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初诊多发性骨髓瘤患者采用来那度胺维持治疗的 RVD 诱导和自体干细胞移植:芬兰骨髓瘤研究组的 2 期研究。

RVD induction and autologous stem cell transplantation followed by lenalidomide maintenance in newly diagnosed multiple myeloma: a phase 2 study of the Finnish Myeloma Group.

机构信息

Comprehensive Cancer Center, Department of Hematology, Helsinki University Hospital and University of Helsinki, Helsinki, Finland.

Hematology-Oncology Unit, Oulu University Hospital, Oulu, Finland.

出版信息

Ann Hematol. 2019 Dec;98(12):2781-2792. doi: 10.1007/s00277-019-03815-7. Epub 2019 Oct 31.

Abstract

Autologous stem cell transplantation (ASCT) combined with novel agents is the standard treatment for transplant-eligible, newly diagnosed myeloma (NDMM) patients. Lenalidomide is approved for maintenance after ASCT until progression, although the optimal duration of maintenance is unknown. In this trial, 80 patients with NDMM received three cycles of lenalidomide, bortezomib, and dexamethasone followed by ASCT and lenalidomide maintenance until progression or toxicity. The primary endpoint was the proportion of flow-negative patients. Molecular response was assessed if patients were flow-negative or in stringent complete response (sCR). By intention to treat, the overall response rate was 89%. Neither median progression-free survival nor overall survival (OS) has been reached. The OS at 3 years was 83%. Flow-negativity was reached in 53% and PCR-negativity in 28% of the patients. With a median follow-up of 27 months, 29 (36%) patients are still on lenalidomide and 66% of them have sustained flow-negativity. Lenalidomide maintenance phase was reached in 8/16 high-risk patients but seven of them have progressed after a median of only 6 months. In low- or standard-risk patients, the outcome was promising, but high-risk patients need more effective treatment approach. Flow-negativity with the conventional flow was an independent predictor for longer PFS.

摘要

自体干细胞移植(ASCT)联合新型药物是适合移植的新诊断多发性骨髓瘤(NDMM)患者的标准治疗方法。来那度胺获批用于 ASCT 后至疾病进展期间的维持治疗,尽管维持治疗的最佳持续时间尚不清楚。在这项试验中,80 例 NDMM 患者接受了 3 个周期的来那度胺、硼替佐米和地塞米松治疗,随后进行 ASCT 和来那度胺维持治疗,直至疾病进展或出现毒性。主要终点是流式阴性患者的比例。如果患者为流式阴性或达到严格完全缓解(sCR),则评估分子缓解情况。根据意向治疗原则,总体缓解率为 89%。无进展生存期和总生存期(OS)均未达到。3 年 OS 为 83%。53%的患者达到流式阴性,28%的患者达到 PCR 阴性。中位随访 27 个月时,29 例(36%)患者仍在接受来那度胺治疗,其中 66%的患者持续达到流式阴性。在 16 例高危患者中,有 8 例进入来那度胺维持期,但其中 7 例在中位时间仅 6 个月后就进展了。在低危或中危患者中,结果是有希望的,但高危患者需要更有效的治疗方法。常规流式细胞术的流式阴性是 PFS 延长的独立预测因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a27a/6900265/3e129515c9b6/277_2019_3815_Fig1_HTML.jpg

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