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Clinical effect of Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy in the treatment of brain metastasis of non-small cell lung cancer |
LI Wenge GE Wei |
Department of Oncology, Renmin Hospital of Wuhan University, Hubei Province, Wuhan 430060, China |
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Abstract Objective To investigate the short-term efficacy and safety of Icotinib Hydrochloride Tablets (Conmana) combined with whole-brain radiotherapy in the treatment of advanced non-small cell lung cancer with brain metastasis. Methods The clinical data of 142 patients with non-small cell lung cancer with brain metastasis admitted to the Renmin Hospital of Wuhan University from February 2013 to February 2016 were retrospectively analyzed. According to the treatment approaches, they were divided into 51 cases in the group of Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy, 51 cases in the group of Icotinib Hydrochloride Tablets and 40 cases in the group of whole-brain radiotherapy. In the Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy group, whole-brain radiotherapy was performed simultaneously with oral administration of Icotinib Hydrochloride Tablets. The radiotherapy dose was 40-50 Gy/20-25 F, and the radiotherapy was completed within one month. Icotinib Hydrochloride Tablets were taken orally once a day at the beginning of radiotherapy, and the dose was 125 mg, 3 times a day. In the Icotinib Hydrochloride Tablets group, one Icotinib Hydrochloride Tablet was taken orally every day at a dose of 125 mg, 3 times a day. The whole-brain radiotherapy group received a radiotherapy dose of 40-50 Gy/20-25 F. The radiotherapy was completed within one month. In the three groups, the drug of parients was discontinued until the disease progressed or an intolerable toxic reaction occurred, and the progression-free survival time was calculated from the start of treatment until the disease progressed. Chi-square test was used to analyze whether there were significant differences in objective response rate, disease control rate and incidence of adverse reactions among the three groups of patients, and Kaplan-Meier test was used to analyze whether there were significant differences in progression-free survival among the three groups of patients. Results The objective response rate and disease control rate of Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy group were higher than those of the Icotinib Hydrochloride Tablets group and the whole-brain radiotherapy group, the differences were statistically significant (all P < 0.05). There was no significant difference in the objective response rate and disease control rate between the Icotinib Hydrochloride Tablets group and the whole-brain radiotherapy group (P > 0.05). Median progression-free survival in the Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy group was higher than that in the Icotinib Hydrochloride Tablets group and higher than that in the whole-brain radiotherapy group, the differences were statistically significant (all P < 0.05). The median progression-free survival time of the Icotinib Hydrochloride Tablets group was not significantly different from that of the whole-brain radiotherapy group (P > 0.05). The one-year survival rate of Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy group was 66.7% higher than that of the Icotinib Hydrochloride Tablets group (41.2%) and the whole-brain radiotherapy group (37.5%), with statistically significant differences (all P < 0.05). There was no significant difference in the incidence of adverse reactions among the three groups of parients (P > 0.05). Conclusion Icotinib Hydrochloride Tablets combined with whole-brain radiotherapy can significantly improve the disease control rate and progression-free survival time of patients with tolerable adverse reactions.
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