Department of Radiation Oncology, Centre Jean Perrin, Clermont Ferrand, France.
Radiother Oncol. 2012 Apr;103(1):57-62. doi: 10.1016/j.radonc.2011.12.010. Epub 2012 Jan 31.
In 2003, the French Authority for Health (HAS) recommended the use of intensity modulated radiotherapy (IMRT) in prospective trial before its routine use. The Oncology and Radiotherapy Group for Head and Neck Cancer (GORTEC) proposed to evaluate prospectively acute and late toxicities, locoregional control and overall survival for patients treated for head and neck cancer (HNC) with IMRT and bilateral neck irradiation.
Between 2002 and 2008, 208 patients with HNC were treated with IMRT in 8 centres. There were 38 nasopharynx, 117 oropharynx, 25 pharyngo-larynx, 24 oral cavity and 4 unknown primary (28.5% stage I-II and 71% Stage III-IV). Ninety-three patients (46%) had postoperative IMRT and 78 patients (37.5%) received concurrent chemotherapy. The doses were 70 Gy to the gross tumour, 66 Gy to the high-risk postoperative sites and 50 Gy to the subclinical disease. Toxicities were graded according to the RTOG-EORTC scales.
The median follow-up was 25.3 months (range: 0.4-72 months). There were 29 local-regional failures: 24 were in-field, three were marginal and one was out-field. The two-year loco-regional control and overall survival were 86% and 86.7%, respectively. At 18 months, grade ≥ 2 xerostomia was 16.1%. A mean dose to the spared parotid below 28 Gy led to significantly less grade ≥ 2 xerostomia (8.5% vs 24%) with a relative risk of 1.2 [95% CI: 1.02-1.41, p = 0.03]. Grade ≥ 2 xerostomia increased by approximately 3% per Gy of mean parotid dose up to 28, Gy then 7% per Gy above 33 Gy.
IMRT for HN cancer seems to reduce late toxicities without jeopardising local control and overall survival.
2003 年,法国卫生署(HAS)建议在常规使用调强放疗(IMRT)之前进行前瞻性试验。头颈部肿瘤放疗协作组(GORTEC)提议前瞻性评估 IMRT 和双侧颈部照射治疗头颈部癌症(HNC)患者的急性和迟发性毒性、局部区域控制和总生存情况。
2002 年至 2008 年间,208 例 HNC 患者在 8 个中心接受 IMRT 治疗。其中 38 例为鼻咽癌,117 例口咽癌,25 例咽-喉癌,24 例口腔癌,4 例原发灶不明(28.5%为 I-II 期,71%为 III-IV 期)。93 例(46%)为术后 IMRT,78 例(37.5%)接受同期化疗。大体肿瘤给予 70Gy,高危术后部位给予 66Gy,亚临床疾病给予 50Gy。毒性按 RTOG-EORTC 量表分级。
中位随访时间为 25.3 个月(0.4-72 个月)。共有 29 例局部区域复发:24 例为肿瘤内,3 例为边缘,1 例为肿瘤外。两年局部区域控制率和总生存率分别为 86%和 86.7%。18 个月时,≥2 级口干症发生率为 16.1%。腮腺受照剂量平均低于 28Gy 可显著降低≥2 级口干症发生率(8.5%比 24%),相对风险为 1.2(95%CI:1.02-1.41,p=0.03)。腮腺平均剂量每增加 1Gy,口干症发生率增加约 3%,达 28Gy 后,每增加 1Gy 口干症发生率增加 7%。
IMRT 治疗头颈部癌症似乎可降低迟发性毒性,而不影响局部控制和总生存率。