King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
King Faisal Hospital and Research Centre, Riyadh, Saudi Arabia.
Hematol Oncol Stem Cell Ther. 2021 Sep;14(3):199-205. doi: 10.1016/j.hemonc.2020.05.005. Epub 2020 May 21.
OBJECTIVE/BACKGROUND: To evaluate the efficacy and outcome of adding low-dose fractionated radiotherapy (LDFRT) to induction chemotherapy plus concurrent chemoradiation in locally advanced nasopharyngeal carcinoma (LANPC).
A single-institute, phase II-III, prospectively controlled randomized clinical trial was performed at King Faisal Specialist Hospital and Research Centre. Patients aged 18-70 years with WHO type II and III, stage III-IVB nasopharyngeal carcinoma, Eastern Cooperative Oncology Group performance score of 0-2, with adequate hematological, renal, and hepatic function were eligible. In total, 108 patients were enrolled in this trial. All patients received two cycles of induction docetaxel and cisplatin (75 mg/m each) chemotherapy on Days 1 and 22, followed by concurrent chemoradiation therapy. Radiation therapy consisted of 70 Gy in 33 fractions, with concurrent cisplatin 25 mg/m for 4 days on Days 43 and 64. Patients were randomly assigned to either adding LDFRT (0.5 Gy twice daily 6 hours apart for 2 days) to induction chemotherapy in the experimental arm (54 patients) or induction chemotherapy alone in the control arm (54 patients).
There was no significant difference in the post-induction response rates (RRs) or in toxicity between the two treatment arms. The 3-year overall survival (OS), locoregional control (LRC), and distant metastases-free survival (DMFS) rates for experimental arm and control arm were 94% versus 93% (p = .8), 84.8% versus 87.5% (p = .58), and 84.1% versus 91.6% (p = .25), respectively.
The results showed no benefit from adding LDFRT to induction chemotherapy in terms of RR, OS, LRC, and DMFS.
目的/背景:评估低剂量分割放疗(LDFRT)联合诱导化疗加同期放化疗治疗局部晚期鼻咽癌(LANPC)的疗效和结局。
这是一项在法萨尔国王专科医院和研究中心进行的单中心、Ⅱ期到Ⅲ期、前瞻性对照随机临床试验。符合条件的患者为年龄在 18-70 岁之间、WHO 类型 II 和 III、III-IVB 期鼻咽癌、东部肿瘤协作组体力状况评分 0-2 分、有足够的血液学、肾脏和肝功能的患者。共有 108 例患者入组本试验。所有患者在第 1 天和第 22 天接受两个周期的诱导多西他赛和顺铂(75mg/m 各)化疗,随后接受同期放化疗。放疗剂量为 70Gy,共 33 次,在第 43 天和第 64 天给予顺铂 25mg/m 连续 4 天。患者被随机分为实验组(54 例),即在诱导化疗的基础上加用 LDFRT(0.5Gy,每日两次,间隔 6 小时,共 2 天),或对照组(54 例),仅接受诱导化疗。
两组患者的诱导后反应率(RR)或毒性无显著差异。实验组和对照组的 3 年总生存率(OS)、局部区域控制率(LRC)和无远处转移生存率(DMFS)分别为 94%比 93%(p=0.8)、84.8%比 87.5%(p=0.58)和 84.1%比 91.6%(p=0.25)。
结果显示,在 RR、OS、LRC 和 DMFS 方面,LDFRT 联合诱导化疗并未带来获益。