[Clinical research on recombinant human Ad-p53 injection combined with cisplatin in treatment of malignant pleural effusion induced by lung cancer].

Wei-Zhu Zhao, Ji-Kun Wang, Wei Li, Xiu-Li Zhang
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引用次数: 21

Abstract

Background and objective: p53 gene is one of cancer suppressor genes and its mutation and deletion induces almost all human cancers. This study was to evaluate the clinical efficacy and toxicity of recombinant human Ad-p53 injection (rAd-p53) combined with cisplatin in treatment of malignant pleural effusion induced by lung cancer.

Methods: A total of 35 cases of malignant pleural effusion were randomly divided into the combined group (n=17) and the single-agent group (n=18). On the basis of systemic treatment (vinorelbine 25 mg/m2, Days 1-8, every 3 weeks), the combined group were given intracavitary administration of rAd-p53 (1x1012 VP) and cisplatin (40 mg/m2) once a week for 4 weeks. The single-agent group were given the same intracavitary administration as the combined group but without rAd-p53 therapy.

Results: The total effective rates in the combined group and the single-agent group were 82.35% and 50.00% (P<0.05), respectively. The total modification rates in the combined group and the single-agent group were 64.70% and 33.33% (P<0.05), respectively. The toxicities in the two groups were fever, stethalgia, nausea/vomiting and leukopenia. The toxic reaction in combined group was mainly self-limited fever (P<0.05), which disappeared automatically after 36 h.

Conclusions: rAd-p53 and cisplatin is safe and effective for malignant pleural effusion induced by lung cancer. It is worthy of application in clinical treatment.

[重组人Ad-p53注射液联合顺铂治疗肺癌所致恶性胸腔积液的临床研究]。
背景与目的:p53基因是肿瘤抑制基因之一,其突变和缺失可诱发几乎所有人类癌症。本研究旨在评价重组人Ad-p53注射液联合顺铂治疗肺癌所致恶性胸腔积液的临床疗效及毒副作用。方法:35例恶性胸腔积液患者随机分为联合用药组(n=17)和单药组(n=18)。联合组患者在全身治疗(长春瑞滨25 mg/m2,第1-8天,每3周)的基础上,给予rAd-p53 (1 × 1012 VP)和顺铂(40 mg/m2)腔内治疗,每周1次,连用4周。单药组给予与联合组相同的腔内给药,但不进行rAd-p53治疗。结果:联合组和单药组的总有效率分别为82.35%和50.00%。结论:rAd-p53联合顺铂治疗肺癌所致恶性胸腔积液安全有效。值得在临床治疗中推广应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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