Background
According to the 2008 global cancer statistics, the morbidity and mortality of lung cancer ranks first worldwide [
1]. China also faces a similar situation. According to the 2010 data released by the National Cancer Control Office of the National Cancer Center, the new cases of lung cancer every year totaled approximately 600,000, and the cases of death number approximately 490,000 [
2]. For unresectable locally advanced non-small cell lung cancer (NSCLC), concurrent radiochemotherapy is the standard treatment [
3,
4]. The classical concurrent radiochemotherapy program uses conventional fractionated radiation with a total dose of 60–66 Gy; however, the local recurrence rate is still as high as 30 % [
4]. Studies have suggested that increasing the tumor radiation dose could increase the local control, thus improving survival [
5,
6]. However, the RTOG06-17 study using the conventional fractionated regimen showed that, compared with the 60-Gy group, the survival was not increased in the 74-Gy high-dose group [
7]. Although the exact reasons were not clear, the very long treatment time (7.4 weeks) in the high-dose group might be one of the reasons [
3].
Studies in head and neck squamous cell carcinoma have shown that tumor cells start to accelerate repopulation after 4 weeks of radiotherapy; at this time, the doubling time of tumor cells shortened from 60 days without interference to 4 days. To eliminate this re-proliferation, an extra 0.6-Gy dose was required each day for compensation [
8]. This result also partially explained the possible reasons behind the poor effect of conventional fractionated radiotherapy. For NSCLC radiotherapy, after 4 weeks, when the treatment time was increased by 1 day, a 0.45-Gy radiation dose was lost. Therefore, extension of the total treatment time might be a key reason causing the failure of local control [
9]. The continuous, hyperfractionated, accelerated radiotherapy (CHART) program continued giving hyperfractionated radiation for 12 days; although the total dose was only 54 Gy, the absolute value of the 2-year survival increases by 9 % compared with the conventional fractionation of 60 Gy (2 Gy/fraction) (29 % vs 20 %, respectively) [
10]. Hypofractionated radiotherapy has a dosimetric advantage; it shortens the treatment time, increases the biological effective dose (BED), and can potentially reduce the effect of accelerated repopulation on local failure [
6,
11]. Compared with hyperfractionated radiation, hypofractionated radiotherapy has the advantages of convenience, economy, and easy implementation; thus, it has increasingly more clinical applications [
12‐
29].
It has been confirmed that combined radiochemotherapy is better than radiotherapy alone [
30], conventional fractionated radiotherapy with concurrent chemotherapy is better than sequential radiotherapy and chemotherapy, and the overall survival (OS) shows benefits with a 5.7 % 3-year OS and a 4.5 % 5-year OS [
4]. Similarly, hypofractionated radiotherapy combined with concurrent chemotherapy can also theoretically further increase the efficacy. Experimental research has shown that hypofractionated radiotherapy with concurrent chemotherapy could increase the efficacy [
31]. However, due to the concern about the aggressive toxicity of hypofractionated radiotherapy with concurrent chemotherapy, this type of clinical research is relatively rare. The applied fractionated dose and chemotherapy regimens have larger differences, and the optimal program of hypofractionated radiotherapy with concurrent chemotherapy has not been confirmed. We previously conducted a phase I study of hypofractionated radiotherapy (3 Gy/fraction) with concurrent chemotherapy and considered that NSCLC could tolerate the high 69-Gy dose [
32]. Base on this finding, we performed the current phase II study to further evaluate the safety and preliminary efficacy of 69-Gy/23-fraction (3 Gy/fraction) hypofractionated radiotherapy with concurrent radiochemotherapy. Only 12 cases were enrolled in this study. Because of the strong esophagus and lung toxicity, this trial was prematurely terminated. The detailed results are reported below.
