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Stereotactic body radiotherapy for very elderly patients (age, greater than or equal to 85 years) with stage I non-small cell lung cancer
Radiation Oncology volume 9, Article number: 138 (2014)
Stereotactic body radiotherapy (SBRT) for non-small cell lung cancer (NSCLC) is primarily a treatment option for medically inoperable patients, who are often elderly. However, few studies report the effects of SBRT in elderly patients. Thus, we retrospectively analyzed clinical outcomes and feasibility following treatment of very elderly patients (age ≥ 85 years) with stage Ι NSCLC and younger patients (age < 85 years) with SBRT in our institution.
From January 2006 to December 2012, 81 patients (20 very elderly; median age, 80 years; age range 64–93 years) with stage Ι NSCLC received SBRT. Prescription doses of 48 Gy were delivered in 4 fractions over 2 weeks or doses of 60 Gy were delivered in 10 fractions over 3 weeks.
Local control was achieved in 91.8% of all patients at 3 years (83.1% and 93.8% of very elderly and younger patients, respectively), and the 3-year overall survival (OS) rate was 69.4% (40.7% and 75.0% of very elderly and younger patients, respectively). OS rates were significantly shorter for the very elderly group than for the younger group, with a 3-year cause-specific survival (CSS) rate of 77.9% (50.4% and 81.6% of very elderly and younger patients, respectively) and a 3-year progression-free survival (PFS) rate of 59.5% (44.7% and 63.5% in very elderly and younger groups, respectively). Multivariate analysis revealed a significant correlation between T stage and OS. Grades 2 and 3 radiation pneumonitis (RP) occurred in 7 (8.6%) and 2 (2.5%) patients, respectively. Among patients of very elderly and younger groups, grade 2 RP occurred in 4 (20%) and 3 (4.9%) patients, and grade 3 occurred in 2 (10%) and 0 (0%) patients, respectively. No grade 4 or 5 toxicity was observed, RP was significantly more severe among very elderly patients.
SBRT for stage Ι NSCLC was well tolerated and feasible in very elderly patients. The efficacy of SBRT was comparable to that achieved in younger patients, although very elderly patients experienced significantly more severe RP. Although this study cohort included only 20 very elderly patients, the present data suggest that decreasing volumes of normal lung tissues exposed to ≥ 20 Gy and mean lung doses reduces the risk of RP in very elderly patients. The present data warrant studies of larger very elderly cohorts.
Numbers of elderly patients with non-small cell lung cancer (NSCLC) are currently increasing . However, these patients are less likely to receive surgical resection due to comorbid conditions, higher intraoperative risks, and personal preference to avoid definitive surgery. Radiotherapy offers a curative alternative for elderly patients with NSCLC, although conventional radiotherapy is not curative . Silbley GS et al. showed that higher than conventional doses of radiotherapy improved survival in patients with medically inoperable stage I NSCLC . Furthermore, stereotactic body radiotherapy (SBRT) presents a promising treatment for patients with stage I NSCLC who are medically inoperable or refuse surgery, with improved efficacy and lower complication rates [4–7]. Previously, the effectiveness of lobectomy, sublobar resection, conventional radiotherapy, SBRT, and observation based treatment strategies were compared with conventional radiotherapy in elderly patients. In this study, overall survival (OS) was significantly improved following SBRT and was similar to that after lobectomy . Other recent reports also indicate that SBRT is an effective treatment option for the elderly (age ≥ 75 years), with minimal toxicity [9–12] and similar OS outcomes to those achieved with surgery . According to reports from Japanese institutions, SBRT is primarily performed in medically inoperable NSCLC patients with median ages of 76–78 years [14–17]. Japan has one of the world’s fastest aging societies, with a mean life expectancy at birth of 83 years in 2011 (79 years for men and 86 years for women) . However, few studies report outcomes of SBRT in elderly patients with NSCLC. Thus, in the present study, we retrospectively analyzed clinical outcomes and feasibility of SBRT in 20 very elderly patients (≥85 years) with stage Ι NSCLC who exceeded the Japanese life expectancy at birth, and made comparisons with NSCLC patients of < 85 years.
