镰仓总医院质子束治疗胰腺癌的初步经验。

IF 1.8 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
In vivo Pub Date : 2025-09-01 DOI:10.21873/invivo.14101
Shintaro Shiba, Sachika Shiraishi, Kazuya Koizumi, Yutaka Fujimoto, Naoto Ishiai, Koichi Tokuuye, Motoko Omura
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引用次数: 0

摘要

背景/目的:在日本,质子束治疗(PBT)在先进的医疗系统下治疗局部晚期胰腺癌,直到2022年;从那时起,它就被纳入国民保险。我院于2022年7月启动胰腺癌PBT治疗。本研究评估了国民保险覆盖范围开始后PBT治疗胰腺癌的临床结果,并评估了我们在我院的初步经验是否再现了先前报道的结果。患者和方法:本研究包括10例因局部晚期、合并症或拒绝手术而确诊不能手术的胰腺癌患者,无远处转移。所有患者接受的PBT总剂量为67.5 Gy(相对生物有效性),分25份给药。结果:所有和存活患者的中位随访时间分别为13.9个月(范围为3.9-24.6个月)和19.5个月(范围为8.1-24.6个月)。1年和2年总生存率分别为70%和35%,局部控制率分别为89%和89%。未观察到与PBT相关的3级或以上急性或晚期非血液学毒性。结论:新建立的PBT设施的临床结果与在以前先进的医疗系统下治疗的患者的临床结果具有可比性和可重复性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Initial Experience With Proton Beam Therapy for Pancreatic Cancer at Shonan Kamakura General Hospital.

Initial Experience With Proton Beam Therapy for Pancreatic Cancer at Shonan Kamakura General Hospital.

Initial Experience With Proton Beam Therapy for Pancreatic Cancer at Shonan Kamakura General Hospital.

Initial Experience With Proton Beam Therapy for Pancreatic Cancer at Shonan Kamakura General Hospital.

Background/aim: In Japan, proton beam therapy (PBT) for locally advanced pancreatic cancer was administered under an advanced medical treatment system until 2022; since then, it has been covered by national insurance. Our hospital initiated PBT for pancreatic cancer in July 2022. This study evaluated the clinical outcomes of PBT for pancreatic cancer after the initiation of national insurance coverage and assessed whether our initial experience at our hospital reproduced previously reported results.

Patients and methods: This study included 10 patients with pancreatic cancer confirmed as inoperable due to locally advanced stage, comorbidity, or refusal to undergo surgery, without distant metastasis. All patients received a total PBT dose of 67.5 Gy (relative biological effectiveness) delivered in 25 fractions.

Results: The median follow-up durations for all and surviving patients were 13.9 months (range=3.9-24.6 months) and 19.5 months (range=8.1-24.6 months), respectively. The 1- and 2-year overall survival and local control rates were 70% and 35%, and 89% and 89%, respectively. No grade 3 or higher acute or late non-hematological toxicities associated with PBT were observed.

Conclusion: The clinical outcomes at the newly established PBT facility were comparable and reproducible to those observed in patients treated under the previous advanced medical treatment system.

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来源期刊
In vivo
In vivo 医学-医学:研究与实验
CiteScore
4.20
自引率
4.30%
发文量
330
审稿时长
3-8 weeks
期刊介绍: IN VIVO is an international peer-reviewed journal designed to bring together original high quality works and reviews on experimental and clinical biomedical research within the frames of physiology, pathology and disease management. The topics of IN VIVO include: 1. Experimental development and application of new diagnostic and therapeutic procedures; 2. Pharmacological and toxicological evaluation of new drugs, drug combinations and drug delivery systems; 3. Clinical trials; 4. Development and characterization of models of biomedical research; 5. Cancer diagnosis and treatment; 6. Immunotherapy and vaccines; 7. Radiotherapy, Imaging; 8. Tissue engineering, Regenerative medicine; 9. Carcinogenesis.
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