Ho A D, Del Valle F, Haas R, Engelhard M, Hiddemann W, Rückle H, Schlimok G, Thiel E, Andreesen R, Fiedler W
Northeastern Ontario Oncology Program, Sudbury, Canada.
Semin Oncol. 1990 Dec;17(6 Suppl 10):14-8; discussion 18-9.
Mitoxantrone (Novantrone, American Cyanamid Company; NO) and high-dose cytarabine (Ara-C; AC) have each been shown to be active in non-Hodgkin's lymphomas (NHL) in various studies. The studies reported here are sequential. The first study (NOAC I) combined high-dose cytarabine (3 g/m2/12 h as a 3 h infusion on day 1) with mitoxantrone (10 mg/m2/d on days 2 and 3). Of 31 patients with relapsed and refractory NHL, 7 achieved complete remission (CR) and 7, partial remission (PR). Myelosuppression was the major toxicity of this regimen. In the second study (NOAC II), the dosage of cytarabine was escalated to 3 g/m2/12 h on days 1 and 2 (4 doses) while mitoxantrone remained 10 mg/m2/d on days 2 and 3. The effects of recombinant human (rh) granulocyte-macrophage colony-stimulating factor (GM-CSF) were simultaneously studied. Twenty-three patients from five centers were treated with NOAC plus rhGM-CSF while 14 patients from four centers received NOAC II alone. A CR was achieved in 9 of 23 patients who received the additional rhGM-CSF and in 2 of 14 patients treated with NOAC alone. With rhGM-CSF, the median duration of severe neutropenia (less than 0.5/nL) after chemotherapy was 8 days versus a median of 13 days without rhGM-CSF, while the duration of severe thrombocytopenia (less than 20/nL) was not significantly different. The rates of infection and mucositis were 25% and 17%, respectively, with rhGM-CSF compared to 53% and 60% without rhGM-CSF. Thus, this last nonrandomized pilot study indicates that administration of rhGM-CSF reduces the duration of chemotherapy-induced cytopenia and the rate of mucositis. This growth factor does not appear to result in stimulation of lymphoma cells. At present, a controlled randomized trial is being conducted using NOAC II with rhGM-CSF or placebo to establish the definitive role of this growth factor in the treatment of NHL.
在各项研究中,米托蒽醌(诺凡托,美国氰胺公司;NO)和大剂量阿糖胞苷(Ara-C;AC)均已显示出对非霍奇金淋巴瘤(NHL)有活性。此处报告的研究是连续性的。第一项研究(NOAC I)将大剂量阿糖胞苷(第1天以3小时输注方式给予3 g/m²/12小时)与米托蒽醌(第2天和第3天给予10 mg/m²/天)联合使用。在31例复发难治性NHL患者中,7例达到完全缓解(CR),7例达到部分缓解(PR)。骨髓抑制是该方案的主要毒性。在第二项研究(NOAC II)中,阿糖胞苷的剂量在第1天和第2天增加至3 g/m²/12小时(4剂),而米托蒽醌在第2天和第3天仍为10 mg/m²/天。同时研究了重组人(rh)粒细胞-巨噬细胞集落刺激因子(GM-CSF)的作用。来自五个中心的23例患者接受了NOAC加rhGM-CSF治疗,而来自四个中心的14例患者仅接受了NOAC II治疗。在接受额外rhGM-CSF治疗的23例患者中有9例达到CR,在仅接受NOAC治疗的14例患者中有2例达到CR。使用rhGM-CSF时,化疗后严重中性粒细胞减少(低于0.5/μL)的中位持续时间为8天,而未使用rhGM-CSF时中位持续时间为13天,而严重血小板减少(低于20/μL)的持续时间无显著差异。使用rhGM-CSF时感染率和粘膜炎发生率分别为25%和17%,而未使用rhGM-CSF时分别为53%和60%。因此,这项最后的非随机初步研究表明,给予rhGM-CSF可缩短化疗引起的血细胞减少持续时间和粘膜炎发生率。这种生长因子似乎不会导致淋巴瘤细胞的刺激。目前,正在进行一项对照随机试验,使用NOAC II加rhGM-CSF或安慰剂来确定这种生长因子在NHL治疗中的明确作用。