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[白血病前期状态(慢性粒细胞白血病和骨髓增生异常综合征)中干扰素的临床研究]

[Clinical investigation of interferons in the preleukemic state (CML and MDS)].

作者信息

Koyama S

机构信息

1st Dept. of Internal Medicine, Niigata University School of Medicine.

出版信息

Gan To Kagaku Ryoho. 1988 Apr;15(4 Pt 2-2):1191-7.

PMID:3132893
Abstract

We treated 11 patients who had Philadelphia-chromosome-positive chronic myelogenous leukemia with natural interferon alpha (human lymphoblastoid interferon; HLBI). HLBI was given at 6-12 X 10(6) u/day i.m. or i.s.c. during induction therapy. Nine patients responded to the treatment, of whom 7 had hematologic remission and 2 had partial remission. Six patients with MDS or hypoplastic leukemia, and 3 patients with overt leukemia from MDS were treated with recombinant interferon gamma (GI-3). GI-3 was given at 0.4 X 10(6) u/m2 of body-surface area per day i.s.c. or i.v. for 4-6 weeks. In 2 patients with RAEB and hypoplastic leukemia, the blast cell count in bone marrow decreased from 8-16% to 2-3% after 4 weeks of administration. In another patient with hypoplastic leukemia, blast cells in the marrow did not decrease, but anemia was improved without transfusion, increasing the bone marrow NCC and erythroblast count. In patients with overt leukemia and CMML, no clinical effect was obtained. Interferons can therefore be offered to patients in a preleukemic state.

摘要

我们用天然干扰素α(人淋巴母细胞干扰素;HLBI)治疗了11例费城染色体阳性的慢性粒细胞白血病患者。诱导治疗期间,HLBI通过肌肉注射或皮下注射给药,剂量为每天6 - 12×10⁶单位。9例患者对治疗有反应,其中7例血液学缓解,2例部分缓解。6例骨髓增生异常综合征(MDS)或低增生性白血病患者以及3例由MDS转化而来的明显白血病患者接受了重组干扰素γ(GI - 3)治疗。GI - 3通过皮下注射或静脉注射给药,剂量为每天0.4×10⁶单位/平方米体表面积,持续4 - 6周。在2例难治性贫血伴原始细胞增多(RAEB)和低增生性白血病患者中,给药4周后骨髓原始细胞计数从8% - 16%降至2% - 3%。在另一例低增生性白血病患者中,骨髓原始细胞未减少,但贫血状况在未输血的情况下得到改善,骨髓有核细胞计数(NCC)和幼红细胞计数增加。在明显白血病和慢性粒 - 单核细胞白血病(CMML)患者中,未观察到临床效果。因此,干扰素可用于处于白血病前期状态的患者。

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