期刊文献+

PEA方案与5-Fu+KSM方案治疗妊娠滋养细胞肿瘤疗效比较 被引量:8

The clinical comparison of effects of PEA regimen and 5- Fu + KSM regimen for treatment of gestational trophoblastic neoplasms
原文传递
导出
摘要 目的 探讨PEA方案是否可以作为妊娠滋养细胞肿瘤联合化疗一线选择。方法 回顾性分析中国医科大学附属盛京医院2004年7月至2013年5月62例妊娠滋养细胞肿瘤患者,评价顺铂+足叶乙甙+更生霉素(PEA方案,30例)与氟尿嘧啶+更生霉素(5-Fu+KSM,32例)方案的疗效和毒副反应。结果 PEA方案治疗妊娠滋养细胞肿瘤完全缓解率为93.33%,高于5-Fu+KSM方案组(90.63%)(P〉0.05)。副反应PEA组Ⅲ~Ⅳ度粒细胞减少、口腔溃疡和腹泻情况明显少于5-Fu+KSM组,差异有统计学意义(P〈0.05)。PEA组恶心呕吐和肝功能损伤的发生率及严重程度均低于5-Fu+KSM组(P〉0.05)。结论 两方案治疗妊娠滋养细胞肿瘤疗效相当,PEA方案副反应小、疗程短、费用少,可以作为妊娠滋养细胞肿瘤联合化疗一线选择之一。 Objective To explore whether the PEA regimen can be used as the first-line chemotherapy drug for gesta- tional trophoblastic neoplasms.Methods Retrospectively analyze 62 cases of gestational trophoblastic neoplasms from July 2004 to May 2013 in our hospital. Compare the treatment efficacy and side effects of these two regimens. Results The effective rate of PEA regimen for the treatment of gestational trophoblastic neoplasms was 93.33%,higher than that of 5-Fu+KSM regimen,but it has no significant difference (P〉0.05). In the aspect of the side effects, Ⅲ~Ⅳ leukopenia, oral cavity ulcer and diarrhea of PEA group were less than those of 52Fu + KSM group,being of significant difference (P〈O.05). In the aspect of nausea, vomiting and liver function damage, the occurrence rate in PEA group was lower than that in 5-Fu + KSM group,but it was of no significant difference (P〉O.O5).Conclusion Two regimens have the same effect, but PEA regimen has fewer side effects, shorter duration of average hospital stay and less treatment cost, which can be used as first-line chemotherapy drug for gestational trophoblastic neoplasms.
出处 《中国实用妇科与产科杂志》 CAS CSCD 北大核心 2014年第9期725-728,共4页 Chinese Journal of Practical Gynecology and Obstetrics
关键词 妊娠滋养细胞肿瘤 顺铂 足叶乙甙 更生霉素 氟尿嘧啶 gestational trophoblastic neoplasms DDP VP 16 KSM 5-Fu
  • 相关文献

参考文献10

  • 1Li MC, Hertz R, Spencer DB. Effects of methotrexate therapy upon choriocarcinoma and chorioadenoma[J].Proc Soc Exp Biol Med,1956,93(2):361-366. 被引量:1
  • 2Kohorn EI.The new FIGO 2000 staging and risk factor scoring system for gestational trophoblastic disease: description and critical assessment[J].Int J Gynecol Cancer,2001,11 (1):73-77. 被引量:1
  • 3Ngan HY.The practicability of FIGO 2000 staging for gestational trophoblastic neoplasia [J].Int J Gynecol Cancer,2004,14(2):202-205. 被引量:1
  • 4曹泽毅.中华妇产科学[M].2版.北京:人民卫生出版社,2004:2163-2169. 被引量:621
  • 5孙燕,周际昌.临床肿瘤内科手册[M].4版.北京:人民卫生出版社,2003:568-569. 被引量:130
  • 6Alazzam M, Tidy J, Hancock BW, et al . First-line chemotherapy in low-risk gestational trophoblastic neoplasia[J].Cochrane Database Syst Rev,2012,11(7):CD007102. 被引量:1
  • 7Cavoretto P,Gentile C,Mangili G,et al. Transvaginal ultrasound predicts delayed response to chemotherapy and drug resistance in stage I low-risk trophoblastic neoplasia[J].Ultrasound Obstet Gynecol,2012,40(1):99-105. 被引量:1
  • 8Chapman-Davis E, Hoekstra AV, Rademaker AW, et al .Treatment of nonmetastatic and metastatic low-risk gestational trophoblastic neoplasia:factors associated with resistance to single-agent methotrexate chemotherapy[J].Gynecol Oncol ,2012 ,125(3):572-575. 被引量:1
  • 9杨焯,钱建华.低危型妊娠滋养细胞肿瘤耐药高危因素探讨[J].中国实用妇科与产科杂志,2011,27(7):526-529. 被引量:11
  • 10Lurain JR,Nejad B.Secondary chemotherapy for high-risk gestational trophoblastic neoplasia [J].Gynecol Oncol,2005,97(2):618-623. 被引量:1

二级参考文献9

  • 1Moodley M, Tunkyi KMo, Odley J. gestational trophoblastic syn- drome : an audit of 112 patients. A south African experience [ J ]. Gynecol Cancer,2003,13 ( 2 ) :234-239. 被引量:1
  • 2Soper JH,Mntch DG. Diagnosis and treatment of gestational ttro- phoblastic disease. ACOG Pratic Bullentin NO. 53 [ J]. Obstet Gyneco1,2004,93 ( 3 ) :575-585. 被引量:1
  • 3Lurain JR. Pharmacotherapy of gestational trophoblastic disease [ J ]. Expert Opin Pharmacother, 2003,4 ( 11 ) : 2005-2017. 被引量:1
  • 4Lurain JR, Eifstand EP. Single-agent methotrexate chemotherapy for the treatement of nonmetastic gestational trophoblastic tumors [J]. Am J Obset Gynecol, 1995,172:574-579. 被引量:1
  • 5Gillespie AM, Kumar S, Hancock BW. Treatment of persis-tent tropholastic disease later than 6 months after diagnosis of molar pregnancy [J]. Br J Cancer,2000,82 : 1393-1395. 被引量:1
  • 6Berkowitz RS, Goldstein DP. Gestational trophoblastic disease// Berek JS, Adashi EY, Hillard PA. Novak' s Gynecol-ogy [ M ]. 12th ed. Canada: WiUiams & Wilkins,2000 : 1261-1252. 被引量:1
  • 7Abrao RA,de Andrade JM,Tiezzi DG, et al. Treatment for low- risk gestational trophoblastic disease:comparison of single-agent methotrxate, dactinomycin and combination regimens [ J ]. Gy- necol 0ncol,2008,108 ( 1 ) : 149-153. 被引量:1
  • 8Mao Y,Wan X,Lv W,et al. Relapsed or refractory gestational trophoblastic neoplasia treated with the etoposide and cisplatin/ etoposide, methotrexate, and actionmycin D (EP-EMA) regimen [J]. Gynecol Obstet,2007,98( 1 ) :44-47. 被引量:1
  • 9杨秀玉 向阳 宋鸿钊.耐药及危重绒癌病例治疗的研究[A]..中国医学科学院中国协和医科大学年鉴[C].,2000.78-80. 被引量:2

共引文献759

同被引文献65

引证文献8

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部