Nicoletto M O, Padrini R, Ferrazzi E, Nascimben O, Visonà E, Tumolo S, Palumbo M, Costa L, Vinante O, Monfardini S
Medical Oncology Division, Padova General Hospital, Italy.
Eur J Cancer. 1993;29A(9):1242-8. doi: 10.1016/0959-8049(93)90065-n.
36 previously treated patients (25 with anthracyclines) with advanced epithelial ovarian cancer have been treated with intraperitoneal (i.p.) mitoxantrone (M) at increasing doses. The response was evaluated through repeated laparoscopy with multiple biopsies and serial measurement of Ovarian Cancer Antigen 125 (CA 125); 11/36 patients had a complete (6 patients) or partial (5 patients) response. Toxicity (both local and general) was observed starting from 25 mg/m2 of M per cycle. The amount of drug reaching systemic circulation was monitored by measuring M plasma value after i.p. treatment. This study showed wide variations in serum levels obtained after i.p. doses ranging from 23 to 36 mg/m2. The area under the curve (AUC) of mitoxantrone plasma samples, did not correlate with the i.p. administered dose. Conversely, a correlation seems to exist between the plasma AUC and the responder status. Patients who showed clinical responses to i.p. treatment with mitoxantrone had AUCs and plasma peak levels of the drug that were significantly higher than those in non-responders (P = 0.03, Fisher's exact test).
36例先前接受过治疗的晚期上皮性卵巢癌患者(25例接受过蒽环类药物治疗)接受了递增剂量的腹腔内米托蒽醌(M)治疗。通过重复腹腔镜检查及多次活检和连续测量卵巢癌抗原125(CA 125)来评估疗效;36例患者中有11例获得完全缓解(6例)或部分缓解(5例)。从每个周期25mg/m²的M开始观察到毒性(局部和全身)。腹腔内治疗后通过测量M血浆值监测进入体循环的药物量。本研究显示腹腔内给予23至36mg/m²剂量后获得的血清水平差异很大。米托蒽醌血浆样本的曲线下面积(AUC)与腹腔内给药剂量无关。相反,血浆AUC与反应者状态之间似乎存在相关性。对腹腔内米托蒽醌治疗有临床反应的患者的药物AUC和血浆峰值水平显著高于无反应者(P = 0.03,Fisher精确检验)。