Eligibility criteria were as follows: (1) identification of T1N0M0 or T2aN0M0 (stage Ι) primary lung cancer according to the Union for International Cancer Control in the 7th lung cancer TNM classification and staging system using computed tomography (CT) of the chest and upper abdomen, bone scintigraphy, and brain magnetic resonance imaging, (2) confirmation of NSCLC from histology or clinical information such as increased maximum standardized uptake valued (SUVmax) on 18-fluoro-deoxyglucose-positron emission tomography (FDG-PET), tumor enlargement on CT images, or elevated tumor marker levels during the observation period, (3) predominantly peripheral localization of the tumor, and (4) arterial oxygen pressure of ≥ 60 mmHg and predicted postoperative forced expiratory volume of ≥ 700 ml at 1 s. These respiratory criteria are identical to those prescribed by the Japan Clinical Oncology Group 0403 . Patients with medicated interstitial pneumonia or a history of radiotherapy to the chest and lungs were excluded, whereas age was not considered a contraindication. Medical operability of tumors was assessed by a multidisciplinary board. Our institutional Medical Ethics Committee approved the treatment protocol, and all patients submitted written informed consent before inclusion in the study.
From January 2006 to December 2012, 81 patients with stage Ι NSCLC received SBRT. Table 1 summarizes the pretreatment characteristics of the 81 patients, who were divided into age groups of very elderly (≥85 years; n = 20, 24.7%) and younger (<85 years; n = 61, 75.3%) patients. The median age of all patients was 80 years (range, 64–93; 3 over 90 years), and 64 were male (79%) and 17 were female (21%). Very elderly patients included 11 females and 9 males. Of the 17 patients for whom histological diagnosis of NSCLC was not possible, 13 were very elderly. Among all patients, 61 (75%) were assessed as inoperable, and only 4 very elderly patients were considered medically operable.
SBRT was performed with 6 MV X-rays using a CLINAC C21EX linear accelerator (2006–2009; Varian Medical Systems, Palo Alto, CA, USA) or a Novalis Tx linear accelerator (2010–2012; BrainLAB, AG, Germany). A CT simulator and a 3D radiotherapy planning system (ECLIPSE, Version 6.5, 7.5; Varian Medical Systems) were used to plan treatments for all patients. A BlueBAG system (Medical Intelligence, Munich, Germany) was used to immobilize patients. To maintain tumor positions during irradiation, patients were instructed in the self-controlled breath-hold technique using an Abches (APEX Medical, Tokyo, Japan) respiratory monitoring system . This system was used during CT scanning for treatment planning and irradiation, and breath was held at inspiration or expiration. CT data sets comprised 3 scans for each patient, with a slice thickness of 2.5 mm. For patients who were unable to hold their breath long enough, irradiation was performed and CT images for treatment planning were obtained under normal breathing during both expiratory and inspiratory phases. Data sets were combined, and gross tumor volumes (GTV) were contoured for each patient. Clinical target volumes (CTV) were equal to GTV and the internal target volume (ITV) was the sum of CTV. Planning target volumes (PTV) were determined by adding 3- to 5-mm margins around the ITV, with a leaf margin of 5 mm. Prescription doses of 48 Gy were predominantly delivered in four fractions at the isocenter using 8–11 conformal static ports, and patients were treated biweekly. For tumors located centrally or adjacent to critical organs with large CTV, the prescribed dose was a total of 60 Gy in 10 fractions over 3 weeks. Dose calculations were performed using the convolution method, and the Batho power-law method was used to correct for tissue heterogeneities. Dose constraints for organs at risk were maintained on the basis of the criteria described by JCOG 0403 [19, 21].
Follow-up after SBRT comprised CT scans at 1 month, and then at 3-month intervals for the first 2 years. Thereafter, follow-up CT scans were performed every 4 months. Local recurrence was diagnosed according to pathological confirmation, high uptake on FDG-PET (SUVmax ≥ 8) [22, 23], enlargement of tumor size, or the presence of a mass-like consolidation shadow with disappearance of air bronchogram [24, 25]. Toxicity was evaluated using the Common Terminology Criteria for Adverse Events, version 4.0. Median follow-up was 29.0 months, ranging from 5.0 to 84.0 months (median 22.5 months) in patients aged ≥ 85 years, and was 30.0 months for all patients < 85 years.
Continuous quantitative variables were compared using Student’s t test, ordinal quantitative variables were compared using Mann–Whitney U test, and qualitative variables were compared using chi-squared test with Fisher’s exact test. The Kaplan–Meier method was used to calculate local control (LC), overall survival (OS), cause-specific survival (CSS), and progression-free survival (PFS) rates, and group comparisons were made using the log-rank test. The Cox proportional hazard model was used to identify predictors of OS in both univariate and multivariate analyses. Multivariate analyses were performed for variables with probability (p) values of < 0.20 in univariate analysis, and differences were considered significant when p < 0.05. All statistical analyses were performed using StatView software version 5.0 (SAS Institute, Cary, NC, USA).
