利用多导管间质近距离放射治疗早期乳腺癌的超短围手术期部分乳房照射的初步报告。

IF 4 3区 医学 Q1 OBSTETRICS & GYNECOLOGY Breast Cancer Pub Date : 2024-05-01 Epub Date: 2024-02-15 DOI:10.1007/s12282-024-01546-w
Kazuhiko Sato, Hiromi Fuchikami, Naoko Takeda, Nana Natsume, Masahiro Kato
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引用次数: 0

摘要

目的:与术后多导管间质近距离放射治疗(MIB)相比,围手术期部分乳房放射治疗(PBI)创伤更小、更方便。本研究旨在比较同期进行的超短围手术期多导管间近距离放射治疗(uPBI)和常规围手术期多导管间近距离放射治疗(cPBI):研究的纳入标准为年龄≥ 40 岁、T0-2(≤ 3 厘米)、N0-mi 和乳腺 X 射线检查边缘阴性的患者。比较了4次分次25.2 Gy剂量的uPBI和8次分次32 Gy剂量的cPBI的局部区域复发率(LRR)和毒性:共对198名患者(151名接受了uPBI治疗,47名接受了cPBI治疗)进行了评估。中位随访时间为 20.1 个月,uPBI 组中有一名患者(0.66%)出现 LRR。uPBI组和cPBI组的两年同侧乳腺肿瘤无复发生存率分别为98.7%和100%。毒性分级最高的是uPBI组,23人(15.2%)为1级,2人(1.3%)为2级;cPBI组,8人(17.0%)为1级,1人(2.1%)为2级。两组患者均未出现 3 级及以上毒性反应。两组患者的毒性反应率没有明显差异。此外,uPBI 组和 cPBI 组分别有 22 名(14.6%)和 8 名(17.0%)患者出现急性和晚期毒性反应,uPBI 组和 cPBI 组分别有 3 名(2.0%)和 1 名(2.1%)患者出现急性和晚期毒性反应。两组患者出现毒性的时间没有明显差异:虽然这份初步报告的样本量较小,随访时间较短,但uPBI组和cPBI组的局部控制率和毒性发生率相似。有必要进一步研究 MIB-PBI 的理想剂量表。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Preliminary report on ultrashort perioperative partial-breast irradiation with multicatheter interstitial brachytherapy for early-stage breast cancer.

Purpose: Perioperative partial-breast irradiation (PBI) with multicatheter interstitial brachytherapy (MIB) is less invasive and more convenient than postoperative one. This study aimed to compare ultrashort perioperative MIB-PBI (uPBI) and conventional perioperative MIB-PBI (cPBI) performed during the same period of time.

Methods: Inclusion criteria of the study were patients aged ≥ 40 years and those with T0-2 (≤ 3 cm), N0-mi, and negative margins on mammography. The locoregional recurrence (LRR) and toxicity rates were compared between uPBI at a dose of 25.2 Gy in four fractions and cPBI at a dose of 32 Gy in eight fractions.

Results: In total, 198 patients (151 with uPBI and 47 with cPBI) were evaluated. At a median follow-up of 20.1 months, one (0.66%) patient in the uPBI group had LRR. The 2-year ipsilateral breast tumor recurrence-free survival rates of the uPBI and cPBI groups were 98.7% and 100%, respectively. The highest toxicity grades were grade 1 in 23 (15.2%) and grade 2 in 2 (1.3%) patients in the uPBI group, and grade 1 in 8 (17.0%) and grade 2 in 1 (2.1%) patient in the cPBI group. None of the patients in the two groups presented with grade 3 and higher toxicities. The toxicity rates between the two groups did not significantly differ. Further, 22 (14.6%) patients in the uPBI group and 8 (17.0%) in the cPBI group, and 3 (2.0%) patients in the uPBI group and 1 (2.1%) in the cPBI had acute and late toxicities, respectively. The timing of toxicity development between the two groups did not significantly differ.

Conclusions: Although this preliminary report included a small sample size and had a short follow-up period, the local control and toxicity rates were similar between the uPBI and cPBI groups. Further research is warranted to investigate the ideal dose schedule of MIB-PBI.

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来源期刊
Breast Cancer
Breast Cancer ONCOLOGY-OBSTETRICS & GYNECOLOGY
CiteScore
6.70
自引率
2.50%
发文量
105
审稿时长
6-12 weeks
期刊介绍: Breast Cancer, the official journal of the Japanese Breast Cancer Society, publishes articles that contribute to progress in the field, in basic or translational research and also in clinical research, seeking to develop a new focus and new perspectives for all who are concerned with breast cancer. The journal welcomes all original articles describing clinical and epidemiological studies and laboratory investigations regarding breast cancer and related diseases. The journal will consider five types of articles: editorials, review articles, original articles, case reports, and rapid communications. Although editorials and review articles will principally be solicited by the editors, they can also be submitted for peer review, as in the case of original articles. The journal provides the best of up-to-date information on breast cancer, presenting readers with high-impact, original work focusing on pivotal issues.
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