%	0.2±0.03%	2.8±0.3%	<0.001*
<1%	239 (93.7%)	3 (5.7%)	<0.001*
≥1%	16 (6.3%)	50 (94.3%)

Notes: *Statistical significance. V105% and V107%=percent volume receiving 105% and 107% of the prescribed dose.

Abbreviations: BCS, breast-conserving surgery; BMI, body mass index; TV, treatment volume.

Skin Toxicity and Dosimetric Parameters for IMRT vs 3D-CRT

We further divided the 308 patients into the group for 3D-CRT and IMRT. Table 2 summarizes the patient numbers and the dosimetry parameters. A comparison of the parameters between the 2 groups revealed that the percentage of patients who had undergone a total mastectomy and nodal irradiation did not significantly differ. The patients treated with IMRT were at significantly lower risk for developing RID. The incidences of acute RID were 26% and 10% of the 3DRT and IMRT groups, respectively (p< 0.001). A review of the IMRT dosimetry showed better target coverage with the volume of PTV and CTV receiving 95% of the prescribed dose and dose conformality compared to the 3D-CRT technique (). There were significantly lower volumes of radiation hotspots (p<0.001) in patients treated with IMRT compared to those treated with 3DRT. On multivariate analysis for RID, patients received total mastectomy and 3D-CRT were associated with higher incidence of radiation dermatitis (Table 3).

Table 2

Difference in Clinical Characteristics and Dosimetry Between IMRT and 3D-CRT Groups

	RT Techniques		p value
	3DRT	IMRT
Patients	134 (100%)	174 (100%)
BMI			0.756
≤24	64 (47.8%)	80 (46.0%)
>24	70 (52.2%)	94 (54.0%)
Surgery type			0.140
BCS	89 (66.4%)	129 (74.1%)
Mastectomy	45 (33.6%)	45 (25.9%)
Nodal irradiation			0.885
No	79 (59.0%)	104 (59.8%)
Yes	55 (41.0%)	70 (40.2%)
Skin toxicity			<0.001*
< grade 2	99 (73.9%)	156 (89.7%)
≥ grade 2	35 (26.1%)	18 (10.3%)
Dosimetry (mean±SD)
CTV-V95%	98.6±0.1%	99±0.1%	0.009*
PTV-V95%	94.5±0.2%	95.2±0.1%	0.001*
TV-V105%	7.8±0.5%	2.9±0.2%	<0.001*
<5.7%	53 (39.6%)	151 (86.8%)	<0.001*
≥5.7%	81 (60.4%)	23 (13.2%)
TV-V107%	1.2±0.2%	0.2±0.03%	<0.001*
<1%	90 (67.2%)	152 (87.4%)	0.001*
≥1%	44 (32.8%)	22 (12.6%)

Notes: *Statistical significance. V105% and V107%=percent volume receiving 105% and 107% of the prescribed dose.

Abbreviations: BCS, breast-conserving surgery; BMI, body mass index; TV, treatment volume.

Table 3

Multivariate Analysis to Determine Factors Associated with RID

Variable	HR	95% CI	P value
Surgery type
Mastectomy	Ref
BCS	0.323	0.19–0.54	<0.001*
Nodal irradiation
Yes	Ref
No	0.811	0.60–1.1	0.18
BMI
≤24	Ref
>24	1.44	0.78–2.63	0.24
RT technique
3D-CRT	Ref
IMRT	0.27	0.14–0.50	<0.001*

Note: *Statistical significance.

Dosimetric Parameters of OAR for IMRT vs 3DRT

OAR Doses

Table 4 summarizes the numbers of patients and the dosimetry parameters of heart and ipsilateral lung. Patients treated with IMRT had a significantly lower cardiac exposure, including the MHD and the V5~V20 based on the DVH for the CT treatment plans. Patient variability was noted in terms of the MHD with a range of values from 1.22 to 16 Gy (4.4 ± 0.12Gy). The distance of heart (DHL) is measured on the CT slice with the thickest section of heart and is defined as the distance between the anterior cardiac contour to the imaginary line connecting middle point of sternum and the left middle axillary line (Figure 2A). Figure 2B reveals that there was a positive correlation between the MHD and DHL (R=0.66). To assess the predictive value of the DHL, DHL was redefined as a binary variable by finding the value from a ROC curve that maximized the percentage correctly classified for predicting MHD ≥4.4Gy. The optimal cut-off for the DHL was 2.47 cm (79% sensitivity and 62% specificity). Accordingly, we divided the patients into high and low-DHL groups. The MHD was 3.42± 0.10Gy in the low-DHL group and 5.48± 0.18 Gy in the high-DHL group. IMRT significantly reduced the MHD both in both groups of DHL (p<0.001) compared to those treated with 3D-CRT (). Furthermore, treatment with IMRT was associated with a lower mean dose, and V20 of the ipsilateral lung. The mean lung dose values for the 3D-CRT and IMRT groups were 11.3± 0.3Gy and 10.4± 0.3 cm3, respectively (p=0.039).