Patient and tumor characteristics
Table 1 summarizes the pretreatment characteristics of 81 patients, and tumors from very elderly (≥85 years) and younger (<85 years) patients. Numbers of females were significantly greater in the very elderly group than in the younger group (p = 0.002). Numbers of patients who were capable of self-controlled breath-holding during irradiation were significantly fewer in the very elderly group than in the younger group (p = 0.02). CTV were similar in each group, whereas PTV, V20 (the percentage of the normal lung volume, after subtracting PTV following radiation with ≥ 20 Gy), and mean lung doses (MLD) were slightly but insignificantly greater in the very elderly group than in the younger group. No other significant differences were found between the groups.
Local control and survival
Among all 81 patients, 1-, 2-, and 3-year LC rates were 97.4%, 95.9%, and 91.8%, respectively, and did not differ significantly between very elderly and younger patient groups (95.0%, 95.0%, and 83.1%, and 98.2%, 96.4%, and 93.8% , respectively; Figure 1a and Table 2). Among all patients, 1-, 2-, and 3-year OS rates for all patients were 95.1%, 82.9%, and 69.4%, respectively. These were significantly shorter among very elderly patients (95.0%, 71.2%, and 40.7%, respectively) than in the younger group (95.1%, 86.4%, and 75.0%, respectively; p = 0.0306; Figure 1b and Table 2). Among all patients, 1-, 2-, and 3-year CSS rates were 97.5%, 87.8%, and 77.9%, respectively, and did not differ significantly between very elderly (100%, 88.2%, and 50.4%, respectively) and younger patients (96.7%, 87.8%, and 81.6%, respectively; Figure 1c and Table 2). Similarly, 1-, 2-, and 3-year PFS rates for all patients were 88.9%, 75.5%, and 59.5%, and did not differ between very elderly (90.0%, 65.2%, and 44.7%, respectively) and younger patients ( 88.5%, 78.3%, and 63.5%, respectively; Figure 1d and Table 2).
Univariate and multivariate analyses of predictors of OS in all patients are shown in Table 3, and age, gender, performance status, T stage (T1a vs. T1b or T2a), CTV, PTV, histology, tumor location, operability, and total doses were identified as independent variables. However, in univariate analyses, only age, CTV, and T stage were correlated with OS, with p values of < 0.20. Because CTV was strongly related to T stage, subsequent multivariate analyses were performed with only age and T stage, and T stage was significantly correlated with OS (p = 0.04; Table 4).
SBRT was well tolerated, and all patients completed the scheduled irradiation course without hospitalization. Grades 2 and 3 RP developed in 7 (8.6%) and 2 (2.5%) patients, respectively. In the very elderly and younger groups, grade 2 RP was observed in 4 (20%) and 3 (10%) patients, and grade 3 RP was observed in 2 (10%) and 0 (0%) patients, respectively. No patients suffered from grade 4 or 5 toxicity. However, RP was more severe in the very elderly group than in the younger group (p = 0.002; Table 5). In multivariate analyses of RP grade, age, CTV, PTV, V20, and MLD, age was significantly related to the severity of RP (p = 0.018), whereas CTV, PTV, V20, and MLD were not. However, V20 and MLD showed predictive tendencies for the severity of RP, with p values of 0.054 and 0.052, respectively (Table 6). Late toxicities included CT diagnosed rib fractures in 15 (18.5%) of 81 patients (5 (25%) in the very elderly group and in 10 patients (16.3%) of the younger group. Only 2 patients (2.4%) in the younger group complained of transient chest pain. Rib fracture rates did not differ significantly between age groups (Table 5). Other adverse events included nonmalignant pleural effusion in 5 patients (2 very elderly patients and 3 and younger patients), atelectasis in 3 younger patients, and pneumothorax in 1 younger patient.
Elderly populations are growing in many countries, including Japan. Although lung cancer is a leading cause of death, patients aged ≥ 80 years account for only 14% of all lung cancer patients . Because the life expectancy of Japanese at birth was 83 years in 2011 for both sexes, and because men and women who are 85 years old are expected to live for an additional 6.0 and 8.1 years, respectively, radical treatment should be considered for elderly patients . Surgery is the standard treatment for stage I NSCLC. However, elderly patients are often unsuitable for surgery and prefer non-surgical options. The prognosis for untreated stage I NSCLC is poor, with a median survival period of only 13 months . Radiotherapy is considered a curative alternative for these patients, primarily because reported outcomes of SBRT are similar to those of surgery . Accordingly, SBRT is often the primary treatment option for patients with stage I NSCLC who are medically inoperable or refuse surgery, and Palma et al.  proposed SBRT as the standard care for inoperable elderly patients.
