Department of Radiotherapy and Nuclear Medicine, South Egypt Cancer Institute, Assiut University, Assiut, Egypt.
Department of Clinical Oncology, Faculty of Medicine, Assiut University, Assiut, Egypt.
J Med Life. 2023 May;16(5):743-750. doi: 10.25122/jml-2023-0003.
To mitigate the risk of COVID-19 infection in cancer patients, it is recommended to utilize hypo-fractionated treatment schedules that aim to minimize the overall duration of treatment. In this study, we aimed to determine whether hypo-fractionated intensity-modulated radiotherapy (hypo-IMRT) with concurrent chemotherapy was practical, effective, and could achieve acceptable tumor control rates for squamous cell carcinoma of the head and neck (SCCHN). We enrolled 62 patients with high-risk stage II, stage III, and IVA SCCHN who received hypo-IMRT (62.5 Gy in 25 fractions over 5 weeks 2.5Gy/fraction with weekly cisplatin 40 mg/m). Our primary endpoint was to assess acute toxicity, while our secondary endpoints were late toxicity, loco-regional control, disease-free survival, and overall survival. The percentages of grade 3 acute pain, dermatitis, mucositis, and dysphagia were 71%, 19.4%, 72.6%, and 41.9%, respectively. The rates of late xerostomia, dysphagia, dental complications, grade 3 pain, and grade 3 weight loss were 72.6%, 62.9%, 27.4%, 4.8%, and 4.3%, respectively. At a median follow-up time of 24 months, 2-year loco-regional control and overall survival were 87.1% and 83.9%, respectively. Disease-free survival was 100%, 89.5%, and 69% in stages II, III, and IV%, respectively, with a significant p-value of 0.024. This regimen was effective and relatively safe, with acceptable and tolerable acute and late toxicity. Given the reduced need for hospital visits, hypo-fractionated schedules may represent an alternative treatment during the COVID-19 outbreak.
为降低癌症患者感染 COVID-19 的风险,建议采用分次剂量降低的治疗方案,以尽量缩短整体治疗时间。本研究旨在确定针对头颈部鳞状细胞癌(SCCHN),采用分次剂量降低的强度调制放疗(hypo-IMRT)联合同期化疗是否可行、有效,能否实现可接受的肿瘤控制率。我们纳入了 62 例高危 II 期、III 期和 IVA 期 SCCHN 患者,接受 hypo-IMRT(5 周内 25 次分割,每次 62.5Gy,2.5Gy/次,每周给予顺铂 40mg/m2)治疗。主要终点为评估急性毒性,次要终点为晚期毒性、局部区域控制、无病生存率和总生存率。3 级急性疼痛、皮炎、黏膜炎和吞咽困难的比例分别为 71%、19.4%、72.6%和 41.9%。晚期口干、吞咽困难、牙齿并发症、3 级疼痛和 3 级体重减轻的发生率分别为 72.6%、62.9%、27.4%、4.8%和 4.3%。中位随访时间 24 个月时,2 年局部区域控制率和总生存率分别为 87.1%和 83.9%。II 期、III 期和 IVA 期的无病生存率分别为 100%、89.5%和 69%,差异有统计学意义(p=0.024)。该方案疗效确切,安全性相对较高,急性和晚期毒性可接受且耐受良好。鉴于分次剂量降低的方案减少了住院需求,在 COVID-19 大流行期间可能成为一种替代治疗选择。