潘巍 孙海 王守华 涂燕玲 付金萍 徐乐.氟西汀联合同步放化疗治疗局部晚期非小细胞肺癌的临床观察[J].,2014,14(3):522-525 |
氟西汀联合同步放化疗治疗局部晚期非小细胞肺癌的临床观察 |
Clinical Observation on the Effect of Continuous Fluoxetine AdministrationCombined with Chemoradiotherapy in the Treatment of LocalAdvanced NSCLC |
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DOI: |
中文关键词: 非小细胞肺癌 同步放化疗 氟西汀 临床疗效 |
英文关键词: Non-small cell lung cancer Chemoradiotherapy Fluoxetine Clinical efficacy |
基金项目:江宁区科技发展项目(2011F05) |
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中文摘要: |
目的:观察氟西汀联合同步放化疗治疗局部晚期非小细胞肺癌(none small cells lung carcinoma,NSCLC)的临床疗效及其安
全性。方法:选择2010 年10 月~2011 年4 月我院收治的Ⅲ期不能手术的NSCLC 患者47 例,根据患者的入院顺序,随机分为两
组,同步放化疗组(对照组)22 例,接受三维适形或调强放疗:肿瘤处方剂量60~66 Gy,常规分割:1.8~2.0 Gy/ 次;放疗期间同步
两周期“紫杉醇+顺铂”方案化疗,放疗后再原方案巩固化疗2~3 个周期;氟西汀联合治疗组(实验组)25 例,从同步放化疗开始
起同时服用氟西汀(20~40 mg/day),持续服药半年。随访至1 年,观察和评价两组的疗效以及不良反应的发生情况。结果:对照组
与实验组的客观有效率分别为77.3 %(17/22)和80%(20/25)(P>0.05);1 年生存率分别为68.2%(15/22)和80 %(20/25)(P>0.05);1
年局控率分别为45.5 %(10/22)和76 %(19/25),差异有统计学意义(P<0.05)。治疗后,实验组患者CD+/CD8+比率由1.34± 0.23 升
至1.58± 0.22(P<0.05),而汉密尔顿抑郁量表(HAMD)总分由13.4± 4.8 降至9.6± 3(P<0.05);全组患者主要不良反应为骨髓抑
制、消化道反应、放射性食管炎和放射性肺炎,未发生4 级不良反应,两组3 级不良反应发生率无明显差异(P>0.05)。结论:对于不
能手术的局部晚期NSCLC 患者,在同步放化疗的基础上联合氟西汀治疗可以提高肿瘤的1 年局控率,促进抗肿瘤免疫,并缓解
患者的抑郁情绪,且不加重不良反应。 |
英文摘要: |
Objective:To evaluate the efficacy and safety of continuous Fluoxetine administration combined with concurrent
chemoradiotherapy (C-CRT) for local advanced non-small cell lung cancer.Methods:From October 2010 to April 2011, 47 patients with
unresectable stage Ⅲ NSCLC were randomly assigned to one of the two treatment arms: C-CRT group were treated with three
dimensional conformal radiation therapy (3D-CRT) or intensity modulated radiation therapy (IMRT) to a total dose of 60-66 Gy at
1.8-2.0 Gy per fraction, 2 cycles of TP chemotherapy was carried concurrent with radiotherapy and followed by 2-3 cycles of TP
chemotherapy thereafter. Fluoxetine group were additionally administered with 20-40 mg Fluoxetine daily for 6 months besides
chemoradiotherapy.Results:The response rates and 1 year overall survival rate were 77.3% (17/22), 68.2% (15/22) and 80%(20/25),
80% (20/25) in C-CRT group and Fluoxetine group, respectively (P>0.05). 1 year local control rate were 45.5% (10/22) and 76 %
(19/25) in C-CRT group and Fluoxetine group, respectively (P<0.05). CD4+/CD8+ ratio raised from 1.34± 0.23 to1.58± 0.22 (P<0.05),
HAMD score decreased from13.4± 4.8 to 9.6± 3 (P<0.05) in Fluoxetine group, meanwhile no changes were observed in C-CRT group.
The main side effects included anemia/leucopenia /thrombocytopenia, nausea/vomiting, radiation esophagitis and radiation pneumonitis.
No differences in grade 3 side-effect was observed between these two groups. Conclusion:Compared with C-CRT alone, additional
Fluoxetine administration provided higher 1 year local control rate for local advanced NSCLC patients. Fluoxetine administration helped
to regain immune balance and alleviate depression without additional side effect. |
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