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信迪利单抗联合安罗替尼治疗三线及以上肺腺癌患者的临床疗效 被引量:10
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作者 陈菊香 朱利群 +2 位作者 费小东 王纯 王军 《现代肿瘤医学》 CAS 北大核心 2022年第14期2543-2547,共5页
目的:观察信迪利单抗联合安罗替尼用于治疗三线及以上晚期肺腺癌的临床疗效和不良反应。方法:将自2019年3月至2020年8月在本院肿瘤科进行诊治的118例晚期肺腺癌患者分为安罗替尼组(n=59)和联合治疗组(n=59),分别采用安罗替尼单药,信迪... 目的:观察信迪利单抗联合安罗替尼用于治疗三线及以上晚期肺腺癌的临床疗效和不良反应。方法:将自2019年3月至2020年8月在本院肿瘤科进行诊治的118例晚期肺腺癌患者分为安罗替尼组(n=59)和联合治疗组(n=59),分别采用安罗替尼单药,信迪利单抗联合安罗替尼进行治疗,采用胸部计算机断层扫描放射,计算机断层扫描,骨扫描等检测患者肿瘤进展,治疗前后采用TDL生命质量测定表(TDL-QOLAS)反映患者生命质量水平,通过酶联免疫吸附法测量血液肿瘤标志物水平,此外,在随访截至时使用Morisky药物依从性量表评估所有患者服药依从性,通过Kaplan-Meier曲线描述两组患者的PFS(无病进展期)和OS(总生存期),并观察用药期间两组患者不良反应发生情况。结果:联合治疗组的ORR、PFS和OS均明显高于安罗替尼组,分别为23.7%vs 10.2%、6.9个月vs 4.7个月、15.7个月vs 9.3个月,差异有统计学意义(P<0.05)。血液学分析显示,联合治疗与安罗替尼单用均可显著降低血清肿瘤标志物水平,而联合治疗效果更佳(P<0.05),此外,相较于安罗替尼单药组,联合治疗可以更好的提高患者生活质量并具有良好的用药依从性(P<0.05),且联合治疗组未明显增加治疗相关不良反应,未发生因不良反应终止治疗的事件,无治疗相关死亡事件。结论:信迪利单抗联合安罗替尼治疗三线及以上肺腺癌患者,可显著改善患者的生存时间,具有良好的用药依从性和安全性,值得临床进一步推广。 展开更多
关键词 信迪利单抗 安罗替尼 肺腺癌患者 用药依从性
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冀东满族肺腺癌患者胸液与相应肿瘤组织EGFR基因突变检测对比分析
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作者 贾瑞 薛雷 +3 位作者 杜海荣 杨宏伟 高鲲 梁华刚 《现代肿瘤医学》 CAS 2015年第12期1676-1678,共3页
目的:分析冀东满族肺腺癌患者胸液与相应肿瘤组织EGFR基因突变检测结果。方法:选取2010年9月至2014年9月间在我院胸外科治疗的74例有胸液的冀东满族肺腺癌患者为研究对象,采用变性高效液相色谱法(DHPLC)检测肺腺癌患者胸液及相应肿瘤组... 目的:分析冀东满族肺腺癌患者胸液与相应肿瘤组织EGFR基因突变检测结果。方法:选取2010年9月至2014年9月间在我院胸外科治疗的74例有胸液的冀东满族肺腺癌患者为研究对象,采用变性高效液相色谱法(DHPLC)检测肺腺癌患者胸液及相应肿瘤组织样本中是否发生EGFR基因突变。结果:肿瘤组织EFGR基因突变检出率为50.00%,胸液样本EGFR基因突变检出率为52.70%,两者间无统计学差异(P>0.05)。胸液上清、胸液沉淀、胸液上清与沉淀以及肿瘤组织EGFR基因检测结果一致性均良好。结论:肺腺癌患者胸液与相应肿瘤组织EGFR基因突变检测结果一致性良好,临床可通过胸液检测代替肿瘤组织检测,以期能够持续监测患者EGFR基因突变状态,以指导患者添加或者实施EGFR-TKIs治疗。 展开更多
关键词 肺腺癌患者 胸液 相应肿瘤组织 EGFR基因突变检测
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癌组织中CD45RO表达水平与肺腺癌患者临床病理特征及生存率的关联分析 被引量:5
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作者 俞达辉 吴道立 +1 位作者 袁冲 褚文炎 《中国医科大学学报》 CAS CSCD 北大核心 2018年第5期448-453,共6页
目的 评估肿瘤组织CD45RO表达水平与肺腺癌手术患者的临床病理参数及预后的相关性。方法 选取121例进行手术的肺腺癌患者,采集肿瘤组织和癌旁组织样本。采用anti-CD45RO抗体进行免疫组织化学染色检测CD45RO表达水平,计算染色强度分数... 目的 评估肿瘤组织CD45RO表达水平与肺腺癌手术患者的临床病理参数及预后的相关性。方法 选取121例进行手术的肺腺癌患者,采集肿瘤组织和癌旁组织样本。采用anti-CD45RO抗体进行免疫组织化学染色检测CD45RO表达水平,计算染色强度分数和染色面积分数的乘积得到总表达评分,并分为高、中和低表达。结果 相对于癌旁组织,CD45RO在肺腺癌组织中高表达;肿瘤组织CD45RO表达水平与肿瘤大小、淋巴结转移呈负相关;Kaplan-Meier(K-M)曲线显示,肺腺癌组织中的CD45RO表达水平越高,无病生存期(DFS)和总体生存期(OS)越长;多因素COX回归发现,肺腺癌组织CD45RO表达量能独立预测良好的DFS,然而,低分化和淋巴结转移均能独立预测不良的DFS;肺腺癌组织CD45RO表达量是较长OS的独立预测因素,而低分化、淋巴转移及远端转移均是OS的独立危险因素。结论 肿瘤组织中CD45RO的表达水平可作为新的、可靠的生物标记物,用于评估肺腺癌手术患者的临床病理特征和预后情况。 展开更多