The median age of patients receiving SBRT for stage I NSCLC in Japanese institutions is 76–78 years [14–17], but was 80 years in the current study, which may reflect the rural location of our hospital. Significantly more women were aged ≥ 85 years than men, reflecting the well known longer average life span of women than men. In this study, we used a self-controlled breath-hold technique to reduce ITV and PTV. However, patients in the very elderly group could not hold their breath for a sufficient period of time, leading to slightly but insignificantly higher mean PTV, V20, and MLD values in the very elderly group. No other significant differences in patients or tumor characteristics were found between very elderly and younger patient groups.
Several recent studies show that SBRT is an effective treatment, causing only minimal toxicity in elderly patients with NSCLC (Table 7), and leads to excellent 3-year LC rates of 82.3%–100% [9, 11, 12]. In the present study, LC rates were 83.1% and 93.8% among very elderly and younger patients, respectively, but did not differ significantly between the groups. LC rates for inoperable patients receiving SBRT for stage I NSCLC were reportedly between 83.0% and 97.6% at 3 years [5–7], and this was similar among elderly patients.
The OS rate for all 81 patients was 69.4% at 3 years, and 1-, 2-, and 3-year OS rates in the very elderly group were 95.0%, 71.2%, and 40.7%, respectively. Although these rates were significantly lower than in the very elderly group, CSF rates did not differ between the groups. Eight patient deaths occurred in the elderly group during the present observation period. Among these, 4 were due to lung cancer (1 with local failure and distant metastases, 2 were due to distant metastases only, and 1 was due to pleuritis carcinomatosa. The other 4 patients died of unrelated illnesses (2 of heart failure, 1 of cerebral infarction, and 1 of pneumonia that was not related to radiation pneumonitis). Thus, very elderly patients tended to die of causes other than NSCLC.
Prognostic factors for OS that were identified in univariate analysis included age, T stage (T1a vs. others), and CTV. However, in subsequent multivariate analyses, only T stage was a significant prognostic factor for OS, indicating that tumor size is a stronger prognostic factor than age. In agreement, Palma et al.  showed that survival after radical treatment (radical radiotherapy or surgery) for stage I NSCLC is dependent on tumor stage but not age. They also suggested that elderly patients should not be excluded from radical treatments based on age alone. Moreover, T stage (T1a vs. T1b or T2a), tumor diameter, and sex were previously reported as significant prognostic factors for NSCLC following SBRT [31, 32]. In the present study, prognostic factors were not evaluated in the very elderly due to low patient numbers and limitations of natural life span. Takeda et al.  reported predictors of short OS in medically inoperable patients aged ≥ 80 years, including low body mass index, high T stage, and high C-protein level. The present data also show that operability was not a significant prognostic factor. However, because this is assessed by multidisciplinary boards, a bias may exist between institutions. Nonetheless, 4 very elderly operable patients remained alive without recurrence during the observation period (18–36 months). In this study, we did not analyze factors associated with FDG-PET because not all patients were assessed using this procedure. However, we previously reported that pretreatment SUVmax values from FDG-PET or CT were predictive of disease-free survival in SBRT-treated patients with pathologically or cytologically confirmed stage I NSCLC . However, some reports show no relationship between SUVmax and SBRT treatment outcomes for NSCLC [33, 34]. Thus, the prognostic value of SUVmax in these patients remains controversial.
