Palumbo A, Rajkumar S V
Divisione di Ematologia dell'Università di Torino, Azienda Ospedaliera S. Giovanni Battista, Ospedale Molinette, Turin, Italy.
Leukemia. 2009 Mar;23(3):449-56. doi: 10.1038/leu.2008.325. Epub 2008 Nov 13.
The introduction of thalidomide, bortezomib and lenalidomide has dramatically changed the treatment paradigm of multiple myeloma (MM). In patients eligible for autologous stem cell transplant (ASCT), combinations including thalidomide/dexamethasone (Thal/Dex) or bortezomib/dexamethasone (Bort/Dex) or lenalidomide/dexamethasone (Rev/Dex) have been introduced as induction regimens in patients eligible for ASCT. New induction regimens have significantly increased complete response rate before and after ASCT with a positive impact on progression-free survival. Maintenance therapy with thalidomide, under investigation with lenalidomide, may further prolong remission duration. In patients not eligible for ASCT, randomized studies have shown that melphalan, prednisone, thalidomide (MPT) and melphalan, prednisone and bortezomib (MPV) are both superior to melphalan and prednisone (MP), and are now considered standard of care. Ongoing trials will soon assess if MP plus lenalidomide may be considered an attractive option. More complex regimens combining thalidomide or bortezomib or lenalidomide with cyclophosphamide or doxorubicin have been also tested. In small cohorts of patients bortezomib or lenalidomide may overcome the poor prognosis induced by deletion 13 or translocation t(4;14) or deletion 17p13. If these data will be confirmed, a cytogenetically risk-adapted strategy might become the most appropriate strategy.
沙利度胺、硼替佐米和来那度胺的引入显著改变了多发性骨髓瘤(MM)的治疗模式。在适合自体干细胞移植(ASCT)的患者中,包含沙利度胺/地塞米松(Thal/Dex)或硼替佐米/地塞米松(Bort/Dex)或来那度胺/地塞米松(Rev/Dex)的联合方案已被用作适合ASCT患者的诱导方案。新的诱导方案显著提高了ASCT前后的完全缓解率,对无进展生存期产生了积极影响。沙利度胺维持治疗以及来那度胺维持治疗的研究,可能会进一步延长缓解期。在不适合ASCT的患者中,随机研究表明,美法仑、泼尼松、沙利度胺(MPT)和美法仑、泼尼松、硼替佐米(MPV)均优于美法仑和泼尼松(MP),目前被视为标准治疗方案。正在进行的试验将很快评估MP加利那度胺是否可被视为一个有吸引力的选择。将沙利度胺或硼替佐米或来那度胺与环磷酰胺或阿霉素联合使用的更复杂方案也已进行了测试。在一小部分患者中,硼替佐米或来那度胺可能克服由13号染色体缺失、t(4;14)易位或17p13缺失所导致的不良预后。如果这些数据得到证实,一种根据细胞遗传学风险调整的策略可能会成为最合适的策略。
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