关键词 组织 CD45RO 临床病理特征 预后 手术患者
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肺腺癌患者PICC置管后静脉血栓形成的危险因素观察 被引量:1
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作者 童群 陈实 《当代临床医刊》 2019年第1期89-89,63,共2页
目的探讨肺腺癌患者PICC置管后静脉血栓形成的危险因素。方法选择我院2015年1月至2018年5月期间收治的进行PICC置管化疗的280例肺腺癌患者作为本次研究对象,使用Logistic多元回归分析方式,对患者数据进行分析,找出PICC置管后静脉血栓形... 目的探讨肺腺癌患者PICC置管后静脉血栓形成的危险因素。方法选择我院2015年1月至2018年5月期间收治的进行PICC置管化疗的280例肺腺癌患者作为本次研究对象,使用Logistic多元回归分析方式,对患者数据进行分析,找出PICC置管后静脉血栓形成的危险因素。结果在280例肺腺癌患者中,发生静脉血栓或及其并发症的有19例,发生率为6. 7%。肺腺癌患者在性别上,女性发生静脉血栓的几率大于男性;体重指数(BMI)、穿刺头静脉、纤维蛋白原(FIB)都是肺腺癌患者PICC置管后静脉血栓形成的危险因素。结论在临床操作中,性别、静脉穿刺点、体重指数(BMI)、纤维蛋白原(FIB)是肺腺癌患者PICC置管后静脉血栓形成的危险因素,女性疾病的发生率高于男性[1]。 展开更多
关键词 PICC置管 静脉血栓 肺腺癌患者 因素观察
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肺腺癌组织中CD8表达水平与患者临床病理特征及生存率的关系 被引量:6
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作者 俞达辉 吴道立 +1 位作者 袁冲 褚文炎 《广东医学》 CAS 2018年第3期398-402,共5页
目的评估CD8表达水平与肺腺癌手术患者临床病理特征及预后的关系。方法纳入121例肺腺癌手术患者,采集肿瘤组织样本和癌旁组织样本。采用anti-CD8抗体(Abcam)进行免疫组织化学染色检测CD8表达水平。最后随访时间为2017年2月,中位随访期... 目的评估CD8表达水平与肺腺癌手术患者临床病理特征及预后的关系。方法纳入121例肺腺癌手术患者,采集肿瘤组织样本和癌旁组织样本。采用anti-CD8抗体(Abcam)进行免疫组织化学染色检测CD8表达水平。最后随访时间为2017年2月,中位随访期为44个月。结果 CD8在肺腺癌组织中相对于癌旁组织高表达;在肺腺癌患者中,组织CD8表达水平与淋巴结转移呈负相关(r=-0.217,P=0.017)。Kaplan-Meier(K-M)曲线和Log Rank检验发现肺腺癌组织CD8表达越高,其手术患者的无病生存期(DFS)(P<0.001)和总体生存期(OS)(P<0.001)越长;单元Cox风险回归模型发现肿瘤组织CD8表达水平与患者较好的DFS显著相关(P<0.001)。然而,低分化(P=0.046)、淋巴转移(P<0.001)及TNM分级(P=0.003)与患者较差的DFS显著相关。进一步采用多元Cox回归结果显示肺腺癌组织CD8高表达水平(P<0.001)和淋巴结转移(P=0.016)分别是肺腺癌手术患者DFS的独立保护因素与独立危险因素。此外,单元Cox分析显示肺腺癌组织CD8表达水平能预测较好的OS(P=0.003),而低分化(P=0.003)、淋巴转移(P<0.001)、远端转移(P=0.029)及TNM分期(P=0.001)均能预测较差的OS。多元Cox分析结果表明肺腺癌组织CD8表达水平(P=0.001)是手术患者较好的OS的独立预测因素,低分化(P=0.009)、淋巴转移(P=0.001)及远端转移(P=0.004)是手术患者OS的独立危险因素。结论肺腺癌组织中CD8表达水平可作为用于评估其手术患者的临床病理特征和预后情况的新颖且可靠的生物标记物。 展开更多
关键词 组织 CD8 临床病理特征 预后 手术患者
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替吉奥联合吉非替尼治疗EGFR突变阳性的老年晚期肺腺癌患者的疗效及对生活质量的影响
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作者 董艳琼 《首都食品与医药》 2020年第4期55-56,共2页
目的探讨替吉奥联合吉非替尼治疗EGFR突变阳性的晚期肺腺癌患者的疗效及对生活质量的影响.方法选取来我院进行治疗的EGFR突变阳性的晚期肺腺癌患者124例,随机分为两组各62例.对照组给予吉非替尼,治疗组在对照组基础上口服替吉奥胶囊,两... 目的探讨替吉奥联合吉非替尼治疗EGFR突变阳性的晚期肺腺癌患者的疗效及对生活质量的影响.方法选取来我院进行治疗的EGFR突变阳性的晚期肺腺癌患者124例,随机分为两组各62例.对照组给予吉非替尼,治疗组在对照组基础上口服替吉奥胶囊,两组患者接受治疗2个疗程.对比两组患者治疗后的临床疗效、生活质量改善情况、CA199、CEA和CYFRA211水平和不良反应发生率.结果经过治疗后,治疗组ORR和CBR显著高于对照组(P<0.05);两组患者CA199、CEA和CYFRA211水平显著降低(P<0.05);并且治疗组降低较多(P<0.05);治疗组生活质量总改善率显著高于对照组(P<0.05).结论采用替吉奥联合吉非替尼治疗EGFR突变阳性的晚期肺腺癌,具有较好的治疗效果. 展开更多