Discussion
The treatment failure of the primary lesions of NSCLC had negative effects on PFS, metastasis-free survival, and OS [
37]. Increasing the tumor radiation dose could increase the local control and improve survival [
5,
38]. A study using model analysis obtained the same conclusion: the radiotherapy dose and survival had a significant dose-effect relationship, and a high radiotherapy dose could obtain a better 2-year PFS [
8]. However, only increasing the radiotherapy dose alone was not sufficient. RTOG0617 used 74 Gy for conventional radiotherapy (concurrent with chemotherapy), and the total treatment time was as long as 7.4 weeks; the results showed that OS was not improved [
7]. The other key factor for the radiotherapy efficacy was the total treatment time [
10,
11]. Shortening the total treatment time could increase the BED [
11]. Application of the hypofractionated radiotherapy not only could obtain higher BED but also could shorten the total treatment time [
36]. Therefore, compared with hyperfractionated radiotherapy, it might obtain more benefits [
8].
Many studies have reported implementing hypofractionated radiotherapy on unresectable early- and middle-stage NSCLC (IA-IIB); the results showed that there was no severe esophagus and lung toxicities, and the survival results were inspiring [
12‐
15]. Hypofractionated radiotherapy (with or without sequential chemotherapy) on locally advanced NSCLC was also safe and effective. Concerning the toxicity of hypofractionated radiotherapy, the single fractionated dose was rarely above 3 Gy/fraction [
16‐
21]. Radiotherapy with 55 Gy/20 fraction and 2.75 Gy/fraction was extensively applied in the UK. Din et al. [
39] retrospectively analyzed 609 cases of hypofractionated radiotherapy, and the results showed that there were 227 cases of IIIA/IIIB, the MST was 20 months, the 2-year OS was 40 %, and toxicity could be tolerated. This regimen could also be implemented safely in the elderly population over the age of 80 years [
18].
Conventional fractionated radiotherapy with concurrent chemotherapy was better than simple radiotherapy or sequential radiochemotherapy [
3,
4]. Theoretically, it was hypothesized that hypofractionated radiotherapy with concurrent chemotherapy could reasonably further increase efficacy. Therefore, studies exploring hypofractionated radiotherapy with concurrent chemotherapy are emerging [
22‐
29]. These studies obtained inspiring survival results: the MST was 13.4–29.5 months, the 1-year OS was 56–90 %, and the 2-year OS was 30–58.3 % [
24‐
29]. However, except for two studies [
24,
27], all other studies had a small sample size and were single-group and phase I/II trials; the number of cases was small with only 10–37 participants. Therefore, these survival results must be confirmed by phase III randomized controlled trials. Although the multivariate analysis in a non-randomized retrospective study showed that radiochemotherapy was the only survival predictive factor [
40], but two prospective studies did not confirm that concurrent radiochemotherapy was better than sequential radiochemotherapy [
24,
27]. EORTC 08912–22973 was a randomized controlled trial with the most cases; it enrolled 158 patients and used the radiotherapy regimen of 66 Gy/24 fractions and 2.75 Gy/fraction. The concurrent chemotherapy used a low dose of cisplatin at 6 mg/m
2 every day. The MST, 2-year OS, and 3-year OS in the concurrent radiochemotherapy group and sequential radiochemotherapy group were 16.5 months and 16.2 months, 39 % and 34 %, and 34 % and 22 %, respectively; there were no significant differences [
27]. The Sequential or Concurrent Chemotherapy and Radiotherapy (SOCCAR) trial enrolled 130 cases. The radiotherapy regimen was 55 Gy/20 fractions and 2.75 Gy/fraction. The chemotherapy was the vinorelbine + cisplatin regimen. Although both groups obtained good survival results, there was no significant difference. The MST, 1-year OS, and 2-year OS in these two groups were 24.3 months and 18.4 months, 70 % and 83 %, and 50 % and 46 %, respectively [
24]. The hypofractionated regimens used in the above studies had very large differences; the fractionated dose ranged from 2.4 Gy/fraction to 3.5 Gy/fraction, the total dose ranged from 52.5 Gy to 66 Gy, and the total treatment time ranged from 26 days to 37 days, and the results were different; therefore, it was difficult to choose the best regimen from these results.
