鬼臼毒素新衍生物4′-去甲基幻鬼臼毒素9-(4,6-o-乙基- β -d -葡萄糖苷)的临床研究(NSC-141540;VP-16-213),实体瘤。

Cancer chemotherapy reports Pub Date : 1975-07-01
W Felix, H J Senn
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引用次数: 0

摘要

新合成的半合成鬼臼毒素4′-去甲基鬼臼毒素9-(4,6-o-乙基- β -d -glucopyranoside) (NSC-141540)对30例实体瘤进行了抗肿瘤活性和临床毒性试验。前两个疗程静脉给药(60mg /m2/天乘5次,每21天一次),后续疗程口服(60 ~ 120mg /m2/天乘5次,每21天一次)。该药主观上耐受性良好,但引起大量白细胞减少和脱发。它在燕麦细胞肺癌(11例患者中有8例有应答)和卵巢癌(6例患者中有-我们的应答)中显示出显著的活性。NSC-141540对这两种肿瘤具有宝贵的细胞抑制活性,值得进一步的临床试验,特别是在联合化疗中。
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Clinical study of the new podophyllotoxin derivative, 4'-demethylepipodophyllotoxin 9-(4,6-o-ethylidene- beta-D-glucopyranoside) (NSC-141540; VP-16-213), in solid tumors.

The new semisynthetic epipodophyllotoxin, 4'-demethylepipodophyllotoxin 9-(4,6-o-ethylidene- beta-D-glucopyranoside) (NSC-141540), was tested for antitumor activity against solid tumors and for clinical toxicity in 30 patients. The first two courses were given intravenously (60 mg/m2/day times 5, every 21 days), and subsequent courses were given orally (60-120 mg/m2/day times 5, every 21 days). The drug was subjectively well tolerated but induced considerable leukothrombocytopenia and alopecia. It demonstrated significant activity in oat cell carcinoma of the lung (eight responses out of 11 patients) and ovarian cancer (-our responses out of six patients). NSC-141540 has valuable cytostatic activity against these two tumors and warrants further clinical trials, especially in combination chemotherapy.

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