Carbon-ion radiotherapy for octogenarians with locally advanced non-small-cell lung cancer



The clinical significance of carbon-ion radiotherapy (CIRT) for octogenarians with locally advanced non-small-cell lung cancer (LA-NSCLC) remains unclear. We aimed to evaluate the clinical outcomes of CIRT alone for octogenarians with LA-NSCLC.

Materials and methods

We evaluated 32 patients who underwent CIRT alone between 1997 and 2015. The median age was 82.0 years (range, 80–88 years). In terms of clinical stage (UICC 7th edition), 7 (21.9%), 10 (31.3%), 11 (34.4%), and 4 (12.5%) patients had stage IIA, IIB, IIIA, and ΙΙΙB disease, respectively. The median CIRT dose was 72.0 Gy (relative biological effectiveness), and the median follow-up period was 33.1 months.


All patients successfully completed CIRT. Regarding grade ≥ 2 toxicities, 1 (3.1%), 3 (9.4%), and 4 (0.7%) patients developed grade 3 radiation pneumonitis, grade 2 radiation pneumonitis, and grade 2 dermatitis, respectively. No grade ≥ 4 toxicities were observed. The 2 year LC, PFS, and OS rates were 83.5%, 46.7%, and 68.0%, respectively.


CIRT alone is safe and effective for octogenarians with LA-NSCLC.


Primary lung cancer is one of the most common cancers worldwide [1]. Japan has one of the fastest aging societies, with a mean life expectancy at birth of 81 years for men and 87 years for women in 2017 [2]. Therefore, almost 40% of deaths owing to primary lung cancer are in octogenarians who are rarely eligible for highly invasive treatment modalities [3]. The standard treatment options for locally advanced non-small-cell lung cancer (LA-NSCLC) generally comprise surgery, chemotherapy, and/or radiotherapy. For inoperable patients, platinum-based chemotherapy or platinum-based chemoradiotherapy (CRT) is used. However, it sometimes induces severe hematologic toxicity, infection, esophagitis, and pneumonitis [4,5,6], thus making it highly toxic for octogenarians. The standard treatment modality for octogenarians with LA-NSCLC is controversial because there are limited data describing the specific therapies for patients aged 80 years or older. CRT, radiotherapy alone, and chemotherapy including an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) can be administered as treatment options [6]. In clinical practice, the treatment for octogenarians with LA-NSCLC is decided based on their performance status, comorbidity, and the patient value.

Carbon-ion radiotherapy (CIRT) is a high linear energy transfer radiotherapy that is used in some countries across Europe and Asia. CIRT has good dose-localizing properties [7], and thus can deliver a higher dose to the target volume than conventional photon radiotherapy while avoiding irradiation to the adjacent critical organs at risk, such as the lung, esophagus, trachea, and heart. CIRT alone can clinically achieve high local control (LC) rates with low toxicity [8,9,10,11,12,13]. Two published studies from our hospital have reported 2 year LC and overall survival (OS) rates of 83.5–93.1% and 51.9–68.0%, respectively, with CIRT alone in patients with LA-NSCLC [8, 13]. The incidence of grade 3–4 toxicities ranged from 3.2% to 4.9%, and none of the evaluated patients experienced grade 5 toxicities. Karube et al. conducted a multicenter study on CIRT alone in 64 patients with LA-NSCLC and reported similar 2 year LC and OS rates of 81.8% and 62.2%, respectively [9]. No grade ≥ 3 toxicities were observed. These clinical outcomes indicated that CIRT alone may be a safe treatment option for LA-NSCLC. However, these studies evaluated patients of all ages together, and no previous study has focused on octogenarians. Therefore, the safety and efficacy of CIRT alone for octogenarians with LA-NSCLC remain to be clarified. As such, this study aimed to investigate the clinical outcomes of CIRT alone for octogenarians with LA-NSCLC.

Material and methods

Study design and patients

This single-center retrospective study was approved by the Institutional Review Board of our institution (16–027) and was conducted according to the tenets of the Helsinki Declaration and its later amendments. The subjects were octogenarians who underwent CIRT alone between June 1997 and December 2015 at our institution. They were identified from a previously reported prospective phase Ι/ΙΙ study of 72 patients of all ages and a previously reported retrospective study of 69 patients of all ages who were deemed ineligible for the phase Ι/ΙΙ study at our institution [8, 13]. The studies have been described in detail previously [8, 13]. The inclusion criteria were as follows: (1) histologically or clinically diagnosed LA-NSCLC of stages ΙΙA to ΙΙΙB (the UICC’s TNM 7th Classification) [14], (2) Eastern Cooperative Oncology Group performance status of 0–2, (3) measurable tumors, (4) inoperable or refusal of surgery, (5) definitive treatments, (6) no other active cancers, and (7) no history of radiotherapy to the concerned region. The exclusion criteria included lung tumors with suspected invasion to the trachea, great vessels, heart, or carina. Consequently, data of 32 patients (18 patients from the prospective phase Ι/ΙΙ study and 12 patients from the retrospective study) who met the inclusion criteria were analyzed.

