Background
The INT0116 study revealed the survival benefits of postoperative radiotherapy for gastric cancer patients [
1,
2]. Moreover, both the 3-year and 11-year follow-up results affirmed the overall survival and disease-free survival benefits of radiotherapy [
1,
2]. Despite these results, however, gastric cancer radiotherapy remains controversial. Specifically, concerns remain regarding radiation-induced toxicity. The toxicity levels reported for the INT0116 study included grade 3 (40 %), grade 4 (32 %), and gastrointestinal toxicity (33 %), and three cases involved treatment-related deaths. Consequently, treatment-related toxicity remains a limiting factor for the application of gastric cancer radiotherapy [
1].
In recent years, three-dimensional conformal radiotherapy (3DCRT) and intensity modulated radiotherapy (IMRT) have been widely used for the treatment of cancer. These techniques address the drawbacks of conventional anteroposterior-posteroanterior techniques, such as under-dosage of target regions and excessive radiation to surrounding normal structures. An advantage of IMRT technology over 3DCRT for the treatment of nasopharyngeal carcinoma, prostate cancer, and lung cancer has been improved dose distribution within the target area, better dose hotspot control, and reduced radiation exposure to organs at risk (OAR), including the brain stem and spinal cord [
3‐
5]. However, it continues to be debated whether IMRT or 3DCRT is better for gastric cancer radiotherapy [
6,
7]. In our previous study, IMRT was found to provide better target uniformity and conformality than four-field 3DCRT. However, IMRT did not reduce the dose applied to the OAR (e.g., the liver and kidneys) [
8]. Therefore, the availability of new technologies is of great interest.
RapidArc (RA) is a type of dynamic IMRT that involves application of a rotation beam according to Otto’s rotation theory of intensity-modulated radiation therapy. Briefly, by dynamically changing the gantry rotation speed, the shape of the multi collimator leaves, and the dose rate, RA can rapidly and efficiently achieve superior radiation dose distribution [
9]. As such, RA technology has the potential to shorten treatment time and reduce the possibility of target movement during treatment, thereby increasing treatment accuracy. Currently, the literature available regarding RA mainly focuses on the treatment of breast, prostate, and lung cancer [
10‐
12]. In contrast, only a few studies have reported clinical applications of RA for gastric cancer [
13].
To date, neither 3D-CRT nor IMRT have shown a clear advantage in gastric cancer radiotherapy. This is mostly attributed to the extensive region of the OAR that is involved. It also remains to be determined whether RA technology would improve the outcome of gastric cancer radiotherapy. Therefore, the goal of this study was to compare the dose distribution of RA, static gantry IMRT, and 3DCRT for the radiotherapy treatment of gastric cancer using dosimetric analysis, and to evaluate which external radiation technology is best for the postoperative treatment of gastric cancer.
Discussion
Currently, postoperative chemoradiation is one of the main treatments for cases of gastric cancer with poor prognosis. However, due to the proximity of this region to many vital organs, it remains a challenge to effectively cover the target area and protect neighboring vital organs. For adjuvant radiotherapy modalities, it has been difficult to achieve an ideal dose distribution with traditional 3DCRT, while IMRT is able to simultaneously optimize target dose and decrease exposure of OAR. IMRT has also been shown to effectively improve local tumor control, to reduce the extent of radiation damage to normal tissues, and to improve patient quality of life [
22]. However, in our previous study of 3DCRT and IMRT for the treatment of gastric cancer, radiation dosimetry data indicated that IMRT did not show a significant advantage over 3DCRT, with 3DCRT being superior to IMRT for V
20 of the left and right kidneys [
8]. Therefore, new radiotherapy techniques for the treatment of gastric cancer are still needed.
