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采用同步整合升压技术的质子束放疗治疗局部晚期胰腺癌的疗效和可行性。

Efficacy and feasibility of proton beam radiotherapy using the simultaneous integrated boost technique for locally advanced pancreatic cancer.

机构信息

Center for Liver and Pancreatobiliary Cancer, National Cancer Center, Goyang, 10408, Republic of Korea.

Center for Proton Therapy, National Cancer Center, Goyang, 10408, Republic of Korea.

出版信息

Sci Rep. 2020 Dec 10;10(1):21712. doi: 10.1038/s41598-020-78875-1.

DOI:10.1038/s41598-020-78875-1
PMID:33303947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7729854/
Abstract

To evaluate the clinical efficacy and feasibility of proton beam radiotherapy (PBT) using the simultaneous integrated boost (SIB) technique in locally advanced pancreatic cancer (LAPC), 81 LAPC patients receiving PBT using SIB technique were analyzed. The prescribed doses to planning target volume (PTV)1 and PTV2 were 45 or 50 GyE and 30 GyE in 10 fractions, respectively. Of 81 patients, 18 patients received PBT without upfront and maintenance chemotherapy (group I), 44 received PBT followed by maintenance chemotherapy (group II), and 19 received PBT after upfront chemotherapy followed by maintenance chemotherapy (n = 16) (group III). The median follow-up time was 19.6 months (range 2.3-57.6 months), and the median overall survival (OS) times of all patients and of those in groups I, II, and III were 19.3 months (95% confidence interval [CI] 16.8-21.7 months), 15.3 months (95% CI 12.9-17.7 months), 18.3 months (95% CI 15.9-20.7 months), and 26.1 months (95% CI 17.8-34.3 months), respectively (p = 0.043). Acute and late grade ≥ 3 toxicities related to PBT were not observed. PBT with the SIB technique showed promising OS for LAPC patients with a safe toxicity profile, and intensive combinations of PBT and chemotherapy could improve OS in these patients.

摘要

为了评估质子束放疗(PBT)联合同步整合推量(SIB)技术在局部晚期胰腺癌(LAPC)中的临床疗效和可行性,我们分析了 81 例接受 PBT 联合 SIB 技术治疗的 LAPC 患者。计划靶区(PTV)1 和 PTV2 的处方剂量分别为 45 或 50 GyE 和 30 GyE,共 10 次。81 例患者中,18 例未接受 upfront 和维持化疗(I 组),44 例接受 PBT 联合维持化疗(II 组),19 例接受 upfront 化疗联合维持化疗(n=16)(III 组)。中位随访时间为 19.6 个月(范围 2.3-57.6 个月),所有患者以及 I、II 和 III 组的中位总生存期(OS)分别为 19.3 个月(95%置信区间 [CI] 16.8-21.7 个月)、15.3 个月(95% CI 12.9-17.7 个月)、18.3 个月(95% CI 15.9-20.7 个月)和 26.1 个月(95% CI 17.8-34.3 个月)(p=0.043)。未观察到与 PBT 相关的急性和迟发性≥3 级毒性。PBT 联合 SIB 技术治疗 LAPC 患者具有良好的 OS 且毒性谱安全,PBT 与化疗的强化联合可能改善这些患者的 OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/d155eee10297/41598_2020_78875_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/52ea94a1edb4/41598_2020_78875_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/1efedb0dc41e/41598_2020_78875_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/d155eee10297/41598_2020_78875_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/52ea94a1edb4/41598_2020_78875_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/1efedb0dc41e/41598_2020_78875_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68e9/7729854/d155eee10297/41598_2020_78875_Fig3_HTML.jpg

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