Levi J A, Diggs C H, Wiernik P H
Cancer. 1977 May;39(5):1967-70. doi: 10.1002/1097-0142(197705)39:5<1967::aid-cncr2820390509>3.0.co;2-2.
Thirteen patients with advanced mycosis fungoides received induction therapy with Adriamycin, 60/m2 I.V. repeated at 21-day intervals. Ten patients had extensive skin tumors; all patients had lymph node enlargement with mycosis fungoides involvement in eight; four patients had biopsy-proven visceral involvement. Only two patients had received no prior therapy. The overall response rate with Adriamycin therapy was 85% with three patients (23%) achieving a biopsy-proven complete remission and five patients (39%) partial remissions. The median number of courses to maximum response was two (range two to four). The principle toxicity was myelosuppression, but this was not severe and the entire group received more than 90% of the intended doses of Adriamycin. One patient developed probable Adriamycin cariotoxicity. Maintenance therapy for patients achieving a remission was methotrexate 15 mg/m2 I.M. twice weekly and cyclophosphamide 750 mg/m2 I.V. every 21 days. The median duration of complete remission was 32+ weeks (range 16+-40+ weeks) while the median duration of partial remission was 18 weeks (range 8-111+ weeks). Adriamycin has proven to be an effective induction agent in the treatment of advanced mycosis fungoides and its incorporation into combination chemotherapy regimens is warranted.
13例晚期蕈样肉芽肿患者接受阿霉素诱导治疗,剂量为60mg/m²静脉注射,每21天重复一次。10例患者有广泛的皮肤肿瘤;所有患者均有淋巴结肿大,其中8例有蕈样肉芽肿累及;4例经活检证实有内脏受累。只有2例患者此前未接受过治疗。阿霉素治疗的总体缓解率为85%,3例患者(23%)经活检证实达到完全缓解,5例患者(39%)部分缓解。达到最大缓解的疗程中位数为2个(范围为2至4个)。主要毒性是骨髓抑制,但并不严重,整个组接受的阿霉素剂量超过预期剂量的90%。1例患者出现可能的阿霉素心脏毒性。达到缓解的患者的维持治疗方案为甲氨蝶呤15mg/m²肌肉注射,每周两次,环磷酰胺750mg/m²静脉注射,每21天一次。完全缓解的中位持续时间为32+周(范围为16+-40+周),而部分缓解的中位持续时间为18周(范围为8-111+周)。阿霉素已被证明是治疗晚期蕈样肉芽肿的一种有效诱导药物,将其纳入联合化疗方案是有必要的。