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接受单磷酸氟达拉滨治疗的患者出现严重免疫缺陷。

Severe immunodeficiency in patients treated with fludarabine monophosphate.

作者信息

Wijermans P W, Gerrits W B, Haak H L

机构信息

Department of Haematology, Leyenburg Hospital, The Hague, The Netherlands.

出版信息

Eur J Haematol. 1993 May;50(5):292-6. doi: 10.1111/j.1600-0609.1993.tb00165.x.

Abstract

Fludarabine monophosphate (FAMP) has been shown to be highly effective against low-grade malignant B-cell lymphoproliferative diseases. Because some opportunistic infections were observed in patients treated with FAMP, we investigated the influence of this drug on several parameters of immunocompetence. For 17 consecutive patients treated with FAMP for CLL or low-grade malignant lymphoma we studied T-cell subpopulations during and after therapy by flow cytometry and our findings were correlated with the clinical course of their disease. A pronounced decrease in the various T-cell subpopulations was seen in all cases, that for CD4+ cells was still present 11-13 months after the end of the therapy. In 7 patients a severe opportunistic infection developed; the outcome was fatal in 2 cases. Only 5 patients did not experience any serious infection. These results show that FAMP therapy in a dose of 25 mg/m2/day for 5 d every 4 weeks might be too toxic for patients with very advanced disease. However, in view of the efficacy of FAMP, the possibility of less intensive schedules for these advanced cases should be explored.

摘要

单磷酸氟达拉滨(FAMP)已被证明对低度恶性B细胞淋巴增殖性疾病非常有效。由于在接受FAMP治疗的患者中观察到一些机会性感染,我们研究了这种药物对免疫能力的几个参数的影响。对于连续17例接受FAMP治疗慢性淋巴细胞白血病(CLL)或低度恶性淋巴瘤的患者,我们通过流式细胞术研究了治疗期间和治疗后的T细胞亚群,我们的发现与他们疾病的临床病程相关。在所有病例中,各种T细胞亚群均有明显减少,治疗结束后11 - 13个月,CD4 +细胞的减少仍然存在。7例患者发生了严重的机会性感染;2例患者死亡。只有5例患者没有经历任何严重感染。这些结果表明,每4周一次、剂量为25 mg/m²/天、持续5天的FAMP治疗对病情非常严重的患者可能毒性过大。然而,鉴于FAMP的疗效,应该探索为这些晚期病例采用强度较低的治疗方案的可能性。

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