Citrin Deborah, Mansueti John, Likhacheva Anna, Sciuto Linda, Albert Paul S, Rudy Susan F, Cooley-Zgela Theresa, Cotrim Ana, Solomon Beth, Colevas A Dimitrios, Russo Angelo, Morris John C, Herscher Laurie, Smith Sharon, Van Waes Carter
Radiation Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Int J Radiat Oncol Biol Phys. 2009 Jul 15;74(4):1040-6. doi: 10.1016/j.ijrobp.2008.09.053. Epub 2008 Dec 29.
To report the long-term outcomes and toxicity of a regimen of infusion paclitaxel delivered concurrently with radiotherapy in patients with locally advanced squamous cell carcinoma of the head and neck.
Between 1995 and 1999, 35 patients with nonmetastatic, Stage III or IV squamous cell carcinoma of the head and neck were treated with three cycles of paclitaxel as a 120-h continuous infusion beginning on Days 1, 21, and 42, concurrent with radiotherapy. The initial 16 patients received 105 mg/m(2)/cycle, and the subsequent 19 patients received 120 mg/m(2)/cycle. External beam radiotherapy was delivered to a dose of 70.2-72 Gy at five fractions weekly. Patients were followed to evaluate the disease outcomes and late toxicity of this regimen.
The median follow-up for all patients was 56.5 months. The median survival was 56.5 months, and the median time to local recurrence was not reached. Of the 35 patients, 15 (43%) developed hypothyroidism. Of the 33 patients who underwent percutaneous endoscopic gastrostomy tube placement, 11 were percutaneous endoscopic gastrostomy tube dependent until death or their last follow-up visit. Also, 5 patients (14%) required a tracheostomy until death, and 3 (9%) developed a severe esophageal stricture. All evaluated long-term survivors exhibited salivary hypofunction. Fibrosis in the radiation field occurred in 24 patients (69%).
The results of our study have shown that concurrent chemoradiotherapy with a 120-h infusion of paclitaxel provides long-term local control and survival in patients with squamous cell carcinoma of the head and neck. Xerostomia, hypothyroidism, esophageal and pharyngeal complications, and subcutaneous fibrosis were common long-term toxicities; however, the vast majority of toxicities were grade 1 or 2.
报告在局部晚期头颈部鳞状细胞癌患者中,紫杉醇静脉输注联合放疗方案的长期疗效和毒性。
1995年至1999年间,35例非转移性Ⅲ期或Ⅳ期头颈部鳞状细胞癌患者接受了三个周期的紫杉醇治疗,于第1天、第21天和第42天开始进行120小时持续静脉输注,同时接受放疗。最初的16例患者接受105mg/m²/周期的治疗,随后的19例患者接受120mg/m²/周期的治疗。外照射放疗每周5次,剂量为70.2 - 72Gy。对患者进行随访,以评估该方案的疾病疗效和晚期毒性。
所有患者的中位随访时间为56.5个月。中位生存期为56.5个月,局部复发的中位时间未达到。35例患者中,15例(43%)发生甲状腺功能减退。在33例行经皮内镜下胃造瘘管置入术的患者中,11例直至死亡或最后一次随访时一直依赖经皮内镜下胃造瘘管。此外,5例患者(14%)直至死亡需要气管造口术,3例(9%)发生严重食管狭窄。所有接受评估的长期存活者均表现出唾液腺功能减退。24例患者(69%)放疗区域出现纤维化。
我们的研究结果表明,120小时输注紫杉醇的同步放化疗可使头颈部鳞状细胞癌患者获得长期局部控制和生存。口干、甲状腺功能减退、食管和咽部并发症以及皮下纤维化是常见的长期毒性反应;然而,绝大多数毒性反应为1级或2级。