Our previous study performed dose escalation of the 3-Gy/fraction radiotherapy. The maximum-tolerated dose (MTD) recommended in the phase II trial was 69 Gy/23 fractions [
32]. However, currently, our phase II trial only enrolled 12 cases. Due to the aggressive esophageal toxicity (mainly esophageal pain) and lung toxicity, the trial was prematurely terminated. The percentage of grade III acute esophagitis in our study was far higher than those in other hypofractionated reports and reached 41.7 % (5/12). Five cases presented with intolerable esophageal pain, and 80 % (4/5) had different degrees of dysphagia, of which one case had very severe dysphagia and could only drink a small amount of water. It was considered that the reasons for the development of such severe esophagitis might be associated with the following factors. First, the total dose was 69 Gy, and the fractionated dose was 3 Gy/fraction in our radiotherapy regimen. The radiation on the esophagus regardless of the total dose or single dose might both be very high [
41,
42]. In addition, since the single fractionated dose was large, the rapidity of dose accumulation on the esophagus might cause severe esophagitis [
36]. Second, the whole group had 41.7 % lymph node metastasis with more than four stations and 50 % N3 lesions, thus causing extensive involvement of the mediastinum. Mediastinal infiltration and extensive lymph node metastasis are factors for the high incidence of esophagitis [
16]. Third, 41.7 % patients had Station 7 metastasis. Station 7 was adjacent to the esophagus; therefore, it was easy to cause the high-dose radiation on esophagus. In our study, the occurrence of esophagitis was early; the earliest case (No. 5) had already developed the complication at the 10
th fraction. Although the corresponding measures such as narcotic analgesic drug administration and nutrition support were provided, the grade III esophagitis persisted for 23 days before being reduced to grade II, thus causing 16 days of radiotherapy interruption. This patient had eight stations of mediastinal lymph node metastasis—1R, 2R, 4R, 4 L, 5, 7, 8, and 10. The V60 reached 49.9 %. The whole circumferential length of esophagus receiving more than 2.7 Gy and 3 Gy per fraction reached 13 cm and 4 cm, respectively. Regardless of the total radiation dose, irradiation length, dose-volume percentage, or irradiation dose per fraction to esophagus, they were all very high.
The dosimetric parameters of the occurrence of radiation esophagitis might be associated with the maximum radiation dose, irradiation length, and dose-volume parameters of the esophagus [
41‐
45]. Our study also confirmed these results. However, there were also some conflicting studies considering that these parameters did not have a clear correlation with esophagitis [
46,
47]. The dosimetric parameters of radiation esophagitis could not draw a very firm conclusion [
36], particularly for hypofractionated radiotherapy with concurrent chemotherapy [
22].
When the five cases of grade III esophagitis occurred in our study, the completed radiation dose was only 43 %, 52 %, 57 %, 57 %, and 65 % of the plan. In addition, at the end, they did not complete the radiation of the total dose (with the exception of the patient who had a 16-day interruption). Therefore, the maximum radiation dose and dose-volume parameters of the esophagus in these patients might not be the most relevant factors to predict severe esophagitis [
36]. Studies have shown that severe esophagitis was closely associated with the rapid accumulation of the radiation dose of the esophagus, a finding that might be more important than the final completed total irradiation dose [
36]. A single large-dose radiation on the esophagus would induce the rapid increase of the radiation dose of the esophagus. Our study also observed this condition: the percentage of severe esophagitis in patients who received one single dose per fraction of ≥2.7-Gy radiation on the esophagus was markedly higher than in those who received a dose lower than 2.7 Gy (80 % vs 0, respectively). Although there was no significant difference, it was considered that the cause might be due to the very small sample size. Therefore, we considered that the severe acute radiation esophagitis might be closely associated with the irradiation dose per fraction to esophagus ≥2.7 Gy.