Tumor stage was evaluated using computed tomography (CT) imaging of the chest and whole abdomen, enhanced magnetic resonance imaging (MRI) of the brain, chest radiography, and blood tests. Bone scans or [18F]-fluorodeoxyglucose positron emission tomography combined with CT (18F-FDG PET/CT) were also performed. Histological or cytological diagnosis was confirmed via bronchoscopic biopsy, CT-guided biopsy, or sputum cytology in 28 (87.5%) patients and via CT, radiography, and/or 18F-FDG PET/CT in the remaining patients.

We collected information on grade ≥ 2 toxicities. Treatment-related toxicities were graded according to the National Cancer Institute’s Common Terminology Criteria for Adverse Events (version 4.0) [15].

Carbon-ion radiotherapy

Patients were fixed using an individually tailored immobilization device (Moldcare; Alcare, Tokyo, Japan; Shellfitter; Kuraray, Osaka, Japan), and CT images were obtained in the supine or prone position using respiratory sensors to monitor the respiratory phase [7, 8]. Target delineation was performed as previously reported [8, 13]. The primary lung lesion and metastatic lymph nodes were contoured as the gross tumor volume (GTV) on CT images. The GTV with a 10 mm margin and any prophylactic lymph nodes (ipsilateral hilar and/or mediastinal lymph nodes) were defined as the clinical target volume (CTV). For N0 cases, prophylactic lymph nodes irradiation was omitted irrespective of T-stage. Planning target volume (PTV) was defined as the CTV + 5 mm safety margin. In cases where the PTV was close to the organs at risk, the margins for creating PTV was reduced.

The prescribed dose ranged from 68.0 to 76.0 Gy [relative biological effectiveness (RBE)] in 12–16 fractions, 4 days per week. Their prescribed doses were converted to 96.9 to 115.0 Gy (RBE) as the biologically effective dose using α/β = 10. A dose escalation study conducted during our investigation showed the potential of short-course CIRT alone at 72 Gy (RBE) [8], and thus the recommended dose was fixed at 72 Gy (RBE) in 16 fractions. Subsequently, this dose was adopted for all remaining patients (n = 21, 65.6%). The total dose was applied to the isocenter, and it enclosed the PTV conformably, with a 95% isodose line. The patients with lymph node metastasis underwent metastatic and prophylactic lymph node irradiation at a median dose of 49.5 Gy (RBE) [8, 13, 16]. The following irradiation dose constraints were applied: main bronchus, 60 Gy (RBE); esophagus, 50 Gy (RBE); and spinal cord, 30 Gy (RBE). Irradiation was performed in 2–5 fields with 250 or 290 meV carbon ions.

Regarding chemotherapy, 2 patients were administered induction chemotherapy, but none of the 32 patients received concurrent or adjuvant chemotherapy.


After treatment, follow-up observations were performed at 1, 3, 6, 9, and 12 months, and every 3–6 months thereafter if serious complications had not occurred. Follow-up comprised chest CT, chest radiography, and blood tests during each evaluation. Brain MRI or F18-FDG PET/CT was performed as necessary.

Statistical analyses

LC, progression-free survival (PFS), and OS were calculated using the Kaplan–Meier method. LC was defined as the time interval between irradiation commencement date and the local tumor regrowth at the PTV date or the last follow-up. PFS was defined as the time interval between irradiation commencement date and the date of disease progression at any site, death from any cause, or the last follow-up. OS was defined as the time interval between the start of irradiation and death or the last follow-up.

All statistical analyses were conducted using JMP statistical software (version 14.0; SAS Institute Inc., Cary, NC, USA).


