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使用递增剂量的重组αA干扰素治疗毛细胞白血病。

Treatment of hairy cell leukemia with increasing doses of recombinant alpha A interferon.

作者信息

Holmes R, Schwarz M A, Whiteside M G, Firkin F C

机构信息

Alfred Hospital, Prahran, Vic, Australia.

出版信息

Aust N Z J Med. 1988 Jun;18(4):557-62. doi: 10.1111/j.1445-5994.1988.tb00124.x.

DOI:10.1111/j.1445-5994.1988.tb00124.x
PMID:3196242
Abstract

Since July 1984, eight patients with advanced hairy cell leukemia have received treatment with recombinant alpha A interferon. At commencement of interferon, seven patients had progressive cytopenia, and one was in leukemic phase (greater than 20 x 10(9)/L circulating hairy cells). All patients had had previous splenectomy. Interferon was administered subcutaneously. The initial dose was 3 x 10(6) U/day, continued until peripheral counts stabilised. Subsequently, patients received 6 x 10(6) U/day, 9 x 10(6) U/day, and finally 12 x 10(6) U/day. The dose increases proceeded every 8-12 weeks, as tolerated. Seven patients had an objective response. There were four complete remissions, two partial remissions, and one minor response. Complete remission was documented only in patients on at least 6 x 10(6) U/day for 12 weeks. The median time to complete remission was 40 weeks (range 35-53). Normalisation of peripheral blood counts preceded histologic marrow improvement. The median times for response (platelets greater than or equal to 100 x 10(9)/L, hemaglobin greater than or equal to 12 gm/dL, neutrophils greater than or equal to 1.5 x 10(9)/L), were six to eight and 17 weeks, respectively. Toxicity included myelosuppression during the first four weeks of therapy. With increasing doses of interferon, myelosuppression did not recur. A transient, mild, flu-like syndrome affected all patients. Two patients developed asymptomatic transaminitis at doses greater than 6 X 10(6) U/day. This resolved with dose reduction. In one case impotence was reported during the first four weeks of each interferon level.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

自1984年7月以来,8例晚期毛细胞白血病患者接受了重组αA干扰素治疗。开始使用干扰素时,7例患者有进行性血细胞减少,1例处于白血病期(循环毛细胞大于20×10⁹/L)。所有患者既往均行脾切除术。干扰素皮下注射。初始剂量为3×10⁶U/天,持续至外周血细胞计数稳定。随后,患者接受6×10⁶U/天、9×10⁶U/天,最终为12×10⁶U/天。剂量增加每8 - 12周进行一次,视耐受情况而定。7例患者有客观反应。4例完全缓解,2例部分缓解,1例轻度反应。仅在至少接受6×10⁶U/天治疗12周的患者中记录到完全缓解。完全缓解的中位时间为40周(范围35 - 53周)。外周血细胞计数正常化先于组织学骨髓改善。反应的中位时间(血小板≥100×10⁹/L、血红蛋白≥12g/dL、中性粒细胞≥1.5×10⁹/L)分别为6至8周和17周。毒性包括治疗前四周的骨髓抑制。随着干扰素剂量增加,骨髓抑制未再出现。所有患者均出现短暂、轻度、流感样综合征。2例患者在剂量大于6×10⁶U/天时出现无症状转氨酶升高。剂量减少后缓解。1例患者在每个干扰素剂量水平的前四周报告有阳痿。(摘要截断于250字)

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