Kushner J P, Hansen V L, Hammar S P
Cancer. 1975 Nov;36(5):1577-84. doi: 10.1002/1097-0142(197511)36:5<1577::aid-cncr2820360507>3.0.co;2-b.
A 22-year-old man with a synovial cell sarcoma attained an excellent response to therapy with adriamycin (NSC-123127) and dimethyltriazeno imidazole carboxamide (NSC-45388). Therapy was discontinued at a cumulative dose of adriamycin of 600 mg/m2. Relapse occurred 13 1/2 months later, and therapy with adriamycin was restarted. Because of tumor progression, therapy was discontinued after a cumulative dose of adriamycin of 120 mg/m2. Ten weeks later, severe congestive heart failure developed which ultimately caused the patient's death. Exacerbations of the heart failure were temporally related to the administration of the antitumor antibiotics actinomycin-D (NSC-3053) and mithramycin (NSC-24559). Electron microscopic examination of the heart revealed changes characteristic of adriamycin cardiomyopathy. Thus, even after a long hiatus, it may not be safe to exceed the recommended maximum cumulative dose level of adriamycin. The pathogenic mechanisms involved in the development of adriamycin cardiomyopathy are reviewed, and the possible synergistic effect of other antitumor antibiotics is discussed.
一名患有滑膜肉瘤的22岁男性对阿霉素(NSC - 123127)和二甲三氮烯咪唑甲酰胺(NSC - 45388)治疗反应良好。当阿霉素累积剂量达到600 mg/m²时停止治疗。13个半月后复发,重新开始阿霉素治疗。由于肿瘤进展,在阿霉素累积剂量达到120 mg/m²后停止治疗。十周后,发生严重充血性心力衰竭,最终导致患者死亡。心力衰竭的加重在时间上与抗肿瘤抗生素放线菌素D(NSC - 3053)和光辉霉素(NSC - 24559)的使用有关。心脏的电子显微镜检查显示出阿霉素心肌病的特征性变化。因此,即使经过长时间的中断,超过阿霉素推荐的最大累积剂量水平可能也不安全。本文回顾了阿霉素心肌病发生的致病机制,并讨论了其他抗肿瘤抗生素可能的协同作用。