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Mitozolomide (NSC 353451), a new active drug in the treatment of malignant melanoma. Phase II trial in patients with advanced disease.

机译:线粒体(NSC 353451),一种新的治疗恶性黑色素瘤的活性药物。晚期疾病患者的II期试验。

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摘要

A phase II trial with mitozolomide was carried out in patients with malignant melanoma, since in preclinical studies this new imidazotetrazine had shown promising effects against human melanoma xenografts. Twenty-one evaluable patients with advanced malignant melanoma were treated with 115 mg m-2 of mitozolomide, given orally every 6 weeks. None of the patients had received prior chemotherapy. Two partial responses (10 and 7+ months) were observed. The responding patients had lung metastases, and one of them had, in addition, a huge (17 X 14 cm) lymph node metastasis in the groin. Also, one patient had a 48% tumour volume reduction of lung metastases. The dose limiting side effect of the treatment was bone marrow depression, with delayed leukopenia and thrombocytopenia. The median white blood cell counts and platelet nadirs were 2.5 X 10(9) 1(-1) (range 1.1-3.8) and 59 X 10(9) 1(-1) (range 14-95), respectively. Non-haematological adverse reactions were limited to mild or moderate nausea. It is concluded that orally administered mitozolomide is active against malignant melanoma and seems to have a response rate comparable to those of the most active established drugs.
机译:在恶性黑色素瘤患者中进行了线粒体II期试验,因为在临床前研究中,这种新的咪唑并四嗪已显示出对人类黑色素瘤异种移植物的有希望的作用。 21例可评估的晚期恶性黑色素瘤患者接受了115 mg m-2的咪唑唑胺治疗,每6周口服一次。所有患者均未接受过化疗。观察到两个部分反应(10和7个月以上)。有反应的患者有肺转移,其中一名在腹股沟处有巨大的(17 X 14 cm)淋巴结转移。另外,一名患者的肺转移瘤体积减少了48%。该治疗的剂量限制副作用是骨髓抑制,白细胞减少症和血小板减少症的延迟。中位数白细胞计数和血小板最低点分别为2.5 X 10(9)1(-1)(范围1.1-3.8)和59 X 10(9)1(-1)(范围14-95)。非血液学不良反应仅限于轻度或中度恶心。结论是,口服施用的线粒体对恶性黑色素瘤具有活性,并且其响应率似乎与最活跃的既定药物相当。

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