Weiss R B
Walter Reed Army Medical Center, Washington, DC.
Oncology (Williston Park). 1989 Jun;3(6):135-41; discussion 141-3, 147-8.
Mitoxantrone is an antitumor agent that was synthesized to try to develop a doxorubicinlike drug with a better therapeutic index. It has clinical activity for acute leukemias, breast carcinoma, non-Hodgkin's lymphoma, and ovarian cancers. There is some lack of cross-resistance to the anthracyclines. Its spectrum of toxicity is advantageous in that it causes less alopecia and can be administered for a slightly longer time than doxorubicin. For selected patients, mitoxantrone can be useful as a substitute for doxorubicin, but doxorubicin will remain the more widely used drug.
米托蒽醌是一种抗肿瘤药物,其合成目的是研发一种治疗指数更佳的类似阿霉素的药物。它对急性白血病、乳腺癌、非霍奇金淋巴瘤和卵巢癌具有临床活性。与蒽环类药物存在一定程度的交叉耐药性缺乏。其毒性谱具有优势,因为它导致脱发较少,且给药时间可比阿霉素稍长。对于特定患者,米托蒽醌可作为阿霉素的替代药物,但阿霉素仍将是使用更广泛的药物。