Department of Surgical, Oncological and Stomatological Disciplines, University of Palermo, Palermo, Italy.
Hematology Unit, Department of Health Promotion, Mother and Child Care, Internal Medicine and Medical Specialties (PROMISE), University of Palermo, Palermo, Italy.
Chemotherapy. 2021;66(3):87-91. doi: 10.1159/000515430. Epub 2021 Mar 30.
Ruxolitinib side effects include the most frequent hematological toxicity along with a more recently evidenced immunosuppressive activity, interfering both with the innate and adaptive immunity, and several cases of reactivation of latent infections by opportunistic agents in patients in treatment with ruxolitinib have been published in the last years. Several pathophysiological mechanisms may explain an association between ruxolitinib and opportunistic infections. From what we know, the only case of an isolated lymph node TBC reactivation in a ruxolitinib-treated myelofibrosis (MF) patient was reported by Patil et al. in 2016 [Int J Med Sci Public Health. 2017;6(3):1]. Other 10 cases describing TBC reactivations in MF patients assuming ruxolitinib and successfully treated with 4-drug anti-TBC therapy are available in the literature to date. The case we reported describes an isolated lymph nodal TBC reactivation in a patient with the diagnosis of post-essential thrombocythemia-MF during ruxolitinib treatment after a long course of interferon-a (IFN-α2b) assumed for the previous diagnosis of ET. The case we report teaches that lymphadenopathy with or without constitutional symptoms developing during ruxolitinib therapy should be considered as a possible manifestation of a TBC reactivation in patients with a previous positive TBC-exposure test. In these cases, Ziel-Nielsen testing on urine and sputum has to be performed to rule out infectiousness and eventually isolate the patient. Moreover, previous long-time exposition to IFN-α2b may be related with a higher risk for TBC reactivation in these subset of patients. We encourage reevaluation of the cohorts of patients treated with ruxolitinib in previous and current large prospective studies to study the possible correlation between previous exposition to IFN-α2b and TBC reactivation.
芦可替尼的副作用包括最常见的血液学毒性,以及最近证实的免疫抑制活性,干扰固有免疫和适应性免疫,近年来已有报道称,接受芦可替尼治疗的患者中,几种潜伏感染的机会性病原体被重新激活。几种病理生理机制可能解释芦可替尼与机会性感染之间的关联。据我们所知,2016 年 Patil 等人报道了唯一一例芦可替尼治疗骨髓纤维化(MF)患者孤立性淋巴结结核(TB)再激活的病例[Int J Med Sci Public Health. 2017;6(3):1]。迄今为止,文献中还报道了其他 10 例 MF 患者在接受芦可替尼治疗后出现 TB 再激活并成功接受 4 药抗 TB 治疗的病例。我们报告的病例描述了一例诊断为原发性血小板增多症-MF 的患者在接受芦可替尼治疗期间出现孤立性淋巴结 TB 再激活,在此之前该患者长期接受干扰素-α(IFN-α2b)治疗以治疗原发性血小板增多症。我们报告的病例表明,在接受芦可替尼治疗期间出现的伴或不伴全身症状的淋巴结病,应被视为 TB 再激活的可能表现,而这些患者之前曾有 TB 暴露试验阳性。在这些情况下,必须进行尿和痰的 Ziel-Nielsen 检测,以排除传染性,并最终对患者进行隔离。此外,先前长期接受 IFN-α2b 治疗可能与这些患者亚组中 TB 再激活的风险增加有关。我们鼓励在之前和当前的大型前瞻性研究中重新评估接受芦可替尼治疗的患者队列,以研究之前接受 IFN-α2b 暴露与 TB 再激活之间的可能相关性。