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白细胞介素-2可能会使晚期急性髓细胞性白血病获得长期缓解。

Interleukin-2 may induce prolonged remissions in advanced acute myelogenous leukemia.

作者信息

Meloni G, Foa R, Vignetti M, Guarini A, Fenu S, Tosti S, Tos A G, Mandelli F

机构信息

Dipartimento di Biopatologia Umana, Università La Sapienza, Roma, Italy.

出版信息

Blood. 1994 Oct 1;84(7):2158-63.

PMID:7919330
Abstract

The administration of interleukin-2 (IL-2) may induce complete remissions in acute myelogenous leukemia (AML) patients with a low proportion of residual bone marrow (BM) blasts. To confirm this preliminary observation, we treated 14 AML patients with advanced disease and with a residual BM blastosis that ranged between 7% and 24% with repeated 5-day cycles of high-dose recombinant IL-2 administered by daily continuous intravenous infusion. Patients who responded have been subsequently submitted to a monthly maintenance scheme with subcutaneous IL-2 at lower doses. While using this schedule and closely monitoring clinical and laboratory conditions, side effects were acceptable and no toxic deaths recorded. Eight of the 14 patients treated with high-dose IL-2 obtained a complete remission (CR). Five remain in persistent CR (four in third CR and one in fourth CR) after a median follow-up time of 32 months (14, 30, 32, 33, and 68 months, respectively). In all five patients, the IL-2-induced remission is the longest in the natural history of the disease. These findings show that IL-2 displays an antileukemic effect in AML with limited residual disease, and suggest that IL-2 should be considered a therapeutic option for resistant or relapsed AML patients.

摘要

给予白细胞介素-2(IL-2)可能会使残留骨髓(BM)母细胞比例较低的急性髓性白血病(AML)患者完全缓解。为了证实这一初步观察结果,我们对14例晚期疾病且残留BM母细胞病介于7%至24%之间的AML患者进行治疗,通过每日持续静脉输注给予重复的5天高剂量重组IL-2周期。有反应的患者随后接受每月低剂量皮下注射IL-2的维持方案。在采用该方案并密切监测临床和实验室情况时,副作用是可接受的,且未记录到毒性死亡病例。14例接受高剂量IL-2治疗的患者中有8例获得完全缓解(CR)。5例患者在中位随访时间32个月(分别为14、30、32、33和68个月)后仍处于持续CR状态(4例处于第三次CR,1例处于第四次CR)。在所有5例患者中,IL-2诱导的缓解是疾病自然史中最长的。这些发现表明,IL-2在残留疾病有限的AML中显示出抗白血病作用,并提示IL-2应被视为耐药或复发AML患者的一种治疗选择。

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