Background
Non-small-cell lung cancer (NSCLC) is one of the leading causes of cancer mortality worldwide, and approximately 25–30% of patients are initially diagnosed with stage III, which is inoperable [
1,
2]. Definitive concurrent chemoradiotherapy (CCRT) was the standard treatment for locally advanced NSCLC, but it showed a short progression-free survival (PFS) of 8–11 months and overall survival (OS) of 20–23 months [
3‐
5]. Many immunotherapy agents have been developed and have demonstrated promising results in locally advanced NSCLC patients, including immune checkpoint inhibitors (ICIs), which activate anti-tumor immune responses [
6‐
8]. Notably, in the PACIFIC trial, the use of consolidative durvalumab after CCRT led to remarkable tumor control results. With the use of durvalumab, the median PFS was extended to 16.8 months versus 5.6 months with a placebo, and the 3-year OS rate with durvalumab and a placebo was 57.0% and 43.5%, respectively [
9,
10]. Therefore, the use of adjuvant durvalumab in patients with unresectable NSCLC, whose conditions did not worsen after definitive CCRT, is now the new standard of care.
With the advent of the immunotherapy era, issues regarding the safety of treatment when administered with CCRT have emerged, although many studies have shown that the combination of ICI and CCRT is generally safe. However, in the PACIFIC trial, despite no observed significant differences, the incidence of any grade of pneumonitis was found to be 9.1% higher in the durvalumab group [
9]. Radiation pneumonitis (RP) is a major complication in patients who have undergone thoracic irradiation, which can lead to a decreased quality of life, decreased performance status, and the early termination of further treatments; therefore, this needs to be carefully considered. Several studies have proven that some clinical and dosimetric factors are closely related to the occurrence of RP [
11‐
13]. However, most have been conducted on CCRT-only groups; a few studies have targeted the patients who were additionally prescribed ICI after CCRT but only as a small cohort or as a single-arm study [
14].
Therefore, we investigated the incidence of RP when ICI is used for any reason after definitive CCRT in patients with NSCLC who are unable to undergo surgery. In addition, we also sought to investigate which clinical and dosimetric factors are associated with the occurrence of RP.
Methods
Patients
We retrospectively reviewed the medical records of 143 consecutive NSCLC patients who underwent definitive CCRT with curative intent at Asan Medical Center from May 2018 to May 2020. Patients treated with ICI after CCRT were classified into the ICI group, and those who had never received ICI were classified into the non-ICI group. Among these patients, 37 were excluded from the analysis for the following reasons: patients with double primary cancer in the 5 years prior to the diagnosis of NSCLC (n = 7), distant metastasis at the time of diagnosis (n = 7), a history of previous lung surgery (n = 1), a history of previous thoracic radiation therapy (RT) (n = 2), radiation dose < 45 Gy (n = 1), use of ICI < 2 cycles (n = 8), and short follow-up period after CCRT of < 3 months (n = 11). Finally, 106 patients were enrolled in this study, and all of them underwent tissue biopsy, chest computed tomography (CT), 18-fluoro-deoxyglucose positron emission tomography (FDG-PET-CT), brain magnetic resonance imaging, and/or a pulmonary function test (PFT) before definitive treatment. The clinical stage of the patients was evaluated based on the 8th edition of the American Joint Committee on Cancer staging system.
Treatments
Radiation targeted the primary tumor and clinically-involved lymph nodes. A lymph node was included in the gross tumor volume if the longest diameter was > 1 cm on its short axis by CT image and/or if the tumor had a hypermetabolic uptake on FDG-PET-CT or was proven to be a metastatic carcinoma by biopsy. No elective nodal irradiation was performed. A median total dose of 66 Gy (range, 46.0–73.0 Gy) was administered, and the fraction size was either 200 or 220 cGy. All patients received RT with the intensity-modulated radiotherapy technique. Radiation was delivered once daily (five times per week) with four to six coplanar or non-coplanar beams, and treatment verification was performed by weekly kV imaging guidance using set-up correction based on the carina and bony anatomy. The organs at risk included both lungs, the esophagus, the spinal cord, and the heart. The normal organ constraints included a maximal dose for the spinal cord of < 50 Gy, a mean lung dose (MLD) of < 20 Gy, a volume of lung receiving at least 20 Gy (V20) of < 30%, a mean esophagus dose of < 35 Gy, and a volume of heart receiving at least 60 Gy (V60) < 1/3, V45 < 2/3 and V40 < 100%. The following dosimetric parameters were generated from the dose-volume histogram (DVH) for the total lung: MLD, size of planning target volume (PTV), and the percentage of lung volume receiving more than a threshold radiation dose (VD), which refers to the relative lung volume receiving radiation above the threshold dose. As for the dose considered in VD, five variables were observed from 5 to 40 Gy (V5, V10, V20, V30, and V40).