Patient characteristics

All patients successfully completed CIRT. The patient characteristics are summarized in Table 1. The median age was 82.0 years (range 80–88 years), and the median follow-up period was 33.1 months (range 2.3–150.1 months) in the overall cohort and 36.9 months for survivors. This study included 28 (87.5%) patients with performance status 1–2. There were 3 (9.4%), 12 (37.5%), 12 (37.5%), and 5 (15.6%) patients who had T1, T2, T3, and T4 disease, respectively. Furthermore, 12 (37.5%), 11 (34.4%), and 9 (28.1%) patients had N0, N1, and N2 disease, respectively. Seven patients (21.9%) had stage IIA disease; 10 (31.3%), stage IIB; 11 (34.4%), stage IIIA; and 4 (12.5%), stage ΙΙΙB. The median dose was 72.0 Gy (RBE).

Table 1 Patient characteristics (n = 32)


Regarding grade ≥ 2 lung toxicities, three (9.4%) and one (3.1%) patient developed grade 2 and grade 3 radiation pneumonitis, respectively (Table 2). In addition, four (0.7%) patients developed grade 2 dermatitis. No grade ≥ 2 toxicities other than dermatitis and pneumonitis were observed. Neither grade ≥ 4 nor cardiac toxicities were observed.

Table 2 Treatment-related toxicities

Local control and survival

By the end of follow-up, 8 and 17 patients had died of cancer and unrelated causes, respectively, while 7 patients were still alive. At the time of first relapse, 3 local recurrences, 5 regional recurrences (regional lymph nodes), and 4 distant metastases were detected.

The 2 and 3 year LC rates were 83.5% [95% confidence interval (CI) 62.9–93.8%] and 77.1% (95% CI 54.3–90.5%), respectively (Fig. 1a). The 2 and 3 year PFS rates were 46.7% (95% CI 32.9–68.8%) and 41.5% (95% CI 29.2–61.2%), respectively (Fig. 1b). The 2 and 3 year OS rates were 68.0% (95% CI 50.0–81.8%) and 54.3% (95% CI 36.7–70.8%), respectively (Fig. 1c). The median PFS and OS durations were 20.8 and 33.1 months, respectively.

Fig. 1

Local control rate (a), progression-free survival rate (b), and overall survival rate (c)

For survival analysis according to clinical stage, the participants were categorized into those with stages ΙΙ and ΙΙΙ LA-NSCLC, and the corresponding median PFS rates were 21.6 months and 15.1 months. Meanwhile, the corresponding median OS rates were 45.9 months and 22.2 months, respectively. In addition, the 2 year LC, PFS, and OS rates of patients with stage ΙΙ disease were 93.3%, 55.8%, and 82.4%, whereas those with stage III disease were 70.7%, 44.4%, and 50.6%, respectively.


CRT as a treatment option for octogenarians with LA-NSCLC induces several toxicities. However, photon radiotherapy also yields unsatisfactory outcomes, and the adoption of EGFR-TKI is rather limited. Therefore, other treatment approaches that are safer and more effective are needed for these patients. The results of this study show that CIRT alone is safe and effective for octogenarians with LA-NSCLC. To our best knowledge, this is the first study to report the clinical usefulness of CIRT alone for octogenarians with LA-NSCLC to date.

Only one study has focused on treatment options for octogenarians with LA-NSCLC [17]. In the study by Corre et al. octogenarians with EGFR-mutated stage Ι–IV lung cancer were treated using EGFR-TKI (Table 3). The main grade ≥ 3 toxicities were diarrhea (17.0% of patients), cutaneous (10.3%), and others (41.0%). With respect to photon CRT or radiotherapy alone, only studies in septuagenarians were conducted. Atagi et al. conducted a phase ΙΙΙ trial of photon radiotherapy with or without low-dose carboplatin for patients older than 70 years [median age 77 years (range 71–93 years)] with stage ΙΙΙ LA-NSCLC [18]. The most common grade ≥ 3 toxicity in the CRT group was leukopenia (63.5%), followed by thrombocytopenia (29.2%), infection (12.5%), radiation pneumonitis (6.5%), and dyspnea (4.2%). In contrast, the most common grade ≥ 3 toxicity in the photon radiotherapy alone group was radiation pneumonitis (5.3%), closely followed by dyspnea (5.1%) and infection (4.1%). Meanwhile, in our study, grade 3 radiation pneumonitis occurred in only 3.1% of all patients, and none of the patients developed other grade ≥ 3 toxicities. These findings indicate that CIRT alone may be safer than photon CRT or chemotherapy, including EGFR-TKI, and approximately comparable to photon radiotherapy alone with respect to grade ≥ 3 toxicity.

