Department of Clinical Oncology, St. James's Institute of Oncology, Leeds, United Kingdom.
Int J Radiat Oncol Biol Phys. 2011 Nov 15;81(4):e237-43. doi: 10.1016/j.ijrobp.2011.03.043. Epub 2011 May 27.
To report the experience of treating selected fit patients with locally advanced head-and-neck squamous cell carcinoma with three cycles of induction TPF (docetaxel 75 mg/m(2), cisplatin 75 mg/m(2), 5-fluorouracil 750 mg/m(2), Days 2-5) followed by concurrent three-weekly bolus cisplatin 100 mg/m(2) chemoradiotherapy.
Between March 2006 and February 2010, 66 patients with nonmetastatic Stage IV head-and-neck squamous cell carcinoma were treated in a single institution with three cycles of induction TPF, followed by radical radiotherapy with concurrent cisplatin 100 mg/m(2).
Median age was 54 years (range, 33-69 years). Median follow-up was 21 months (range, 4-55 months). During TPF, Grade 3 toxicity occurred in 18 patients (27%), dose modifications in 10 (15%), delays in 3 (5%), and unplanned admissions in 6 (9%); a clinical tumor response was documented in 60 patients (91%). Median time from the final cycle of TPF to commencing radiotherapy was 22 days. Sixty-two patients (94%) received radical radiotherapy, and all completed treatment with no delays ≥3 days. One, two, and three cycles of concurrent cisplatin were delivered to 18 patients (29%), 38 patients (61%), and 3 patients (5%), respectively. Ninety-two percent of patients received enteral feeding; median weight loss during treatment was 7%. Forty-two patients (68%) had unplanned admissions with no on-treatment deaths. Three unrelated deaths occurred after treatment. At 1 year after treatment, 21% of patients without disease progression remained gastrostomy dependent. Of 58 assessable patients, 50 (86%) achieved a complete response after treatment. One- and 2-year progression-free survival, cause-specific survival, and overall survival were 88%, 92%, and 86% and 80%, 85%, and 80%, respectively.
The combination of induction TPF with concurrent cisplatin chemoradiotherapy in patients with locally advanced head and neck squamous cell carcinoma is tolerable, with encouraging efficacy.
报告对选定的局部晚期头颈部鳞状细胞癌患者采用三周期诱导 TPF(多西他赛 75mg/m(2)、顺铂 75mg/m(2)、5-氟尿嘧啶 750mg/m(2),第 2-5 天)治疗,随后进行同期三周高剂量顺铂 100mg/m(2)放化疗的经验。
在 2006 年 3 月至 2010 年 2 月期间,在一家机构对 66 例非转移性 IV 期头颈部鳞状细胞癌患者采用三周期诱导 TPF 治疗,随后进行根治性放疗,并同时给予顺铂 100mg/m(2)。
中位年龄为 54 岁(范围,33-69 岁)。中位随访时间为 21 个月(范围,4-55 个月)。在 TPF 期间,18 例(27%)患者发生 3 级毒性,10 例(15%)需要调整剂量,3 例(5%)出现延迟,6 例(9%)需要计划外住院;60 例(91%)患者有临床肿瘤反应。从 TPF 的最后一个周期到开始放疗的中位时间为 22 天。62 例(94%)患者接受根治性放疗,所有患者均无≥3 天的延迟,完成了治疗。18 例(29%)、38 例(61%)和 3 例(5%)患者分别接受了 1 个、2 个和 3 个周期的同期顺铂治疗。92%的患者接受了肠内喂养;治疗期间中位体重减轻 7%。42 例(68%)患者计划外住院,无治疗相关死亡。3 例患者在治疗后死亡。治疗 1 年后,21%的无疾病进展患者仍依赖胃造口术。58 例可评估患者中,50 例(86%)治疗后达到完全缓解。1 年和 2 年无进展生存率、疾病特异性生存率和总生存率分别为 88%、92%和 86%、80%、85%和 80%。
在局部晚期头颈部鳞状细胞癌患者中,诱导 TPF 联合同期高剂量顺铂放化疗是耐受的,疗效令人鼓舞。