Department of Clinical Therapeutics, National and Kapodistrian University of Athens, Athens, Greece.
Dana-Farber Cancer Institute, Boston, Massachusetts.
Eur J Haematol. 2019 Jun;102(6):494-503. doi: 10.1111/ejh.13231. Epub 2019 May 8.
To evaluate the safety and efficacy of maintenance therapy with the oral proteasome inhibitor ixazomib in patients with newly diagnosed multiple myeloma (NDMM) not undergoing transplantation.
Data were pooled from four NDMM phase I/II studies; patients received induction therapy with once- or twice-weekly ixazomib plus lenalidomide-dexamethasone (IRd), melphalan-prednisone (IMP), or cyclophosphamide-dexamethasone (ICd), followed by single-agent ixazomib maintenance, given at the last tolerated dose during induction, until disease progression, death, or unacceptable toxicity.
A total of 121 patients achieved stable disease or better after induction (weekly IRd, n = 25; twice-weekly IRd, n = 18; weekly or twice-weekly IMP, n = 35; weekly ICd, n = 43) and received ≥ 1 dose of ixazomib maintenance. Grade ≥ 3 drug-related adverse events occurred in 24% of patients during maintenance; each event was reported in ≤2% of patients. Rates of complete response were 22% after induction and 35% after maintenance. A total of 28 patients (23%) improved their response during maintenance.
Ixazomib maintenance following ixazomib-based induction is associated with deepening of responses and a positive safety profile with no cumulative toxicity in patients with NDMM not undergoing transplantation, suggesting that ixazomib is feasible for long-term administration. Phase III investigation of ixazomib maintenance is ongoing.
评估口服蛋白酶体抑制剂伊沙佐米维持治疗未经移植的初诊多发性骨髓瘤(NDMM)患者的安全性和疗效。
数据来自四项 NDMM I/II 期研究;患者接受每周或每两周一次伊沙佐米联合来那度胺-地塞米松(IRd)、马法兰-泼尼松(IMP)或环磷酰胺-地塞米松(ICd)诱导治疗,随后给予单药伊沙佐米维持治疗,剂量为诱导治疗期间最后耐受剂量,直至疾病进展、死亡或不可接受的毒性。
共有 121 例患者在诱导后达到稳定疾病或更好(每周 IRd,n=25;每两周 IRd,n=18;每周或每两周 IMP,n=35;每周 ICd,n=43),并接受了至少 1 剂伊沙佐米维持治疗。维持期间,24%的患者发生了≥3 级与药物相关的不良事件;每种事件均≤2%的患者报告。诱导后完全缓解率为 22%,维持后为 35%。共有 28 例患者(23%)在维持期间改善了缓解情况。
在未接受移植的 NDMM 患者中,伊沙佐米诱导后应用伊沙佐米维持治疗与加深缓解和良好的安全性相关,无累积毒性,提示伊沙佐米可长期应用。正在进行伊沙佐米维持治疗的 III 期研究。