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Erlotinib Plus Capecitabine as First-Line Treatment for Older Chinese Patients With Advanced Adenocarcinoma of the Lung (C-TONG0807)

机译:厄洛替尼加卡培他滨作为一线治疗老年中国晚期肺腺癌的患者(C-TONG0807)

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摘要

Preclinical studies have shown synergism between epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors and antifolates in solid tumors. This study is to investigate the efficacy and tolerability of erlotinib plus capecitabine as first-line treatment in older Chinese patients (≥ 65 years) with lung adenocarcinoma.This is an open-label, single arm, multicenter phase II clinical trial. Sixty- two patients with previously untreated stage IIIB/IV adenocarcinoma and age 65 years or above were enrolled at four tertiary teaching hospitals and 2 provincial hospitals in China; 58 patients fulfilled the study requirements. Erlotinib (150 mg/day) and capecitabine (1000 mg/m2 twice daily on days 1–14) were administered during every 21-day cycle. The primary endpoint was the non-progression rate at 12 weeks. EGFR and K-ras mutation rates were determined using PCR. Tumor expression of different biomarkers was assessed using immunohistochemistry.In a cohort of 58 patients, 34 patients had no disease progression at 12 weeks following treatment. The objective response rate was 29.3%, and the disease control rate was 75.9%. The objective response rate was significantly higher in patients with EGFR mutations than in those with wild-type EGFR. Patients with thymidine phosphorylase-negative tumors had significantly longer overall survival after one year than patients with thymidine phosphorylase-positive tumors. Forty-four patients had at least one primary adverse events (AEs), including skin rash (n = 30), grade 3 AEs (n = 17), and grade 4 AEs (n = 7).This is the first phase II clinical trial to assess erlotinib plus capecitabine combination therapy as first-line treatment in older patients with lung adenocarcinoma. Erlotinib/capecitabine chemotherapy was significantly better in patients with EGFR mutations and in those with thymidine phosphorylase-negative tumors. The use of fluorouracil derivatives for the treatment of lung adenocarcinoma warrants further study.
机译:临床前研究表明,实体瘤中表皮生长因子受体(EGFR)酪氨酸激酶抑制剂与抗叶酸药物之间存在协同作用。本研究旨在探讨厄洛替尼联合卡培他滨在中国65岁以上老年肺腺癌患者中的一线治疗的疗效和耐受性,这是一项开放标签,单组,多中心II期临床试验。在中国的四家三级教学医院和两家省立医院中纳入了62例先前未经治疗的IIIB / IV期腺癌且年龄在65岁以上的患者; 58位患者满足了研究要求。在每个21天的周期中,分别服用厄洛替尼(150μmg/天)和卡培他滨(1000μmg/ m2,在第1-14天每天两次)。主要终点是12周时的非进展率。使用PCR确定EGFR和K-ras突变率。使用免疫组化方法评估了不同生物标志物的肿瘤表达。在58名患者中,有34名患者在治疗后12周没有疾病进展。客观缓解率为29.3%,疾病控制率为75.9%。 EGFR突变患者的客观缓解率明显高于野生型EGFR患者。与胸苷磷酸化酶阳性肿瘤患者相比,胸苷磷酸化酶阴性肿瘤患者一年后的总生存期明显更长。四十四名患者至少发生了一次主要不良事件(AE),包括皮疹(n = 30),3级AE(n = 17)和4级AE(n = 7),这是第一阶段的II期临床研究。一项评估厄洛替尼联合卡培他滨联合治疗作为老年肺腺癌患者一线治疗的试验。 EGFR突变患者和胸苷磷酸化酶阴性肿瘤患者的厄洛替尼/卡培他滨化疗效果显着。氟尿嘧啶衍生物在治疗肺腺癌中的应用值得进一步研究。

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