Niitsu N, Iijima K, Chizuka A
First Department of Internal Medicine, Toho University School of Medicine, Japan.
Ann Hematol. 2001 Jul;80(7):411-6. doi: 10.1007/s002770100313.
Irinotecan hydrochloride (CPT-11) is a topoisomerase I inhibitor with a broad antitumor spectrum. In the present study, we combined CPT-1 and mitoxantrone (MIT) with dexamethasone because the effect elicited by this combination was additive or better in a preclinical study. This study was performed to determine the efficacy and toxicities of this combination. Thirty-two patients were evaluable. CPT-11 combined with MIT achieved a complete remission in 11 patients (34.4%) and a partial remission in 9 patients (28.1%). The median follow-up period was 20 months. The 4-year survival rate was 31.8% (95% confidence intervals: 11.2-64.6%), and the 3-year event-free survival rate was 16.1% (95% confidence intervals: 8.2-24.6%). Grade 3 or higher hematological toxicity included neutropenia in 96.9%, anemia in 3.1%, and thrombocytopenia in 15.6%. Grades 1, 2, and 3 nonhematological toxicity included diarrhea in one patient, nausea/vomiting in five patients, and hematuria in one patient, respectively. CPT-11 combined with MIT was safe even for elderly patients and was effective even in patients who had received pretreatment with doxorubicin. In addition, this regimen can be used on an outpatient basis. This combination should be tested further to determine the optimum doses and administration schedule.
盐酸伊立替康(CPT-11)是一种具有广泛抗肿瘤谱的拓扑异构酶I抑制剂。在本研究中,我们将CPT-11和米托蒽醌(MIT)与地塞米松联合使用,因为在一项临床前研究中,这种联合使用产生的效果是相加的或更好的。进行本研究以确定这种联合使用的疗效和毒性。32例患者可进行评估。CPT-11联合MIT使11例患者(34.4%)达到完全缓解,9例患者(28.1%)达到部分缓解。中位随访期为20个月。4年生存率为31.8%(95%置信区间:11.2 - 64.6%),3年无事件生存率为16.1%(95%置信区间:8.2 - 24.6%)。3级或更高的血液学毒性包括96.9%的中性粒细胞减少、3.1%的贫血和15.6%的血小板减少。1级、2级和3级非血液学毒性分别包括1例患者出现腹泻、5例患者出现恶心/呕吐和1例患者出现血尿。CPT-11联合MIT即使对老年患者也是安全的,并且即使对接受过阿霉素预处理的患者也有效。此外,该方案可在门诊使用。这种联合用药应进一步进行试验,以确定最佳剂量和给药方案。