摘要
目的:探索高剂量强度的化疗方案VIP(VP16,IFO,PDD)能否提高小细胞肺癌的疗效,以及在小剂量GCSF支持下能否保证其剂量强度。方法:19例小细胞肺癌患者,接受高剂量强度的VIP方案化疗:VP16100mg/m2ivd1~5,IFO1.5g/m2ivd1~5,Mesna0.4giv,于IFO注射后0、4、8h各一次;DDP20mg/m2ivd1~5;于d7开始应用GCSF2~3μg/kg·d,皮下注射直至血白细胞>5×109/L时停药。每3周重复,共4~6疗程,局限期病人进行辅助胸部放疗。结果:初治的16例中,CR7例(448%)、PR9例(562%),CR+PR为100%。4例PR的局限期病例中,通过放射治疗又有2例获得CR,3例复治病例亦有2例PR。相对剂量强度为928%。初治的病例,中位生存期11个月,范围为5~36个月,2例CR的病例获得了2年无病生存。主要的不良反应为骨髓抑制及恶心、呕吐。结论:高剂量强度的VIP方案化疗能获得较高的有效率及完全缓解率,毒性能耐受。
Purpose:To explore the effect of intensive VIP regimen in the treatment of small cell lung cancer,and to evaluate the possibility of intensive chemotherapy supported with low dose G CSF. Method:Nineteen patients with small cell lung cancer (SCLC) received 4 6 cycles of VIP chemotherapy:Vp 16 100mg/m2 iv d 1~5,IFO 1.5g/m2 iv d1~5. Mesna 0.4 iv following IFO 0、4、8 h, d 1~5, DDP 20 mg/ iv d 1~5. G CSF 2 3 μg/kg·d was administered daily,started from d7 followed chemotherapy till WBC>5.0×109/L.In the limited stage patients,adjuvant chest irradiation was given following 4 cycles of chemotherapy.Result:In the 16 previous untreated patients,the complete response rate and the partial response rate was 44.8%(7/16) and 52.8%(9/16) respectively.The overall response rate was 100%.The median survival was 11 months(range 5 36 months).Two patients got 2 year disease free survival.In the 3 previous treated cases,2 patients was PR.The relative dose intensity was 92.8%.The main side effects were myelosuppression,nausea and vomting.Conclusion:The intensive VIP regimen can improve the efficacy of SCLC,and the toxicity was moderate.Low dose G CSF can increase the dose intensity of chemotherapy.
出处
《癌症》
SCIE
CAS
CSCD
北大核心
1998年第6期453-455,共3页
Chinese Journal of Cancer