RA technology has the potential to shorten treatment time and reduce the possibility of target movement during treatment, which would serve to increase treatment accuracy [
18]. RA has previously been applied to the treatment of many types of tumors [
23,
24]. For example, in work by Verbakel et al. [
25], twelve patients with advanced head and neck cancer received IMRT versus RA radiation therapy. Treatment with RA was found to improve target dose uniformity and to reduce exposure of neighboring OAR. Furthermore, double arc RA provided additional dosimetric advantages compared to single arc RA and IMRT. These advantages were confirmed with the treatment of lung cancer and prostate cancer with double arc RA [
11,
12]. However, for gastric cancer radiation therapy, the shape of the radiation target is irregular and the surrounding organs, including the liver and kidneys, have a low tolerance for radiation. Thus, it remains to be determined whether a rotary volumetric IMRT technique will be advantageous for gastric cancer radiotherapy.
The cohort studied included 15 postoperative gastric cancer patients. Based on the location of their lesions and CT imaging, 3DCRT (4-field), IMRT (5-field), or RA treatment plans were applied. The prescription dose included 45 Gy/25 F applied to the PTV, with >95 % of the PTV receiving 45 Gy and 99 % of the PTV receiving 42.75 Gy. All three plans met the dose requirements and there were no significant differences between them. Furthermore, IMRT and RA reduced the target maximum dose and the high dose range (D
1%, V
107%) compared to 3DCRT. IMRT and RA were also superior to 3DCRT for target volume uniformity. The CI value for RA was significantly closer to one than the CI values for IMRT and 3DCRT, suggesting an improved conformality was achieved. For targets with larger and more complex shapes, RA was found to provide better dose distribution, better PTV target conformality, and better target dose distribution, and these results are consistent with previous studies [
13]. Thus, RA has the potential to reduce treatment-related side effects.
In the early studies of organ tolerance to ionizing radiation, radiosensitivity of the liver may have been underestimated. Tolerance doses were limited according to the risk of RT-induced liver disease, and the mean dose and V30 for the liver were considered important dosimetric parameters associated with increased toxicity risk [
26]. Meanwhile, more recent studies have shown that normal liver cells are sensitive to radiation, especially when the liver is infected with hepatitis B virus [
26]. Accordingly, Dawson et al. [
27] have suggested that the tolerance dose for the liver should be less than 30 % for V
30, and the D
mean should be less than 30 Gy. For cases involving hepatitis B infection, the D
mean should be less than 23 Gy. Furthermore, according to the Quantitative Analyses of Normal Tissue Effects in the Clinic (QUANTEC) effort, the mean liver dose should be less than 28 Gy in 2-Gy fractions for primary liver cancer, and should be less than 32 Gy in 2-Gy fractions for liver metastases [
26]. In the present study, liver V
30 was (12.32 ± 1.61) % for 3DCRT, (12.73 ± 1.33) % for IMRT, and (6.90 ± 1.41) % for RA, with the latter being significantly lower than the two former values (
P <0.05). Liver D
mean was 17.61 ± 0.82 Gy for 3DCRT, 14.22 ± 0.23 Gy for IMRT, and 15.31 ± 1.11 Gy for RA, and these did not significantly differ. Compared with 3DCRT and IMRT, RA significantly reduced liver V
30, yet did not affect the average liver dose. Furthermore, despite the significant reduction in liver V
30, an analysis of volume from the DVH showed that V
10 increased. These results are consistent with those reported for a liver cancer radiation treatment study performed by Kuo et al. [
28].
The kidney is another important organ that is threatened by gastric cancer radiotherapy. Kidney tissue is radiosensitive, and the recommended radiation tolerance doses are 23 Gy for the whole kidney, 30 Gy for 2/3 of the kidney, and 50 Gy for 1/3 of the kidney. A study by Jansen et al. further suggested that the average renal dose was less important than V
20. Therefore, it is recommended that <70 % of the kidney volume should receive 20 Gy (V
20 <70 %), while the V
20 for the contralateral kidney should be <30 % [
29]. In total, kidney tissues exposed to more than 20 Gy should not exceed 50 % of the whole kidney, otherwise, radiation-induced damage to the kidney may occur, such as a decrease in the glomerular filtration rate and/or renal failure. Thus, an ongoing goal is to reduce the radiation dose to kidneys during postoperative radiotherapy for gastric cancer. Minn et al. [
30] studied the dosimetry, efficacy, and toxicity of radiotherapy planning with 3DCRT and IMRT for 57 cases of gastric cancer, and IMRT was found to reduce kidney V
20. In our previous study, no obvious difference in the V
20 of kidney between IMRT and 3D-CRT was observed, although IMRT exhibited favorable tumor coverage and superiority in protecting the spinal cord and liver. However, this superiority was not observed in the kidney compared with 3D-CRT. Thus, IMRT does not appear to represent a superior treatment for gastric cancer [
8]. Similarly, in our subsequent single arc RA study, kidney radiation dose was not significantly reduced, yet double arc RA significantly decreased kidney V
20 compared to IMRT and 3DCRT for both kidneys. Meanwhile, there was no obvious difference in the D
mean for both kidneys among the 3D-CRT, IMRT, and RA treatments. Taken together, these results suggest that RA can provide a protective effect for kidneys compared to IMRT.