Toxicity of SBRT is primarily related to RP. However, whereas grades 2 and 3 RP reportedly occur in 4.6%–13.8% and 0%–20% of patients, respectively [7, 9–11, 19, 2, 30, 31], reported rates of grade 4 and 5 RP are very low. According to a survey of SBRT in Japan, grade 5 RP occurs in 0.6% of cases and is predominantly associated with interstitial pneumonia [21, 35]. Similarly, among the present patients, rates of grades 2 and 3 RP were 8.5% and 2.5%, respectively, and no grade 4 or 5 RP was observed. However, grades 2 and 3 RP were observed in 20% and 10% of very elderly patients, respectively. Severe RP was observed more frequently in the very elderly group than in the younger group. However, no younger patients, and only two very elderly patients, suffered from grade 3 RP, and the severity of RP was significantly correlated with age. The incidence of ≥ grade 2 RP in the very elderly group was greater than that reported in other studies of elderly patients (Table 7). However, previous reports included patients aged ≥ 75 or 80 years, and and did not include data from patients aged ≥ 85 years. Nonetheless, the increased severity of RP among very elderly patients may reflect reduced cardiopulmonary functions and physical conditions. PTV, V20, and MLD are reportedly risk factors for RP in SBRT treated patients with NSCLC [30, 36–38]. In the present study, CTV values were similar between the groups, whereas PTV, V20, and MLD values were slightly higher in the very elderly group, and V20 and MLD were almost significant predictors of RP severity (Table 6). Very few of the present elderly patients were able to perform the breath-hold technique sufficiently to maintain tumor position during irradiation and reduce the volume of irradiated healthy lung tissue, which may have increased PTV, V20, and MLD values. Hence, efforts to decrease these values should be prioritized to reduce the risk of RP using methods such as four-dimensional CT with respiratory gating or real-time tumor-tracking radiation therapy systems [31, 39].
Rib fracture was observed on follow-up CT in 18.5% of all patients (25% in the very elderly group and 16.3% in the younger group). Only two (2.4%) patients in the younger group complained of chest pain, and no patients exhibited symptoms of grade 3 or more. All elderly patients with rib fractures were asymptomatic, and no significant differences in rib fracture rates were found between the groups. In a study by Nambu et al. , rib fractures occurred in 23.2% of patients, and pain to the chest wall was reported in 10.2% of patients. The rib fracture rate in the current study was much higher than that reported in other studies of elderly patients, but was similar to that reported by Nambu et al. . Potentially, the follow-up period, tumor locations, and parameters of CT scanning may have increased rib fracture rates in the present study. Previous studies showed that female gender, lateral tumor location, small tumor-chest distance, doses to 8 cc of the chest wall, and doses to 2 cm3 of the rib were significant prognostic factors for rib fracture [41–43], However, age was not a risk factor for rib fracture in the present study, and symptoms were generally mild or asymptomatic if present. Thus, rib fracture is not a major concern during treatment of very elderly patients with SBRT.
SBRT for very elderly patients (age ≥ 85 years) with stage Ι NSCLC was well tolerated and feasible, with comparable efficacy to that observed in younger patients. Although very elderly patients suffered significantly more severe RP than younger patients, SBRT decreased V20 and MLD and reduced the risk of RP in very elderly patients. Although only 20 very elderly patients with NSCLC were included, the present analyses indicate that SBRT is curative, and warrant future studies with larger patient numbers.
Makrantonakis PD, Galani E, Harper PG: Non-small cell lung cancer in the elderly. Oncologist 2004, 9: 556-560. 10.1634/theoncologist.9-5-556
Wisnivesky JP, Bonomi M, Henschke C, Iannuzzi M, McGinn T: Radiation therapy for treatment of unresected stage Ι-ΙΙ non-small cell lung cancer. Chest 2005, 128: 1461-1467. 10.1378/chest.128.3.1461
Sibley GS: Radiotherapy for patients with medically inoperable stage Ι non small cell lung carcinoma: smaller volumes and higher doses, a review. Cancer 1998, 82: 433-438. 10.1002/(SICI)1097-0142(19980201)82:3<433::AID-CNCR2>3.0.CO;2-Q
Palma D, Visser O, Lagerwaard FJ, Belderbos J, Slotman BJ, Senan S: Impact of introducing stereotactic lung radiotherapy for elderly patients with stage Ι non-small-cell lung cancer: a population-based time-trend analysis. J Clin Oncol 2010, 28: 5153-5159. 10.1200/JCO.2010.30.0731
Timmerman R, Paulus R, Galvin J, Michalski J, Straube W, Bradley J, Fakiris A, Bezjak A, Videtic G, Johnstone D, Fowler J, Gore E, Choy H: Stereotactic body radiation therapy for inoperable early stage lung cancer. JAMA 2010, 303: 1070-1076. 10.1001/jama.2010.261
Baumann P, Nyman J, Hoyer M, Wennberg B, Gagliardi G, Lax I, Drugge N, Ekberg L, Friesland S, Johansson K, Lund J, Morhed E, Nilsson K, Levin N, Paludan M, Sederholm C, Traberg A, Wittgren L, Lewensohn R: Outcome in prospective phase ΙΙ trial of medically inoperable stage Ι non-small-cell lung cancer patients treated with stereotactic body radiotherapy. J Clin Oncol 2009, 27: 3290-3296. 10.1200/JCO.2008.21.5681
Andratschke N, Zimmermann F, Boehm E, Schill S, Schoenknecht C, Thamm R, Molls M, Nieder C, Geinitz H: Stereotactic radiotherapy of histologically proven inoperable stage Ι non-small cell lung cancer: Patterns of failure. Radiother Oncol 2001, 101: 245-249.
