Pezzullo Luca, Giudice Valentina, Serio Bianca, Fontana Raffaele, Guariglia Roberto, Martorelli Maria Carmen, Ferrara Idalucia, Mettivier Laura, Bruno Alessandro, Bianco Rosario, Vaccaro Emilia, Pagliano Pasquale, Montuori Nunzia, Filippelli Amelia, Selleri Carmine
Hematology and Transplant Center, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", Salerno, 84131, Italy.
Clinical Pharmacology, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", Salerno, 84131, Italy.
Open Med (Wars). 2021 Apr 21;16(1):672-682. doi: 10.1515/med-2021-0274. eCollection 2021.
Cytomegalovirus (CMV) reactivation during chemotherapy or after organ or hematopoietic stem cell transplantation is a major cause of morbidity and mortality, and the risk of reactivation increases with patients' age. Bendamustine, an alkylating agent currently used for treatment of indolent and aggressive non-Hodgkin lymphomas, can augment the risk of secondary infections including CMV reactivation. In this real-world study, we described an increased incidence of CMV reactivation in older adults (age >60 years old) with newly diagnosed and relapsed/refractory indolent and aggressive diseases treated with bendamustine-containing regimens. In particular, patients who received bendamustine plus rituximab and dexamethasone were at higher risk of CMV reactivation, especially when administered as first-line therapy and after the third course of bendamustine. In addition, patients with CMV reactivation showed a significant depression of circulating CD4 T cell count and anti-CMV IgG levels during active infection, suggesting an impairment of immune system functions which are not able to properly face viral reactivation. Therefore, a close and early monitoring of clinical and laboratory findings might improve clinical management and outcome of non-Hodgkin lymphoma patients by preventing the development of CMV disease in a subgroup of subjects treated with bendamustine more susceptible to viral reactivation.
化疗期间或器官或造血干细胞移植后巨细胞病毒(CMV)再激活是发病和死亡的主要原因,且再激活风险随患者年龄增加而升高。苯达莫司汀是一种目前用于治疗惰性和侵袭性非霍奇金淋巴瘤的烷化剂,可增加包括CMV再激活在内的继发感染风险。在这项真实世界研究中,我们描述了使用含苯达莫司汀方案治疗的新诊断及复发/难治性惰性和侵袭性疾病的老年患者(年龄>60岁)中CMV再激活发生率增加。特别是,接受苯达莫司汀联合利妥昔单抗和地塞米松治疗的患者CMV再激活风险更高,尤其是作为一线治疗以及在苯达莫司汀第三个疗程之后使用时。此外,CMV再激活患者在活跃感染期间循环CD4 T细胞计数和抗CMV IgG水平显著降低,提示免疫系统功能受损,无法有效应对病毒再激活。因此,密切且早期监测临床和实验室检查结果,可能通过预防在接受苯达莫司汀治疗且更易发生病毒再激活的亚组患者中出现CMV疾病,改善非霍奇金淋巴瘤患者的临床管理和预后。