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Five-Year Survival Outcomes After Carbon-Ion Radiotherapy for Operable Stage I NSCLC: A Japanese National Registry Study (J-CROS-LUNG).
Kubo, Nobuteru; Suefuji, Hiroaki; Nakajima, Mio; Tokumaru, Sunao; Okano, Naoko; Yoshida, Daisaku; Suzuki, Osamu; Ishikawa, Hitoshi; Satouchi, Miyako; Nakayama, Haruhiko; Shimizu, Kimihiro; Shioyama, Yoshiyuki.
Afiliação
  • Kubo N; Gunma University Heavy Ion Medical Center, Gunma, Japan. Electronic address: kubo@gunma-u.ac.jp.
  • Suefuji H; Ion Beam Therapy Center, SAGA-HIMAT Foundation, Saga, Japan.
  • Nakajima M; National Institutes for Quantum and Radiological Science and Technology, QST Hospital, Chiba, Japan.
  • Tokumaru S; Department of Radiology, Hyogo Ion Beam Medical Center, Hyogo, Japan.
  • Okano N; Gunma University Heavy Ion Medical Center, Gunma, Japan.
  • Yoshida D; Department of Radiation Oncology, Kanagawa Cancer Center, Kanagawa, Japan.
  • Suzuki O; Osaka Heavy Ion Therapy Center, Osaka, Japan.
  • Ishikawa H; National Institutes for Quantum and Radiological Science and Technology, QST Hospital, Chiba, Japan.
  • Satouchi M; Department of Thoracic Oncology, Hyogo Cancer Center, Hyogo, Japan.
  • Nakayama H; Kanagawa Prefectural Hospital Organization, Kanagawa, Japan.
  • Shimizu K; Division of General Thoracic Surgery, Department of Surgery, Shinshu University School of Medicine, Nagano, Japan.
  • Shioyama Y; Ion Beam Therapy Center, SAGA-HIMAT Foundation, Saga, Japan.
J Thorac Oncol ; 19(3): 491-499, 2024 Mar.
Article em En | MEDLINE | ID: mdl-37924974
ABSTRACT

INTRODUCTION:

The standard therapy for stage I NSCLC is surgery, but some operable patients refuse this option and instead undergo radiotherapy. Carbon-ion radiotherapy (CIRT) is a type of radiotherapy. The Japanese prospective nationwide registry study on CIRT began in 2016. Here, we analyzed real-world clinical outcomes of CIRT for operable patients with stage I NSCLC.

METHODS:

All patients with operable stage I NSCLC treated with CIRT in Japan between 2016 and 2018 were enrolled. The dose fractionations for CIRT were selected from several options approved by the Japanese Society for Radiation Oncology. CIRT was delivered to the primary tumor, not to lymph nodes.

RESULTS:

The median follow-up period was 56 months. Among 136 patients, 117 (86%) had clinical stage IA NSCLC and 19 (14%) had clinical stage IB NSCLC. There were 50 patients (37%) diagnosed clinically without having been diagnosed histologically. Most tumors (97%) were located in the periphery. The 5-year overall survival, cause-specific survival, progression-free survival, and local control rate were 81.8% (95% confidence interval [CI] 75.1-89.2), 91.2% (95% CI 86.0-96.8), 65.9% (95% CI 58.2-74.6), and 95.8% (95% CI 92.3-99.5), respectively. Multivariate analysis identified age as a significant factor for overall survival (p = 0.018), whereas age and consolidation/tumor ratio (p = 0.010 and p = 0.004) were significant factors for progression-free survival. There was no grade 4 or higher toxicity. Grade 3 radiation pneumonitis occurred in one patient.

CONCLUSIONS:

This study reports the long-term outcomes of CIRT for operable NSCLC in the real world. CIRT for operable patients has been found to have favorable outcomes, with tolerable toxicity.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Carcinoma Pulmonar de Células não Pequenas / Neoplasias Pulmonares Limite: Humans País como assunto: Asia Idioma: En Ano de publicação: 2024 Tipo de documento: Article