Tian Jing, Shang Ming, Shi Sheng-Bin, Han Yong, Xu Jun
Department of Medical Oncology, Shan Dong Tumor Hospital, 440 Jiyan Road, Jinan, Shandong, People's Republic of China.
Cancer Chemother Pharmacol. 2015 Oct;76(4):829-34. doi: 10.1007/s00280-015-2854-0. Epub 2015 Sep 2.
The aim of this study was to evaluate the efficacy and toxicity of cetuximab and pemetrexed as the second-line treatment for advanced esophageal cancer patients, who had undergone treatment with the standard cisplatin and 5-FU regimens.
A total of 29 patients accepted this treatment. Cetuximab was administered at an initial dose of 400 mg/m(2) IV followed by weekly doses of 250 mg/m(2) IV, whereas pemetrexed 500 mg/m(2) was administered on day 1 every 3 weeks.
Twelve patients (41.4 %) presented PR, ten (34.5 %) had SD, and seven (24.1 %) had PD. The response rate was 41.4 %. The median PFS was 4.5 months (95 % CI 4.1-4.9), and the median OS was 9.4 months (95 % CI 8.4-10.5). The expression levels of serum miR-335 were determined, and the subsequent analysis suggested that PFS was significantly different between the patients with higher level of serum miR-335 and those with low level of serum miR-335. The former had a PFS of 4.9 months (95 % CI 4.2-5.7) and the latter 4.1 months (95 % CI 3.7-4.5) (log rank = 0.025). None of the patients experienced grade 4 toxicity. Twenty-four patients presented rash.
A combination of cetuximab plus pemetrexed was marginally effective and well tolerated in patients with advanced esophageal squamous cell carcinoma as the second-line treatment.
本研究旨在评估西妥昔单抗和培美曲塞作为晚期食管癌患者二线治疗方案的疗效和毒性,这些患者此前已接受过标准的顺铂和5-氟尿嘧啶治疗方案。
共有29例患者接受了该治疗。西妥昔单抗初始剂量为400mg/m²静脉注射,随后每周剂量为250mg/m²静脉注射,而培美曲塞500mg/m²每3周的第1天给药。
12例患者(41.4%)出现部分缓解(PR),10例(34.5%)疾病稳定(SD),7例(24.1%)疾病进展(PD)。缓解率为41.4%。中位无进展生存期(PFS)为4.5个月(95%置信区间4.1 - 4.9),中位总生存期(OS)为9.4个月(95%置信区间8.4 - 10.5)。测定了血清miR - 335的表达水平,随后的分析表明,血清miR - 335水平高的患者与血清miR - 335水平低的患者之间的PFS有显著差异。前者的PFS为4.9个月(95%置信区间4.2 - 5.7),后者为4.1个月(95%置信区间3.7 - 4.5)(对数秩检验=0.025)。没有患者出现4级毒性反应。24例患者出现皮疹。
西妥昔单抗加培美曲塞联合方案作为晚期食管鳞状细胞癌患者的二线治疗方案,疗效尚可且耐受性良好。