Table 4

Dosimetric Differences Between 3D-CRT and IMRT for OAR

	3D-CRT	IMRT	p value
Heart
Dmean (Gy)	5.31± 0.20	3.77± 0.12	<0.001*
V5Gy (%)	16.5± 0.8%	13.9± 0.6%	0.014*
V10Gy (%)	10.6± 0.6%	7.6± 0.4%	<0.001*
V20Gy (%)	7.7± 0.4%	4.6± 0.2%	<0.001*
Left Lung
Dmean (Gy)	11.28± 0.28	10.40 ± 0.3	0.039*
<10.2Gy	52	101	0.001*
≥10.2Gy	82	73
V20Gy (%)	21.6± 0.6	19.8 ± 0.4	0.024*
<20%	58	98	0.023*
≥20%	76	76
V5Gy (%)	38.6± 0.7	36.6 ± 0.6	0.051

Note: *Statistical significance.

Figure 2

Relationship between MHD and the distance of heart (DHL) for left-sided breast cancer patients. (A) Representative images of the distance of heart (DHL) is shown (A: the midline of the sternum; B: the left middle axillary line; DHL: orange; PTV: light green). (B) The values of DHL plotted against mean heart dose. DHL indicated good positive linear correlation with mean heart dose for all patients.

Clinical Findings

There were no deaths related to cardiac toxicity or major coronary events during the follow-up. The median follow-up time was 51.7 months (range 2.7–112.3 months). In term of lung toxicity, no patients had grade 2 symptomatic radiation pneumonitis during the follow-up. The most common pulmonary changes in the imaging included patchy, ground-glass opacities, and fibrosis. In all, 81 patients (26%) developed radiographic changes within the RT field in follow-up images (Figure 3, Table 5). The data revealed that total mastectomy, simultaneous nodal irradiation, and 3D-CRT technique were associated with a higher risk of developing RT-induced radiologic changes. The incidence was 41% (37/90) in patients with a total mastectomy compared to 20% (44/218) in patients who had undergone BCS (p<0.001), and 17% (31/183) in patients without nodal irradiation compared to 40% (50/125) in patients with nodal irradiation (p<0.001). Furthermore, RT-induced pulmonary changes occurred in 34% and 20% of the 3D-CRT and IMRT groups, respectively. The MLD and the ipsilateral lung V20 were, the important predictors of radiation pneumonitis, being significantly associated with incidence of developing RT-induced pulmonary changes. We used the median of MLD (10.2 Gy) and V20 (20%) as a cut-off value to divide the 308 patients into lower and higher groups. The patients in the lower MLD and V20 group had a significantly lower risk for developing RT-induced pulmonary injury compared to those in the higher groups. Furthermore, there were significantly more patients who had undergone 3D-CRT in the higher MLD and V20 group compared to those treated with IMRT. By multivariate analysis, patients received total mastectomy and 3D-CRT was associated with higher incidence of RT-induced pulmonary changes (Table 6).

Figure 3

Relationship between RT-induced radiologic changes and V20 of ipsilateral lung Representative pictures of a selected patient with RT-induced radiologic changes and the isodose distribution are shown, respectively (prescribed dose: yellow curve; V20: orange curve).

Table 5

Factors Correlated with the RT-Induced Radiologic Changes for Ipsilateral Lung

	Pulmonary Changes		p value
	(-)	(+)
Patients	227 (100%)	81 (100%)
BMI			0.38
≤24	111 (48.9%)	35 (43.2%)
>24	116 (51.1%)	46 (56.8%)
Surgery type			<0.001
BCS	174 (76.7%)	44 (54.3%)
Mastectomy	53 (23.3%)	37 (45.7%)
RT technique			0.005*
3DRT	88 (38.7%)	46 (56.8%)
IMRT	139 (61.2%)	35 (43.2%)
Nodal irradiation			<0.001*
No	152 (67.0%)	31 (38.3%)
Yes	75 (33.0%)	50 (61.7%)
Dosimetry (mean±SD)
MLD (Gy)	10.32±0.25	12.09± 0.34	<0.001*
<10.2Gy	130 (57.3%)	23 (28.4%)
≥10.2Gy	97 (42.7%)	58 (71.6%)
V20Gy (%)	19.6±0.4%	23.5± 0.7%	<0.001*
<20%	129 (56.8%)	27 (33.3%)
≥20%	98 (43.2%)	54 (66.7%)

Note: *Statistical significance.