Shirvani SM, Jiang J, Chang JY, Welsh JW, Gomez DR, Swisher S, Buchholz TA, Smith BD: Comparative effectiveness of 5 treatment strategies for early-stage non-small cell lung cancer in the elderly. Int J Radiat Oncol Biol Phys 2012, 84: 1065-1070.
Haasbeek CJA, Lagerwaard FJ, Antonisse ME, Slotman BJ, Senan S: Stage Ι nonsmall cell lung cancer in patients aged ≥75 years. Cancer 2010, 15: 406-414.
Samuels MA, Kandula S, Koru-Sengul T, Bogart JA, Salama JK, Aridgides PD, Gajra A, Lilenbaum RC: Stereotactic body radiotherapy in patients with stage Ι non-small-cell lung cancer aged 75 years and older: Retrospective results from a multicenter consortium. Clin Lung Cancer 2013, 14: 446-451. 10.1016/j.cllc.2013.03.004
Sandhu AP, Lau SK, Rahn D, Nath SK, Kim D, Song WY, Gulaya S, Fuster MM, Bazhenova L, Mundt AJ: Stereotactic body radiation therapy in octogenarians with stage Ι lung cancer. Clin Lung Cancer 2014, 15: 131-135. 10.1016/j.cllc.2013.08.007
Takeda A, Sanuki N, Eriguchi T, Kaneko T, Morita S, Handa H, Aoki Y, Oku Y, Kuniueda E: Stereotactic ablative body radiation therapy for octogenarians with non-small cell lung cancer. Int J Radiat Oncol Biol Phys 2013, 86: 257-263. 10.1016/j.ijrobp.2013.01.006
Palma D, Visser O, Lagerwaard FJ, Belderbos J, Slotman B, Senan S: Treatment of stage Ι NSCLC in elderly patients: A population-based matched-pair comparison of stereotactic radiotherapy versus surgery. Radiother Oncol 2011, 101: 240-244. 10.1016/j.radonc.2011.06.029
Nagata Y, Takayama K, Matsuo Y, Norihisa Y, Mizowaki T, Sakamoto T, Sakamoto M, Mitumori M, Shibuya K, Araki N, Yano S, Hiraoka M: Clinical outcomes of a phase Ι/ΙΙ study of 48 Gy of stereotactic body radiotherapy in 4 fractions for primary lung cancer using a stereotactic body frame. Int J Radiat Oncol Biol Phys 2005, 63: 1427-1431. 10.1016/j.ijrobp.2005.05.034
Onishi H, Kuriyama K, Komiyama T, Tanaka S, Sano N, Marino K, Ikenaga S, Araki T, Uematsu M: Clinical outcomes of stereotactic radiotherapy for stage Ι non-small cell lung cancer using a novel irradiation technique: patient self-controlled breath-hold and beam switching using a combination of linear accelerator and CT scanner. Lung Cancer 2004, 45: 45-55. 10.1016/j.lungcan.2004.01.004
Onimaru R, Fujino M, Yamazaki K, Onodera Y, Taguchi H, Katoh N, Hommura F, Oizumi S, Nishimura M, Shirato H: Steep dose–response relationship for stage Ι non-small-cell lung cancer using hypofractionated high-dose irradiation by real-time tumor-tracking radiotherapy. Int J Radiat Oncol Biol Phys 2008, 70: 374-381. 10.1016/j.ijrobp.2007.06.043
Takeda A, Sanuki N, Kunieda E, Ohashi T, Oku Y, Takeda T, Shigematsu N, Kubo A: Stereotactic body radiotherapy for primary lung cancer at a dose of 50 Gy total in five fractions to the periphery of the planning target volume calculated using superposition algorithm. Int J Radiat Oncol Biol Phys 2009, 73: 442-448. 10.1016/j.ijrobp.2008.04.043
Population Statistics. http://www.ipss.go.jp/index-e.asp
Nagata Y, Hiraoka M, Shibata T, Onishi H, Kokubo M, Karasawa K, Shioyama Y, Onimaru R, Kunieda E, Ishikura S: A Phase ΙΙ trial of stereotactic body radiation therapy for operable T1N0M0 non-small cell lung cancer: Japan clinical oncology group (JCOG0403). Int J Radiat Oncol Biol Phys 2010,78(Issue 3):S27-S28.
