Ueno Hirona, Nishiyama Yuta, Maruo Takuya, Fukuda Yohei, Katayama Takayuki, Yoda Shinichiro, Nishi Kotaro, Kayanuma Hideki
Laboratory of Veterinary Radiology, School of Veterinary Medicine, Azabu University, Sagamihara, Japan.
Veterinary Teaching Hospital, Azabu University, Sagamihara, Japan.
Open Vet J. 2025 Feb;15(2):827-834. doi: 10.5455/OVJ.2025.v15.i2.32. Epub 2025 Feb 28.
Despite an initial favorable response to hypofractionated radiotherapy (RT), intranasal neoplasia has a poor long-term prognosis. Re-irradiation (re-RT) has been shown to result in clinical remission in dogs with recurrent intranasal tumors. Hypofractionated re-RT is indicated in cases of recurrence.
This study aimed to investigate the response of patients with recurrent intranasal tumors who were initially treated with repeated hypofractionated RT and subsequently underwent re-RT.
Medical records of dogs with intranasal tumors that relapsed after undergoing hypofractionated RT at Azabu University Veterinary Teaching Hospital and who underwent re-RT between 2008 and 2022 were retrospectively analyzed.
Among the 30 dogs included, 20 had adenocarcinomas. Eleven patients underwent a second re-RT, and five patients underwent a third re-RT. The median total isocenter dose and total number of fractions were 56 Gy (range, 37.5-102) and 8 fractions (range, 5-14), respectively. The first, second, and third progression-free intervals (PFIs) were 315 ( = 30), 185 ( = 11), and 218 days ( = 4), respectively. Overall survival (OS) was 504 days ( = 30). Adverse events such as alopecia ( = 7), white hair ( = 8), cataracts ( = 9), pigmentation ( = 5), keratitis ( = 3), and corneal ulceration ( = 1) were limited to grades 1 and 2. The medians of the first PFI for one course and two or more courses of re-RT were 298 and 331 days, respectively, indicating no significant differences between the groups. The OS after two or more courses of re-RT (758 days) was significantly longer than after one course of re-RT alone (414 days) ( = 0.048). However, the cases were not randomized, and most of the tumor types were adenocarcinomas.
Since it is expected to prolong survival time with few life-threatening adverse events, the findings of the present study suggest that hypofractionated re-RT can be used in dogs with recurrent intranasal tumors initially treated with hypofractionated RT. Therefore, repeated hypofractionated re-RT may be a reasonable option for young dogs with a good initial response and recurrent intranasal tumors.
尽管鼻内肿瘤对分割放疗(RT)最初有良好反应,但其长期预后较差。再放疗(re-RT)已被证明可使复发性鼻内肿瘤犬达到临床缓解。复发情况下可采用分割再放疗。
本研究旨在调查最初接受重复分割放疗并随后接受再放疗的复发性鼻内肿瘤患者的反应。
回顾性分析了麻布大学兽医教学医院接受分割放疗后复发且在2008年至2022年间接受再放疗的鼻内肿瘤犬的病历。
纳入的30只犬中,20只患有腺癌。11只犬接受了第二次再放疗,5只犬接受了第三次再放疗。等中心总剂量中位数和总分割次数分别为56 Gy(范围37.5 - 102)和8次分割(范围5 - 14)。第一次、第二次和第三次无进展生存期(PFI)分别为315天(n = 30)、185天(n = 11)和218天(n = 4)。总生存期(OS)为504天(n = 30)。脱发(n = 7)、白毛(n = 8)、白内障(n = 9)、色素沉着(n = 5)、角膜炎(n = 3)和角膜溃疡(n = 1)等不良事件仅限于1级和2级。一个疗程和两个或更多疗程再放疗的首次PFI中位数分别为298天和331天,表明两组之间无显著差异。两个或更多疗程再放疗后的OS(758天)明显长于仅一个疗程再放疗后的OS(414天)(P = 0.048)。然而,病例未随机分组,且大多数肿瘤类型为腺癌。
由于预计能延长生存时间且危及生命的不良事件较少,本研究结果表明分割再放疗可用于最初接受分割放疗的复发性鼻内肿瘤犬。因此,对于初始反应良好且患有复发性鼻内肿瘤的幼犬,重复分割再放疗可能是一个合理的选择。