Hug V, Hortobagyi G N, Buzdar A U, Blumenschein G R, Grose W, Burgess M A, Bodey G P
Cancer. 1980 May 15;45(10):2524-8. doi: 10.1002/1097-0142(19800515)45:10<2524::aid-cncr2820451010>3.0.co;2-m.
A phase II trial of Peptichemio (PTC) was conducted on 56 patients with advanced breast cancer that had been resistant to treatment with cyclophosphamide. The overall response rate was 32%, with one complete remission, seven partial remissions, and ten instances of improved disease status. Soft tissue and bone lesions were the primary sites of response. The median duration of response was 11 weeks, with a range of 6--30 weeks. Major toxicities were myelosuppression, affecting predominantly the platelets, and sclerosing phlebitis. Myelosuppression was cumulative and thrombocytopenic bleeding was a likely contributing factor in the death of 2 patients. This trial showed that PTC is another alkylating agent with definite activity in the treatment of breast cancer. More importantly, it showed that cross-resistance with cyclophosphamide does not exist, at least in breast carcinoma.
对56例对环磷酰胺治疗耐药的晚期乳腺癌患者进行了甲氮咪胺(PTC)的II期试验。总缓解率为32%,其中1例完全缓解,7例部分缓解,10例疾病状态改善。软组织和骨病变是主要的缓解部位。缓解的中位持续时间为11周,范围为6 - 30周。主要毒性为骨髓抑制,主要影响血小板,以及硬化性静脉炎。骨髓抑制是累积性的,血小板减少性出血可能是2例患者死亡的一个促成因素。该试验表明,PTC是另一种在乳腺癌治疗中具有明确活性的烷化剂。更重要的是,它表明至少在乳腺癌中不存在与环磷酰胺的交叉耐药性。