A 54 Gy in three fractions of stereotactic body radiotherapy using CyberKnife for T1b-2aN0M0 pathologically confirmed non-small cell lung cancer

Author:

Abe Takanori1ORCID,Ryuno Yasuhiro1,Iino Misaki1,Saito Satoshi1,Aoshika Tomomi1,Ohta Tomohiro1,Igari Mitsunobu1,Hirai Ryuta1,Kumazaki Yu1,Kaira Kyoichi2ORCID,Kagamu Hiroshi2,Ishida Hironori3,Noda Shin-ei1,Kato Shingo1

Affiliation:

1. Departments of Radiation Oncology, International Medical Center, Saitama Medical University, Hidaka, Japan

2. Respiratory Medicine, International Medical Center, Saitama Medical University, Hidaka, Japan

3. General Thoracic Surgery, International Medical Center, Saitama Medical University, Hidaka, Japan

Abstract

Abstract Objective Optimal dose-fractionation regimen of stereotactic body radiotherapy for peripheral early-stage non-small cell lung cancer remains unclear. We retrospectively investigated outcomes of stereotactic body radiotherapy using CyberKnife at 54 Gy in three fractions in 26 patients (median age: 76 years) with pathologically confirmed T1b–T2aN0M0 non-small cell lung cancer. Methods A 54 Gy in three fractions was prescribed to cover the 99% of gross tumor volume. We estimated cumulative local control, progression-free survival and overall survival rates (Kaplan–Meier method), and toxicity (Common Toxicity Criteria for Adverse Events, version 5.0). Results All the tumors were located at peripheral area of lung. Mean distance from chest wall to tumor was 6.5 mm (range: 0–32 mm). The patients’ pathological diagnoses were: adenocarcinoma: n = 18, squamous cell carcinoma: n = 7 and non-small cell carcinoma: n = 1. Their stages were T1b: n = 9, T1c: n = 14 and T2a: n = 3. Median follow-up was 24 months (range: 6–54). Cumulative 2-year effect rates were local control: 100%, progression-free survival 70% and overall survival: 92%. Twenty patients developed grade one radiation pneumonitis, but grade 2 or greater radiation pneumonitis was not observed. Conclusions We found CyberKnife-stereotactic body radiotherapy for pathologically confirmed T1b–T2aN0M0 non-small cell lung cancer to be effective and safe. However, these results should be validated with a larger patient cohort and prospective follow-up monitoring.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Radiology, Nuclear Medicine and imaging,Oncology,General Medicine

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