Tarohda TI, Ishiguro M, Hasegawa K, Kohda Y, Onishi H, Aoki T, Takanaka T: The management of tumor motions in the stereotactic irradiation to lung cancer under the use of Abches to control active breathing. Med Phys 2011, 38: 4141-4146. 10.1118/1.3604151
Nagata Y, Wulf J, Lax I, Timmerman R, Zimmermann F, Stojkovski I, Jeremic B: Stereotactic radiotherapy of primary lung cancer and other targets: Results of consultant meeting of the International Atomic Energy Agency. Int J Radiat Oncol Biol Phys 2011, 79: 442-448.
Tanaka H, Hayashi S, Hoshi H: Pretreatment maximum standardized uptake value on 18F-fluorodeoxyglucose positron emission tomography is a predictor of outcome for stage Ι non-small cell lung cancer after stereotactic body radiotherapy. Asia Pac J Clin Oncol 2013, 31: 1743-7563.
Hang K, Dahele M, Senan S, Guckenberger M, Rodrigues GB, Ward A, Boldt G, Palma DA: Radiographic changes after lung stereotactic ablative radiotherapy. Can we distinguish recurrence from fibrosis? A systematic review of the literature. Radiother Oncol 2012, 102: 335-342. 10.1016/j.radonc.2011.12.018
Matsuo Y, Nagata Y, Mizowaki T, Takayama K, Sakamoto T, Sakamoto M, Norihisa Y, Hiraoka M: Evaluation of mass-like consolidation after stereotactic body radiation therapy for lung tumors. Int J Clin Oncol 2007, 12: 356-362. 10.1007/s10147-007-0691-9
Kato S, Nambu A, Onishi H, Saito A, Kuriyama K, Komiyama T, Marino K, Araki T: Computed tomography appearance of local recurrence after stereotactic body radiotherapy for stage Ι non-small-cell lung carcinoma. Jpn J Radiol 2010, 28: 259-265. 10.1007/s11604-009-0415-3
Owonikoko TK, Ragin CC, Belani CP, Oton AB, Gooding WE, Taioli E, Ramalingam SS: Lung cancer in elderly patients: An analysis of the surveillance, epidemiology, and end results database. J Clin Oncol 2007, 25: 5570-5577. 10.1200/JCO.2007.12.5435
Raz DJ, Zell JA, Ou I, Gandara DR, Aoton-Culver H, Jablons DM: Natural History of stage Ι non-small cell lung cancer. Chest 2007, 132: 193-199. 10.1378/chest.06-3096
Onishi H, Nagata Y, Hiraoka M, Fujino M, Gomi K, Karasawa K, Hayakawa K, Niibe Y, Takai Y, Kimura T, Takeda A, Ouchi A, Hareyama M, Kokubo M, Kozuka T, Arimoto T, Hara R, Itami J, Araki T: Stereotactic body radiotherapy for operable stage Ι non-small cell lung cancer. Can SBRT be comparable to surgery? Int J Radiat Oncol Biol Phys 2011, 81: 1352-1358. 10.1016/j.ijrobp.2009.07.1751
Palma DA, Senan S: Early-stage non-small cell lung cancer in elderly patients: Should stereotactic radiation therapy be the standard of care? Int J Radiat Oncol Biol Phys 2011, 84: 1058-1359.
Palma DA, Tyldersley , Sheehan F, Mohamed IG, Smith S, Wai E, Murray N, Senan S: Stage Ι non-small cell lung cancer in patients aged 75 years and older. J Thorac Oncol 2010, 5: 818-824. 10.1097/JTO.0b013e3181d6e052
Inoue T, Katho N, Onimaru R, Shimizu S, Tsuchiya K, Suzuki R, Sakakibara-konishi J, Shinagawa N, Oizumi S, Shirato H: Stereotactic body radiotherapy using gated radiotherapy with real-time tumor tracking for stage Ι non-small cell lung cancer. Radiat Oncol 2013, 8: 69. 10.1186/1748-717X-8-69
Matsuo Y, Shibuya K, Nagata Y, Takayama K, Norihisa Y, Mizowaki T, Narabayashi M, Sakanaka K, Hiraoka M: Prognostic factors in stereotactic body radiotherapy for non-small-cell lung cancer. Int J Radiat Oncol Biol Phys 2011, 79: 1104-1111. 10.1016/j.ijrobp.2009.12.022
Burdick MJ, Stephans KL, Reddy CA, Djemil T, Srinivas SM, Videtic GMM: Maximum standardized uptake value from staging FDG-PET/CT does not predict treatment outcome for early-stage non-small-cell lung cancer treated with stereotactic body radiotherapy. Int J Radiat Oncol Biol Phys 2011, 78: 1033-1039.
