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随机对照试验:在 CLL 一线化疗免疫治疗后,采用个体化、低剂量、固定疗程来那度胺维持治疗与观察的比较。

Randomized controlled trial of individualized, low dose, fixed duration lenalidomide maintenance versus observation after frontline chemo-immunotherapy in CLL.

机构信息

Department of Internal Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Leuk Lymphoma. 2021 Jul;62(7):1674-1681. doi: 10.1080/10428194.2021.1885668. Epub 2021 Feb 21.

Abstract

Lenalidomide maintenance after frontline chemo-immunotherapy (CIT) in chronic lymphocytic leukemia (CLL) has not been standard due to the availability of novel therapies, though these remain out of reach for most in low-middle income countries. This single-center, open-label study randomized CLL patients (non-deletion 17p) after frontline therapy to lenalidomide maintenance (dose-escalated 2.5-10mg, 20/28 days per cycle for six months) or observation (2:1 allocation). Forty patients were included over 2018-2020. At a median follow-up of 22 months, median progression-free survival (PFS) with lenalidomide was not significantly different than observation (26 vs. 18 months,  = 0.4). Patients with minimal residual disease >10 had a trend toward better PFS with lenalidomide (19 vs. 7 months,  = 0.07). Grade 3 neutropenia was seen in 16.7% of patients on lenalidomide. Quality of life was comparable between the two arms. Low dose, fixed duration lenalidomide maintenance is not an effective strategy after frontline CIT in CLL.

摘要

来那度胺维持治疗在一线化疗免疫治疗(CIT)后在慢性淋巴细胞白血病(CLL)中尚未标准化,因为新型疗法的出现,尽管这些疗法在中低收入国家对大多数人来说仍然遥不可及。这项单中心、开放标签研究在一线治疗后将 CLL 患者(非 17p 缺失)随机分配至来那度胺维持治疗组(剂量递增 2.5-10mg,每 28 天 20/28 天,共 6 个月)或观察组(2:1 分配)。2018 年至 2020 年期间共纳入 40 例患者。在中位随访 22 个月时,来那度胺组与观察组的中位无进展生存期(PFS)无显著差异(26 个月 vs. 18 个月,  = 0.4)。微小残留病灶 >10 的患者接受来那度胺治疗的 PFS 有改善趋势(19 个月 vs. 7 个月,  = 0.07)。来那度胺组有 16.7%的患者出现 3 级中性粒细胞减少症。两组之间的生活质量相当。低剂量、固定疗程的来那度胺维持治疗在 CLL 患者一线 CIT 后并不是一种有效的策略。

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