Yu Bowen, Li Kai-Wen, Fan Yingyi, Pei Xiaohua
Galactophore Department, Beijing University of Chinese Medicine Third Affiliated Hospital, Beijing, China.
Department of Technology, CAS Ion Medical Technology Co., Ltd., Beijing, China.
Int J Part Ther. 2024 Aug 30;14:100629. doi: 10.1016/j.ijpt.2024.100629. eCollection 2024 Dec.
To explore the challenges and future of carbon-ion radiation therapy (CIRT) in breast cancer, we summarized the progress of nonclinical and clinical studies on CIRT for breast cancer in this review. A total of 6 nonclinical studies have been reported, which demonstrated a better effect of Carbon-ion irradiation compared with X-ray in breast cancer cell lines (including triple-negative breast cancer and Human Epidermal Growth Factor Receptor 2-negative breast cancer). Combination with Hh inhibitor, dual tyrosine kinase inhibitor, and PARP inhibitor is promising as demonstrated in the in vitro studies. Approximately 34 patients with breast cancer went through CIRT treatment, as reported in 5 clinical studies. All studies demonstrated promising treatment effects with acceptable and manageable risks. In these studies, a total of 21 patients were reported with post-treatment response assessments, among whom 19 patients (90.48%) reported a response of complete response or partial response. The complete response rate was 66.67%. The time to complete the response ranged from 3 months to 24 months. No adverse events were observed in these studies except for grade 1 acute skin reaction in 14 out of the 21 patients (66.67%). Although the time to respond was longer than expected in some studies, the persistent responses and satisfactory safety profile provided the rationale for further research on this new therapy.
为探讨碳离子放射治疗(CIRT)在乳腺癌治疗中的挑战与未来发展,我们在本综述中总结了CIRT治疗乳腺癌的非临床和临床研究进展。共报道了6项非临床研究,这些研究表明,在乳腺癌细胞系(包括三阴性乳腺癌和人表皮生长因子受体2阴性乳腺癌)中,碳离子照射比X射线具有更好的效果。体外研究表明,联合使用Hh抑制剂、双酪氨酸激酶抑制剂和PARP抑制剂具有良好前景。据5项临床研究报道,约34例乳腺癌患者接受了CIRT治疗。所有研究均显示出有前景的治疗效果,且风险可接受和可控。在这些研究中,共报道了21例患者的治疗后反应评估情况,其中19例患者(90.48%)报告为完全缓解或部分缓解。完全缓解率为66.67%。达到缓解的时间为3个月至24个月。除21例患者中有14例(66.67%)出现1级急性皮肤反应外,这些研究中未观察到其他不良事件。尽管在一些研究中达到缓解的时间比预期长,但持续的缓解效果和令人满意的安全性为进一步研究这种新疗法提供了依据。