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米托蒽醌、依托泊苷和中剂量阿糖胞苷(MEC):一种用于既往未治疗的急性非淋巴细胞白血病的有效诱导方案。

MEC (mitoxantrone, etoposide and intermediate dose cytarabine): an effective induction regimen for previously untreated acute non-lymphocytic leukemia.

作者信息

Visani G, Petti M C, Cenacchi A, Manfroi S, Tosi P, Spadea A, Latagliata R, Amadori S, Mandelli F, Tura S

机构信息

Institute of Hematology L. e A. Seràgnoli, University of Bologna, Italy.

出版信息

Leuk Lymphoma. 1995 Nov;19(5-6):447-51. doi: 10.3109/10428199509112203.

Abstract

Twenty-three patients with acute non lymphocytic leukemia (ANLL), were treated with a single-6 day course of Mitoxantrone 6mg/m2/day, Etoposide 80mg/m2/day and intermediate dose Cytarabine (ara-C) 1g/m2/day (MEC). Patients who achieved complete remission (CR) were submitted to a 4-day-course of MEC as consolidation. Seventeen patients (73.9%) obtained CR, five patients (22.7%) were resistant to the treatment and one patient died during induction. Median remission duration was 11 months; overall median survival was 16 months. Relapses occurred in 11 patients; eight patients are still alive: 6 in 1st, 2 in 2nd CR (mean survival 20.1 months, range 17-26). All patients experienced severe myelosuppression comparable to that observed after classical induction cycles including ara-C in continuous intravenous infusion; none, however, died of infection. Non-hematologic toxicity was minimal; in particular, neurotoxicity was not observed. According to our results, the MEC regimen, which was previously demonstrated to be active in refractory patients, represents an effective induction treatment in ANLL, with an acceptable toxicity.

摘要

23例急性非淋巴细胞白血病(ANLL)患者接受了米托蒽醌6mg/m²/天、依托泊苷80mg/m²/天和中剂量阿糖胞苷(ara-C)1g/m²/天的单一6天疗程治疗(MEC方案)。达到完全缓解(CR)的患者接受4天疗程的MEC方案巩固治疗。17例患者(73.9%)获得CR,5例患者(22.7%)对治疗耐药,1例患者在诱导治疗期间死亡。中位缓解期为11个月;总体中位生存期为16个月。11例患者复发;8例患者仍存活:6例处于首次CR,2例处于第二次CR(平均生存期20.1个月,范围17 - 26个月)。所有患者均经历了与经典诱导周期(包括持续静脉输注阿糖胞苷)后观察到的严重骨髓抑制相当的情况;然而,无一例死于感染。非血液学毒性极小;特别是未观察到神经毒性。根据我们的结果,先前已证明在难治性患者中有效的MEC方案是ANLL一种有效的诱导治疗方法,且毒性可接受。

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