Fryen Anneke, Brandes Iris, Wichmann Jörn, Christiansen Hans, Tavassol Frank, Durisin Martin, Merten Roland
Department of Radiation Oncology, Hanover Medical School, Hanover, Germany;
Department of Epidemiology, Social Medicine and Public Health, Hanover Medical School, Hanover, Germany.
In Vivo. 2022 May-Jun;36(3):1259-1266. doi: 10.21873/invivo.12825.
Comorbidity and frailty are relevant limitations of normofractionated combined radiochemotherapy for squamous cell head and neck cancer (HNSCC), especially in elderly patients. This retrospective study aimed to evaluate the efficacy and toxicity of moderately hypofractionated radiotherapy (HRT) without chemotherapy in patients ineligible for concurrent radiochemotherapy.
Between 2011 and 2018, 51 elderly/frail patients with HNSCC were treated with either definitive (n=23) or adjuvant (n=28) moderate HRT. A dose of 45 Gy was given to the primary tumour region and cervical nodes with a sequential boost up to 50 in the adjuvant and 55 Gy in the definitive cure setting (2.5 Gy/fraction). Patient outcomes of locoregional control, overall survival, and acute and late toxicity were analysed.
After a median follow-up of 6 months for the definitive HRT group and 28.5 months for the adjuvant HRT group, we found a median overall survival of 6 vs. 55 months (log-rank test: p<0.001) and a median locoregional control of 9 months vs. not reached (log-rank test: p=0.008), respectively. The 2-year rates of locoregional control were 28.5% for the definitive HRT group vs. 75.2% for the adjuvant HRT group. No acute or late grade 4-5 toxicity occurred; grade 3 toxicity was rarely documented.
HRT in elderly/frail patients with HNSCC who are unfit for chemotherapy leads to acceptable local control with moderate toxicity in a short overall treatment time. Especially in the postoperative situation, HRT can be considered an appropriate alternative to normofractionated radio(chemo)therapy. Definitive HRT can be a treatment alternative, especially for multimorbid patients.
合并症和虚弱是头颈部鳞状细胞癌(HNSCC)常规分割放化疗的相关限制因素,尤其是在老年患者中。本回顾性研究旨在评估不适合同步放化疗的患者接受中度低分割放疗(HRT)且不进行化疗的疗效和毒性。
2011年至2018年期间,51例老年/虚弱的HNSCC患者接受了根治性(n = 23)或辅助性(n = 28)中度HRT治疗。对原发肿瘤区域和颈部淋巴结给予45 Gy的剂量,在辅助治疗中序贯增加至50 Gy,在根治性治疗中增加至55 Gy(每次分割2.5 Gy)。分析患者的局部区域控制、总生存以及急性和晚期毒性的结果。
根治性HRT组的中位随访时间为6个月,辅助性HRT组为28.5个月,我们发现总生存中位数分别为6个月和55个月(对数秩检验:p<0.001),局部区域控制中位数分别为9个月和未达到(对数秩检验:p = 0.008)。根治性HRT组的2年局部区域控制率为28.5%,辅助性HRT组为75.2%。未发生4 - 5级急性或晚期毒性;3级毒性很少有记录。
对于不适合化疗的老年/虚弱HNSCC患者,HRT在较短的总治疗时间内可实现可接受的局部控制且毒性适中。特别是在术后情况下,HRT可被视为常规分割放(化)疗的合适替代方案。根治性HRT可以是一种治疗选择,尤其是对于患有多种疾病的患者。