Dufour P, Mors R, Berthaud P, Lamy T, Bergerat J P, Herbrecht R, Maloisel F, Audhuy B, Lioure B, Giron C, Hurteloup P, Oberling F
Département Onco-Hématologie, Hôpitaux, Universitaires de Strasbourg, France.
Leuk Lymphoma. 1996 Jul;22(3-4):329-34. doi: 10.3109/10428199609051764.
Twenty three patients with relapsing (n = 11) or refractory (n = 12) non-Hodgkin's lymphoma (NHL) to one or two prior anthracycline based combination chemotherapy regimens were treated as second or third line regimen with 3 induction cycles of Idarubicin (IDA) (7 mg/m2/d i.v. d1-d3) and high dose cytarabine (HD Ara-C) (1 g/m2/12 h i.v. d1-d3), each cycle was repeated every 3 weeks. Responding patients received a maintenance therapy with monthly cycles of IDA: 15 mg/m2 d1-d3, Etoposide 100 mg/m2 d1-d3, both by oral route. Twenty two patients are evaluable and we observed 13 CR and 1 PR with an overall response rate of 61% (14/23: 95% Cl = 38.5% 80.3%). The median time to progression was 32 months (6.5 - 63 + m.). The response rate to IDA-HD Ara C was not different for patients with (n = 14) or without (n = 9) objective response to the last prior therapy. The main toxicity was hematological: all patients experienced grade 4 neutropenia and 22 patients had grade 4 thrombopenia, but there were no toxic deaths. IDA and HD-Ara-C combination is highly effective in refractory or relapsed. NHL. As hematological toxicity was the limiting factor for further escalation of dose-intensity, further studies might include hematopoietic growth factors support in the therapeutic scheme.
23例对一或两种含蒽环类药物的既往联合化疗方案复发(n = 11)或难治(n = 12)的非霍奇金淋巴瘤(NHL)患者,接受伊达比星(IDA)(7mg/m²/d,静脉滴注,第1 - 3天)和大剂量阿糖胞苷(HD Ara - C)(1g/m²/12h,静脉滴注,第1 - 3天)的3个诱导周期治疗作为二线或三线方案,每个周期每3周重复一次。缓解患者接受每月一次的IDA维持治疗:15mg/m²,第1 - 3天;依托泊苷100mg/m²,第1 - 3天,均口服给药。22例患者可评估,我们观察到13例完全缓解(CR)和1例部分缓解(PR),总缓解率为61%(14/23:95%置信区间 = 38.5% - 80.3%)。疾病进展的中位时间为32个月(6.5 - 63 + 月)。对于对最后一次既往治疗有(n = 14)或无(n = 9)客观缓解的患者,对IDA - HD Ara C的缓解率无差异。主要毒性为血液学毒性:所有患者均经历4级中性粒细胞减少,22例患者有4级血小板减少,但无毒性死亡。IDA和HD - Ara - C联合方案对难治性或复发性NHL非常有效。由于血液学毒性是剂量强度进一步增加的限制因素,进一步的研究可能包括在治疗方案中加入造血生长因子支持。