Thongprasert S
Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Thailand.
J Med Assoc Thai. 2000 May;83(5):549-53.
Twenty patients with small cell lung cancer (SCLC) were entered to the study. Fourteen cases were male and six cases were female. Twelve cases were extensive disease, eight cases were limited disease. Median age was 60 years (range = 40-72 years), median performance status was 70 per cent (range = 60-80%). All patients were treated with combination chemotherapy consisting of ifosfamide 5 g/m2 intravenous infusion over 4 hours with mesna uroprotection, carboplatin 300 mg/m2 intravenous infusion over 2 hours on day 1, and etoposide 120 mg/m2 intravenous infusion over 4 hours on day 1-3. Chemotherapy was re-cycled every 28 days. Assessment of hematologic toxicity (CBC) was performed two times per week. If there was grade 3 or 4 neutropenia on any cycle of chemotherapy, GM-CSF was administered for febrile neutropenia and on the next cycle it was administered prophylactically on day 4-14.
Seventeen cases were evaluable for response and toxicity (three cases were inevaluable due to loss to follow-up after the first cycle of chemotherapy). Fourteen cases (five limited disease, nine extensive disease) achieved partial response (82.5%). Two cases had stable disease, one case died on day 7. One year survival was 23.5 per cent. Seventy and a half percent grade 3 and 4 neutropenia was seen during the first cycle. One patient had febrile neutropenia. After being prophylactically treated with GM-CSF, grade 3 and 4 neutropenia was reduced from 70.5 per cent to 56.2 per cent, 46.7 per cent, 63.6 per cent, 42.8 per cent and 0 per cent in cycle 2-6 respectively. Major toxicity of GM-CSF consisted of transient chest distress, chills, sweating and hypotension which subsided in 5-10 minutes. No fever or skin rash was observed.
Combination of ifosfamide, carboplatin and etoposide (ICE) is an active regimen for small cell lung cancer. However, because of its severe myelosuppression, this regimen needs hematopoietic growth factor support, and GM-CSF was used in this study. The administration of GM-CSF rendered ICE chemotherapy to be given safely.
20例小细胞肺癌(SCLC)患者进入本研究。14例为男性,6例为女性。12例为广泛期疾病,8例为局限期疾病。中位年龄为60岁(范围=40 - 72岁),中位体能状态为70%(范围=60 - 80%)。所有患者均接受联合化疗,包括异环磷酰胺5 g/m²静脉输注4小时并给予美司钠尿路保护,卡铂300 mg/m²静脉输注2小时于第1天进行,依托泊苷120 mg/m²静脉输注4小时于第1 - 3天进行。化疗每28天重复一次。每周进行两次血液学毒性评估(全血细胞计数)。如果在任何化疗周期出现3级或4级中性粒细胞减少,对于发热性中性粒细胞减少给予粒细胞巨噬细胞集落刺激因子(GM - CSF),并在下一周期于第4 - 14天预防性给予。
17例可评估疗效和毒性(3例因在第一个化疗周期后失访而不可评估)。14例(5例局限期疾病,9例广泛期疾病)达到部分缓解(82.5%)。2例病情稳定,1例在第7天死亡。1年生存率为23.5%。在第一个周期中70.5%出现3级和4级中性粒细胞减少。1例患者出现发热性中性粒细胞减少。在接受GM - CSF预防性治疗后,3级和4级中性粒细胞减少在第2 - 6周期分别从70.5%降至56.2%、46.7%、63.6%、42.8%和0%。GM - CSF的主要毒性包括短暂的胸部不适、寒战、出汗和低血压,这些症状在5 - 10分钟内消退。未观察到发热或皮疹。
异环磷酰胺、卡铂和依托泊苷(ICE)联合方案是小细胞肺癌的一种有效方案。然而,由于其严重的骨髓抑制,该方案需要造血生长因子支持,本研究中使用了GM - CSF。GM - CSF的应用使ICE化疗能够安全进行。