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CHOP-VP_(16) 与 ProMACE-CytaBOM 方案治疗 NHL 疗效观察 被引量:1

Comparison Between Therapeutic Effects of CHOP-VP_(16)and ProMACE-CytaBOM Regimen in the Non-Hodgkin′s lymphoma
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摘要 分别采用CHOP-VP16方案对52例和ProMACE-CytaBOM方案对30例非霍奇金淋巴瘤(NHL)进行化疗,结果显示,CHOP-VP16方案组的完全缓解率为51.9%(27/52),总有效率为92.3%(48/52);ProMACE-CytaBOM方案组的完全缓解率为43.3%(13/30),总有效率为90.0%(27/30)。两组的完全缓解率及总有效率比较,无显著性差异(P>0.05)。两组的主要毒副反应是骨髓抑制,CHOP-VP16方案组和ProMACE-CytaBOM方案组的白细胞下降(Ⅰ~Ⅲ度)分别为82.7%(43/52)和83.3%(25/30),但均无Ⅳ度下降发生,均无与毒性有关的死亡发生。结果表明,CHOP-VP16方案治疗NHL可以达到ProMACE-CytaBOM方案相近的疗效,且使用方便,毒副反应较轻。 82 patients with intermediatehigh grade non-Hodgin′s lymphoma entered to this study.52 cases received CHOP-VP_(16) regimen,the complete remission rate was 51.9%(27/52),the overall response rate was 92.3%(48/52).30 cases received ProMACE-CytaBOM regimen,the complete remission rate was 43.3%(13/30),the overall response rate was 90.0%(27/30).There was no significant difference((P>0.05) in response rate between the two groups.The main toxicity were myelosuppression,the leukocytopenia rate was 82.7% in CHOP-VP_(16) and 83.3% in ProMACE-CytaBOM(P>0.05).No fatal toxicity was encountered in both groups.The results demonstrate that CHOP-VP_(16) regimen is similar to ProMACE-CytaBOM reigmen in the therapeutic effect.
机构地区 江西省肿瘤医院
出处 《实用癌症杂志》 1998年第3期215-217,共3页 The Practical Journal of Cancer
关键词 淋巴瘤 NHL 药物疗法 联合化疗 Non-Hodgkin′s lymphoma CHOP-VP_(16) regimen ProMACE-CytaBOM regimen
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  • 1团体著者,肿瘤,1985年,6卷,277页

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  • 1汪安兰,罗永忠,王肇炎.不同方案治疗中高度恶性非霍奇金淋巴瘤的临床探讨[J].中华肿瘤杂志,1997,19(3):215-217. 被引量:5
  • 2Monteserrat E,Garcia-Conde J,Vinolas N,et al. CHOP vs Promace-cytaBOM in the treatment ofaggressive nonHodgkin's lympkomas: long-term results of a multicenter randomized trial[J ]. Eur J Haematol, 1996,57:377.
  • 3Meller TP, Dahlberg S, Weick JK, et al. Unfavorable hisologies of non-Hodgkin's lymphoma treated with Promace-cytaBOM: a group wide southwest oncolgy group study[J ]. J Clin Oncol, 1990,8 (12) : 1951.
  • 4Federico M, Clo V, Brugiatelli M, et al. Efficacy of two different Promace-cytaBOM derived regimens in advanced aggressive non-Hodgkin's lymphoma. Final report of a multicenter trial condiucted by GISL[J ]. Haematologica, 1998,83: 800.

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