Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Seoul, Republic of Korea.
Lung Cancer. 2010 Oct;70(1):71-6. doi: 10.1016/j.lungcan.2009.12.015. Epub 2010 Jan 21.
Although platinum-based doublet chemotherapy is considered as standard of care for patients with advanced non-small cell lung cancer (NSCLC), most of them are eventually supposed to experience disease progression. Pemetrexed, docetaxel, erlotinib, and gefitinib have been shown to be active as monotherapy for pretreated patients. In this study, the efficacy of pemetrexed and carboplatin as a salvage therapy for patients with advanced NSCLC is evaluated.
From March 2007 to February 2009, 32 patients who were diagnosed with inoperable NSCLC and treated with one or more prior cisplatin-based chemotherapies were enrolled. Treatment consisted of pemetrexed 500 mg/m(2) over a 10-min intravenous infusion and carboplatin at an AUC 5 mg/mL/min over a 30-min intravenous infusion on Day 1 of a 21-day cycle. All patients were supplemented with folic acid and vitamin B12 to reduce the hematological toxicity of pemetrexed.
There were one (3.1%) complete response and five partial (15.6%) responses. The overall response rate was 18.8% and the median response duration was 4.4 months. Among the responders, four patients had adenocarcinoma and two had squamous cell carcinoma. Nine patients had stable disease, and the disease control rate was 46.9%. With a median follow up duration of 9.4 months, the median time to progression was 2.3 months and the median OS was 9.4 months. Seven patients (21.9%) experienced grade 3 and 4 hematologic toxicities; one anemia (3.1%), six neutropenia (18.8%), and six thrombocytopenia (18.8%). Two patients experienced grade 4 febrile neutropenia with infection. Four patients (12.5%) experienced grade 3 non-hematologic toxicities; four asthenia (12.5%), two anorexia (6.3%), and one stomatitis (3.1%). Grade 1-2 peripheral neuropathy developed in 13 patients (40.6%).
The combination of pemetrexed and carboplatin showed favorable toxicity profiles and activity in the pretreated patients with advanced NSCLC. It is suggested that this regimen can be a good chemotherapeutic option as a salvage therapy for patients with NSCLC.
铂类双联化疗被认为是晚期非小细胞肺癌(NSCLC)患者的标准治疗方法,但大多数患者最终都会出现疾病进展。培美曲塞、多西他赛、厄洛替尼和吉非替尼已被证明可作为预处理患者的单药治疗有效。本研究评估培美曲塞和卡铂作为晚期 NSCLC 挽救治疗的疗效。
2007 年 3 月至 2009 年 2 月,纳入 32 例诊断为不可切除 NSCLC 且接受过一种或多种顺铂为基础的化疗的患者。治疗方案为培美曲塞 500mg/m2,静脉输注 10 分钟;卡铂 AUC 5mg/mL/min,静脉输注 30 分钟,每 21 天为一个周期。所有患者均补充叶酸和维生素 B12 以降低培美曲塞的血液毒性。
1 例(3.1%)完全缓解,5 例(15.6%)部分缓解。总缓解率为 18.8%,中位缓解持续时间为 4.4 个月。在缓解者中,4 例为腺癌,2 例为鳞癌。9 例病情稳定,疾病控制率为 46.9%。中位随访 9.4 个月时,中位疾病进展时间为 2.3 个月,中位总生存期为 9.4 个月。7 例(21.9%)出现 3 级和 4 级血液学毒性;1 例贫血(3.1%),6 例中性粒细胞减少症(18.8%),6 例血小板减少症(18.8%)。2 例患者发生 4 级发热性中性粒细胞减少伴感染。4 例(12.5%)出现 3 级非血液学毒性;4 例乏力(12.5%),2 例厌食(6.3%),1 例口腔炎(3.1%)。13 例(40.6%)出现 1-2 级周围神经病变。
培美曲塞联合卡铂在晚期 NSCLC 预处理患者中显示出良好的毒性特征和疗效。该方案可作为 NSCLC 患者挽救治疗的一种较好的化疗选择。