关键词 替吉奥 吉非替尼 EGFR突变阳性的晚期肺腺癌患者 生活质量影响
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埃克替尼治疗17例晚期肺腺癌非吸烟患者的早期临床疗效观察 被引量:3
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作者 孙婧华 张阳 +5 位作者 赵金波 刘芳 戴朝霞 蒋葵 冯仲珉 孙秀华 《中国新药杂志》 CAS CSCD 北大核心 2012年第14期1651-1653,共3页
目的:观察埃克替尼(icotinib)治疗晚期肺腺癌非吸烟患者的早期临床疗效。方法:收集17例口服埃克替尼晚期肺腺癌非吸烟患者的临床资料,统计症状缓解时间、KPS评分变化、客观有效率、不良反应。结果:症状缓解时间4~10 d,KPS评分升高率为7... 目的:观察埃克替尼(icotinib)治疗晚期肺腺癌非吸烟患者的早期临床疗效。方法:收集17例口服埃克替尼晚期肺腺癌非吸烟患者的临床资料,统计症状缓解时间、KPS评分变化、客观有效率、不良反应。结果:症状缓解时间4~10 d,KPS评分升高率为70.6%(12例),完全缓解率(CR)0%,部分缓解率(PR)为52.9%(9例),疾病稳定率(SD)为35.3%(6例),疾病进展率(PD)为11.8%(2例)。一线治疗9例,CR 0%,PR 66.7%(6例),SD 11.1%(1例),PD 22.2%(2例)。二线及以上治疗8例,CR 0%,PR37.5%(3例),SD 62.5%(5例),PD 0%(0例)。轻度皮肤干燥、皮疹、腹泻不良反应发生率分别为23.5%,11.8%,11.8%,均为轻度。结论:埃克替尼治疗晚期肺腺癌非吸烟患者疗效较好,一线治疗疗效显著,不良反应轻微。 展开更多
关键词 埃克替尼 非吸烟患者 表皮生长因子受体酪氨酸激酶抑制剂
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Clinical study on gefitinib combined with γ-ray stereotactic radiotherapy for senile patients with adenocarcinoma of lung as the first-line regimen
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作者 Dejian Pan Biao Wang +1 位作者 Xijian Zhou Donglin Wang 《The Chinese-German Journal of Clinical Oncology》 CAS 2011年第7期386-390,共5页
Objective: The aim of our study was to evaluate the efficacy and safety of gefitinib combined with γ-ray stereo-tactic radiotherapy for senile patients with adenocarcinoma of lung as the first-line regimen. Methods: ... Objective: The aim of our study was to evaluate the efficacy and safety of gefitinib combined with γ-ray stereo-tactic radiotherapy for senile patients with adenocarcinoma of lung as the first-line regimen. Methods: The 153 senile patients with adenocarcinoma of lung were divided into 4 groups according to the therapy method. Group A was the 35 patients treated with gefitinib combined with γ-ray stereotactic radiotherapy. Group B was the 45 patients treated with γ-ray stereotactic radio-therapy. Group C was the 42 patients treated with gefitinib. Group D was the 31 patients treated with best supportive therapy. The patients received gefitinib of 250 mg/d from the first day until disease progression or other reasons. The patients were treated with γ-ray stereotactic radiotherapy from the second day. Dose curve of this group of cases was 50%-80%. Encircled dose was 4.0-6.5 Gy per fraction and the range of total dose was 36-48 Gy. The total number of treatment was 8-12 and treated six times every week. Results: All the patients were examined by enhanced double helix CT