Several studies on photon radiotherapy alone for patients older than 70 years with stage ΙΙΙ LA-NSCLC reported that the median PFS and OS of radiotherapy alone were 6.8 months and 11–18.1 months, respectively [18,19,20,21]. Driessen et al. reported a median OS of 5 months when patients older than 70 years with stage ΙΙΙ LA-NSCLC selected non-curative treatment [19]. Meanwhile, although our study included only patients with N0–2 metastatic lymph node status, and consequently did not include all stage ΙΙΙ patients, the median PFS and OS for stage ΙΙΙ LA-NSCLC were 15.1 and 22.2 months, respectively, despite the median age being 82.0 years. Further, all the patients completed CIRT on schedule. These findings indicate that CIRT alone would be an effective treatment option for patients classified as N0–2.

The side effects of definitive treatment are generally more severe in elderly patients than in younger patients. Therefore, for elderly patients, the clinical goals must be decided by considering not only survival, but also quality of life and treatment tolerance. Administration of EGFR-TKI is limited to patients with NSCLC with activating EGFR mutation, although it is effective and relatively safe [22]. In addition, sustained disease control is uncommon [22]. Further, while CRT is effective, it is highly toxic for octogenarians and may worsen quality of life [21]. Unfortunately, photon radiotherapy alone also yields poor prognosis despite the relatively low incidence of severe toxicity. Meanwhile, CIRT alone achieved both a low incidence of severe toxicities and favorable local control, thus making it a promising treatment option for octogenarians with LA-NSCLC.

Table 3 Comparison of photon chemoradiotherapy, radiotherapy, EGFR-TKI, and CIRT alone for elderly patients with locally advanced NSCLC

Our study had several limitations. First, the present study was a single-center retrospective analysis. Second, our results were derived from a small sample size of only 32 patients. Third, only octogenarians with Eastern Cooperative Oncology Group performance status of 0–2 were treated with CIRT alone, and thus there might have been patient bias. Finally, the total doses and fractionation varied (68–76 Gy (RBE) in 12–16 fractions) among the patients. Further large-scale multicenter prospective trials are warranted.

In conclusion, CIRT alone is a relatively safe and effective treatment modality for octogenarians with LA-NSCLC.


  1. 1.

    de Groot PM, Wu CC, Carter BW, Munden RF. The epidemiology of lung cancer. Transl Lung Cancer Res. 2018;7:220–33.

    Article  Google Scholar 

  2. 2.

    Statistics of Japan. Published 2017.

  3. 3.

    Cancer Information Service. Published 2018.

  4. 4.

    Oh IJ, Ahn SJ. Multidisciplinary team approach for the management of patients with locally advanced non-small cell lung cancer: searching the evidence to guide the decision. Radiat Oncol J. 2017;35:16–24.

    Article  Google Scholar 

  5. 5.

    Schild SE, Stella PJ, Geyer SM, Bonner JA, McGinnis WL, Mailliard JA, et al. The outcome of combined-modality therapy for stage III non–small-cell lung cancer in the elderly. J Clin Oncol. 2003;21:3201–6.

    CAS  Article  Google Scholar 

  6. 6.

    Gajra A, Jatoi A. Non-small-cell lung cancer in elderly patients: a discussion of treatment options. J Clin Oncol. 2014;32:2562–9.

    CAS  Article  Google Scholar 

  7. 7.

    Kanai T, Endo M, Minohara S, Miyahara N, Koyama-ito H, Tomura H, et al. Biophysical characteristics of HIMAC clinical irradiation system for heavy-ion radiation therapy. Int J Radiat Oncol Biol Phys. 1999;44(4):201–10.

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Takahashi W, Nakajima M, Yamamoto N, Yamashita H, Nakagawa K, Miyamoto T, et al. A prospective nonrandomized phase I/II study of carbon ion radiotherapy in a favorable subset of locally advanced non-small cell lung cancer (NSCLC). Cancer. 2015;121:1321–7.

    CAS  Article  Google Scholar 

  9. 9.

    Karube M, Yamamoto N, Shioyama Y, Saito J, Matsunobu J, Okimoto J, et al. Carbon-ion radiotherapy for patients with advanced stage non–small-cell lung cancer at multicenters. J Radiat Res. 2017;58:761–4.

    CAS  Article  Google Scholar 

  10. 10.

    Yamamoto N, Miyamoto T, Nishimura H, Koto M, Tsujii H, Ohwada H, et al. Preoperative carbon ion radiotherapy for non-small cell lung cancer with chest wall invasion–pathological findings concerning tumor response and radiation induced lung injury in the resected organs. Lung Cancer. 2003;42:87–95.

    Article  Google Scholar 

  11. 11.

