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A preliminary experience of moderate-intensity stereotactic body radiation therapy for ultra-central lung tumor

Authors
Park, SunminKim, YoungYoon, Won SupRim, Chai Hong
Issue Date
2-Sep-2019
Publisher
TAYLOR & FRANCIS LTD
Keywords
Stereotactic body radiotherapy; ultra-central tumor; feasibility; radiotherapy
Citation
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, v.95, no.9, pp.1287 - 1294
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY
Volume
95
Number
9
Start Page
1287
End Page
1294
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/62923
DOI
10.1080/09553002.2019.1626026
ISSN
0955-3002
Abstract
Purpose: Administration of stereotactic body radiation therapy (SBRT) to ultra-central (UC) lung tumors, generally defined as those abutting the proximal bronchial trees, is difficult due to concerns about serious toxicities. Therefore, our institution has performed moderate-intensity SBRT. Patients and methods: Patients with UC tumors underwent SBRT at a dose of 50-60 Gy in 10 fractions, with D-max in the target volume not exceeding 110% of the prescribed dose. The primary outcomes were tumor response and overall survival (OS). Results: From January 2017 to September 2018, we treated eight patients who had been diagnosed with UC tumors. The median follow-up time was 8.6 months (range: 2.7-14.9). Five of the eight patients (62.5%) showed a complete response (CR), two (25%) had a partial response (PR), and one (12.5%) had stable disease (SD); the response and disease control rates were 87.5% and 100%, respectively. Seven patients were alive with no evidence of disease or with controlled disease until the last follow-ups, except for one patient who died due to a non-RT cause at 3 months after SBRT. One patient experienced grade 2 esophageal pain and another had grade 1 cough. No grade 3 or higher toxicities were reported. Conclusion: Moderate-intensity SBRT might aid in achieving good control of UC tumors without excessive toxicities. Future studies involving larger numbers of patients and longer follow-up times are warranted to confirm the efficacy and feasibility.
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