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小细胞肺癌的门诊强化化疗:改良“ICE”(异环磷酰胺、卡铂和依托泊苷)方案的五年经验

Outpatient intensive chemotherapy for small cell lung cancer: five years experience of modified 'ICE' ifosfamide carboplatin and etoposide.

作者信息

Hand S, Baker J, Smith A P, Macbeth F R

机构信息

Llandough Hospital, Penarth, Cardiff, UK.

出版信息

Clin Oncol (R Coll Radiol). 2002 Oct;14(5):367-71. doi: 10.1053/clon.2002.0097.

Abstract

INTRODUCTION

Small Cell Lung Cancer (SCLC) is increasingly being treated in the district general hospital setting. The search for an active regimen which can be given with the least toxicity and best outcomes led us to use a modified ICE (Ifosfamide, Carboplatin and Etoposide) regimen and modify it further by using oral mesna instead of intravenous mesna.

METHOD

All patients selected to receive the modified ICE regime over a 5-year period were included in our study. All patients were assessed for performance status and prognostic factors. Only those with WHO performance status 0-1 and Manchester prognostic score 0-3 were considered for ICE chemotherapy. All patients were followed up for 1 year after recruitment was completed.

RESULTS

Median survival for all 32 patients was 18.4 months (CI 12.2-24.6) and for the 28 patients with limited disease the median survival was 19.9 months (CI 8.2-31.6). Toxicity levels were low with no neutropenic deaths. One patient died three days after treatment was started due to disease progression. A total of 6 patients remained alive one year after recruitment was completed. Five out of the 6 were followed up for at least 2 years.

CONCLUSION

Using this out-patient modified ICE regime we have achieved a median survival comparable to other active chemotherapy regimes for SCLC with no significant increase in toxicity.

摘要

引言

在地区综合医院环境中,小细胞肺癌(SCLC)的治疗越来越普遍。为了寻找一种毒性最小且疗效最佳的有效治疗方案,我们采用了改良的ICE(异环磷酰胺、卡铂和依托泊苷)方案,并通过使用口服美司钠替代静脉注射美司钠对其进一步改良。

方法

我们的研究纳入了在5年期间内所有选择接受改良ICE方案治疗的患者。对所有患者进行了体能状态和预后因素评估。仅将世界卫生组织体能状态为0 - 1且曼彻斯特预后评分为0 - 3的患者纳入ICE化疗。所有患者在入组完成后随访1年。

结果

32例患者总的中位生存期为18.4个月(可信区间12.2 - 24.6),28例局限性疾病患者的中位生存期为19.9个月(可信区间8.2 - 31.6)。毒性水平较低,无中性粒细胞减少导致的死亡。1例患者在治疗开始三天后因疾病进展死亡。入组完成后共有6例患者存活1年。6例中的5例接受了至少2年的随访。

结论

使用这种门诊改良ICE方案,我们实现了与其他SCLC有效化疗方案相当的中位生存期,且毒性没有显著增加。

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