机构地区:[1]暨南大学附属第一医院肿瘤科,广东广州510630
出 处:《癌症》2005年第12期1514-1517,共4页Chinese Journal of Cancer
摘 要:背景与目的:以铂类药物为基础的化疗方案对晚期非小细胞肺癌(non-smallcelllungcancer,NSCLC)治疗效果较其他方案好,“第三代”化疗药物比“第二代”有优势。本文旨在比较含铂药物的“第二代”和“第三代”化疗方案联合放疗治疗晚期(Ⅲ~Ⅳ期)NSCLC的疗效。方法:全组病例均采用化疗、放疗、化疗的“夹心”治疗。采用“第二代”的化疗方案为MVP、IVP、EP、VDS+DDP共24例。“第三代”的化疗方案为NP、TP和GP共23例,两组患者资料经χ2检验具有可比性。两组放疗均采用60Coγ射线常规外照射,剂量为65~76Gy。用Kaplan-Meier法计算生存率,两组间差异比较用log-rank检验。结果:“第二代”治疗组的有效率(CR+PR)为41.7%(10/24),“第三代”治疗组的有效率(CR+PR)为56.5%(13/23),差异无显著性(χ2=0.53,P=0.47)。“第二代”治疗组和“第三代”治疗组的中位肿瘤进展时间(mediantimetoprogression,MTTP)分别为6.00个月和12.60个月,差异有显著性(χ2=6.93,P=0.01)。第二代和第三代治疗组中位生存期分别为9.0个月、14.0个月,差异有显著性(U检验:Z=-2.17,P=0.03);1年生存率分别为30.7%、56.3%。“第二代”治疗组中无2年生存者,“第三代”治疗组中2年生存率为15.6%,差异有显著性(χ2=6.59,P=0.01)。两组的主要不良反应为骨髓抑制、恶心呕吐以及放疗引起的放射性肺部反应、放射性食管反应。Ⅲ~Ⅳ级的中性粒细胞减少发生率以“第二代”治疗组较多见,而Ⅲ~Ⅳ级的放射性食管反应以“第三代”治疗组较多见,但均无统计学意义。结论:初步显示含铂药物的“第三代”化疗方案联合放疗治疗晚期NSCLC比“第二代”在生存时间上有一定优势,值得进一步进行临床研究。BACKGROUND & OBJECTIVE: Platinum-based chemotherapy regimens are better than other regimens when treating patients with advanced non-small cell lung cancer (NSCLC). The third generation of platinum-based regimens {NP [Navelbine (NVB), cisplatin (DDP)], TP (Taxol, DDP), GP (Gemzar, DDP)} is better than the second generation {MVP [mitomycin (MMC), desacetylvinblastin amide (VDS), DDP], MIP [MMC, ifosfamide (IFO), DDP], EP [etopside (VP-16), DDP], VDS+DDP}. This study was to compare the efficacy between the second and the third generations of platinum-based regimens combined with radiotherapy on advanced non-small cell lung cancer (NSCLC). METHODS: From Jul. 1999 to Dec. 2001, 47 pathologically confirmed advanced NSCLC patients received chemoradiotherapy. 24 received the second generation of platinum-based regimens, 23 received the third generation; all patients received routine external irradiation of ^60Co (65-76 Gy). Characteristics of the patients were comparable. Kaplan-Meier analysis was used to evaluate survival rates, and log-rank test to study differences between the 2 groups. RESULTS: The objective response rates were 41.7% in the second generation group, and 56.5% in the third generation group (χ^2=0.53, P=0.47). The median time to progression and median survival time were significantly longer in the third generation group than in the second generation group (12.6 months vs. 6.0 months, χ^2=6.93, P=0.01; 14.0 months vs. 9.0 months, Z=-2.17, P=0.03). The 1-, and 2-year survival rates were significantly higher in the third generation group than in the second generation group (56.3% vs. 30.7%, 15.6% vs. 0%, χ^2=6.59, P=0.01). The major adverse events were leukocytopenia, nausea and vomiting, radiation-induced esophagitis and pneumonia, which were tolerable. CONCLUSIONS: The third generation of platinum-based regimens in combination with radiotherapy for advanced non-small lung cancer may be more advantageous over the second generation of
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