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免疫调节药物在骨髓增生异常综合征中的应用。

Immunomodulating drugs in myelodysplastic syndromes.

机构信息

Hôpital Avicenne, Assistance Publique-Hôpitaux de Paris, Paris, France.

出版信息

Hematology Am Soc Hematol Educ Program. 2011;2011:556-60. doi: 10.1182/asheducation-2011.1.556.

Abstract

Based on immune mechanisms that appear to play an important role in the pathophysiology of at least part of the lower-risk myelodysplastic syndrome (MDS), the immunomodulating drug (IMID) thalidomide and its derivative lenalidomide (LEN) have been used in MDS, principally in lower-risk MDS. LEN has become the first-line US Food and Drug Administration (FDA)-approved treatment for lower-risk MDS with 5q deletion (del5q), in which its main mechanism of action is probably a direct cytotoxic activity on the del5q clone. This possibly specific effect is currently being investigated in higher-risk MDS-and even acute myeloid leukemia (AML)-with del5q, but LEN has also demonstrated some efficacy in MDS and AML without del5q. Thalidomide also has some activity in lower-risk MDS without del5q, but its side effects limit its practical use in these patients.

摘要

基于免疫机制似乎在至少部分低危骨髓增生异常综合征(MDS)的病理生理学中发挥重要作用,免疫调节药物(IMID)沙利度胺及其衍生物来那度胺(LEN)已被用于 MDS,主要是在低危 MDS 中。LEN 已成为美国食品和药物管理局(FDA)批准用于治疗伴有 5q 缺失(del5q)的低危 MDS 的一线药物,其主要作用机制可能是对 del5q 克隆的直接细胞毒性活性。目前正在高危 MDS 甚至急性髓系白血病(AML)中对具有 del5q 的患者进行这一可能具有特异性的疗效研究,但 LEN 在不具有 del5q 的 MDS 和 AML 中也显示出一定的疗效。沙利度胺在不具有 del5q 的低危 MDS 中也有一定的活性,但因其副作用限制了其在这些患者中的实际应用。

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