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Drug resistance analysis of gefitinib-targeted therapy in non-small cell lung cancer

机译:吉非替尼靶向治疗非小细胞肺癌的耐药性分析

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The aim of the study was to examine the drug resistance analysis of gefitinib-targeted therapy in non-small cell lung cancer (NSCLC). In total, 156 NSCLC patients without surgical treatment were selected, including 117 cases of adenocarcinoma (75%), to receive single gefitinib 0.25 g/day or combined with platinum chemotherapy. Computed tomography was used to evaluate tumor growth for the response and non-response groups. The chemotherapy regimen was changed or combined with radiotherapy in the non-response group. Tumor progression or metastasis in the response group was considered as the generation of drug resistance. The chemotherapy regimen was altered in the response group. Eleven cases had tumor response in the non-response group after the chemotherapy regimen was adjusted (20%), 33 cases had complete response (CR) (32.7%), 44 cases had partial response (PR) (43.6%), and 24 cases had stable disease (SD) (23.8%) in the response group. The drug resistance rates of CR, PR, and SD showed no significant difference (P>0.05). However, the drug-resistant time of CR was significantly delayed and the difference was statistically significant (P<0.05). The response rates of CR, PR, and SD patients regaining the response rate showed no statistical significance after the chemotherapy regimen was adjusted, and the difference was not statistically significant (P>0.05). In conclusion, gefitinib-targeted therapy in NSCLC showed certain drug resistance, which may not be related to the response.
机译:这项研究的目的是检查针对非小细胞肺癌(NSCLC)的吉非替尼靶向治疗的耐药性分析。总共选择了156例未经手术治疗的NSCLC患者,包括117例腺癌(75%),接受单次0.25 g /天的吉非替尼或联合铂化疗。计算机断层扫描用于评估反应和非反应组的肿瘤生长。无反应组改变化疗方案或联合放疗。应答组中的肿瘤进展或转移被认为是耐药性的产生。反应组改变了化疗方案。调整化疗方案后无反应组中有11例肿瘤反应(20%),完全反应(CR)(33.7%)33例,部分反应(PR)(43.6%)44例和24例应答组中有稳定疾病(SD)的病例(23.8%)。 CR,PR和SD的耐药率差异无统计学意义(P> 0.05)。但是,CR的耐药时间显着延迟,差异有统计学意义(P <0.05)。调整化疗方案后,CR,PR和SD患者恢复缓解率的反应率无统计学意义,差异无统计学意义(P> 0.05)。总之,以吉非替尼为靶点的非小细胞肺癌治疗显示出一定的耐药性,这可能与反应无关。

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