Antwerp University Hospital, Edegem, Belgium.
Eur J Cancer. 2013 Sep;49(13):2877-83. doi: 10.1016/j.ejca.2013.05.002. Epub 2013 May 30.
Platinum/5-fluorouracil plus cetuximab is a standard systemic treatment for recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN). Pemetrexed has shown activity in SCCHN. This phase II study evaluated pemetrexed with cisplatin and cetuximab in recurrent/metastatic SCCHN.
Patients received cetuximab 250 mg/m(2) (loading dose: 400mg/m(2))days 1, 8 and 15; pemetrexed 500 mg/m(2)+cisplatin 75 mg/m(2) on day 1, q3w up to six cycles and folic acid, vitamin B12 and prophylactic medications. After a minimum of four cycles, responding patients were eligible for maintenance with pemetrexed and cetuximab, or either as monotherapy, until progression or toxicity. Efficacy (primary end-point: progression-free survival [PFS]) and toxicity were evaluated.
Sixty-six patients received ≥1 cycle of the triplet. Most patients were male (80.3%), with a median age of 62 years and Eastern Cooperative Oncology Group (ECOG) performance status of 1 (71.2%). Diagnoses included oropharynx (45.5%) and larynx (24.2%) cancers, with locoregional disease (51.5%) alone, or combined with distant metastases (48.5%). Median (m) PFS was 4.4 months (95% confidence interval [CI]: 3.6, 5.4); median overall survival was 9.7 months (95% CI: 6.5, 13.1). Objective response rate was 29.3%; 23 patients had stable disease (39.7%). Drug-related grade 3/4 toxicities included neutropaenia (33.3%), fatigue (24.2%), anorexia (12.1%) and infection (10.6%). Five treatment-related deaths (7.6%) occurred.
Efficacy results were consistent with current standard treatment for this patient population, but the pre-specified mPFS of 5.5 months was not achieved. Grade 3/4 toxicities were also consistent with standard treatment, although treatment-related deaths were higher than expected.
铂类/5-氟尿嘧啶联合西妥昔单抗是治疗复发性或转移性头颈部鳞状细胞癌(SCCHN)的标准系统治疗方法。培美曲塞在 SCCHN 中显示出活性。这项 II 期研究评估了培美曲塞联合顺铂和西妥昔单抗在复发性/转移性 SCCHN 中的应用。
患者接受西妥昔单抗 250mg/m2(负荷剂量:400mg/m2),第 1、8 和 15 天;培美曲塞 500mg/m2+顺铂 75mg/m2,每 3 周一次,最多 6 个周期,同时给予叶酸、维生素 B12 和预防药物。至少完成 4 个周期后,有反应的患者有资格接受培美曲塞和西妥昔单抗维持治疗,或单独使用培美曲塞或西妥昔单抗维持治疗,直至疾病进展或出现毒性。评估疗效(主要终点:无进展生存期[PFS])和毒性。
66 例患者接受了至少 1 个周期的三联治疗。大多数患者为男性(80.3%),中位年龄为 62 岁,东部肿瘤协作组(ECOG)体能状态为 1 分(71.2%)。诊断包括口咽(45.5%)和喉(24.2%)癌,局部区域疾病(51.5%)单独存在,或合并远处转移(48.5%)。中位(m)PFS 为 4.4 个月(95%CI:3.6,5.4);中位总生存期为 9.7 个月(95%CI:6.5,13.1)。客观缓解率为 29.3%;23 例患者病情稳定(39.7%)。与药物相关的 3/4 级毒性包括中性粒细胞减少症(33.3%)、疲劳(24.2%)、厌食症(12.1%)和感染(10.6%)。5 例治疗相关死亡(7.6%)。
疗效结果与该患者人群的当前标准治疗一致,但未达到预设的 5.5 个月 mPFS。3/4 级毒性也与标准治疗一致,尽管治疗相关死亡高于预期。