Department of Radiation Oncology, Fudan University Shanghai Cancer Center, 200032, Shanghai, China.
Eur Arch Otorhinolaryngol. 2012 Mar;269(3):1027-33. doi: 10.1007/s00405-011-1669-9. Epub 2011 Jun 26.
The purpose of this study was to evaluate the efficacy and toxicity of cisplatin plus gemcitabine chemotherapy and intensity-modulated radiation therapy (IMRT) for locoregionally advanced nasopharyngeal carcinoma (NPC). A total of 54 patients (stage IIB: 6, stage III: 24, stage IVA-B: 24) with locoregionally advanced NPC were treated with cisplatin 25 mg/m(2) intravenously on days 1-3, and gemcitabine 1,000 mg/m(2) of 30-min intravenous infusion on days 1 and 8, every 3 weeks for two cycles as neoadjuvant chemotherapy. Two cycles of the same regimen were administered as adjuvant chemotherapy 28 days after the end of radiotherapy. The prescription doses were 66-70.4 Gy to the gross tumor volume (GTV), 66 Gy to positive neck nodes, 60 Gy to the high-risk clinical target volume and 54 Gy to the low-risk clinical target volume. The overall response rate to neoadjuvant chemotherapy was 88.6%. Toxicity was mainly grade 1/2 myelosuppression. All patients completed IMRT. The median follow-up duration was 30 months (range, 12-60 months). The 3-year locoregional control, metastasis-free rate and overall survival were 94.9%, 86.2% and 87.7%, respectively. Severe late toxicities included grade 3 trismus in one patient, grade 3 hearing impairment in one patient and cranial nerve XII palsy in one patient. No grade 4 late toxicities were observed. A combination of cisplatin plus gemcitabine chemotherapy and intensity-modulated radiotherapy for locoregionally advanced NPC is well-tolerated, convenient, effective and warrants further studies.
本研究旨在评估顺铂联合吉西他滨化疗和调强放疗(IMRT)治疗局部晚期鼻咽癌(NPC)的疗效和毒性。共 54 例局部晚期 NPC 患者(IIB 期:6 例,III 期:24 例,IVA-B 期:24 例)接受顺铂 25mg/m²静脉滴注,第 1-3 天,吉西他滨 1000mg/m²静脉滴注 30 分钟,第 1 天和第 8 天,每 3 周为一个周期,作为新辅助化疗。放疗结束后 28 天,再进行两个周期相同方案的辅助化疗。大体肿瘤体积(GTV)处方剂量为 66-70.4Gy,阳性颈部淋巴结 66Gy,高危临床靶区 60Gy,低危临床靶区 54Gy。新辅助化疗的总缓解率为 88.6%。毒性主要为 1/2 级骨髓抑制。所有患者均完成了调强放疗。中位随访时间为 30 个月(12-60 个月)。3 年局部区域控制、无转移率和总生存率分别为 94.9%、86.2%和 87.7%。严重的晚期毒性包括 1 例 3 级牙关紧闭,1 例 3 级听力障碍和 1 例颅神经 XII 麻痹。未观察到 4 级晚期毒性。顺铂联合吉西他滨化疗和调强放疗治疗局部晚期 NPC 耐受性好,方便,有效,值得进一步研究。