at the second month. The tumor response rate (RR) of group A was 68.6% (24/35). Disease control rate (DCR) was 88.6% (31/35). The median survival time (MST) was 13.4 months (range 3-34 months ) and the progression-free survival (PFS) was 7.8 months. The overall 1-year survival rate was 40.0% (14/35). The main side effects included skin rash and diarrhea. The RR of group B was 51.1% (23/45). DCR was 71.1% (32/45). MST was 9.6 months (range, 3-18 months ) and PFS was 5.3 months. The overall 1-year survival rate was 15.6 % (7/45). The RR of group C was 40.5 % (17/42). DCR was 61.9% (26 /42). MST was 10.3 months (range, 3-26 months ) and PFS was 5.1 months. The overall 1-year survival rate was 35.7 % (15/42). The main side effects included skin rash and diarrhea. The MST of group D was 5.6 months (range, 2-11 months ) and PFS was 1.7 months. The overall 1-year survival rate was 0. The short-term therapeutic effects (RR) of group A was higher than group C (P = 0.014 < 0.05, χ2 = 6.053) but has no significant difference with group B (P = 0.116 > 0.05, χ2 = 2.477). The long-term therapeutic effects (overall 1-year survival rate) of group A was higher than group B (P = 0.014 < 0.05, χ2 = 6.077) but has no significant difference with group C (P = 0.642 > 0.05, χ2 = 0.216). Conclusion: Gefitinib combined with γ-ray stereotactic radiotherapy is feasible and effective for treatment in senile patients with adenocarcinoma of lung as the first-line regimen. 展开更多
关键词 GEFITINIB γ-ray stereotactic radiotherapy adenocarcinoma of lung SENILE first-line regimen
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Gefitinib combined with γ-ray stereotactic body radiation therapy has better efficacy than gefitinib alone for senile lung adenocarcinoma patients with EGFR mutations as first-line regimen
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作者 Dejian Pan Biao Wang +3 位作者 Weibing Wang Yuanwen Wu Xijian Zhou Donglin Wang 《The Chinese-German Journal of Clinical Oncology》 CAS 2014年第7期299-304,共6页
Objective: The senile lung adenocarcinoma patients harboring an activating epidermal growth factor receptor (EGFR) mutation shows good and rapid response to EGFR tyrosine kinase inhibitors (TKIs). Whether gefitin... Objective: The senile lung adenocarcinoma patients harboring an activating epidermal growth factor receptor (EGFR) mutation shows good and rapid response to EGFR tyrosine kinase inhibitors (TKIs). Whether gefitinib combined with y-ray stereotactic body radiation