2024/04/11 更新

写真a

ナガイ ナオヤ
長井 尚哉
NAGAI Naoya
所属
医学部附属病院 放射線部 病院助教
職名
病院助教
 

論文 1

  1. Palliative radiotherapy for painful non-bone lesions in patients with advanced cancer: a single center retrospective study

    Shindo, Y; Koide, Y; Nagai, N; Kitagawa, T; Aoyama, T; Shimizu, H; Hashimoto, S; Tachibana, H; Kodaira, T; Ishihara, S; Naganawa, S

    JAPANESE JOURNAL OF RADIOLOGY     2024年2月

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    記述言語:英語   出版者・発行元:Japanese Journal of Radiology  

    Purpose: This retrospective study aimed to assess the efficacy and safety of palliative radiotherapy for painful non-bone lesions in patients with advanced cancer. Materials and methods: We enrolled patients with painful non-bone lesions who underwent conventional palliative radiotherapy between September 2018 and September 2022. The treatment targets included primary tumor lesions, lymph node metastases, non-bone hematogenous metastases, and other lesions. The primary endpoint was the overall pain response rate in evaluable patients, determined based on the International Consensus Pain Response Endpoint criteria. The secondary endpoints included overall survival, pain recurrence, and adverse events. Results: Of the 420 screened patients, 142 received palliative radiotherapy for painful non-bone lesions, and 112 were evaluable. A pain response was achieved in 67 patients (60%) of the 112 evaluable patients within a median of 1.2 months. Among these patients, 25 exhibited complete response, 42 partial response, 18 indeterminate response, and 27 pain progression. The median survival time was 5.5 months, recorded at a median follow-up of 6.0 months, during which 67 patients died. Multivariate analysis identified poor performance status scores of 2–4, opioid use, and re-irradiation as independent factors associated with a reduced likelihood of achieving a pain response. Pain recurrence occurred in 18 patients over a median of 4.1 months. Seventeen patients had grade 1–2 adverse events, while none experienced grade 3 or higher toxicity. Conclusion: Palliative radiotherapy can potentially be a safe and well-tolerated modality for managing painful non-bone lesions, with a low rate of adverse events.

    DOI: 10.1007/s11604-024-01536-0

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