Muss H B, Bundy B N, Christopherson W A
Department of Medicine, Bowman Gray School of Medicine of Wake Forest University, Winston-Salem, North Carolina.
Am J Clin Oncol. 1989 Apr;12(2):142-4. doi: 10.1097/00000421-198904000-00011.
Nineteen evaluable patients with advanced carcinoma of the vulva or vagina were treated with mitoxantrone, 12 mg/m2, every 3 weeks. All patients had good performance status and measurable disease and only nine had received prior chemotherapy. No complete or partial responses were noted. The major toxicity was myelosuppression; other toxicity was mild, and no cardiac toxicity or drug deaths occurred. The median progression-free interval was 1.3 months for patients with vulvar cancer and 1.6 months for patients with vaginal cancer. Median survival was 3.2 months for patients with vulvar cancer and 2.7 months for patients with vaginal cancer. Mitoxantrone displays no activity in patients with advanced carcinoma of the vulva or vagina.
19例可评估的晚期外阴癌或阴道癌患者接受了米托蒽醌治疗,剂量为12mg/m²,每3周一次。所有患者的身体状况良好且疾病可测量,只有9例曾接受过化疗。未观察到完全缓解或部分缓解。主要毒性为骨髓抑制;其他毒性较轻,未发生心脏毒性或药物相关死亡。外阴癌患者的无进展生存期(PFS)中位数为1.3个月,阴道癌患者为1.6个月。外阴癌患者的中位生存期为3.2个月,阴道癌患者为2.7个月。米托蒽醌对晚期外阴癌或阴道癌患者无活性。