Other hypofractionated radiotherapy studies also exhibited similar phenomena [
26,
27]. Koukourakis et al. applied the 3.5 Gy/fraction concurrent radiochemotherapy, although there was a routine 9-day interval, and also applied the cytoprotective adjuvant amifostine; however, the grade III esophagitis still reached 22.5 % [
26]. A study that applied 2.75 Gy/fraction had 17 % grade III/IV esophagitis [
27]. In these two high single-dose hypofractionated studies, the percentages of esophagitis were significantly higher than those in hypofractionated studies using a relatively smaller single dose [
25,
28,
29]. EORTC 08912 [
23] applied a large fractionated dose of 2.75 Gy/fraction; 17 cases received a total radiation dose >60 Gy of the esophagus that was one single irradiation dose of >2.5 Gy/fraction, and the mean length reached 11.4 cm. However, there were only two cases of grade III esophagitis; the radiation doses of the esophagus of these two cases were 65 Gy and 66 Gy, respectively—that is, the single irradiation doses were 2.71 Gy and 2.75 Gy, respectively. These results were consistent with our study results suggesting that the single dose equal to or larger than 2.7 Gy would induce severe esophagitis. Research in the Netherlands reported two cases of grade IV esophageal toxicity of which the radiation dose of the esophagus in one case was 66 Gy/27 fraction and 2.75 Gy/fraction [
40]. The above analyses supported the following conclusion. A single dose radiation per fraction ≥2.7 Gy in hypofractionated radiotherapy with concurrent chemotherapy might induce severe radiation esophagitis. In the three studies applying relatively small fractionated doses (2.5 Gy, 2.4 Gy, and 2.4 Gy, respectively), two studies did not have grade III or higher esophagitis [
25,
29], and the other one only had 3 % of grade III esophagitis [
28]. However, the number of cases in these studies was small, and the number of severe esophagitis cases was even smaller; therefore, this phenomenon was not a confirmed conclusion. In our study, among the five cases of grade III acute esophagitis, only one case was finally transformed into late grade III esophageal injury, indicating that 69 Gy might not cause a severe late esophageal toxicity. However, this result should be treated cautiously because only one case among these five cases completed 69 Gy of radiation (the radiotherapy was interrupted for 16 days due to esophagitis). This case showed rapid disease progression and died after 4 months of completion of the radiotherapy; the observation time was short and was not sufficient to exclude the possibility of the occurrence of grade III and above late esophageal injury. Three of other four cases completed only 74–78 % of the radiation dose; therefore, it could not verify the safety of the 69 Gy of radiation.
In our study, two cases of grade III radiation pneumonitis (16.7 %) transformed into one case of late grade III lung injury and one case of late grade II lung injury after 90 days. It was worth noting that patients who completed 69 Gy of radiation according to the plan had 28.6 % grade III radiation pneumonitis (2/7), and the actual incidence of lung injury might be underestimated (one case died due to disease progression after 4 months of the completion of radiotherapy; thus, the evaluation time for lung injury was short). Currently, there are no established data to guide the prevention and reduction of the development of radiation pneumonia during hypofractionated radiotherapy. Studies have shown that application of hypofractionated radiotherapy using the dose parameters obtained mainly from conventional hypofractionated radiotherapy might induce severe lung toxicity [
48,
49]. Therefore, the possibility of developing severe radiation pneumonia during hypofractionated radiotherapy is highly vigilant.
In our study, at the median 10-month follow-up, as high as 41.7 % grade III acute esophagitis and 28.6 % grade III acute pneumonitis (patients who completed the radiotherapy plan) were already observed. The late lung toxicity might be underestimated because of short follow-up time [
48]. Because a late lung toxicity was usually fatal [
48,
49], we considered that this hypofractionated radiochemotherapy regimen was not safe. In addition, grade III esophagitis in this study presented prominently esophageal pain; thus, 33.3 % patients in this group could not complete the whole 69-Gy radiotherapy, and the compliance of this regimen was poor. Therefore, this phase II trial was terminated early.
