Takano Seiya, Tomita Natsuo, Kuno Mayu, Niwa Masanari, Torii Akira, Takaoka Taiki, Kita Nozomi, Okazaki Dai, Yamamoto Shintaro, Kawai Tatsuya, Sugie Chikao, Ogawa Yasutaka, Matsumoto Kenichi, Uchiyama Kaoru, Otsuka Shinya, Matsui Tooru, Miyakawa Akifumi, Mizuno Tomoki, Iida Masato, Tanikawa Motoki, Mase Mitsuhito, Hiwatashi Akio
Department of Radiology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-Cho, Mizuho-Ku, Nagoya, Aichi, 467-8601, Japan.
Department of Radiation Oncology, Ichinomiya Municipal Hospital, 2-2-22 Bunkyo, Ichinomiya, Aichi, 491-8558, Japan.
Sci Rep. 2024 Apr 23;14(1):9283. doi: 10.1038/s41598-024-60154-y.
We compared survival outcomes of high-dose concomitant boost radiotherapy (HDCBRT) and conventional dose radiotherapy (CRT) for newly diagnosed glioblastoma (GB). Patients treated with intensity-modulated radiation therapy for newly diagnosed GB were included. In HDCBRT, specific targets received 69, 60, and 51 Gy in 30 fractions, while 60 Gy in 30 fractions was administered with a standard radiotherapy method in CRT. Overall survival (OS) and progression-free survival (PFS) were compared using the Log-rank test, followed by multivariate Cox analysis. The inverse probability of treatment weighting (IPTW) method was also applied to each analysis. Among 102 eligible patients, 45 received HDCBRT and 57 received CRT. With a median follow-up of 16 months, the median survival times of OS and PFS were 21 and 9 months, respectively. No significant differences were observed in OS or PFS in the Kaplan-Meier analyses. In the multivariate analysis, HDCBRT correlated with improved OS (hazard ratio, 0.49; 95% confidence interval, 0.27-0.90; P = 0.021), and this result remained consistent after IPTW adjustments (P = 0.028). Conversely, dose suppression due to the proximity of normal tissues and IMRT field correlated with worse OS and PFS (P = 0.008 and 0.049, respectively). A prospective study with a stricter protocol is warranted to validate the efficacy of HDCBRT for GB.
我们比较了高剂量同步加量放疗(HDCBRT)与传统剂量放疗(CRT)对新诊断胶质母细胞瘤(GB)的生存结局。纳入了接受调强放射治疗的新诊断GB患者。在HDCBRT中,特定靶区接受30次分割照射,总剂量分别为69、60和51 Gy,而在CRT中,采用标准放疗方法给予30次分割照射,总剂量60 Gy。使用对数秩检验比较总生存期(OS)和无进展生存期(PFS),随后进行多因素Cox分析。每种分析均应用治疗权重逆概率(IPTW)方法。在102例符合条件的患者中,45例接受HDCBRT,57例接受CRT。中位随访16个月,OS和PFS的中位生存时间分别为21个月和9个月。在Kaplan-Meier分析中,OS或PFS未观察到显著差异。在多因素分析中,HDCBRT与改善的OS相关(风险比,0.49;95%置信区间,0.27 - 0.90;P = 0.021),IPTW调整后该结果仍保持一致(P = 0.028)。相反,由于正常组织和调强放疗野接近导致的剂量抑制与较差的OS和PFS相关(分别为P = 0.008和0.049)。有必要进行一项采用更严格方案的前瞻性研究,以验证HDCBRT对GB的疗效。