Multi-institutional phase II study of ultra-hypofractionated whole-breast irradiation after breast-conserving surgery for breast cancer in Japan: Kyoto Radiation Oncology Study Group (UPBEAT study)

被引:5
|
作者
Mitsuyoshi, Takamasa [1 ,6 ]
Ono, Yuka [2 ]
Ashida, Ryo [1 ]
Yamashita, Mikiko [3 ]
Tanabe, Hiroaki [3 ]
Takebe, Sayaka [4 ]
Tokiwa, Mariko [4 ]
Suzuki, Eiji [4 ]
Imagumbai, Toshiyuki [1 ]
Yoshimura, Michio [2 ]
Yamauchi, Chikako [5 ]
Mizowaki, Takashi [2 ]
Kokubo, Masaki [1 ]
机构
[1] Kobe City Med Ctr Gen Hosp, Dept Radiat Oncol, Kobe, Hyogo 6500057, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Radiat Oncol & Image Appl Therapy, Kyoto 6068501, Japan
[3] Kobe City Med Ctr Gen Hosp, Dept Radiol Technol, Kobe, Hyogo 6500057, Japan
[4] Kobe City Med Ctr Gen Hosp, Dept Breast Surg, Kobe, Hyogo 6500057, Japan
[5] Shiga Gen Hosp, Dept Radiat Oncol, Moriyama, Shiga 5240022, Japan
[6] Kobe City Med Ctr Gen Hosp, Dept Radiat Oncol, 2-1-1 Minatojima Minamimachi, Chuo Ku, Kobe, Hyogo 6500047, Japan
关键词
breast cancer; phase II study; ultra-hypofractionated; whole-breast irradiation; THERAPY; UK;
D O I
10.1093/jjco/hyac174
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The UK-FAST-Forward study showed that ultra-hypofractionated whole-breast irradiation (ultra-HF-WBI) involving five fractions of 26 Gy radiation over 1 week was not inferior to HF-WBI. However, it is not used in Japan due to safety concerns. In April 2022, we commenced a multi-institutional, single-arm, phase II trial. Our aim is to confirm the safety of ultra-HF-WBI after breast-conserving surgery (BCS) for breast cancer in Japanese women. Method We plan to enroll 98 patients from 13 institutions. The primary endpoint is the proportion of late adverse events of grades >= 2 within 3 years. Discussion We believe that this highly promising clinical study can positively impact the Japanese guidelines for breast cancer treatment. The results will help us decide whether or not ultra-HF-WBI can be used as a more convenient alternative to WBI. Registration number and date This trial was registered in the UMIN Clinical Trials Registry (UMIN000047080) on March 4, 2022. This multi-institutional, single-arm, phase II trial is aimed at confirming the safety of ultra-HF-WBI after BCS for breast cancer in Japanese women.
引用
收藏
页码:174 / 178
页数:5
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