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Clinical Observation and Prognostic Analysis of Pemetrexed plus Platinum as First-line Treatment in Patients with Advanced Non-small Cell Lung Cancer

机译:培美曲塞加铂金为一线治疗晚期非小细胞肺癌的临床观察和预后分析

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Objective: To determine clinical efficacy, safety and prognostic factors of pemetrexed plus platinum as firstlinetreatment in patients with advanced non-small cell lung cancer (NSCLC). Materials and Methods: Clinicalcharacteristics, short-term efficacy, survival and adverse reactions of 47 advanced non-squamous NSCLCpatients who had received pemetrexed plus platinum as first-line treatment in Shanghai Pulmonary Hospitalfrom January 2009 to June 2011 were retrospectively analyzed. The Chi-squared test was applied to statisticallyanalyze the overall response rate (ORR), disease control rate (DCR) and toxicity reactions in both groups, whilesurvival data wereanalyzed by Kaplan-Meier and logrank methods, and the COX proportional hazards modelwas adopted for a series of multi-factor analyses. Results: Only two patients were lost to follow-up. The ORR,DCR, medium progression-free survival time (PFS) and medium overall survival (OS) were 31.9%, 74.5%, 5months and 15.2 months, while 1- and 2-year survival rates were 63.8% (30/47) and 19.2% (9/47), respectively.Single-factor analysis showed that tumor pathological patterns and efficacy were in association with mediumPFS (P<0.05), whereas tumor pathological patterns, smoking history and efficacy were closely connectedwith medium OS (P<0.05). Multi-factor analyses demonstrated that pathological patterns and efficacy wereindependent factors influencing OS (P<0.05). The rate of toxicity reactions in degree Ⅲ/Ⅳ was low, includinghematologic toxicity marked by decline in white blood cell count and decrease in the platelet count (PLT), andnon-hematologic toxicity manifested by gastrointestinal reactions, such as nausea and vomiting. Conclusions:Pemetrexed plus platinum as first-line treatment has excellent efficacy and slight adverse reactions with favorabledrug-tolerance in patients with advanced non-squamous NSCLC.
机译:目的:确定培美曲塞加铂金作为一线治疗晚期非小细胞肺癌(NSCLC)患者的临床疗效,安全性和预后因素。资料与方法:回顾性分析2009年1月至2011年6月在上海肺科医院接受培美曲塞加铂金作为一线治疗的47例晚期非鳞状NSCLC患者的临床特点,近期疗效,生存率和不良反应。卡方检验用于统计学分析两组的总缓解率(ORR),疾病控制率(DCR)和毒性反应,同时通过Kaplan-Meier和logrank方法分析生存数据,并采用COX比例风险模型进行风险评估。系列多因素分析。结果:仅两名患者失去随访。 ORR,DCR,中度无进展生存时间(PFS)和中度总生存期(OS)分别为31.9%,74.5%,5个月和15.2个月,而1年和2年生存率为63.8%(30/47)单因素分析表明,肿瘤的病理类型和疗效与中度PFS相关(P <0.05),而肿瘤的病理类型,吸烟史和有效性与中度OS密切相关(P <0.05)。 0.05)。多因素分析表明,病理类型和疗效是影响OS的独立因素(P <0.05)。 Ⅲ/Ⅳ度的毒性反应发生率较低,包括以白细胞计数下降和血小板计数(PLT)下降为标志的血液学毒性,以及以恶心和呕吐等胃肠道反应表现的非血液学毒性。结论:培美曲塞加铂金一线治疗晚期非鳞状非小细胞肺癌的疗效好,不良反应小,耐药性好。

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