Chang A Y, Asbury R F, Boros L, Garrow G C, Hsieh S
Department of Medicine, Genesee Hospital, University of Rochester, NY 14607-4055, USA.
Semin Oncol. 1995 Jun;22(3 Suppl 7):9-12.
We have evaluated the combination of ifosfamide, carboplatin, and etoposide (ICE) along with mesna in 46 patients with stage IV non-small cell lung cancer. Treatment consisted of ifosfamide (1.25 g/m2/d with mesna) and etoposide (80 mg/m2/d) given intravenously on days 1 to 3 and carboplatin (300 mg/m2) given intravenously on day 1 every 4 weeks. Eligibility criteria included measurable disease; adequate hematologic, hepatic, and renal functions; no prior chemotherapy; and an Eastern Cooperative Oncology Group performance status (PS) of 0 to 3. Two patients were lost to follow-up and one had received prior chemotherapy, leaving 43 patients evaluable for response and toxicities. There were 27 male and 16 female patients. Twenty-three patients had a PS of 0 or 1 and 20 had a PS of 2 or 3. Eighteen patients had received prior radiotherapy. There were two complete responses and nine partial responses. The response rate was 35% in PS 0 or 1 patients and 15% in PS 2 or 3 patients. The most frequent toxicity was myelosuppression; 44% of patients experienced grade 3 or 4 leukopenia and 14%, grade 3 or 4 thrombocytopenia. Patients receiving prior radiation were significantly more prone to develop leukopenia (P = .01). Five patients developed leukopenic fever, and three died of sepsis. Gastrointestinal toxicities were mostly mild. No neurologic or genitourinary toxicities were observed. The median length of survival was 209 days for patients with a PS of 0 or 1 and 123 days for the entire group. The 1-year survival rate was 22% and 19%, respectively, in these two patient subgroups. ICE is an active regimen in patients with metastatic non-small cell lung cancer and a good PS. Myelosuppression is the major dose-limiting toxicity. Hematopoietic growth factors may be indicated in subsequent studies, especially in patients who had prior radiation therapy. The therapeutic effect of ICE on patients with a poor PS remains unsatisfactory and requires further investigation.
我们评估了异环磷酰胺、卡铂和依托泊苷(ICE)联合美司钠方案对46例IV期非小细胞肺癌患者的疗效。治疗方案为:异环磷酰胺(1.25 g/m²/d,同时给予美司钠)和依托泊苷(80 mg/m²/d)于第1至3天静脉滴注,卡铂(300 mg/m²)于第1天静脉滴注,每4周重复一次。入选标准包括:可测量的病灶;血液学、肝脏和肾脏功能良好;未曾接受过化疗;东部肿瘤协作组(ECOG)体能状态(PS)为0至3。2例患者失访,1例曾接受过化疗,最终43例患者可评估疗效及毒性反应。其中男性27例,女性16例。23例患者PS为0或1,20例患者PS为2或3。18例患者曾接受过放疗。2例患者完全缓解,9例部分缓解。PS为0或1的患者缓解率为35%,PS为2或3的患者缓解率为15%。最常见的毒性反应为骨髓抑制;44%的患者出现3或4级白细胞减少,14%的患者出现3或4级血小板减少。曾接受放疗的患者更易发生白细胞减少(P = 0.01)。5例患者发生白细胞减少性发热,3例死于败血症。胃肠道毒性反应大多较轻。未观察到神经或泌尿生殖系统毒性反应。PS为0或1的患者中位生存期为209天,全组患者中位生存期为123天。这两个亚组患者的1年生存率分别为22%和19%。ICE方案对转移性非小细胞肺癌且PS良好的患者是一种有效的治疗方案。骨髓抑制是主要的剂量限制性毒性反应。后续研究中可能需要使用造血生长因子,尤其是对曾接受过放疗的患者。ICE方案对PS较差的患者的治疗效果仍不令人满意,需要进一步研究。