4th Department of Internal Medicine-Hematology, University Hospital Hradec Kralove, Hradec Kralove, Czech Republic.
Faculty of Medicine in Hradec Kralove, Charles University, Hradec Kralove, Czech Republic.
Cancer Med. 2024 Aug;13(15):e7399. doi: 10.1002/cam4.7399.
The impact of chemoimmunotherapy (CIT) on immunoglobulin (Ig) quantities in patients with chronic lymphocytic leukemia (CLL) has not been extensively studied.
We analyzed Ig levels in 45 stable patients with indolent CLL (without indication for treatment) and 87 patients with progressive disease before first-line treatment. Fifty-five patients were evaluated again after the treatment with CIT.
We observed significantly lower levels of all Ig classes and subclasses in patients with progressive disease compared to patients with indolent disease. After treatment, median IgA increased from 0.59 g/L to 0.74 g/L (p = 0.0031). In stable patients, lower IgA2 was associated with shorter time to first treatment, although it did not reach statistical significance (p = 0.056). Shorter overall survival was observed in patients with progressive disease and lower IgG2 (p = 0.043). Surprisingly, among the patients with progressive CLL, unmutated IGHV genes were associated with higher levels of IgG, IgG1 and IgM, while TP53 mutation and/or 17p deletion were associated with higher levels of IgA and IgA1.
CIT may lead to increase in IgA levels. Hypogammaglobulinemia is more common in patients with progressive CLL and unmutated IGHV or TP53 dysfunction.
化疗免疫疗法(CIT)对慢性淋巴细胞白血病(CLL)患者免疫球蛋白(Ig)数量的影响尚未得到广泛研究。
我们分析了 45 例稳定的惰性 CLL 患者(无治疗指征)和 87 例一线治疗前进展性疾病患者的 Ig 水平。55 例患者在接受 CIT 治疗后再次进行评估。
与惰性疾病患者相比,我们观察到进展性疾病患者的所有 Ig 类和亚类水平均显著降低。治疗后,IgA 中位数从 0.59g/L 增加到 0.74g/L(p=0.0031)。在稳定的患者中,较低的 IgA2 与首次治疗的时间较短相关,尽管未达到统计学意义(p=0.056)。进展性疾病和较低 IgG2 的患者总生存期较短(p=0.043)。令人惊讶的是,在进展性 CLL 患者中,未突变的 IGHV 基因与 IgG、IgG1 和 IgM 水平较高相关,而 TP53 突变和/或 17p 缺失与 IgA 和 IgA1 水平较高相关。
CIT 可能导致 IgA 水平升高。进展性 CLL 患者和未突变的 IGHV 或 TP53 功能障碍患者更容易出现低丙种球蛋白血症。