含米托蒽醌方案治疗恶性肿瘤97例的近期疗效与毒性  被引量:3

Effect and Toxicity of Mitoxantrone Contained Regimen irl the Treatment of Malignancies

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作  者:翁方纪 马菊颖[2] 朱松英 陈唤青[4] 毛玉文 龚皓 龚振夏[7] 蔡浩[2] 

机构地区:[1]浙江省德清县第一医院,德清县313200 [2]浙江省肿瘤医院 [3]117医院 [4]南通医学院附院 [5]无锡市一院 [6]武汉市一院 [7]南通肿瘤医院

出  处:《中国肿瘤临床》1993年第11期861-864,共4页Chinese Journal of Clinical Oncology

摘  要:本文采用含Mx方案治疗恶性肿瘤97例,完全缓解27例,部分缓解30例,总有效率58.7%。其中急性白血病44例有效率63.6%,ALL69.2%(9/13),AML67.8%(19/28)。实体瘤有效率54.7%,恶性淋巴瘤 75%(12/16),乳癌 47%(8/17),肺癌 40%(6/15)。Mx的血液毒性较重,白细胞,血小板,血红蛋白减少发生率分别为69%,27%与47.4%。非血液毒性较轻,Ⅰ-Ⅱ°居多,未见严重心脏毒性与不可逆的毒性反应。提示Mx为一强效、广谱抗肿瘤药物。A Mitoxantrone contained regimen was und in treating 97 cases of malignant tumors and achieved an overall responsive rate of 58.7% with 27% CRs and 30 PRs. The RRs were 63. 6% for acute leukemias and 54.7%for solid tumors. In cases of malignant lymphoma, breast cancers and lung cancers the respective responsive rates were 25%, 47%and 40%in that order. Haematologic side effects were considerably noteworthy with declining of leucocyte, platelet and hemoglobin in 69%, 27% and 47. 4 % respectively. Whereas non-hemotologic side effects were mild, with Ⅰ°- Ⅱ° prevailing, and no serious heart toxicity nor irreversible adverse reactions were encountered. In consequence mitoxantrone is a higher potent anticancer agent with broad spectrum of target tumors.

关 键 词:米托蒽醌 肿瘤 毒性  

分 类 号:R730.53[医药卫生—肿瘤]

 

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