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长春地辛与泼尼松用于儿童急性淋巴细胞白血病的诱导缓解治疗

Vindesine and prednisone for remission induction in children with acute lymphocytic leukemia.

作者信息

Vats T S, Mehta P, Trueworthy R C, Smith S D, Klopovich P

出版信息

Cancer. 1981 Jun 15;47(12):2789-92. doi: 10.1002/1097-0142(19810615)47:12<2789::aid-cncr2820471205>3.0.co;2-x.

Abstract

Vinca alkaloids are effective anticancer agents. Vindesine is a recent vinca alkaloid derivative with anti-tumor effects shown in in vitro systems and in patients with acute lymphocytic leukemia (ALL). The present study was designed to investigate the therapeutic effectiveness and toxicity of vindesine in combination with prednisone for remission induction in late stage ALL in children. Sixteen children with late-stage ALL were treated with vindesine 4.0 mg/m2/week intravenously and prednisone 60 mg/m2/day orally in four divided doses for minimum of three weeks. Thirteen children were evaluable. Of these patients, four had complete remission and four had partial response. Toxicity was well tolerated and consisted of bone pain, paresthesias, loss of deep tendon reflexes, leukopenia, and thrombocytopenia primarily. Abnormal liver function tests and fever were also noted in some patients. All patients had received vincristine and prednisone prior to vindesine prednisone combination. All patients had been resistant to vincristine prednisone combination prior to vindesine prednisone treatment. This study suggests effectiveness of vindesine in late stage ALL and lack of cross-resistance of vindesine and vincristine.

摘要

长春花生物碱是有效的抗癌药物。长春地辛是一种新的长春花生物碱衍生物,在体外系统和急性淋巴细胞白血病(ALL)患者中显示出抗肿瘤作用。本研究旨在探讨长春地辛联合泼尼松诱导晚期儿童ALL缓解的治疗效果和毒性。16例晚期ALL患儿接受长春地辛4.0mg/m²/周静脉注射,泼尼松60mg/m²/天口服,分4次给药,至少3周。13例患儿可评估。其中,4例完全缓解,4例部分缓解。毒性耐受性良好,主要包括骨痛、感觉异常、深腱反射消失、白细胞减少和血小板减少。部分患者还出现肝功能检查异常和发热。所有患者在接受长春地辛联合泼尼松治疗前均接受过长春新碱和泼尼松治疗。所有患者在长春地辛联合泼尼松治疗前对长春新碱联合泼尼松耐药。本研究表明长春地辛对晚期ALL有效,且长春地辛与长春新碱不存在交叉耐药。

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