Gotoh T, Tanaka Y, Fujita Y, Hiramori N, Fujii T, Arimoto T, Iwasaki Y, Fukabori T, Nakamura T, Ono N, Nakagawa M
Second Department of Medicine, Kyoto Prefectural University of Medicine.
Jpn J Clin Oncol. 1996 Oct;26(5):328-34. doi: 10.1093/oxfordjournals.jjco.a023241.
Pirarubicin (4'-O-tetrahydropyranyladriamycin), a new anthracyline derivative, was administered as a single agent into the pleural cavity of 42 patients (total 46 courses) with malignant pleural effusion at a dose of 20, 40, 60 or 80 mg/body. All 46 courses were evaluable for non-hematological toxicities. Fever and chest pain (> or = WHO grade 2) were seen in 67.4% and 13.0% of courses, respectively. Patients receiving a dose of 80 mg/body developed fever of > or = 39 degrees C in 45.5%, and chest pain lasting more than three days and requiring pentazocine more than three times in 36.4%. In contrast, patients receiving a dose of < or = 60 mg/body presented these toxicities in only 8.6% and 2.9%, respectively. Nausea-vomiting (> or = WHO grade 2) was observed in only 4.3% of the total 46 courses and alopecia was not observed. Thirty-eight courses (36 patients) were evaluable for hematological toxicities. Myelosuppression (leukocyte nadir count < or = 1900, WHO grade 3 or 4) was seen in four courses (10.5%), and thrombocytopenia (< or = 49,000, WHO grade 3 or 4) in only two (5.3%). Although the mean AUC (0-24) for pirarubicin in plasma during the four courses that produced myelosuppression was significantly higher than that during the 11 courses without myelosuppression, the difference in the mean dose was not significant. Furthermore, no significant correlation was shown between dose (mg/m2) and AUC in plasma. It is considered that myelosuppression is not a dose-related toxicity at a dose of 20-80 mg/body. The dose-limiting toxicity was fever or chest pain, although unexpected myelosuppression was also encountered. The maximum tolerated dose was 80 mg/body. With regard to clinical efficacy, the overall response rate was 73.7% in 38 evaluable courses (38 patients). The mean T(1/2) of pirarubicin concentration in pleural effusion and plasma was 22.1 h and 8.8 h, respectively. We recommend a dose of 40 or 60 mg/body pirarubicin for this pleurodesic treatment.
吡柔比星(4'-O-四氢吡喃阿霉素)是一种新的蒽环类衍生物,作为单一药物以20、40、60或80mg/体的剂量注入42例恶性胸腔积液患者的胸腔(共46个疗程)。所有46个疗程均可评估非血液学毒性。发热和胸痛(≥WHO 2级)分别见于67.4%和13.0%的疗程。接受80mg/体剂量的患者中,45.5%出现≥39℃的发热,36.4%出现持续超过三天且需要喷他佐辛超过三次的胸痛。相比之下,接受≤60mg/体剂量的患者中,这些毒性分别仅为8.6%和2.9%。恶心呕吐(≥WHO 2级)仅在46个疗程中的4.3%观察到,未观察到脱发。38个疗程(36例患者)可评估血液学毒性。骨髓抑制(白细胞最低点计数≤1900,WHO 3级或4级)见于4个疗程(10.5%),血小板减少(≤49,000,WHO 3级或4级)仅见于2个疗程(5.3%)。虽然产生骨髓抑制的4个疗程中吡柔比星血浆平均AUC(0 - 24)显著高于无骨髓抑制的11个疗程,但平均剂量差异无统计学意义。此外,剂量(mg/m2)与血浆AUC之间未显示显著相关性。认为在20 - 80mg/体剂量下骨髓抑制不是剂量相关毒性。剂量限制性毒性是发热或胸痛,尽管也遇到了意外的骨髓抑制。最大耐受剂量为80mg/体。关于临床疗效,38个可评估疗程(38例患者)的总缓解率为73.7%。胸腔积液和血浆中吡柔比星浓度的平均T(1/2)分别为22.1小时和8.8小时。我们推荐吡柔比星40或60mg/体的剂量用于这种胸膜固定治疗。