[1]李静敏,王华庆.培美曲塞二线治疗晚期肺大细胞癌的疗效和安全性分析[J].天津医科大学学报,2015,21(04):332-334.
LI Jing-min,WANG Hua-qing. Effect and safety of second-line pemetrexed in patients with advanced large cell lung cancer[J].Journal of Tianjin Medical University,2015,21(04):332-334.
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培美曲塞二线治疗晚期肺大细胞癌的疗效和安全性分析(PDF)
《天津医科大学学报》[ISSN:1006-8147/CN:12-1259/R]
- 卷:
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21卷
- 期数:
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2015年04期
- 页码:
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332-334
- 栏目:
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临床医学
- 出版日期:
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2015-07-15
文章信息/Info
- Title:
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Effect and safety of second-line pemetrexed in patients with advanced large cell lung cancer
- 文章编号:
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1006-8147(2015)04-0332-03
- 作者:
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李静敏; 王华庆
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(天津医科大学肿瘤医院淋巴瘤内科,国家肿瘤临床医学研究中心,天津市“肿瘤防治”重点实验室,天津 300060)
- Author(s):
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LI Jing-min; WANG Hua-qing
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(Department of Lymphoma, Cancer Institute and Hospital, Tianjin Medical University, National Clinical Research Center of Cancer, Tianjin Key Laboratory of Cancer Prevention and Therapy, Tianjin 300060, China)
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- 关键词:
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培美曲塞; 多西他赛; 晚期肺大细胞癌; 疗效
- Keywords:
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pemetrexed; docetaxel; advanced large cell lung cancer; efficacy
- 分类号:
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R734.2
- DOI:
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- 文献标志码:
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A
- 摘要:
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目的: 以多西他赛为阳性对照,评价培美曲塞单药二线治疗大细胞癌的疗效及安全性。方法: 该研究选取了19例一线化疗方案失败的ⅢB或Ⅳ期肺大细胞癌患者。随机将患者分为试验组(n=11),接受培美曲塞(500 mg/m2),第1天,21 d为1周期;对照组(n=8),应用多西他赛(75 mg/m2),第1天,21 d为1周期。比较两组患者无进展生存期(PFS)、总缓解率(ORR)、临床获益率(CBR)、总生存期(OS)以及不良反应。分析两种单药化疗方案的疗效和安全性。结果: 试验组和对照组ORR分别为18.18%,12.50%,差异无统计学意义,P=0.735。两组中位PFS分别为112 d、86 d;CBR分别为57.26%和48.72%;OS分别为355 d、312 d;以上3个观察指标试验组均高于对照组,但差异无统计学意义,P值分别为0.165、0.190、0.606。试验组、对照组分别完成(3.27+1.78)、(2.76+1.54)个化疗周期,差异有统计学意义(P<0.05)。培美曲塞组粒细胞、血小板减少发生率及脱发症状明显低于多西他赛组(P<0.05);而培美曲塞组皮疹发生率高于多西他赛组,具有统计学意义(P<0.05)。结论: 培美曲塞单药二线治疗晚期肺大细胞癌,疗效与多西他赛相似,且不良反应少,耐受性、依从性较好,安全性更高,适合晚期肺大细胞癌的临床应用。
- Abstract:
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Objective: To evaluate the effect and safety of pemetrexed in large cell lung cancer(LCLC). Methods: Nineteen patients with stage IIIB/IV LCLC were included, and all patients failed on first-line chemotherapy treatment. Patients were randomly divided into experimental group (n=11) and control group (n=8), receiving pemetrexed (500 mg/m2) and docetaxel (75 mg/m2), respectively on day 1 of each 21-day cycle. The progression-free survival (PFS), overall response rate (ORR), clinical benefit rate (CBR), overall survival (OS) and the occurrence of adverse reactions were observed. Results: ORR values were 18.18% in pemetrexed versus 12.50% (P=0.735) in docetaxel group. Median PFS values were 112 days and 86 days (P=0.165), CBR were 57.26% and 48.72% (P=0.190), OS were 355 days and 312 days (P=0.606) for pemetrexed and docetaxel group, respectively. No statistical differences were found between the above indicators. Experimental group and control group completed (3.27+1.78), (2.76+1.54) cycles respectively, and the difference was statistically significant (P < 0.05). Adverse reactions were myelosuppression, nausea and vomiting, alopecia, and transient liver function abnormalities. Pemetrexed-treated patients had significantly lower hematologic toxicity (P<0.05), on the contrary, the rash incidence is lower in docetaxel group (P<0.05). Conclusion: The similar effect, superior tolerability and obedience of pemetrexed comparing with docetaxel in this study support the use of single-agent, second-line pemetrexed for advanced LCLC.
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更新日期/Last Update:
2015-07-17