In our phase I study, the 69-Gy group enrolled six patients. There were only two cases of grade II esophagitis, and there was no grade III and above esophagitis. The esophageal toxicity was significantly lower than that in the current study [
32]. We reviewed the dosimetric parameters of the six patients and found that the maximum total doses of the esophagus of all patients were all ≤55.2 Gy—that is, the maximum single dose per fraction of radiation was ≤2.4 Gy. In the phase II study, the maximum irradiation dose per fraction to esophagus of four patients was ≤2.4 Gy, and there was no grade III esophagitis, findings that were consistent with the result of the hypofractionated concurrent radiochemotherapy using a relatively small single dose [
25,
28,
29]. In our phase I study, the 69-Gy group did not have grade III radiation pneumonitis. The latter finding was considered to be associated with the selection bias caused by the small number of cases. A similar phenomenon was also observed in a Canadian report. The maximum single dose per fraction of the dose-escalation was 3.24 Gy/fraction, the total dose was 70.7 Gy, the concurrent full-dose etoposide/cisplatin (EP) chemotherapy regimen was conducted for 2 cycles, and the median 22-month follow-up showed no grade III and above toxicity. Because there were only 10 patients in the group, the authors considered that the results should be cautiously treated with optimism because of the small sample size [
25]. Therefore, if the case number in the dose-escalation group was small, the result was not sufficient to exhibit the safety of this dose level, particularly with high-dose hypofractionated radiation [
48]. The survival data in our study are still not mature, and the MST was not achieved; however, for the 1-year OS of 78.6 %, these results were comparable to those of other literature reports (OS from 56 % to 90 %) [
24‐
29].
The studies on conventional fractionated radiotherapy in NSCLC focused heavily on lung toxicity However, they did not focus on the protection of the esophagus, and some studies did not even have limitation of irradiation dose to esophagus [
28,
29,
50]. Currently, the predictive factors and dose-volume parameters for esophagitis still cannot provide a confirmed conclusion, and the hypofractionated radiotherapy even requires new dosimetric parameters and other factors for evaluation [
36]. Although esophagitis, particularly acute esophagitis, is not fatal, it might affect the completion of the radiotherapy plan, interrupt radiotherapy, or decrease the radiation dose, thus reducing the local control rate. This situation is even more prominent in hypofractionated radiotherapy. Some studies have considered that the major obstacle of dose-escalation in hypofractionated radiotherapy was caused by the esophagus [
37,
40,
48], a finding that was also confirmed in our phase II study. Therefore, during hypofractionated radiotherapy, particularly concurrent radiochemotherapy, in addition to lung toxicity, acute esophageal toxicity should also be given close attention. The toxicity analysis in hypofractionated concurrent radiochemotherapy showed that the traditional dosimetric parameters did not have a good correlation with esophagitis [
22]. Therefore, exploring new predictive factors for esophagitis, particularly for late esophageal injury, has very important clinical significance.
Most radiotherapy studies used the unified prescription dose. However, the application of a fixed dose to all patients might have two consequences. First, some patients might receive a very low radiotherapy dose with insufficient treatment intensity, while other patients might receive a very high radiotherapy dose with strong side effects. The so-called “
in silico” dose prescription refers to the radiation dose limitation of normal tissues being set up in advance and is used as a standard to allow each patient to receive individualized different maximum radiation doses without increasing toxicity; thus, the treatment intensity is sufficient and safe; this dose is also called the “isotoxic” prescription dose [
37,
50‐
52]. In hyperfractionated studies, the application of this method effectively allows escalation of the radiotherapy dose; in addition, the mature survival results showed that the MST at the IIIB phase reached 17.2 months. This series of studies only conducted limitations of radiation dose on the lung and spinal cord [
50‐
52]. Hoffmann et al. [
37] applied the
in silico method to perform a study on individualized dose prescription for hypofractionation and pre-set the limits of radiation dose on the esophagus, lung, spinal cord, heart, and brachial plexus. The results of the model analysis showed that 79 % of cases had a therapeutic gain in dose escalation. During the pre-set of the radiation dose for normal tissues, the “physical dose” was transformed into the “biological effective dose”; thus, it was more in line with the radiation injury reaction of normal tissues after radiation and might be beneficial for reducing toxicity [
16,
25].
Modern advance radiotherapy technologies, including intensity-modulated radiation therapy (IMRT), image-guided radiation therapy (IGRT), 4D-CT, breathing adapted radiotherapy, particle radiotherapy [
53], and tomotherapy [
54], can more accurately irradiate tumors; at the same time, the radiation dose of surrounding normal tissues can be reduced. Using the
in silico method combined with advanced radiotherapy technology to perform radiotherapy with an individualized maximum dose based on the isotoxicity of normal tissues can theoretically achieve the dose-escalated hypofractionated concurrent radiochemotherapy more safely.