Regarding chemotherapy, patients were prescribed paclitaxel-based paclitaxel and cisplatin (TP), paclitaxel and carboplatin (TC) regimen, an etoposide-based etoposide and cisplatin (EP), etoposide and carboplatin regimen, or cisplatin with pemetrexed. Of 106 patients, 51 received ICI after CCRT (Additional File
1). As the analysis was performed regardless of the treatment aim, all patients with consolidative, salvage, and palliative aims were enrolled together. PD-1/PDL-1 inhibitors were used as ICIs, including durvalumab, atezolizumab, pembrolizumab, and nivolumab. Durvalumab was prescribed at 10 mg /kg every 2 weeks, atezolizumab at 1200 mg every 3 weeks, pembrolizumab at 200 mg every 3 weeks, and nivolumab at 3 mg/kg every 2 weeks (all injected intravenously). All ICIs were discontinued when patients were determined to be intolerant due to adverse events or progressive disease.
Follow-up and outcomes
During the CCRT period, chest X-rays (CXR) and complete blood counts were performed weekly. All patients were regularly followed up by a radiation oncologist and a medical oncologist after the termination of CCRT. At each follow-up, history taking, physical examination, CXR, and blood tests were performed. Chest CT was performed every 6 months for 2 years and annually for 5 years.
The primary endpoint was RP ≥ grade 2. RP was assessed according to the toxicity criteria of the lung fibrosis established by Radiation Therapy Oncology Group and the European Organization for Research and Treatment of Cancer. The definitions were as follows: Grade 1, with no symptoms such as cough or shortness of breath and/or no opacity changes on chest CT; Grade 2, with moderate symptoms which require outpatient steroid treatment and/or patchy image changes; Grade 3, with severe symptoms which need hospitalization and/or increased density imaging changes; Grade 4, with severe symptoms requiring continuous O2 or assisted ventilation; Grade 5, expired. Based on the readings of the experienced chest radiologist, the RP was assessed by two radiation oncologists blindly on whether ICI was administered or not. Otherwise, all toxicity excluding RP, was assessed according to the National Cancer Institute’s Common Terminology Criteria for Adverse Events ver. 5.0. The secondary endpoints were survival rate, locoregional failure (LRF) rate, distant metastasis (DM) rate, and acute and late toxicity. The LRF rate was evaluated by dividing cases into in-field and out-of-field failures based on whether the failure occurred inside or outside the PTV field. Recurrence in the ipsilateral lung was considered as LRF, and nodules in the contralateral lung or any pleural metastasis were considered as DM.
Statistical analysis
Statistical analyses were performed using SPSS version 22.0 (SPSS Inc., Chicago, IL, USA) and R version 3.6.1 (web-r.org). To compare the distribution of patient, disease, and treatment characteristics between the ICI group and non-ICI group, an independent-sample t-test was performed for continuous variables and chi-square test was performed for non-continuous variables. A receiver operating characteristic (ROC) curve was drawn to evaluate how well each DVH parameter could distinguish the incidence of RP, and through this, a suitable cut-off value and significance probability were calculated. Based on the cut-off values estimated from here, univariate and multivariate analyses for the occurrence of pneumonitis for the ICI and non-ICI groups were assessed with Fine and Gray competing risk regression analysis. P-values below 0.05 were considered statistically significant.
