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CAR-T 疗法治疗骨髓瘤中早期骨髓微小残留病灶状态的预后价值。

Prognostic value of early bone marrow MRD status in CAR-T therapy for myeloma.

机构信息

Division of Hematology, Mayo Clinic, Rochester, MN, USA.

Division of Hematology and Oncology, Mayo Clinic, Jacksonville, FL, USA.

出版信息

Blood Cancer J. 2023 Apr 5;13(1):47. doi: 10.1038/s41408-023-00820-y.

Abstract

Bone marrow (BM) assessment of minimal residual disease (MRD) is prognostic for survival in multiple myeloma (MM). BM is still hypocellular at month 1 post CAR-T, thus the value of MRD negative (MRDneg) status at this timepoint is unclear. We examined the impact of month 1 BM MRD status in MM patients who received CART at Mayo Clinic between 8/2016 and 6/2021. Among 60 patients, 78% were BM-MRDneg at month 1; and 85% (40/47) of these patients also had decreased to less than normal level of both involved and uninvolved free light chain (FLC < NL). Patients who achieved CR/sCR had higher rates of month 1 BM-MRDneg and FLC < NL. The rate of sustained BM-MRDneg was 40% (19/47). Rate of conversion from MRDpos to MRDneg was 5%(1/20). At month 1, 38%(18/47) of the BM-MRDneg were hypocellular. Recovery to normal cellularity was observed in 50%(7/14) with a median time to normalization at 12 months (range: 3-Not reached). Compared to Month 1 BM-MRDpos patients, patients who were BM-MRDneg had longer PFS irrespective of BM cellularity [PFS: 2.9 months (95% CI, 1.2-NR) vs. 17.5 months (95% CI, 10.4-NR), p < 0.0001]. Month 1 BM-MRDneg and FLC below normal were associated with prolonged survival. Our data support the continued evaluation of BM early post-CART infusion as a prognostic tool.

摘要

骨髓(BM)微小残留病灶(MRD)评估对多发性骨髓瘤(MM)的生存具有预后价值。CAR-T 治疗后 1 个月时骨髓仍呈低细胞状态,因此此时 MRD 阴性(MRDneg)状态的价值尚不清楚。我们研究了在 2016 年 8 月至 2021 年 6 月期间在梅奥诊所接受 CART 的 MM 患者中,1 个月时 BM MRD 状态的影响。在 60 例患者中,78%在 1 个月时为 BM-MRDneg;其中 85%(40/47)的患者同时也使受累和未受累游离轻链(FLC)均降至低于正常值(FLC<NL)。达到完全缓解/严格意义完全缓解(CR/sCR)的患者 1 个月时 BM-MRDneg 和 FLC<NL 的比例更高。持续 BM-MRDneg 的比例为 40%(19/47)。从 MRDpos 转为 MRDneg 的转化率为 5%(1/20)。在 1 个月时,47%的 BM-MRDneg 骨髓呈低细胞状态。有 50%(7/14)的患者恢复到正常细胞状态,中位恢复正常细胞时间为 12 个月(范围:3-未达到)。与 1 个月时 BM-MRDpos 患者相比,无论 BM 细胞数量如何,BM-MRDneg 的患者无进展生存期(PFS)更长[PFS:2.9 个月(95%CI,1.2-NR)与 17.5 个月(95%CI,10.4-NR),p<0.0001]。1 个月时 BM-MRDneg 和 FLC 低于正常与生存期延长相关。我们的数据支持在 CAR-T 输注后早期继续评估 BM 作为一种预后工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e728/10076306/ede6a4242b84/41408_2023_820_Fig1_HTML.jpg

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