不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Lenalidomide maintenance fails to overcome the unfavourable prognosis of low NK-cell counts in rituximab-chemotherapy responsive elderly DLBCL patients: A LYSA group study.
Lenalidomide maintenance fails to overcome the unfavourable prognosis of low NK-cell counts in rituximab-chemotherapy responsive elderly DLBCL patients: A LYSA group study.
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弥漫大 B 细胞淋巴瘤(DLBCL)患者基线 NK 细胞计数(NKCC)偏低与预后不良相关。REMARC III 期试验(NCT01122472)显示,对利妥昔单抗联合化疗应答者进行来那度胺维持治疗可延长无进展生存期(PFS)。
我们开展 REMARC 附属研究,分析来那度胺维持治疗对低基线 NKCC 预后价值的影响。研究采用流式细胞术分析 REMARC 试验中 335 例法国老年患者的血样,获得诊断时(n=220)、随机分组时(n=186)和/或随机分组后 6 个月(n=184)的 NKCC。基线 NKCC<100 个细胞/μL 与较短 PFS 和总生存期(OS)相关(风险比分别为 2.2[1.4–3.3],P<0.001;2.8[1.7–4.5],P<0.001),且独立于 aaIPI。在竞争风险分析中,基线 NKCC 低与较高复发/进展风险相关(P=0.0025),但与无进展死亡风险无关(P=0.33)。来那度胺不影响低基线 NKCC 的预后价值(P=0.6349)。随机分组时 NKCC 低也得到类似结果。研究显示,诊断时及利妥昔单抗联合化疗后 NKCC 低是 DLBCL 稳健的预后因素,来那度胺不影响这一指标。其他旨在改善 NK 细胞功能的治疗策略可能改善 DLBCL 结局。
Low baseline NK-cell counts (NKCCs) in patients with diffuse large B-cell lymphoma (DLBCL) are associated with a poor prognosis. The REMARC phase III trial (NCT01122472) showed that lenalidomide maintenance prolonged PFS in rituximab-chemotherapy responders.
We conducted a REMARC ancillary study analysing the impact of lenalidomide maintenance on the prognostic value of low NKCCs. Blood samples from 335 elderly French patients enrolled in the REMARC trial were analysed by flow cytometry to obtain NKCCs at diagnosis (n = 220), at randomization (n = 186) and/or six months after randomization (n = 184). Baseline NKCCs < 100 cells/ l were associated with shorter PFS and OS (HRs = [2.
2 (1. 4, 3. 3), p < 0. 001] and [2. 8 (1. 7, 4. 5), p < 0. 001], respectively), independently of aaIPI. In a competing risk analysis, low NKCCs at baseline were associated with a higher risk of relapse/progression (p = 0. 0025), but not of death without progression (p = 0. 33). Lenalidomide did not affect the prognosis value of low baseline NKCCs (p = 0. 6349). Similar results were obtained for low NKCCs at randomization.
Our results demonstrate that low NKCCs at baseline and post rituximab-chemotherapy are robust prognostic factors in DLBCL and reveal that lenalidomide has no impact on this parameter. Other therapeutic strategies aiming at improving NK-cell function could improve outcomes in DLBCL.
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