Department of Central Laboratory, The Affiliated People's Hospital of Ningbo University, Ningbo, People's Republic of China.
Department of Hematology, The Affiliated People's Hospital of Ningbo University, Ningbo, People's Republic of China.
Hematology. 2024 Dec;29(1):2329378. doi: 10.1080/16078454.2024.2329378. Epub 2024 Mar 12.
Multiple myeloma (MM) varies in clinical behavior, response to treatment and prognosis due to the heterogeneity of the disease. Data on the association between the immunoparesis status during treatment and prognosis in nontransplant MM patients are limited.
In a retrospective analysis of 142 patients with MM, we examined the relationship between immunoparesis status and prognosis during treatment. All patients received novel agent-based therapy and did not undergo autologous stem cell transplantation. One, two, or three uninvolved immunoglobulins (Igs) below the lowest thresholds of normalcy were used to identify immunoparesis.
Patients with a greater degree of immunoparesis during treatment had shorter progression-free survival (PFS) and overall survival (OS). A total of 46.5% of the patients had severe and continuous immunoparesis (at least two uninvolved Igs suppressed continuously during treatment), representing a worse prognosis than those with complete or partial normalization of Igs during treatment. Among patients who achieved at least complete remission, PFS was poor in patients with severe and continuous immunoparesis. Furthermore, severe and continuous immunoparesis during treatment was a poor prognostic factor for PFS and OS according to multivariate analyses.
The degree of immunoparesis during treatment is a follow-up indicator for survival in nontransplant myeloma patients, and severe and continuous immunoparesis in nontransplant myeloma patients might be a sign of poor prognosis.
由于疾病的异质性,多发性骨髓瘤(MM)在临床行为、对治疗的反应和预后方面存在差异。关于治疗期间免疫抑制状态与非移植 MM 患者预后之间关联的数据有限。
我们对 142 例 MM 患者进行了回顾性分析,研究了治疗期间免疫抑制状态与预后之间的关系。所有患者均接受了新型药物治疗,未进行自体干细胞移植。使用一种、两种或三种低于正常下限的未受累免疫球蛋白(Igs)来确定免疫抑制状态。
治疗期间免疫抑制程度较高的患者无进展生存期(PFS)和总生存期(OS)较短。共有 46.5%的患者存在严重且持续的免疫抑制(至少有两种未受累的 Ig 在治疗期间持续抑制),这比治疗期间 Ig 完全或部分正常化的患者预后更差。在至少达到完全缓解的患者中,严重且持续的免疫抑制患者的 PFS 较差。此外,根据多变量分析,治疗期间严重且持续的免疫抑制是 PFS 和 OS 的不良预后因素。
治疗期间免疫抑制程度是非移植 MM 患者生存的随访指标,非移植 MM 患者严重且持续的免疫抑制可能是预后不良的标志。