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[80例接受吉非替尼治疗超过6个月的晚期非小细胞肺癌患者的预后因素分析]

[Analysis of prognostic factors of 80 advanced NSCLC patients treated with gefitinib for more than 6 months].

作者信息

Dai Ling, Fang Jian, Nie Jun, Hu Weiheng, Chen Xiaoling, Han Jindi, Tian Guangming, Han Sen, Liu Xuyi

机构信息

Key Laboratory of Carcinogenesis and Translational Research, Ministry of Education, Peking University Cancer Hospital and Institute, Beijing 100142, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2010 Nov;13(11):1050-5. doi: 10.3779/j.issn.1009-3419.2010.11.10.

DOI:10.3779/j.issn.1009-3419.2010.11.10
PMID:21081047
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6000485/
Abstract

BACKGROUND

Some clinical predictors can be used to evaluate the efficacy of epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) therapy for non-small cell lung cancer (NSCLC), including female, East-Asian, non-smoker, adenocarcinoma, skin rash, etc. The aim of this study is to explore the prognosis of advanced NSCLC patients treated with gefitinib for more than 6 months.

METHODS

Eighty advanced NSCLC patients treated with gefitinib for more than 6 months were collected from January, 2005 to March, 2010. The association of their clinical characteristics with median progression-free survival time (PFS) was analysed.

RESULTS

Significantly longer median PFS were found in patients with > 70 years old, earlier clinical stage (IIIb), non-bone metastasis (27 months vs 12 months; 32 months vs 12 months; 16 months vs 10 months, P < 0.05). There was no significant difference in median PFS between ECOG performance status 0-1 group and 2-4 group, between more than 4 cycles of chemotherapy and 1-4 cycles, between PFS of chemotherapy > 6 months group and ≤6 months group, however, ECOG 0-1 group and more than 4 cycles of chemotherapy or PFS of chemotherapy > 6 months group seemed to have longer median PFS (15 months vs 10 months; 16 months vs 12 months; 14 months vs 12 months). Compared with no skin rash and grade 0-I rash group, the patients with rash or grade ≥II rash had longer median PFS (16 months vs 13 months, P=0.171; 19 months vs 11 months, P=0.085). The median PFS was not related with sex, smoking index, pathological types, metastatic sites except bone, treatment strategy, etc (P > 0.05).

CONCLUSIONS

For gefitinib treatment, longer median PFS is likely to be obtained in patients with > 70 years old, earlier clinical stage (IIIb), non-bone metastasis.

摘要

背景

一些临床预测指标可用于评估表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)治疗非小细胞肺癌(NSCLC)的疗效,包括女性、东亚人、不吸烟者、腺癌、皮疹等。本研究旨在探讨吉非替尼治疗6个月以上的晚期NSCLC患者的预后情况。

方法

收集2005年1月至2010年3月期间接受吉非替尼治疗6个月以上的80例晚期NSCLC患者。分析其临床特征与中位无进展生存时间(PFS)的相关性。

结果

年龄>70岁、临床分期较早(IIIb期)、无骨转移的患者中位PFS明显更长(27个月对12个月;32个月对12个月;16个月对10个月,P<0.05)。ECOG体能状态0-1组与2-4组之间、化疗4个周期以上与1-4个周期之间、化疗PFS>6个月组与≤6个月组之间的中位PFS无显著差异,然而,ECOG 0-1组、化疗4个周期以上或化疗PFS>6个月组的中位PFS似乎更长(15个月对10个月;16个月对12个月;14个月对12个月)。与无皮疹和0-I级皮疹组相比,有皮疹或≥II级皮疹的患者中位PFS更长(16个月对13个月,P=0.171;19个月对11个月,P=0.085)。中位PFS与性别、吸烟指数、病理类型、除骨以外的转移部位、治疗策略等无关(P>0.05)。

结论

对于吉非替尼治疗,年龄>70岁、临床分期较早(IIIb期)、无骨转移的患者可能获得更长的中位PFS。

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Screening for epidermal growth factor receptor mutations in lung cancer.肺癌中表皮生长因子受体突变的筛查
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