therapy has better efficacy than gefitinib alone for senile lung adenocarcinoma patients with EGFR mutations as first-line regimen is still under investigation. Methods: The 42 senile lung adenocarcinoma patients with EGFR mutations were divided into 2 groups according to the therapy method. Group A was the 22 patients treated with gefitinib combined with y-ray stereotactic body radiation therapy (SBRT). Group B was the 20 patients treated with gefitinib alone. All of the patients received gefitinib of 250 mg/d from the first day until disease progression or other reasons. The patients of Group A were treated with y-ray stereotactic body radiation therapy from the second day. Radiation fields included the primary lesions and the integration of lymph nodes. Dose curve of this group was 50%-80%. Encircled dose was 4.0-6.5 Gy per fraction and the range of total dose was 40-52 Gy. We treated the patients 8-12 times and treated five times every week. Results: All the patients were examined by enhanced double helix CT at the second month. The tumor response rate (RR) of group A was 81.8% (18/22). Disease control rate (DCR) was 90.9% (20/22). The median overall survival (OS) was 24.2 months (range 8-58 months ) and the progression-free survival (PFS) was 18.6 months. The overall 1-year survival rate was 72.3% (16/22) and 2-year survival rate was 54.5% (12/22). The main side effects included skin rash and diarrhea. The RR of group B was 50.0 % (10/20). DCR was 75.0% (15/20). OS was 17.4 months (range 6-32 months ) and PFS was 12.1 months. The overall 1-year survival rate was 60.0% (12/20) and 2-year survival rate was 40.0% (8/20). The main side effects included skin rash and diarrhea. The group A who were treated with gefitinib combined with y-ray stereotactic body radiation therapy had a higher short term therapeutic effects (RR) and long term therapeutic effects (OS) than group B who were treated with gefitinib alone respectively (81.8% vs 50.0%, P = 0.029 〈 0.05, x2 = 4.773 and 24.2 vs 17.4, P = 0.024 〈 0.05, X2 = 5.098). Conclu. sion: Gefitinib combined with y-ray stereotactic body radiation therapy has better efficacy than gefitinib alone for senile lung adenocarcinoma patients with EGFR mutations as first-line regimen. The side affects are acceptable. 展开更多
关键词 GEFITINIB y-ray stereotactic body radiation therapy (SBRT) epidermal growth factor receptor (EGFR) mutations SENILE first-line regimen
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