倪炜1 罗林1△ 左频1 袁红平1 李佳2 范耀东1.体外药物敏感实验为依据的恶性脑胶质瘤个体化化疗初步研究[J].现代生物医学进展英文版,2012,12(6):1075-1077. |
体外药物敏感实验为依据的恶性脑胶质瘤个体化化疗初步研究 |
Preliminary Study on Individualized Chemotherapy Based on DrugSensitivity and Resistance Assay in Patients with Malignant Glioma |
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DOI: |
中文关键词: 脑胶质瘤 药物敏感耐药性 化学药物治疗 |
英文关键词: Glioma Drug sensitivity and resistance Chemotherapy |
基金项目:云南省教育厅基金资助(06y132C) |
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中文摘要: |
目的:建立胶质瘤细胞体外原代培养模型,利用MTT 法进行体外药物敏感实验,为临床化疗方案的设计提供理论指导,实
施个体化化疗。方法:32 例术后病理证实为胶质瘤(WHO Ⅲ级)的新鲜标本,制备肿瘤单细胞悬液进行体外原代培养,与7 种抗肿
瘤药物在临床血浆峰值浓度(PPC)条件下作用72 小时,MTT 法标记存活的肿瘤细胞,用酶标仪检测光密度值(OD),计算出抑制
率(IR),检测不同肿瘤个体对化疗药物的敏感和耐药情况,从而指导临床个体化化疗方案的制定。另选取同期符合上述入选标准
的20 例间变型星形细胞瘤患者作为对照组,按照VM-26 加DDP 方案经验化疗,化疗4 个疗程结束后,复查影像学,按照WHO
肿瘤疗效评价标准评价治疗效果,分为稳定(SD),进展(PD),缓解(PR)。结果:32 例临床标本的原代培养及药敏试验,其PPC 下的
抑制率(IR%)>50%者,DDP 有20 例;VCR 有9 例;VM-26 有12 例;VP-16 有17 例;Procarbazine 有7 例;BCNU 有6 例;Taxol
有3 例;其敏感性依次为:DDP>VP-16>VM-26>VCR> Procarbazine>BCNU >Taxol。根据体外药物敏感实验结果制定个体化化疗
方案治疗29 例,肿瘤缓解率为47.2%,对照组为29.4%,2 组x2 检验统计P<0.05。结论:7 种常用的抗肿瘤药物均有耐药的情况,进
行化疗药物的敏感测定可以避免耐药药物的使用。根据体外药物敏感实验结果制定个体化化疗方案化疗与对照组相比近期疗效
较满意。 |
英文摘要: |
Objective: To establish neurogliocytoma cells ex-vitro primary culture model and carry out chemosensitivity experiment
by the MTT assay. To provide theory guidance for designing and optimizing clinical chemotherapy regimen, to practice individualization
chemotherapy. Methods: Using 32 fresh specimen which were proved to be neurogliocytoma (WHO grade 3) to produce monoplast
suspension and carry out vitro primary culture, add 7 antineoplastic drugs with peak plasma concentration to primary culture glioma
cells, after 72 hours measure the survival tumor cell with the MTT colorimetric assay, get the optical density and the inhibition ratio, then
judge the sensitiveness and drug fast of every drugs to every tumors, to guide the clinical individual Chemotherapy. Another 20 patients
with anaplastic glioma received VM-26 and DDP regimen chemotherapy. Radiology evaluation of 2 groups is done in the light of WHO
malignant tumor treatment effect assessment following 4 periodic of chemotherapy. Results: 32 clinical gliomas specimen were subject to
primary culture and susceptibility test. The rank of sensitivity from high to low is: DDP> VP-16> VM-26>VCR >procarbazine>BCNU>
paclitaxe. Based on the ex-vivo chemotherapy sensitivity and resistance assay, individualized chemotherapy is implemented in 29 patients.
Glioma remission ratio in individualized chemotherapy is 47.2%, in comparision with contral group the difference is significant.
Conclusion: MTT colorimetric assay is convenient,objective and simple method with good repeatability. Every one of 7 drugs commonly
used has the situation of drug resistance. Chemosensitivity assay can avoid using the resistant drugs and provide guidance to improve the
clinical chemotherapy effect. Individualized chemotherapy on the basis of vitro sensitivity and resistance assay for patients with malignant
glioma could improved treatment efficacy. |
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