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吉西他滨联合铂类化疗治疗老年晚期非小细胞肺癌的回顾性分析。

Gemcitabine Plus Platinum Combination Chemotherapy for Elderly Patients with Advanced Non-small Cell Lung Cancer: A Retrospective Analysis.

机构信息

Division of Oncology, Department of Internal Medicine, The Catholic University of Korea School of Medicine, Seoul, Korea.

出版信息

Cancer Res Treat. 2011 Dec;43(4):217-24. doi: 10.4143/crt.2011.43.4.217. Epub 2011 Dec 27.

Abstract

PURPOSE

This study aimed to analyze the efficacy and toxicity of gemcitabine plus platinum chemotherapy for patients aged 70 years or older with advanced non-small-cell lung cancer (NSCLC).

MATERIALS AND METHODS

We reviewed the records of stage IIIB, IV NSCLC patients or surgically inoperable stage II, IIIA NSCLC patients who were aged 70 years or older when treated with gemcitabine (1,250 mg/m(2)) plus cisplatin (75 mg/m(2)) or carboplatin (AUC5) chemotherapy from 2001 to 2010 at Seoul St. Mary's Hospital, Uijeongbu St. Mary's Hospital and St. Vincent's Hospital. Gemcitabine was administered on days 1 and 8, and cisplatin or carboplatin was administered on day 1. Treatments were repeated every 3 weeks for a maximum of 4 cycles.

RESULTS

The median age of the 62 patients was 73.5 years (range, 70 to 84 years). Forty-one (66%) patients exhibited comorbidity. The mean number of treatment cycles was 3.9. The compared average relative dose intensity of gemcitabine plus platinum chemotherapy was 84.8%. The median progression-free survival and overall survival (OS) were 5.0 months and 9.4 months, respectively. Reduced Eastern Cooperative Oncology Group (ECOG) performance status (none vs. ≥1) and weight loss (<5% vs. ≥5%) after treatment were found to have a significant effect on OS (p=0.01).

CONCLUSION

Gemcitabine plus platinum chemotherapy is an effective treatment option with an acceptable level of toxicity in patients aged 70 years or older with good performance status in advanced NSCLC.

摘要

目的

本研究旨在分析吉西他滨联合铂类化疗治疗 70 岁及以上晚期非小细胞肺癌(NSCLC)患者的疗效和毒性。

材料与方法

我们回顾性分析了 2001 年至 2010 年期间在首尔圣玛丽医院、Uijeongbu 圣玛丽医院和圣文森特医院接受吉西他滨(1250mg/m²)联合顺铂(75mg/m²)或卡铂(AUC5)化疗的 70 岁及以上的 IIIB、IV 期 NSCLC 患者或不能手术的 II、IIIA 期 NSCLC 患者的病历资料。吉西他滨于第 1 和第 8 天给药,顺铂或卡铂于第 1 天给药。每 3 周重复治疗,最多 4 个周期。

结果

62 例患者的中位年龄为 73.5 岁(范围为 70-84 岁)。41 例(66%)患者存在合并症。平均治疗周期数为 3.9 个。吉西他滨联合铂类化疗的平均相对剂量强度为 84.8%。中位无进展生存期和总生存期(OS)分别为 5.0 个月和 9.4 个月。治疗后 Eastern Cooperative Oncology Group(ECOG)表现状态(0 级 vs. ≥1 级)和体重减轻(<5% vs. ≥5%)与 OS 显著相关(p=0.01)。

结论

对于体能状态良好的晚期 NSCLC 老年患者,吉西他滨联合铂类化疗是一种有效且毒性可接受的治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abee/3253863/9b57d06e1ef7/crt-43-217-g001.jpg

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