Mattsson W, Borgström S, Landberg T
Clin Ther. 1982;5(2):193-203.
A phase II study of weekly low-dose doxorubicin (6 to 12 mg/m2) showed it to be an effective, well-tolerated therapy in advanced breast cancer. Although most of the 34 patients studied had been clinically resistant to previous endocrine measures and/or other kinds of chemotherapy, had a median score of 60 on Karnofsky's index, and had predominantly visceral metastases, an objective response was obtained in 20 of 34 patients (four complete remissions, 16 partial remissions) for a median duration of 12+ months. Ten patients experienced no change in their condition for three to 12 months (median, six months). Eight of the 17 patients who had myelosuppression at the beginning of the study had an objective response lasting 4+ to 27+ months (median, 11 months). Eleven of the patients had previously received 500 or more mg/m2 of doxorubicin and were retreated with additional doses of doxorubicin (median cumulative dose, 800 mg/m2) without any clinical signs of toxicity.
一项关于每周低剂量阿霉素(6至12毫克/平方米)的II期研究表明,它在晚期乳腺癌中是一种有效且耐受性良好的治疗方法。尽管所研究的34例患者中大多数对先前的内分泌治疗措施和/或其他类型的化疗具有临床耐药性,卡氏评分中位数为60,且主要有内脏转移,但34例患者中有20例获得了客观缓解(4例完全缓解,16例部分缓解),中位缓解持续时间为12个多月。10例患者病情在3至12个月内无变化(中位时间为6个月)。在研究开始时出现骨髓抑制的17例患者中,有8例获得了持续4个多月至27个多月的客观缓解(中位时间为11个月)。11例患者先前已接受过500毫克/平方米或更多剂量的阿霉素治疗,此次再次接受额外剂量的阿霉素治疗(中位累积剂量为800毫克/平方米),未出现任何临床毒性迹象。