Department of Radiation Oncology, Nagoya Proton Therapy Center, Nagoya City West Medical Center, 1-1-1 Hirate-cho, Kita-ku, Nagoya, Japan.
Department of Radiology, Nagoya City University Graduate School of Medical Sciences, 1 Kawasumi, Mizuho-cho, Mizuho-ku, Nagoya, Japan.
J Radiat Res. 2019 Oct 23;60(5):612-621. doi: 10.1093/jrr/rrz036.
To investigate optimal treatment planning using proton beams for non-squamous cell carcinoma of the head and neck (NSCHN), the dose distributions of plans involving pencil beam scanning (PBS) with or without a patient-specific aperture system (PSAS), passive-scattering proton therapy (PSPT) and X-ray intensity-modulated radiotherapy (IMRT) were compared. As clinical results, toxicities of PBS with PSAS, including changes in quality of life, were reported. Between April 2014 and August 2016, a total of 30 patients were treated using PBS with PSAS. In 20 patients selected at random, the dose distributions of PBS with or without the PSAS, PSPT and IMRT plans were compared. Neutron exposure by proton therapy was calculated using a Monte Carlo simulation. Toxicities were scored according to CTCAE ver. 4.0. Patients completed EORTC quality of life survey forms (QLQ-C30 and QLQ-HN35) before and 0-12 months after proton therapy. The 95% conformity number of PBS with the PSAS plan was the best, and significant differences were detected among the four plans (P < 0.05, Bonferroni tests). Neutron generation by PSAS was ~1.1-fold higher, but was within an acceptable level. No grade 3 or higher acute dermatitis was observed. Pain, appetite loss and increased weight loss were more likely at the end of treatment, but recovered by the 3 month follow-up and returned to the pretreatment level at the 12 month follow-up. PBS with PSAS reduced the penumbra and improved dose conformity in the planning target volume. PBS with PSAS was tolerated well for NSCHN.
为了研究适形调强质子放疗(IMRT)与笔形束扫描质子放疗(PBS)联合或不联合个体化孔径系统(PSAS)、散射式质子放疗(PSPT)治疗头颈部非鳞状细胞癌(NSCHN)的最优计划,比较了这 4 种计划的剂量分布。同时,报道了 PBS 联合 PSAS 的毒性,包括生活质量的变化。2014 年 4 月至 2016 年 8 月,共对 30 例患者采用 PBS 联合 PSAS 进行治疗。随机选择 20 例患者,比较了 PBS 联合或不联合 PSAS、PSPT 和 IMRT 计划的剂量分布。利用蒙特卡罗模拟计算质子治疗中的中子暴露。根据 CTCAE 第 4 版对毒性进行评分。治疗前和治疗后 0-12 个月,患者均完成 EORTC 生活质量问卷(QLQ-C30 和 QLQ-HN35)。PBS 联合 PSAS 计划的 95%适形度最好,4 种计划之间存在显著差异(P<0.05,Bonferroni 检验)。PSAS 产生的中子约增加 1.1 倍,但仍在可接受范围内。未见 3 级或以上急性皮肤毒性。治疗结束时,疼痛、食欲下降和体重增加更常见,但在 3 个月随访时恢复,在 12 个月随访时恢复至治疗前水平。PBS 联合 PSAS 可减少半影,提高计划靶区的剂量适形度。PBS 联合 PSAS 治疗 NSCHN 患者毒性可耐受。