Department of Hematology, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Department of Pathology, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
J Clin Exp Hematop. 2020 Jun 20;60(2):41-50. doi: 10.3960/jslrt.19039. Epub 2020 May 13.
Regressive lymphoproliferative disorders (R-LPD) after methotrexate (MTX) withdrawal are one of the specific features of methotrexate - associated lymphoproliferative disorders (MTX-LPD). Although the impact of the absolute lymphocyte count (ALC) on the pathogenesis of R-LPD has been recently emphasized, understanding relapse/regrowth events (RRE) and differences among LPD subtypes is necessary. In this study, we confirmed ALC recovery in the regressive group (R-G; R-LPD without RRE) and relapse/regrowth group (R/R-G; R-LPD with RRE). The increase in ALC lasted at least 2 years in R-G, whereas it decreased within 3 years in R/R-G, supporting the better overall survival (OS) in R-G, as previously reported. In addition, our study suggested that an ALC of 1000/µL at the time of development of LPD is a significant predictor for treatment-free survival (TFS). Furthermore, an ALC of 1000/µL at 6 months after MTX withdrawal was found to be a significant indicator of TFS and OS for R-G and R/R-G. The ALC decreased gradually before LPD development in R/R-G, whereas it decreased 6 months before LPD development in R-G, confirming the important role of ALC in the pathogenesis of MTX-LPD such as regressive events and RRE. In addition to ALC, other predictive factors, such as serum C-reactive protein and soluble interleukin-2 receptors, may be helpful in the management of MTX-LPD, including the decision making for an additional chemotherapy for regressive LPD after MTX withdrawal.
甲氨蝶呤相关性淋巴增生性疾病(MTX-LPD)患者在停用甲氨蝶呤(MTX)后出现退行性淋巴增生性疾病(R-LPD)是其特征之一。虽然最近强调了绝对淋巴细胞计数(ALC)对 R-LPD 发病机制的影响,但了解复发/再生长事件(RRE)和 LPD 亚型之间的差异是必要的。在这项研究中,我们证实了退行性组(R-G;无 RRE 的 R-LPD)和复发/再生长组(R/R-G;有 RRE 的 R-LPD)中 ALC 的恢复。R-G 中的 ALC 增加至少持续 2 年,而 R/R-G 中在 3 年内降低,这与之前报道的 R-G 的总体生存(OS)更好相吻合。此外,我们的研究表明,LPD 发生时的 ALC 为 1000/µL 是无治疗生存(TFS)的显著预测因子。此外,在 MTX 停药后 6 个月时的 ALC 为 1000/µL 是 R-G 和 R/R-G 的 TFS 和 OS 的显著指标。在 R/R-G 中,ALC 在发生 LPD 之前逐渐降低,而在 R-G 中则在发生 LPD 之前 6 个月降低,证实了 ALC 在 MTX-LPD 发病机制中的重要作用,如退行性事件和 RRE。除了 ALC,其他预测因子,如血清 C 反应蛋白和可溶性白细胞介素-2 受体,可能有助于 MTX-LPD 的管理,包括在 MTX 停药后对退行性 LPD 进行额外化疗的决策。