Abbreviations: BCS, breast-conserving surgery; BMI, body mass index; MLD, mean lung dose.

Table 6

Multivariate Analysis to Determine Factors Associated with RT-Induced Pulmonary Injury

Variable	HR	95% CI	P value
Surgery type
Mastectomy	Ref
BCS	0.343	0.22–0.54	<0.001*
Nodal irradiation
Yes	Ref
No	0.802	0.53–1.22	0.31
BMI
≤24	Ref
>24	1.16	0.68–1.98	0.58
MLD (Gy)
<10.2Gy	Ref
≥10.2Gy	1.83	0.98–3.45	0.06
RT technique
3D-CRT	Ref
IMRT	0.49	0.29–0.85	0.01*

Note: *Statistical significance.

Propensity Score Analysis

To further corroborate the results observed in the whole series, a propensity score analysis was performed. After IPTW adjustment, the distributions of most demographic and clinicopathological characteristics were similar between the 3D-CRT and IMRT groups. The effect of the adjustment is depicted in Table 7. The analyses showed that IMRT was associated with significant benefits for the reduction of RID and RT-induced pulmonary changes after adjustment by IPTW (Table 8).

Table 7

Baseline Characteristics for Unweighted Sample and Inverse Probability of Treatment-Weighted (IPTW-ATE) Sample

Variables	Unweighted Sample		Standardized Mean Difference	IPTW-ATE		Standardized Mean Difference
	3D-CRT (n=134)	IMRT (n=174)		3D-CRT (n=307)	IMRT (n=308)
Age (mean, SD)	54.9 (10.6)	55.5 (10.9)	0.053	55.1 (15.8)	55.1 (14.4)	0.006
BMI (%)			−0.036			−0.006
≤24	64 (47.8)	80 (46.0)		144 (46.9)	144 (46.8)
>24	70 (52.2)	94 (54.0)		163 (53.1)	164 (53.2)
Surgery type (%)			−0.170			0.005
BCS	89 (66.4)	129 (74.1)		217 (70.8)	218 (70.9)
Mastectomy	45 (33.6)	45 (25.9)		90 (29.2)	90 (29.1)
Nodal irradiation (%)			0.016			0.005
No	79 (59.0)	104 (59.8)		183 (59.4)	183 (59.5)
Yes	55 (41.0)	70 (40.2)		124 (40.6)	125 (40.5)
Hypofraction (%)			0.179			−0.010
No	112 (83.6)	156 (89.7)		267 (86.9)	268 (87.0)
Yes	22 (16.4)	18 (10.3)		40 (13.1)	40 (13.0)

Table 8

Odds Ratios for Study Outcomes Between IMRT and 3D-CRT Groups by Different Analysis Approaches

	Acute Skin Toxicity		Toxicity (Chest–Lung)
	OR (95% CI)	P-value	OR (95% CI)	P-value
Unweighted Sample
RT type
3D-CRT	Reference	-	Reference	-
IMRT	0.26 (0.13–0.51)	<0.001	0.47 (0.27–0.80)	0.006
IPTW-ATE
RT type
3D-CRT	Reference	-	Reference	-
IMRT	0.24 (0.15–0.40)	<0.001	0.46 (0.31–0.67)	<0.001

Note: Models were adjusted by age, BMI group, surgery type, and nodal irradiation.

Discussion

In recent years, promising RT techniques have been developed to improve dose conformality and homogeneity for BC patients. However, the correlation between dosimetric parameters and the incidence of radiation-induced OAR toxicity requires further investigation. First, we examined the incidence of radiation dermatitis and its relationship with volume of radiation hotspots and RT techniques. According to previous finding,12 we applied the constraint of TV-V110% <5% in treatment planning for BC. As a result, the incidence of grade 3 skin toxicity decreased from 1.9% to 1% compared to that our previous study. We suggest that further significant advancements in conformal treatment delivery have helped to reduce the volume exposed to higher doses; this in turn has resulted in decreased toxicity outcomes. In the present study, we demonstrated that the larger volumes of radiation hotpots (TV-V105% and V107%) were significant predictors of radiation dermatitis. Furthermore, we demonstrated that IMRT significantly improved dose inhomogeneity and decreased volumes of radiation hotspots compared with 3D-CRT. In addition to dose parameters, we found that BMI > 24, total mastectomy, and simultaneous nodal irradiation were associated with a higher incidence of radiation dermatitis. There are still no well-established prophylactic treatments available to prevent RT-induced skin toxicity.26 We previously reported that prophylactic skincare significantly attenuated the risk of radiation dermatitis.12 Greater than 90% of patients in the study received prophylactic skin treatment. It may explain why the use of prophylactic treatment did not significantly decrease the incidence of radiation dermatitis in the present study.

