Directorate of Clinical Haematology, Royal Liverpool & Broadgreen University Hospitals NHS Trust, Liverpool, UK.
Eur J Haematol. 2011 Oct;87(4):372-5. doi: 10.1111/j.1600-0609.2011.01667.x. Epub 2011 Aug 11.
Lenalidomide is an immunomodulatory agent with activity in a range of haematological cancers including chronic lymphocytic leukaemia (CLL). However, major questions remain concerning its effectiveness in patients with T-cell depletion or deletion of TP53 on chromosome 17p. This case report provides insight into these questions by showing that lenalidomide/dexamethasone in combination can be highly effective as induction therapy for refractory 17p-CLL, that remission quality can be improved by subsequent maintenance with lenalidomide alone and that the anti-leukaemic effects of lenalidomide and its stimulatory effects on non-malignant B cells are preserved despite prolonged T-cell depletion resulting from prior alemtuzumab/methylprednisolone.
来那度胺是一种免疫调节药物,在多种血液系统恶性肿瘤中具有活性,包括慢性淋巴细胞白血病(CLL)。然而,在 T 细胞耗竭或 17p 染色体 TP53 缺失的患者中,其有效性仍存在诸多问题。本病例报告通过显示来那度胺/地塞米松联合治疗对难治性 17p-CLL 具有高度有效性,随后单独使用来那度胺维持可改善缓解质量,以及尽管先前使用阿仑单抗/甲基强的松龙导致 T 细胞耗竭延长,但来那度胺的抗白血病作用及其对非恶性 B 细胞的刺激作用仍得以保留,为这些问题提供了深入了解。