Yamada K, Shirakawa S, Ohno R, Yamada H, Hirota Y, Ohara K, Yamagata K, Kobayashi M, Hirano M, Ikeda Y
Department of Internal Medicine, Branch Hospital, University of Nagoya, Japan.
Invest New Drugs. 1987;5(3):299-305. doi: 10.1007/BF00175302.
A phase II study of new anthracycline, THP, was conducted in 46 patients with hematological malignancies in a cooperative study. THP was given intravenously either at a dose of 13-34 mg/m2 for 3-5 consecutive days or 35-50 mg/m2 at 3-4 week intervals. Of 21 patients with acute leukemia, complete response (CR) was observed in 3 patients and partial response (PR) in 4. Of 22 patients with malignant lymphoma, CR was observed in 2 and PR in 6. The predominant toxicity was myelosuppression. Leukopenia was noted in 73% of patients and thrombocytopenia in 14%. Anorexia, nausea and vomiting were observed in 49%, 26% and 23%, respectively. Alopecia and acute cardiac toxicities were mild and recovered quickly on discontinuation of THP. Thus, THP was found to be effective for acute leukemia and malignant lymphoma.
在一项合作研究中,对46例血液系统恶性肿瘤患者进行了新型蒽环类药物吡柔比星(THP)的II期研究。THP通过静脉注射给药,剂量为13 - 34mg/m²,连续3 - 5天,或35 - 50mg/m²,每3 - 4周一次。21例急性白血病患者中,3例达到完全缓解(CR),4例部分缓解(PR)。22例恶性淋巴瘤患者中,2例CR,6例PR。主要毒性为骨髓抑制。73%的患者出现白细胞减少,14%出现血小板减少。厌食、恶心和呕吐的发生率分别为49%、26%和23%。脱发和急性心脏毒性较轻,停用THP后恢复迅速。因此,发现THP对急性白血病和恶性淋巴瘤有效。