    Sugane T, Baba M, Imai R, Nakajima M, Yamamoto N, Miyamoto T, et al. Carbon ion radiotherapy for elderly patients 80 years and older with stage I non-small cell lung cancer. Lung Cancer. 2009;64:45–50.

    Article  Google Scholar 

  12. 12.

    Anzai M, Yamamoto N, Hayashi K, Nakajima M, Nomoto A, Ogawa K, et al. Safety and efficacy of carbon-ion radiotherapy alone for stage ΙΙΙ non-small cell lung cancer. Anticancer Res. 2020;40:379–86.

    CAS  Article  Google Scholar 

  13. 13.

    Hayashi K, Yamamoto N, Nakajima M, Nomoto A, Tsuji H, Ogawa K, et al. Clinical outcomes of carbon-ion radiotherapy for locally advanced non-small-cell lung cancer. Cancer Sci. 2019;110:734–41.

    CAS  Article  Google Scholar 

  14. 14.

    Sobin LH, Gospodarowicz MK, Wittekind C, editors. International union against cancer. TNM classification of malignant tumours. 7th ed. New York: Wiley-Blackwell Inc; 2009.

    Google Scholar 

  15. 15.

    Services UDOHAH, ed. Common terminology criteria for adverse events v4.0. NIH publication; 2009.

  16. 16.

    Hayashi K, Yamamoto N, Karube M, Nakajima M, Matsufuji N, Tsuji H, et al. Prognostic analysis of radiation pneumonitis: carbon-ion radiotherapy in patients with locally advanced lung cancer. Radiat Oncol. 2017;12:91.

    Article  Google Scholar 

  17. 17.

    Corre R, Gervais R, Guisier F, Tassy L, Vinas F, Lamy R, et al. Octogenarians with EGFR-mutated non-small cell lung cancer treated by tyrosine-kinase inhibitor: a multicentric real-world study assessing tolerance and efficacy (OCTOMUT study). Oncotarget. 2018;9:8253–62.

    Article  Google Scholar 

  18. 18.

    Atagi S, Kawahara M, Yokoyama A, Okamoto H, Yamamoto N, Ohe Y, et al. Thoracic radiotherapy with or without daily low-dose carboplatin in elderly patients with non-small-cell lung cancer: a randomized, controlled, phase 3 trial by the Japan Clinical Oncology Group (JCOG0301). Lancet Oncol. 2012;13:671–8.

    CAS  Article  Google Scholar 

  19. 19.

    Driessen EJM, Bootsma GP, Hendriks LEL, van den Berkmortel FW, Bogaarts BA, van Loon JG, et al. Stage III non-small cell lung cancer in the elderly: patient characteristics predictive for tolerance and survival of chemoradiation in daily clinical practice. Radiother Oncol. 2016;121:26–31.

    Article  Google Scholar 

  20. 20.

    Miller ED, Fisher JL, Haglund KE, Grecula JC, Xu-Welliver M, Bertino EM, et al. The addition of chemotherapy to radiation therapy improves survival in elderly patients with stage III non–small cell lung cancer. J Thorac Oncol. 2018;13:426–35.

    CAS  Article  Google Scholar 

  21. 21.

    Kim DY, Song C, Kim SH, Kim YJ, Lee JS, Kim JS. Chemoradiotherapy versus radiotherapy alone following induction chemotherapy for elderly patients with stage iii lung cancer. Radiat Oncol J. 2019;37:176–84.

    Article  Google Scholar 

  22. 22.

    Bunn PA, Dimou A. Systemic therapy for elderly patients with advanced non-small-cell lung cancers. J Clin Oncol. 2018;36:2571–4.

    Article  Google Scholar 

Download references


We thank the members of the Our Institution Working Group for Lung Cancer. This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.


No funding was received.

Author information



Corresponding author

Correspondence to Naoyoshi Yamamoto.

Ethics declarations

Conflict of interest

The authors have no conflict of interest.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

This article is published under an open access license. Please check the 'Copyright Information' section either on this page or in the PDF for details of this license and what re-use is permitted. If your intended use exceeds what is permitted by the license or if you are unable to locate the licence and re-use information, please contact the Rights and Permissions team.

About this article

Verify currency and authenticity via CrossMark

Cite this article

Hayashi, K., Yamamoto, N., Nakajima, M. et al. Carbon-ion radiotherapy for octogenarians with locally advanced non-small-cell lung cancer. Jpn J Radiol (2021).

Download citation


  • Carbon-ion radiotherapy
  • Locally advanced non-small-cell lung cancer
  • Octogenarians
  • Radiotherapy
  • Safety