Discussion
Several small cohort studies have reported the occurrence of RP in patients with NSCLC after the use of ICI with CCRT. In a study by Narek et al., RP ≥ grade 2 occurred in 18% of patients using durvalumab after CCRT, which was significantly higher than that of the CCRT-only group, which was only 9% (
p = 0.09) [
15]. A single-arm study by Moore et al. found that 54% of patients who took durvalumab after CCRT had RP ≥ grade 2 [
14]. In our study, the incidence was 16.5% higher in the ICI group than the non-ICI group, showing a similar tendency to the previous studies (ICI group 52.9% vs. non-ICI group 36.4%,
p = 0.043). In the PACIFIC trial, any grade of RP was 9.1% higher in the ICI group (durvalumab group 33.9% vs. placebo group 24.8%), and the difference in the incidence of RP between the treatment groups was slightly greater in our study. However, for RP ≥ grade 3, similar incidence rates were observed between the two groups in both our study and the PACIFIC study [
16].
In general, RP ≥ grade 2 is known to occur in 10–40% of patients with NSCLC who undergo CCRT with conventional fraction [
17]. In our study, 44.3% of patients developed RP ≥ grade 2, a higher incidence than that observed in other studies. There are likely to be several reasons for this result. First, the PACIFIC trial subgroup analysis found that Asians and patients with EGFR mutations had a high incidence of RP [
16]. As the participants in our study were all Koreans, racial factors could explain the high RP incidence. Second, a high percentage of patients had EGFR mutations in this study; even if the mutation itself was not identified as a risk factor in univariate analysis in this study, in the PACIFIC trial, mutations were found in 8.2% of those tested and in 23.4% in this study. Third, patients who received neoadjuvant chemotherapy before CCRT were not included in this study. If the tumor size is reduced through induction chemotherapy, it can be expected that the radiation administered to the normal lung can also be reduced. In the PACIFIC trial, approximately a quarter of patients underwent induction treatment before CCRT. Finally, the high incidence of RP in the current study may be due to the early initiation of steroid therapy when the patient complained of a mild cough or dyspnea, which might be less associated with RP.
Some studies have indicated that clinical factors, including the presence of chronic lung disease, stage IIIA or higher disease, tumors located in the lower lobe, and previous history of RT, can significantly increase the probability of RP ≥ grade 2 [
13]. However, none of these were found to be associated with the occurrence of RP in our study. Among clinical factors, only the use of ICI was found to be a significant factor. On the other hand, we found that initiating ICI at any point after the end of CCRT did not affect the development of RP; thus, it would be unnecessary to deliberately initiate immunotherapy late due to concerns about the potential side effects.
In our study, only V20 was identified as a factor correlated with RP in the non-ICI group. However, in the ICI group, significant HR were shown with V30 and V40, and the incidence of RP was found to increase in the high VD area. Usually, the lung volume irradiated with a high dose tends to correlate with target size. However, when observing the correlation between the PTV size and RP, the HR was 1.459, and there was no significant difference between the two groups; thus, V30 and V40 may have had a relationship with RP distinct from the field size. In addition, a similar study by Satoshi et al. also found that V30 had the largest AUC among various parameters in patients receiving adjuvant durvalumab after CCRT [
18]. Previous studies have shown that sufficient lymphocytic infiltration is achieved through RT, which turns “cold” tumors “hot” and creates a tumor microenvironment (TME) that can respond well to various ICIs [
19]. However, there remains controversy regarding the optimal dose and fraction scheme that can induce a change in the TME, and no definite conclusions have been drawn. In a preclinical study based on NSCLC cell line, the most potent T cell infiltration was induced by high-dose radiation; according to another study by Marconi et al., the probability of the occurrence of the abscopal effect based on changes in the immunologic environment is 50% with a biologically effective dose of at least 60 Gy [
20,
21]. Therefore, there is a high possibility that a “hot” tumor environment will be created in the high dose area, which may be beneficial in terms of tumor cell control but is also the reason for the increased incidence of RP.
The survival and local control rate were superior in the ICI group, showing similar trends as those reported in the PACIFIC trial. However, these results were not significant, and we predict that this is due to an insufficient follow-up period of < 1 year. In addition, patients with varying responses after CCRT were recruited into one group despite receiving different types of ICI, which makes it difficult to compare oncological outcomes directly. Future studies should be conducted on a larger number of patients with more uniform conditions and treatment characteristics, after which it is expected that results similar to those of other prospective studies will be obtained.
The limitations of this study were the small number of patients and the short follow-up time. Additionally, owing to the study's retrospective nature, the patient characteristics were somewhat different. Nonetheless, it would be of great significance to establish the frequency of adverse events in the new treatment combination and which factors affect them in the actual clinical situation.
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