The lung is sensitive to radiation and side effects may arise, as acute pneumonitis and late lung fibrosis. RT-induced lung toxicity may arise, either acutely or as a chronic disorder following RT.27–29 Clinically, symptomatic RP is one of the major toxicity for irradiated BC patients.30 In our study, none of the patients developed significant symptomatic RP, but there were 81 patients (26%) did develop radiographic changes within RT field, as noted in follow-up images. In the present study, total mastectomy and adding regional nodal irradiation were associated with a higher risk for developing RT-induced radiological changes. The risk for RT-induced lung toxicity is reported to be influenced by the irradiated lung volume, dose and RT field.31,32 The incidence of pulmonary complications in adjuvant 3D-CRT for BC is clinically significant.33 We demonstrated that IMRT significantly decreased the incidence of RT-induced pulmonary changes from 34% in 3D-CRT to 20% in IMRT. With today’s CT-based-planning techniques, we can individually quantify and limit the amount of incidentally irradiated lung volume.16 The MLD and the ipsilateral lung V20 were reported to be critical to induce RP in cancer patients with lung irradiation34,35. For left-BC patients with RT, we demonstrated that MLD and V20 of the ipsilateral lung were significantly associated with the risk of developing RT-induced pulmonary changes. We further used the median value of by MLD (10.2Gy) and V20 (20%) to divide the 308 patients into lower and higher groups. The data revealed that both V20<20% and MLD <10.2Gy for ipsilateral lung were associated with significantly lower RT-induced radiologic changes. Based on our data, individual CT-based dose planning and dosimetric analysis of ipsilateral lung is important for the reduction of RT-induced lung injury.

It has described that adjuvant RT contributed to the induction of ischemic heart disease for left-sided BC population.15,36 A comparison of all patients in our series revealed that BMI>24, total mastectomy and nodal irradiation were significantly associated with increased MHD. It has been reported that variations in chest shape can impact the cardiopulmonary dose received.37,38 In the present study, there was a positive correlation between the MHD and DHL. The patients with DHL ≥ 2.47 cm were associated with higher MHD compared to those lower DHL. As the incidence of ischemic heart disease is proportional to the MHD,14,39 it was advised a reduction of the dose to the heart by as much as possible. Furthermore, the risk of cardiac events is likely to be related to dose and irradiated volume.25,40 In our study, patients treated with IMRT had significantly lower MHD associated with reduced the irradiated volume and dose in the heart for left-BC patients compared to 3D-CRT.

In the present study, the benefits of IMRT compared to conventional 3D have been evaluated. Dosimetry studies have shown that IMRT results in similar target volume coverage, better conformity, and a reduced volume of normal tissues that are irradiated at a high dose. Dosimetric studies showed that volumetric modulated arc therapy (VMAT) also improved target volume coverage and delivered better dose homogeneity.14 The potential risk existing in IMRT and VMAT are that these techniques expose the heart to a substantial “low dose bath” from multiple beam angles. Furthermore, research has shown a further reduction in cardiac exposure by implementing respiratory management methods during radiation delivery, such as deep inspiration breath hold (DIBH). In our preliminary study,23 a regimen using IMRT and DIBH resulted in a significantly lower MHD and Dmean of the LAD compared to FB plans for left BC. However, there were variability of dose reductions by DIBH, and not all patients receive the same benefit from the DIBH technique. In general, choosing which kind (one or more) of methods to use is mainly based on individual characteristics and RT regions. Therefore, to enroll more left-BC patients using IMRT and DIBH would be helpful to find factors to identify which patients derive the most benefit from the IMRT and DIBH technique. The main limitation of this study was that was retrospective in nature and lacked data on long term follow-up for cardiopulmonary toxicity. Therefore, longer follow-up and further investigations that include more patients in a prospective trial are needed.

Conclusion

In general, the choice of adjuvant RT, and the type of methods used are mainly based on individual characteristics and target regions. Our data suggest that IMRT spared high-dose levels to OARs, and offers better dose conformity than 3D-CRT technique for left-BC patients.