Hastürk S, Kurt B, Kocabas A, Orüç O, Burgut R
Cukurova University Faculty of Medicine, Department of Pulmonary Medicine Adana, Turkey.
J Chemother. 1997 Feb;9(1):66-71. doi: 10.1179/joc.1997.9.1.66.
This study was aimed to evaluate the effect of ifosfamide, cisplatin and etoposide (ICE) combined chemotherapy in small cell lung cancer (SCLC), and to test the feasibility of adding recombinant human granulocyte colony-stimulating factor (rhG-CSF) to aggressive chemotherapy. Thirty consecutive, previously untreated, patients with SCLC (17 with limited disease and 13 with extensive disease) entered this study. The ICE regimen consisted of ifosfamide (I) 4 g/m2 i.v. with same dose mesna i.v. on first day, cisplatin (C) 25 mg/m2 i.v. on days 1 to 3 and etoposide (E) 100 mg/m2 i.v. on days 1 to 3. A total of 30 MU rhG-CSF i.v. were given from day 7 to 14 if WBC were lower than 3000 x 10(6)/L, neutrophils were lower than 1000 x 10(6)/L. Overall response (OR) rate was 93% with a complete response (CR) rate of 23%. Median survival was 12 months [95% confidence interval (CI): 11-14] and median response duration was 10 months [95% CI: 8-10]. Thirty-seven percent of patients had grade 3 neutropenia, 40% had grade 3 anemia, and 1% had grade 2 thrombocytopenia. Nonhematologic toxicity was mild with nausea and vomiting being the most common. RhG-CSF, which reduced leukopenic nadirs and shortened the neutropenic period, was also well tolerated. This chemotherapy protocol seems to be active, well tolerated and is currently being compared with various conventional chemotherapies.
本研究旨在评估异环磷酰胺、顺铂和依托泊苷(ICE)联合化疗在小细胞肺癌(SCLC)中的疗效,并测试在强化化疗中添加重组人粒细胞集落刺激因子(rhG-CSF)的可行性。连续30例既往未接受过治疗的SCLC患者(17例为局限性疾病,13例为广泛性疾病)进入本研究。ICE方案包括:异环磷酰胺(I)4 g/m²静脉滴注,首日给予相同剂量的美司钠静脉滴注;顺铂(C)25 mg/m²静脉滴注,第1至3天给药;依托泊苷(E)100 mg/m²静脉滴注,第1至3天给药。如果白细胞低于3000×10⁶/L,中性粒细胞低于1000×10⁶/L,则从第7天至第14天静脉给予总共30 MU的rhG-CSF。总缓解(OR)率为93%,完全缓解(CR)率为23%。中位生存期为12个月[95%置信区间(CI):11 - 14],中位缓解持续时间为10个月[95% CI:8 - 10]。37%的患者出现3级中性粒细胞减少,40%的患者出现3级贫血,1%的患者出现2级血小板减少。非血液学毒性较轻,最常见的是恶心和呕吐。rhG-CSF可降低白细胞减少的最低点并缩短中性粒细胞减少期,且耐受性良好。该化疗方案似乎有效且耐受性良好,目前正在与各种传统化疗方案进行比较。