出 处:《临床肺科杂志》2019年第5期890-895,共6页Journal of Clinical Pulmonary Medicine
基 金:沧州市重点研发计划指导项目(No 172302176)
摘 要:目的探究射频消融术治疗EGFR-TKIs耐药的非小细胞肺癌患者的疗效及对预后的影响。方法选择2012年6月至2016年6月我院救治的105例非小细胞肺癌患者作为研究对象,最终将符合实验设计的88例非小细胞肺癌患者纳入本次研究。根据EGFR-TKIs耐药后治疗方式不同,将88例非小细胞肺癌患者分为2组,即射频消融组(46例)和化疗组(42例)。比较两组患者治疗后客观有效率、不良反应和并发症发生率。随访3年,比较两组患者生存率,并对影响患者预后的因素进行生存分析。结果射频消融组和化疗组患者患者治疗后客观有效率分别为95.65%(44/46)和78.57%(33/42),差异有统计学意义(P<0.05)。15例(32.61%)患者射频消融治疗后出现咯血,5例(10.87%)发生胸痛,7例(15.22%)气紧,6例(13.04%)发生气胸。37例(88.10%)患者化疗后出现骨髓抑制,43例(100.00%)患者化疗后均有不同程度消化道反应。射频消融组患者1a、2a、3a无瘤生存率分别为47.83%(22/46)、30.43%(14/46)和17.39%(8/46);化疗组患者1a、2a、3a无瘤生存率分别为35.71%(15/42)、16.67%(7/42)和4.76%(2/42)。两组患者1a、2a、3a无瘤生存率比较,差异不具统计学意义(P>0.05)。射频消融组患者1a、2a、3a总生存率分别为67.39%(31/46)、36.96%(17/46)和17.39%(8/46);化疗组患者1a、2a、3a无瘤生存率分别为64.29%(27/42)、33.33%(14/42)和9.52%(4/42)。两组患者1a、2a、3a总生存率比较,差异不具统计学意义(P>0.05)。单因素分析结果显示TNM分期、淋巴结转移、ECOG评分和肿瘤直径与非小细胞肺癌患者无瘤生存时间和总生存时间均有关。多因素Cox回归分析结果显示TNM分期、淋巴结转移和ECOG评分是非小细胞肺癌患者无瘤生存时间的独立危险因素;TNM分期、淋巴结转移、ECOG评分和肿瘤直径是非小细胞肺癌患者总生存时间的独立危险因素。结论射频消融可抑制非小细胞肺癌患者EGFR-TKIs耐药后肿瘤局部进展,提�Objective To investigate the efficacy and prognosis of patients with non-small cell lung cancer treated with radio-frequency ablation for EGFR-TKIs resistant. Methods 105 patients with non-small cell lung cancer treated in our hospital from June 2012 to June 2016 were selected as the research subjects, and 88 cases of non small cell lung cancer patients were included in this study. According to the different treatment modalities after EGFR-TKIs resistance, 88 patients with non-small cell lung cancer were divided into 2 groups, the radio-frequency ablation group (46 cases) and the chemotherapy group (42 cases). Objective efficiency, adverse reactions and incidence of complications were compared between the two groups after treatment. During 3-year follow-up, their survival rates of the two groups were compared, and survival factors were analyzed. Results The objective effective rate of the radiofrequency ablation group and the chemotherapy group was 95.65%(44/46) and 78.57%(33/42) respectively ( P< 0.05). 15 cases (32.61%) had hemoptysis after radiofrequency ablation, 5 cases (10.87%) developed chest pain, 7 cases (15.22%) were tightened, 6 cases (13.04%) had pneumothorax, 37 patients (88.10%) developed myelosuppression after chemotherapy, and 43 patients (100%) had varying degrees of digestive tract reactions after chemotherapy. The tumor free survival rates of 1a, 2a and 3a in the radio-frequency ablation group were 47.83%(22/46), 30.43%(14/46) and 17.39%(8/46), respectively. The tumor free survival rates of 1a, 2a and 3a were 35.71%(15/42), 16.67%(7/42) and 4.76%(2/42) in the chemotherapy group. There was no significant difference in the 1a, 2a and 3a tumor free survival rates between the two groups ( P> 0.05). The total survival rates of 1a, 2a and 3a in the radio-frequency ablation group were 67.39%(31/46), 36.96%(17/46) and 17.39%(8/46), respectively. The survival rates of 1a, 2a and 3a were 64.29%(27/42), 33.33%(14/42) and 9.52%(4/42) in the chemotherapy group. There was no significant difference in the ove
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