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自体造血干细胞移植后 PET 阳性多发性骨髓瘤患者的强化治疗。

Intensifying treatment in PET-positive multiple myeloma patients after upfront autologous stem cell transplantation.

机构信息

Oslo Myeloma Center, Department of Hematology, Oslo University Hospital, Oslo, Norway.

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

出版信息

Leukemia. 2023 Oct;37(10):2107-2114. doi: 10.1038/s41375-023-01998-7. Epub 2023 Aug 11.

DOI:10.1038/s41375-023-01998-7
PMID:37568010
Abstract

F-Fluorodeoxyglucose positron emission tomography/computed tomography (PET) positivity after first-line treatment with autologous stem cell transplantation (ASCT) in multiple myeloma is strongly correlated with reduced progression-free and overall survival. However, PET-positive patients who achieve PET negativity after treatment seem to have comparable outcomes to patients who were PET negative at diagnosis. Hence, giving PET-positive patients additional treatment may improve their outcome. In this phase II study, we screened first-line patients with very good partial response (VGPR) or better after ASCT with PET. PET-positive patients received four 28-day cycles of carfilzomib-lenalidomide-dexamethasone (KRd). Flow cytometry-based minimal residual disease (MRD) analysis was performed before and after treatment for correlation with PET. Overall, 159 patients were screened with PET. A total of 53 patients (33%) were PET positive and 57% of PET-positive patients were MRD negative, demonstrating that these response assessments are complementary. KRd consolidation converted 33% of PET-positive patients into PET negativity. MRD-negative patients were more likely to convert than MRD-positive patients. In summary, PET after ASCT detected residual disease in a substantial proportion of patients in VGPR or better, even in patients who were MRD negative, and KRd consolidation treatment changed PET status in 33% of patients.

摘要

自体造血干细胞移植(ASCT)一线治疗后氟代脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(PET)阳性与多发性骨髓瘤患者无进展生存期和总生存期降低密切相关。然而,治疗后达到 PET 阴性的 PET 阳性患者似乎与诊断时即为 PET 阴性的患者具有可比的结局。因此,给予 PET 阳性患者额外的治疗可能会改善其结局。在这项 II 期研究中,我们对 ASCT 后达到非常好的部分缓解(VGPR)或更好的一线患者进行了 PET 筛选。PET 阳性患者接受了四个 28 天周期的卡非佐米-来那度胺-地塞米松(KRd)治疗。在治疗前后进行基于流式细胞术的微小残留病(MRD)分析,以与 PET 相关联。总共对 159 例患者进行了 PET 筛选。共有 53 例(33%)患者为 PET 阳性,57%的 PET 阳性患者为 MRD 阴性,表明这些反应评估是互补的。KRd 巩固治疗使 33%的 PET 阳性患者转为 PET 阴性。MRD 阴性患者比 MRD 阳性患者更有可能转为 PET 阴性。总之,ASCT 后的 PET 在 VGPR 或更好的患者中检测到了相当一部分患者的残留疾病,即使在 MRD 阴性的患者中也是如此,KRd 巩固治疗使 33%的患者的 PET 状态发生了改变。

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