Department of Infectious Diseases, Beijing You An Hospital, Beijing Institute of Hepatology, Capital Medical University, Beijing, China.
Department of Hematology, Nanjing Medical University Affiliated Nanjing First Hospital, Nanjing, Jiangsu, China.
J Med Virol. 2021 Jun;93(6):3907-3914. doi: 10.1002/jmv.26655. Epub 2020 Nov 15.
The lymphocyte-to-monocyte ratio (LMR) and platelet-to-lymphocyte ratio (PLR) have been reported to be useful for predicting the prognosis of various malignancies, including diffuse large B-cell lymphoma (DLBCL). However, little is known about the role of LMR and PLR in the prognosis of DLBCL patients with human immunodeficiency virus (HIV) infection. We retrospectively evaluated the prognostic value of the LMR and PLR in patients with newly diagnosed AIDS-related diffuse large B-cell lymphoma (AR-DLBCL) who were treated with CHOP-like chemotherapy at a single institution. In 33 AR-DLBCL patients, the median follow-up period was 32 months (range: 7-85 months), with an estimated 2-year overall survival (OS) rate of 79.9%. The univariate analysis confirmed the LMR ≤ 2.74 (p = .015), PLR ≥ 337.7 (p = .019), and moderate anemia (p = .045) were associated with inferior survival. The independent significant association between low LMR and poor OS in the multivariate analysis was identified (HR: 0.033, 95% CI: 0.001-0.853, p = .040). However, PLR (p = .459) and moderate anemia (p = .102) did not retain an independent significance in the multivariate analysis. Moreover, compared with the high-LMR group, patients with low-LMR more frequently had B symptoms (p = .010) and lower CD4+T cell count (p < .001). The pretreatment LMR may be an effective prognostic factor for predicting OS in patients with AR-DLBCL.
淋巴细胞与单核细胞比值(LMR)和血小板与淋巴细胞比值(PLR)已被报道可用于预测各种恶性肿瘤的预后,包括弥漫性大 B 细胞淋巴瘤(DLBCL)。然而,关于 LMR 和 PLR 在人类免疫缺陷病毒(HIV)感染相关弥漫大 B 细胞淋巴瘤(AR-DLBCL)患者预后中的作用知之甚少。我们回顾性评估了单中心接受 CHOP 样化疗治疗的新发 AIDS 相关弥漫大 B 细胞淋巴瘤(AR-DLBCL)患者的 LMR 和 PLR 的预后价值。在 33 例 AR-DLBCL 患者中,中位随访时间为 32 个月(范围:7-85 个月),估计 2 年总生存率(OS)为 79.9%。单因素分析证实,LMR≤2.74(p=0.015)、PLR≥337.7(p=0.019)和中度贫血(p=0.045)与生存不良相关。多因素分析中发现,LMR 较低与 OS 不良之间存在独立显著相关性(HR:0.033,95%CI:0.001-0.853,p=0.040)。然而,PLR(p=0.459)和中度贫血(p=0.102)在多因素分析中未保留独立意义。此外,与高 LMR 组相比,低 LMR 组患者更常出现 B 症状(p=0.010)和更低的 CD4+T 细胞计数(p<0.001)。治疗前 LMR 可能是预测 AR-DLBCL 患者 OS 的有效预后因素。