Gastrointestinal toxicity is the main limiting factor for the application of radiation therapy to gastric cancer. Correspondingly, the key to reducing toxicity due to radiotherapy is to control the exposure of the gastrointestinal tract to radiation. In many studies, IMRT and RA have been shown to reduce the radiation dose to the gastrointestinal tract during abdominal radiation therapy. For example, Minn et al. [
30] demonstrated that IMRT reduced intestinal V
45 compared to 3DCRT. In another study of 14 cases of abdominal metastases treated with radiation therapy, Mario et al. [
30] reported that RA and IMRT reduced the average dose and maximum dose to the stomach and small intestine compared to 3DCRT. However, the difference was not significant. In the present study, the average dose (D
mean) for the small intestine, as well as V
30 and V
40, were examined. D
mean for the small intestine did not significantly differ among the three planning methods, yet a DVH chart analysis showed that IMRT and RA increased V
10 and reduced V
30 and V
40 compared to 3DCRT. Thus, the volume of the low dose region increased concomitant with a decrease in the volume of the high dose region. These results are consistent with the observation that the average dose did not show a significant difference.
The spinal cord is a long, thin, tubular bundle of nervous tissue and it is susceptible to injury from local high doses of radiation. Kirkpatrick et al. [
31] reported that the incidence rate for radiation myelitis is 0.2, 6, and 50 % the total dose for 50 Gy, 60 Gy, and_69 Gy, respectively, when administered at the conventional fraction of 2-Gy per day. In addition, according to the Radiation Oncology Group of the European Organisation for Research and Treatment of Cancer, the maximal radiation dose that should be applied to the spinal cord is 45 Gy, and it should not exceed 40 Gy if oxaliplatin chemotherapy is administered as well [
16]. Therefore, the maximum dose for the spinal cord is generally set at no more than 45 Gy. In the present study, the doses applied to the spinal cord with each of the three techniques were all within the tolerated dose. Moreover, compared to 3DCRT, the D
max for the spinal cord with RA was significantly reduced by up to 15.71 %.
RA is an adjuvant radiotherapy modality that has recently been developed and has been used to deliver high doses of radiation to a variety of tumors. However, its role in the treatment of gastric cancer remains controversial due to the irregular target volumes involved and the low radiation tolerance of surrounding critical organs. In our previous study, RA provided superior dose homogeneity compared with 3DCRT and IMRT, but not better protection of the OAR. Moreover, while the single arc technique was unsuccessful, the double arc technique was able to achieve the same dose distribution as IMRT, while significantly sparing the OAR and proximal healthy tissue. This improved protection of liver and kidney tissues compared with IMRT suggests a higher dose could be applied to a target volume using double arc RA. However, it is important to consider the limitations of our study as well. First, a respiratory gating technique was not used, and its influence on the dose distribution was not investigated. In addition, the present study had a small sample size and did not evaluate clinical efficacy and toxicity. Therefore, further studies are needed to confirm the technical feasibility of applying double arc RA to the treatment of gastric cancer, and these should include a larger sample size and evaluations of clinical efficacy and toxicity.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
TZ and Z-WL contributed significantly to the design and concept of this study, HM drafted the manuscript. JH, J-PB, and Z-YY contributed to optimization of the treatment plans. All of the authors have read and approved the final manuscript.