Altay-Langguth Alev, Balermpas Panagiotis, Brandts Christian, Balster Sven, Ghanaati Shahram, Winkelmann Ria, Burck Iris, Rödel Franz, Martin Daniel, Rödel Claus, von der Grün Jens
Department of Radiotherapy and Oncology, University Hospital, Goethe University, Theodor-Stern-Kai 7, 60590 Frankfurt am Main, Germany.
Department of Radiation Oncology, University Hospital Zurich, Rämistrasse 100, 8091 Zurich, Switzerland.
Clin Transl Radiat Oncol. 2021 Mar 26;28:71-78. doi: 10.1016/j.ctro.2021.03.004. eCollection 2021 May.
The rate of loco-regional recurrences for locally advanced head and neck squamous cell carcinoma (HNSCC) following standard treatment reaches up to 50%, accompanied by a probability of 20% to develop a second primary tumor in the head and neck region.
Ten patients with inoperable, in-field recurrence of HNSCC following previous primary or adjuvant radiotherapy (RT) in combination with concurrent platinum-based chemotherapy were re-irradiated with 60 Gray in 30 fractions between December 2017 and January 2020 with concurrent and maintenance nivolumab administration. Data were retrospectively collected and compared with patients who underwent re-irradiation (ReRT) with concurrent cisplatin following propensity score matching (PSM). Local progression-free survival (LPFS) and overall survival (OS) were visualized using Kaplan-Meier method (log-rank test).
All patients completed ReRT. Median number of applied courses of nivolumab was 12 (range, 3-38). OS rate was 50% at 12 months and the median OS was 11 (range, 2-23) months. Six and 12 month LPFS rates were 60% and 30%, respectively. Median LPFS was 8 (range, 2-19) months. OS and LPFS rates were not inferior to those of patients treated with concurrent cisplatin. No unexpected radiation-related toxicity occurred. A total of four patients developed any-grade immune-related adverse events of which two presented with grade 3 toxicities. One patient died within 3 weeks after ReRT. Higher blood levels of CRP (p = 0.004), lower levels of hemoglobin (p = 0.029) and higher neutrophil/lymphocyte ratio (p = 0.004) were associated with impaired LPFS. Higher recursive portioning analysis (RPA) class was associated with impaired LPFS (p = 0.022) and OS (p = 0.024).
The combination of ReRT and nivolumab for locally recurrent HNSCC was feasible without occurrence of unexpected toxicities. Combined radioimmunotherapy might offer an effective treatment option for carefully selected pre-irradiated patients ineligible for salvage surgery.
局部晚期头颈部鳞状细胞癌(HNSCC)经标准治疗后的局部区域复发率高达50%,同时有20%的概率在头颈部区域发生第二原发性肿瘤。
2017年12月至2020年1月期间,对10例先前接受过原发性或辅助放疗(RT)联合顺铂同步化疗后出现不可手术的、野内复发的HNSCC患者进行再次放疗,剂量为60格雷,分30次给予,同时给予纳武单抗并维持给药。回顾性收集数据,并与倾向评分匹配(PSM)后接受顺铂同步再次放疗(ReRT)的患者进行比较。使用Kaplan-Meier方法(对数秩检验)可视化局部无进展生存期(LPFS)和总生存期(OS)。
所有患者均完成了再次放疗。纳武单抗的中位应用疗程数为12(范围3 - 38)。12个月时的总生存率为50%,中位总生存期为11(范围2 - 23)个月。6个月和12个月时的LPFS率分别为60%和30%。中位LPFS为8(范围2 - 19)个月。总生存率和LPFS率不低于接受顺铂同步治疗的患者。未发生意外的放疗相关毒性。共有4例患者发生任何级别的免疫相关不良事件,其中2例出现3级毒性。1例患者在再次放疗后3周内死亡。较高的CRP血水平(p = 0.004)、较低的血红蛋白水平(p = 0.029)和较高的中性粒细胞/淋巴细胞比值(p = 0.004)与LPFS受损相关。较高的递归分割分析(RPA)类别与LPFS受损(p = )和总生存期受损(p = 0.024)相关。
再次放疗与纳武单抗联合用于局部复发性HNSCC是可行的,未出现意外毒性。联合放射免疫疗法可能为精心挑选的不符合挽救性手术条件的放疗前患者提供一种有效的治疗选择。