首页> 中文期刊> 《中国全科医学》 >促红细胞生成素对晚期卵巢癌经紫杉醇化疗所致神经毒性损伤的保护作用研究

促红细胞生成素对晚期卵巢癌经紫杉醇化疗所致神经毒性损伤的保护作用研究

摘要

Objective To explore the role of erythropoietin( EPO)in neurovirulent damages( NVD)caused by pa-clitaxel chemotherapy in patients with advanced ovarian cancers( AOC). Methods A total of 124 Ⅲ-Ⅳ stage AOC patients admitted to Center Hospital of Xiangyang from February 2009 to March 2012 were divided,according to receiving EPO treatment or not,into groups early EPO,advanced EPO,non-EPO. FACT/GO-NTX questionnaire was used to evaluate the neuroviru-lence of 3 groups. The neurovirulence,time of NVD appearance,accumulated paclitaxel were compared among 3 groups. NVDs compared between patients with different grades of anemia in EPO group. Results The incidences of NVD of groups early EPO, advanced EPO,non-EPO were 24. 4%(10/41),42. 5%(17/40),53. 5%(23/43),respectively,the difference was significant(H=6. 862,P =0. 032). There was difference in incidences of different grades of NVD among 3 groups(P <0. 05). There was difference in NVD incidence between patients with different grades of anemia in early EPO group( u =-3. 810,P<0. 05). The earliest time of neurovirulence occurrence was longer in early EPO group〔(12. 3 ± 2. 2) weeks〕than in groups advanced EPO〔(10. 7 ±1. 6)weeks〕,non-EPO〔(7. 7 ±1. 2)weeks,P<0. 05〕. The mean paclitaxel dosage was(785. 3 ± 67. 5) mg in early EPO group at earliest time of neurovirulence occurrence,higher than in groups ad-vanced EPO〔(511. 6 ± 61. 7) mg〕,non-EPO〔(354. 2 ± 47. 5) mg,P<0. 05〕. Conclusion EPO can reduce the NVD caused by paclitaxel chemotherapy in Ⅲ-Ⅳ AOC patients. Early use of EPO is of more remarkable effects.%目的:探讨促红细胞生成素( EPO)对晚期(Ⅲ~Ⅳ期)卵巢癌经紫杉醇化疗后诱发的神经毒性损伤的保护作用。方法选取2009年2月-2012年3月襄阳市中心医院收治的Ⅲ~Ⅳ期卵巢癌患者124例,根据其是否接受EPO治疗及接受治疗的时间分为早期EPO组、晚期EPO组、非EPO组。根据癌症治疗功能评估/妇科肿瘤神经毒性问卷( FACT/GOG-NTX问卷)评分对3组患者行神经毒性评估。比较3组患者神经毒性分级、最早出现神经毒性损伤的时间以及累积紫杉醇用量;比较早期EPO组不同贫血分级患者的神经毒性损伤分级。结果3组患者神经毒性分级间差异有统计学意义( H=6.862,P=0.032)。早期EPO组不同贫血分级患者的神经毒性损伤分级间差异有统计学意义(u=-3.810,P <0.05)。早期 EPO 组发生神经毒性损伤最早时间〔(12.3±2.2)周〕长于晚期 EPO 组〔(10.7±1.6)周〕及非EPO组〔(7.7±1.2)周,P<0.05〕。早期EPO组最早发生神经毒性损伤时紫杉醇用量平均为(785.3±67.5) mg,高于晚期EPO组〔(511.6±61.7) mg〕及非EPO组〔(354.2±47.5) mg,P<0.05〕。结论 EPO能够有效减轻以紫杉醇为基础化疗的Ⅲ~Ⅳ期卵巢癌患者神经毒性,早期应用EPO效果更显著。

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