Division of Hospital Medicine, Department of Internal Medicine, University of Kentucky, Lexington, KY.
Harvey Cushing/John Hay Whitney Medical Library, Yale University, New Haven, CT.
Clin Lymphoma Myeloma Leuk. 2024 Nov;24(11):e870-e877. doi: 10.1016/j.clml.2024.07.008. Epub 2024 Jul 19.
Immunoparesis, defined as suppression of uninvolved polyclonal immunoglobulins, occurs in up to 80% of patients with newly diagnosed multiple myeloma (NDMM). Infections are the second most common cause of mortality in this population, yet evidence regarding prognostic impact of immunoparesis in NDMM remains unclear.
Using a prepublished protocol (CRD42022308687), we searched seven bibliographic databases from inception to February 2023 for studies reporting the impact of immunoparesis on clinical outcomes among adults with NDMM. The primary outcome of interest was overall survival (OS) and secondary outcomes were progression free survival (PFS) and infection risk. Effect sizes were quantified in terms of hazards ratio (HR) and pooled across studies using a random effects restricted maximum likelihood method. Heterogeneity was assessed using Cochran Q and the I statistic. Publication bias was assessed using contour enhanced funnel plots.
Of 5175 studies screened, 7 studies involving 6091 patients met our search criteria. Immunoparesis was not associated with worse OS (pooled hazard ratio 1.30; 95% CI, 0.91-1.84; P-value .11), with significant heterogeneity among the studies (I2 = 72.9%; Cochran's Q P-value .003). However, immunoparesis was associated with a significantly worse PFS (pooled hazard ratio 1.42; 95% CI 1.11-1.82; p value 0.013), with moderate heterogeneity (I2 statistic = 51%; Cochran's Q P-value .056). Infection rates were not uniformly reported precluding meta-analysis. Visual examination of funnel plot revealed the possibility of publication bias.
Overall, our findings suggest that immunoparesis did not have a detrimental impact on OS, but was associated with a significantly shorter PFS. Further studies are needed to understand the complexity of immune system perturbations in NDMM.
免疫抑制,定义为未受累多克隆免疫球蛋白的抑制,在多达 80%的新诊断多发性骨髓瘤(NDMM)患者中发生。在该人群中,感染是第二大常见死亡原因,但免疫抑制在 NDMM 中的预后影响的证据仍不清楚。
使用预先发布的方案(CRD42022308687),我们从成立到 2023 年 2 月在七个文献数据库中搜索了报告免疫抑制对 NDMM 成人临床结局影响的研究。主要研究结果是总生存期(OS),次要结果是无进展生存期(PFS)和感染风险。使用随机效应受限极大似然法,以风险比(HR)的形式量化效应大小,并对研究进行汇总。使用 Cochran Q 和 I 统计量评估异质性。使用轮廓增强漏斗图评估发表偏倚。
在筛选的 5175 项研究中,有 7 项研究涉及 6091 名患者符合我们的检索标准。免疫抑制与较差的 OS 无关(汇总风险比 1.30;95%置信区间,0.91-1.84;P 值.11),但研究之间存在显著异质性(I2 = 72.9%;Cochran's Q P 值.003)。然而,免疫抑制与明显更差的 PFS 相关(汇总风险比 1.42;95%置信区间 1.11-1.82;p 值 0.013),异质性中度(I2 统计量 = 51%;Cochran's Q P 值.056)。感染率未统一报告,因此无法进行荟萃分析。漏斗图的视觉检查显示存在发表偏倚的可能性。
总体而言,我们的研究结果表明,免疫抑制对 OS 没有不利影响,但与明显更短的 PFS 相关。需要进一步研究以了解 NDMM 中免疫系统紊乱的复杂性。