Garcia de Veas Silva Jose Luis, Gonzalez Cejudo Maria Trinidad, Garcia Perojil Jimenez Alberto, Garcia Lopez Velez Maria Del Señor, Garcia Rios Tamayo Rafael, Garcia Bermudo Guitarte Carmen, Garcia De Haro Muñoz Tomas
Department of Laboratory Medicine, Hospital Universitario San Cecilio, Granada, Spain.
Department of Hematology, Hospital Universitario Virgen de las Nieves, Granada, Spain.
Front Oncol. 2021 Mar 9;11:599532. doi: 10.3389/fonc.2021.599532. eCollection 2021.
Despite the outstanding progresses in Multiple Myeloma treatment options in the last decades, it remains an incurable disease nowadays. Infectious events are a complication due to an impaired immune system associated with MM, sometimes a life-threatening one, particularly on the first months after the diagnosis. Both the underlying disease and treatment can contribute to the infection risk, so a biomarker that assess this risk could be highly relevant for a more tailored management of the patient. The measurement of the heavy+light chain (HLC) pairs of immunoglobulins in serum allows the quantification of both the monoclonal component and the non-monoclonal immunoglobulin of the same isotype. This approach has demonstrated high sensitivity for the detection of the clonality and prognostic value for MM. HLC pair suppression itself has prognostic power and it has been proposed to be a reflection of the immune system' attempt to control the tumor. In this study we evaluated the impact of the HLC pair suppression on the rate of bloodstream infections (BSI) and early death in 115 newly diagnosed MM patients. Twenty-one percent of the patients suffered a BSI in the first 6 months after diagnosis, of which 58% died within this period, accounting to 67% of the early deaths in global and highlighting the major impact of infections on MM patients in a "real world" setting. Severe HLC pair suppression identified patients with a higher risk of early BSI (HR: 6,97, p=0,009), and extreme HLC pair suppression together with BSI event and age >65 were independent risk factors for early death (p<0,001). Based on these factors, a stratification model was generated to allow identify patients at a higher risk of early death and poorer OS, with an apparently better performance than the ISS on the early death context. In conclusion, HLC pair suppression associates with both a higher risk of life-threatening early infection and early death in newly diagnosed MM patients. Patients older than 65 with extreme HLC pair suppression and BSI are at a high risk of early death, and thus patients presenting with these criteria have a very adverse prognosis.
尽管在过去几十年中多发性骨髓瘤的治疗选择取得了显著进展,但如今它仍然是一种无法治愈的疾病。感染事件是与多发性骨髓瘤相关的免疫系统受损导致的并发症,有时甚至会危及生命,尤其是在诊断后的头几个月。潜在疾病和治疗都可能增加感染风险,因此,一种能够评估这种风险的生物标志物对于更有针对性地管理患者可能具有重要意义。血清中免疫球蛋白重链+轻链(HLC)对的测量可以对单克隆成分和同型非单克隆免疫球蛋白进行定量。这种方法已被证明对多发性骨髓瘤的克隆性检测具有高灵敏度和预后价值。HLC对抑制本身具有预后能力,有人认为它反映了免疫系统控制肿瘤的尝试。在本研究中,我们评估了HLC对抑制对115例新诊断的多发性骨髓瘤患者血流感染(BSI)发生率和早期死亡的影响。21%的患者在诊断后的前6个月发生了BSI,其中58%在该期间内死亡,占全球早期死亡人数的67%,突出了感染在“现实世界”中对多发性骨髓瘤患者的重大影响。严重的HLC对抑制可识别出早期BSI风险较高的患者(HR:6.97,p = 0.009),而极端的HLC对抑制与BSI事件和年龄>65岁是早期死亡的独立危险因素(p<0.001)。基于这些因素,生成了一个分层模型,以识别早期死亡风险较高和总生存期较差的患者,在早期死亡方面其表现明显优于国际分期系统(ISS)。总之,HLC对抑制与新诊断的多发性骨髓瘤患者危及生命的早期感染风险和早期死亡均相关。年龄大于65岁、HLC对极度抑制且发生BSI的患者早期死亡风险很高,因此符合这些标准的患者预后非常差。