Luo Dong-Hua, Li Xiao-Yun, Guo Shan-Shan, Guo Wan-Ping, Liu Li-Ting, Mo Hao-Yuan, Guo Ling, Lv Xiao-Fei, Liu Li-Zhi, Li Ji-Bin, Liu Qing, Wang Pan, Sun Xue-Song, Liu Sai-Lan, Chen Qiu-Yan, Tang Lin-Quan, Mai Hai-Qiang
Department of Nasopharyngeal Carcinoma, Sun Yat-sen University Cancer Centre, State Key Laboratory of Oncology in South China, Collaborative Innovation Centre for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, 651 Dongfeng Road East, Guangzhou 510060, People's Republic of China.
Department of Radiology, Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, 651 Dongfeng Road East, Guangzhou 510060, People's Republic of China.
Lancet Reg Health West Pac. 2023 Aug 31;40:100895. doi: 10.1016/j.lanwpc.2023.100895. eCollection 2023 Nov.
Previous studies demonstrated that induction chemotherapy (IC) followed by de-escalated chemoradiotherapy adapted to tumor response was effective in treating childhood nasopharyngeal carcinoma (NPC), but the toxicity profile of this treatment strategy, and whether childhood patients with advanced stages can obtain enough benefits from it requires further investigation.
We conducted a single-center phase II trial (NCT03020329). All participants received 3 cycles of paclitaxel liposome, cisplatin and 5-fluorouracil (TPF)-based IC. Patients who showed complete or partial response received de-escalated radiotherapy of 60 Gy with 3 cycles of concurrent cisplatin, and those who showed stable or progressive disease received standard-dose radiotherapy of 70 Gy with concurrent cisplatin. The primary endpoint was the complete response (CR) rate at the end of concurrent chemoradiotherapy (CCRT).
From November 2016 to March 2021, 44 patients were recruited in the cohort. The CR rate was 80% (35/44, 95% CI, 65-90) of the whole cohort. All patients achieved CR 3 months after CCRT. By the last follow-up, the 3-year progression-free survival and overall survival were 91% (95% CI, 82-99) and 100% respectively. Dry mouth was the most common late toxicity, with an incidence of 41% (18/44), followed by skin fibrosis and hearing impairment. No patient suffered from severe late toxicity and growth retardation.
Our results proved the efficacy and safety of TPF regimen followed by de-escalated radiotherapy with concurrent cisplatin in treating stage IVa-b childhood NPC patients.
A full list of funding bodies that contributed to this study can be found in the Acknowledgements section.
先前的研究表明,诱导化疗(IC)后根据肿瘤反应进行降阶梯放化疗对儿童鼻咽癌(NPC)有效,但这种治疗策略的毒性特征以及晚期儿童患者是否能从中获得足够益处仍需进一步研究。
我们开展了一项单中心II期试验(NCT03020329)。所有参与者接受3个周期以紫杉醇脂质体、顺铂和5-氟尿嘧啶(TPF)为基础的IC。显示完全缓解或部分缓解的患者接受60 Gy的降阶梯放疗并同步3个周期顺铂,显示疾病稳定或进展的患者接受70 Gy的标准剂量放疗并同步顺铂。主要终点是同步放化疗(CCRT)结束时的完全缓解(CR)率。
2016年11月至2021年3月,该队列共招募了44例患者。整个队列的CR率为80%(35/44,95%CI,65-90)。所有患者在CCRT后3个月均实现CR。截至最后一次随访,3年无进展生存率和总生存率分别为91%(95%CI,82-99)和100%。口干是最常见的晚期毒性反应,发生率为41%(18/44),其次是皮肤纤维化和听力障碍。没有患者出现严重晚期毒性反应和生长发育迟缓。
我们的结果证明了TPF方案序贯降阶梯放疗并同步顺铂治疗IVa-b期儿童NPC患者的有效性和安全性。
对本研究有贡献的资助机构完整列表见致谢部分。