Clinical results of carbon-ion radiotherapy for stage I non-small cell lung cancer with concomitant interstitial lung disease: a Japanese national registry study (J-CROS-LUNG)

Author:

Okano Naoko1,Suefuji Hiroaki2,Nakajima Mio3,Tokumaru Sunao4,Kubo Nobuteru1,Yoshida Daisaku5,Suzuki Osamu6,Ishikawa Hitoshi3,Satouchi Miyako7,Nakayama Haruhiko8,Shioyama Yoshiyuki2

Affiliation:

1. Gunma University Heavy Ion Medical Center , 3-39-15 Showa-machi, Maebashi, Gunma 371-8511, Japan

2. SAGA-HIMAT Foundation Ion Beam Therapy Center, , 3049, Koga-machi, Tosu, Saga 841-0071, Japan

3. National Institutes for Quantum and Radiological Science and Technology , 4-9-1, Anagawa, Inage-ku, Chiba, Chiba 263-8555, Japan

4. Hyogo Ion Beam Medical Center Department of Radiology, , 1-2-1 Kouto, Shingu-cho, Tatsuno, Hyogo 679-5165, Japan

5. Kanagawa Cancer Center , 2-3-2 Nakao, Asahi-ku, Yokohama, Kanagawa 241-8515, Japan

6. Osaka Heavy Ion Therapy Center , 3-1-10 Otemae, Chuo-ku, Osaka, Osaka, 540-0008, Japan

7. Hyogo Cancer Center Department of Thoracic Oncology, , 13-70, Kitaoji-cho, Akashi, Hyogo 673-8558, Japan

8. Kanagawa Cancer Center Department of Thoracic Surgery, , 2-3-2, Nakao, Asahi-ku, Yokohama, Kanagawa 241-8515, Japan

Abstract

Abstract Anti-cancer treatments for lung cancer patients with interstitial lung disease (ILD) are challenging. The treatment options for ILD are often limited because of concerns that treatments can cause acute exacerbation (AE) of ILD. This study aimed to analyze the outcomes of carbon-ion radiotherapy (CIRT) for stage I non-small cell lung cancer (NSCLC) with ILD, using a multi-institutional registry. Patients with ILD who received CIRT for stage I NSCLC in CIRT institutions in Japan were enrolled. The indication for CIRT was determined by an institutional multidisciplinary tumor board, and CIRT was performed in accordance with institutional protocols. Thirty patients were eligible. The median follow-up duration was 30.3 months (range, 2.5–58 months), and the total dose ranged from 50 Gy (relative biological effectiveness [RBE]) to 69.6 Gy (RBE), and five different patterns of fractionation were used. The beam delivery method was passive beam in 19 patients and scanning beam in 11 patients. The 3-year overall survival (OS), cause-specific survival, disease-free survival (DFS) and local control (LC) rates were 48.2%, 62.2%, 41.2% and 88.1%, respectively. Grade > 2 radiation pneumonitis occurred in one patient (3.3%). In conclusion, CIRT is a safe treatment modality for stage I NSCLC with concomitant ILD. CIRT is a safe and feasible treatment option for early lung cancer in ILD patients.

Funder

Gunma University Heavy Ion Medical Center

Publisher

Oxford University Press (OUP)

Subject

Health, Toxicology and Mutagenesis,Radiology, Nuclear Medicine and imaging,Radiation

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