Hoopes DJ, Tann M, Fletcher , Forquer JA, Lin P, Lo SS, Timmerman RD, McGarry RC: FDG-PET and stereotactic body radiotherapy for non-small-cell lung cancer. Lung Cancer 2007, 56: 229-234. 10.1016/j.lungcan.2006.12.009
Nagata Y, Hiraoka M, Mizowaki T, Narita Y, Matsuo Y, Norihisa Y, Onishi H, Shirato H: Survey of stereotactic body radiation therapy in Japan by the Japan 3D conformal external beam radiotherapy group. Int J Radiat Oncol Biol Phys 2009, 75: 343-347. 10.1016/j.ijrobp.2009.02.087
Barriger RB, Forquer JA, Brabham JG, Andolino DL, Shapiro RH, Henderson MA, Johnstone PAS, Fakiris AJ: A dose-volume analysis of radiation pneumonitis in non-small cell lung cancer patients treated with stereotactic body radiation therapy. Int J Radiat Oncol Biol Phys 2012, 82: 457-462. 10.1016/j.ijrobp.2010.08.056
Guckenberger M, Baier K, Polat B, Richter A, Krieger T, Wilbert J, Mueller G, Flentje M: Dose–response relationship for radiation-induced pneumonitis after pulmonary stereotactic body radiotherapy. Radiother Oncol 2010, 97: 65-70. 10.1016/j.radonc.2010.04.027
Matsuo Y, Shibuya K, Nakamura M, Narabayashi M, Sakanaka K, Ueki N, Miyagi K, Norihisa Y, Mizowaki T, Nagata , Hiraoka M: Dose-volume metrics associated with radiation pneumonitis after stereotactic body radiotherapy for lung cancer. Int J Radiat Oncol Biol Phys 2012, 83: e545-e549. 10.1016/j.ijrobp.2012.01.018
van Zyp NC V d V, Van der Holt B, Van Klaveren RJ, Pattynama P, Maat A, Nuyttens JJ: Stereotactic body radiotherapy using real-time tumor tracking in octogenarians with non-small cell lung cancer. Lung Cancer 2010, 69: 296-301. 10.1016/j.lungcan.2009.12.008
Nambu A, Onishi H, Aoki S, Koshiishi T, Kuriyama K, Komiyama T, Marino K, Araya M, Saito R, Tominaga L, Maehata Y, Sawada E, Araki T: Rib fracture after stereotactic radiotherapy on follow-up thin-section computed tomography in 177 primary lung cancer patients. Radiat Oncol 2011, 6: 137. 10.1186/1748-717X-6-137
Nambu A, Onishi H, Aoki S, Tominaga L, Kuriyama K, Araya M, Saito R, Maehata Y, Komiyama T, Marino K, Koshiishi T, Sawada E: Rib fracture after stereotactic radiotherapy for primary lung cancer: prevalence, degree of clinical symptoms, and risk factors. BMC Cancer 2013, 13: 68. 10.1186/1471-2407-13-68
Petterson N, Nyman , Johansson K: Radiation-induced fractures after hypofractionated stereotactic body radiation therapy of non-small cell lung cancer: A dose- and volume-response analysis. Radiother Oncol 2009, 91: 360-368. 10.1016/j.radonc.2009.03.022
Kim SS, Song SY, Kwak J, Ahn SD, Kim JH, Lee JS, Kim WS, Kim S, Choi EK: Clinical prognostic factors and grading system for rib fracture following stereotactic body radiation therapy in patients with peripheral lung tumors. Lung Cancer 2013, 79: 161-166. 10.1016/j.lungcan.2012.10.011
The authors thank all staff members of the Division of Radiation Oncology (Gifu University Hospital) for their valuable support.
The authors declare that they have no competing interests.
All authors read and approved the final manuscript. SH contributed to the study design, data collection, and analysis, and drafted the manuscript. HT contributed to the study design, data collection and analysis, and approved the final version of the manuscript. YK participated in data analysis and interpretation. YO performed clinical evaluations of patients at follow-up and collected data. HH contributed to study data abstraction, critical reviewed and improved intellectual content, and approved the final version of the manuscript.
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