Paccagnella A, Salvagno L, Chiarion-Sileni V, Bolzonella S, De Besi P, Frizzarin M, Pappagallo G L, Fosser V P, Fornasiero A, Segati R
Eur J Cancer Clin Oncol. 1986 Sep;22(9):1053-8. doi: 10.1016/0277-5379(86)90005-2.
Twenty-one patients with alkylator-resistant plasmacell neoplasms were treated with Peptichemio (PTC) at a dose of 40 mg/m2 for 3 days every 3 weeks or, in the case of persistent leukopenia and/or thrombocytopenia, at the single dose of 70 mg/m2 every 2-3 weeks according to haematological recovery. Seventeen patients, 10 with multiple myeloma and seven with extramedullary plasmacytoma (EMP), were fully evaluable. Six of 17 patients (35%) responded: three of seven EMP patients had a complete remission and 3 of 10 multiple myeloma patients had an objective response greater than 50%. The median duration of response was 8.5 months. An EMP patient obtained a complete response lasting for 16 months. The most frequent toxic effect were phlebosclerosis, occurring in all the patients, and myelosuppression, which was severe in only one case. PTC appears to be an active drug in patients with plasmacell neoplasms even if resistant to alkylating agents.
21例对烷化剂耐药的浆细胞肿瘤患者接受了派普他滨(PTC)治疗,剂量为40mg/m²,每3周连用3天;若出现持续性白细胞减少和/或血小板减少,则根据血液学恢复情况,每2 - 3周单剂量给予70mg/m²。17例患者可进行全面评估,其中10例为多发性骨髓瘤,7例为髓外浆细胞瘤(EMP)。17例患者中有6例(35%)有反应:7例EMP患者中有3例完全缓解,10例多发性骨髓瘤患者中有3例客观反应率大于50%。反应的中位持续时间为8.5个月。1例EMP患者获得了持续16个月的完全缓解。最常见的毒性反应是静脉硬化,所有患者均出现,骨髓抑制仅1例严重。PTC似乎是浆细胞肿瘤患者的一种有效药物,即使对烷化剂耐药。