Swedish Cancer Institute, Swedish Medical Center, 1221 Madison St., Seattle, WA 98104, USA.
J Thorac Oncol. 2010 Sep;5(9):1472-6. doi: 10.1097/JTO.0b013e3181e77a92.
Esophageal adenocarcinomas commonly express the epidermal growth factor receptor. This trial assessed the 6-month overall survival probability in metastatic esophageal cancer patients treated with cetuximab as second-line therapy.
This was a multicenter, open-label phase II study of single-agent cetuximab for metastatic esophageal adenocarcinoma patients who failed one prior chemotherapy regimen. Adequate organ function and Zubrod performance status of 0 to 2 were required. Patients received cetuximab 400 mg/m intravenously (IV) on week 1 and 250 mg/m IV weekly thereafter. The primary objective was to determine 6-month overall survival. Secondary end points included progression-free survival, response rate, and toxicity. Tumor tissue was collected for correlative studies.
Sixty-three patients were registered, with eight ineligible or never treated. Fifty-five eligible patients (49 men, 6 women; median age = 61.2 years [range, 30.7-88.5]) were enrolled. Twenty patients survived more than 6 months for a 6-month overall survival rate of 36% (95% confidence interval [CI]: 24-50%). The median overall survival was 4.0 months (95% CI: 3.2-5.9). Median progression-free survival was 1.8 months (95% CI: 1.7-1.9). One partial response and two unconfirmed partial responses were observed. Two patients experienced grade 4 fatigue. There was one treatment-related death due to pneumonitis. Germline polymorphisms of epidermal growth factor receptor, epidermal growth factor, interleukin (IL)-8, cyclooxygenase (COX)-2, vascular epidermal growth factor receptor (VEGF), CCND1, neuropilin 1 (NRP1), and K-ras mutational status were not associated with response or survival.
The 6-month overall survival rate of 36% observed on this study failed to meet the primary survival objective. Thus, cetuximab alone cannot be recommended in the second-line treatment of metastatic esophageal cancer.
食管腺癌通常表达表皮生长因子受体。本试验评估了二线治疗转移性食管腺癌患者接受西妥昔单抗治疗的 6 个月总生存率。
这是一项多中心、开放性的Ⅱ期研究,评估了接受过一线化疗方案治疗失败的转移性食管腺癌患者使用单药西妥昔单抗的疗效。要求患者有足够的器官功能和 Zubrod 表现状态 0-2 分。患者在第 1 周和第 2 周接受 400mg/m 静脉注射(IV)西妥昔单抗,此后每周接受 250mg/m IV 治疗。主要终点是确定 6 个月的总生存率。次要终点包括无进展生存期、缓解率和毒性。收集肿瘤组织进行相关研究。
共登记了 63 例患者,其中 8 例不符合入组条件或从未接受治疗。55 例符合条件的患者(49 例男性,6 例女性;中位年龄 61.2 岁[范围 30.7-88.5])入组。20 例患者生存时间超过 6 个月,6 个月总生存率为 36%(95%CI:24-50%)。中位总生存期为 4.0 个月(95%CI:3.2-5.9)。中位无进展生存期为 1.8 个月(95%CI:1.7-1.9)。观察到 1 例部分缓解和 2 例未确认的部分缓解。2 例患者出现 4 级疲劳。有 1 例治疗相关死亡归因于肺炎。表皮生长因子受体、表皮生长因子、白细胞介素(IL)-8、环氧化酶(COX)-2、血管表皮生长因子受体(VEGF)、CCND1、神经纤毛蛋白 1(NRP1)和 K-ras 突变状态的种系多态性与反应或生存无关。
本研究观察到的 6 个月总生存率为 36%,未能达到主要生存终点。因此,西妥昔单抗不能单独推荐用于转移性食管腺癌的二线治疗。