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氟达拉滨:一种对慢性淋巴细胞白血病有显著活性的新型药物。

Fludarabine: a new agent with major activity against chronic lymphocytic leukemia.

作者信息

Keating M J, Kantarjian H, Talpaz M, Redman J, Koller C, Barlogie B, Velasquez W, Plunkett W, Freireich E J, McCredie K B

机构信息

Department of Hematology, University of Texas, M.D. Anderson Cancer Center, Houston 77030.

出版信息

Blood. 1989 Jul;74(1):19-25.

PMID:2473795
Abstract

Fludarabine was used to treat 68 patients with previously treated chronic lymphocytic leukemia (CLL). Nine (13%) patients achieved a complete remission and 30 (44%) a partial remission. The response rates for Rai stages 0 to 2, 3, and 4 were 64%, 58%, and 50% respectively. Seventeen (43%) of the 40 Rai stage 1 to 3 patients and four (19%) of the Rai stage 4 patients returned to Rai stage 0. Survival was strongly correlated with the final Rai stage achieved. The survival of the 11 partial responders with residual disease consisting only of residual bone-marrow nodules was similar to the complete responders (36+ months) and superior to the other partial response patients (16 months). The response to fludarabine was rapid, with 36 (92%) of the 39 responders having achieved at least a partial response following the first three courses. Complete responses occurred in the blood, liver, spleen, and lymph nodes in 48% to 69% of the patients. Eradication of all disease in the bone marrow occurred in only 13% of the cases. Neutropenia and thrombocytopenia occurred in 56% and 25% of evaluable courses. Major infections occurred in 9% of evaluable courses and fevers of unknown origin or minor infections in 12% of courses respectively. Myelosuppression and infection were more common in patients with initial Rai stages 3 and 4 and in nonresponding patients. Other toxicity was mild. No CNS toxicity was noted.

摘要

氟达拉滨用于治疗68例曾接受过治疗的慢性淋巴细胞白血病(CLL)患者。9例(13%)患者获得完全缓解,30例(44%)患者获得部分缓解。Rai分期0至2期、3期和4期的缓解率分别为64%、58%和50%。40例Rai分期1至3期患者中有17例(43%)、Rai分期4期患者中有4例(19%)恢复至Rai分期0期。生存率与最终达到的Rai分期密切相关。11例仅残留骨髓结节的部分缓解患者的生存期与完全缓解患者相似(36个多月),且优于其他部分缓解患者(16个月)。对氟达拉滨的反应迅速,39例有反应的患者中有36例(92%)在前三个疗程后至少获得部分缓解。48%至69%的患者在血液、肝脏、脾脏和淋巴结中出现完全缓解。仅13%的病例骨髓中的所有疾病被清除。在可评估疗程中,中性粒细胞减少症和血小板减少症的发生率分别为56%和25%。在可评估疗程中,严重感染发生率为9%,不明原因发热或轻微感染发生率分别为12%。骨髓抑制和感染在初始Rai分期3期和4期患者及无反应患者中更为常见。其他毒性较轻。未观察到中枢神经系统毒性。

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