Urbano Teresa Guerrero, Clark Catharine H, Hansen Vibeke N, Adams Elizabeth J, Miles Elizabeth A, Mc Nair Helen, Bidmead A Margaret, Warrington Jim, Dearnaley David P, Harmer Clive, Harrington Kevin J, Nutting Christopher M
Head and Neck Unit, Royal Marsden Hospital, London, UK.
Radiother Oncol. 2007 Oct;85(1):58-63. doi: 10.1016/j.radonc.2007.07.020. Epub 2007 Sep 27.
This phase 1 study was designed to determine the toxicity of accelerated fractionation IMRT in locally advanced thyroid cancer.
Patients with high risk locally advanced thyroid cancer who required post-operative EBRT were recruited. A single-phase inverse-planned-simultaneous-boost was delivered by IMRT: 58.8 Gy/28F (daily) to the primary tumour and involved nodes and 50 Gy/28F to the elective nodes. Acute (NCICTCv.2.0) and late toxicity (RTOG and modified LENTSOM) was collected.
Thirteen patients were treated (7 medullary thyroid, 2 Hurthle cell and 4 well differentiated thyroid cancer). G3 and G2 radiation dermatitis rates were 38.5% and 31%; G3 and G2 mucositis rates 8% and 53% and G3 and G2 pain 23% and 54%. Thirty-one percentage required enteral feeding. G3 and G2 xerostomia rates were 0% and 31%. Recovery was seen, with 62% patients having dysphagia G< or =1 2 months after IMRT. Thirty percent of patients developed L'Hermitte's syndrome. No grade 4 toxicity was observed. No dose limiting toxicity was found.
Accelerated fractionation IMRT in this group of patients is feasible and safe. The acute toxicity appeared acceptable and early indicators of late toxicity moderate and similar to what would be expected with conventional RT. Longer follow up is required to quantify late side effects.
本1期研究旨在确定局部晚期甲状腺癌加速分割调强放疗(IMRT)的毒性。
招募需要术后体外放疗(EBRT)的高危局部晚期甲状腺癌患者。通过IMRT进行单相逆向计划同步推量:对原发肿瘤及受累淋巴结给予58.8 Gy/28次(每日),对选择性淋巴结给予50 Gy/28次。收集急性毒性(NCICTC v.2.0)和晚期毒性(RTOG和改良LENTSOM)。
13例患者接受治疗(7例髓样甲状腺癌、2例许特耳细胞癌和4例高分化甲状腺癌)。3级和2级放射性皮炎发生率分别为38.5%和31%;3级和2级黏膜炎发生率分别为8%和53%,3级和2级疼痛发生率分别为23%和54%。31%的患者需要肠内营养。3级和2级口干发生率分别为0%和31%。可见恢复情况,62%的患者在IMRT后2个月吞咽困难分级≤1级。30%的患者出现莱尔米特综合征。未观察到4级毒性。未发现剂量限制毒性。
该组患者采用加速分割IMRT是可行且安全的。急性毒性似乎可以接受,晚期毒性的早期指标为中度,与传统放疗预期情况相似。需要更长时间的随访以量化晚期副作用。