Zhang Qin, Cai Xu-Wei, Zhu Zheng-Fei, Yu Wen, Liu Qi, Feng Wen, Xue Meng-Chen, Fu Xiao-Long
aDepartment of Radiation Oncology, Fudan University Shanghai Cancer Center bDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Anticancer Drugs. 2015 Apr;26(4):456-63. doi: 10.1097/CAD.0000000000000215.
Compared with other platinum-based doublet chemotherapy, pemetrexed plus platinum is more effective and tolerable as the first-line treatment for nonsquamous non-small cell lung cancer (NSCLC). Thus, we examined the feasibility of using thoracic radiotherapy combined with concurrent full-dose pemetrexed as the first-line treatment for advanced nonsquamous NSCLC patients. From January 2009 to July 2012, 41 patients with stage IIIB or IV nonsquamous NSCLC were treated with full-dose pemetrexed plus cisplatin as the first-line chemotherapy combined with concurrent thoracic radiotherapy, with or without radiotherapy for metastases. The status of mutations in the epidermal growth factor receptor was unknown before the treatment, and no tyrosine-kinase inhibitor and cytotoxic drug maintenance therapy were administered to the patients after the chemotherapy. The median follow-up duration was 26.3 months (range, 5.8-57.5 months). Twenty-one patients had stage IIIB disease (19 with stage N3-IIIB). Of the 20 patients with stage IV disease, 16 had oligometastases (≤5) and four had polymetastases. The median number of chemotherapy cycles was 4. The median radiation dose was 60 Gy. Thirty-six patients received radical doses of radiotherapy. Toxicities were highly tolerated. The median progression-free survival was 12 months and the median overall survival was 32 months. The 1-, 2-, and 3-year overall survival rates were 87.5, 67.1, and 43.4%, respectively. As the first-line treatment for selected patients with advanced nonsquamous NSCLC, thoracic radiotherapy combined with concurrent full-dose pemetrexed plus cisplatin was safe and highly tolerable. In addition, the survival rate was encouraging. Prospective clinical trials are needed to verify the results.
与其他铂类双联化疗相比,培美曲塞联合铂类作为非鳞状非小细胞肺癌(NSCLC)的一线治疗更有效且耐受性更好。因此,我们研究了采用胸部放疗联合同步全剂量培美曲塞作为晚期非鳞状NSCLC患者一线治疗的可行性。2009年1月至2012年7月,41例IIIB期或IV期非鳞状NSCLC患者接受全剂量培美曲塞联合顺铂作为一线化疗,并同步进行胸部放疗,有或无转移灶放疗。治疗前表皮生长因子受体的突变状态未知,化疗后未对患者给予酪氨酸激酶抑制剂和细胞毒性药物维持治疗。中位随访时间为26.3个月(范围5.8 - 57.5个月)。21例患者为IIIB期疾病(19例为N3 - IIIB期)。在20例IV期疾病患者中,16例有寡转移(≤5个),4例有多转移。化疗周期的中位数为4个。中位放射剂量为60 Gy。36例患者接受了根治性放射剂量。毒性反应耐受性良好。中位无进展生存期为12个月,中位总生存期为32个月。1年、2年和3年总生存率分别为87.5%、67.1%和43.4%。作为选定的晚期非鳞状NSCLC患者的一线治疗,胸部放疗联合同步全剂量培美曲塞加顺铂是安全且耐受性良好的。此外,生存率令人鼓舞。需要进行前瞻性临床试验来验证结果。