Kambe Ryosuke, Sato Masamichi, Uehara Daisuke, Iizuka Yutaka, Kakizaki Satoru
Department of General Internal Medicine National Hospital Organization Takasaki General Medical Center Takasaki Gunma Japan.
Department of Clinical Research National Hospital Organization Takasaki General Medical Center Takasaki Gunma Japan.
Clin Case Rep. 2023 Aug 28;11(9):e7861. doi: 10.1002/ccr3.7861. eCollection 2023 Sep.
SARS-CoV-2 infection has been associated with a prolonged course and a poor prognosis in patients who receive anti-CD20 antibodies. However, there are no established treatments for such patients. Serial changes in the SARS-CoV-2 antigen titer during the clinical course and treatment strategies for immunosuppressed patients are discussed.
We report a case of prolonged SARS-CoV-2 infection during obinutuzumab and bendamustine treatment for follicular lymphoma. Four years previously, the patient had been diagnosed with follicular lymphoma (Stage IIIA, Grade 2). She received several chemotherapy regimens, including rituximab and radiation therapy. Although these therapies achieved complete response temporally, they did not continue and recurred at 8 months before. Obinutuzumab and bendamustine therapy was selected, and she received five courses of obinutuzumab and bendamustine. She also received a SARS-CoV-2 mRNA vaccine two times. Although she did not have any symptoms, a routine check-up just before the 6th course of obinutuzumab and bendamustine revealed SARS-CoV-2 infection. Because she was immunosuppressed and was considered to be at high risk for the exacerbation of her disease, molnupiravir was immediately administered, and her SARS-CoV-2 antigen decreased. However, it was not completely cleared and flared-up at 6 weeks, with symptoms of COVID-19 appearing. Despite intensive treatment for SARS-CoV-2 infection, including remdesivir, baricitinib, tocilizumab and intravenous immunoglobulin, her SARS-CoV-2 antigen titer never became negative, and she finally died of respiratory failure caused by prolonged SARS-CoV-2 infection. Serial changes in the SARS-CoV-2 antigen titer during the clinical course and treatment strategies for immunosuppressed patients are discussed.
对于接受抗CD20抗体治疗的患者,严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染与病程延长及预后不良有关。然而,此类患者尚无既定的治疗方法。本文讨论了临床病程中SARS-CoV-2抗原滴度的系列变化以及免疫抑制患者的治疗策略。
我们报告了1例在接受奥妥珠单抗和苯达莫司汀治疗滤泡性淋巴瘤期间发生SARS-CoV-2感染时间延长的病例。4年前,该患者被诊断为滤泡性淋巴瘤(ⅢA期,2级)。她接受了包括利妥昔单抗和放射治疗在内的多种化疗方案。尽管这些治疗暂时取得了完全缓解,但未持续,8个月前复发。选择了奥妥珠单抗和苯达莫司汀治疗,她接受了5个疗程的奥妥珠单抗和苯达莫司汀治疗。她还接种了2次SARS-CoV-2信使核糖核酸(mRNA)疫苗。尽管她没有任何症状,但在第6个疗程的奥妥珠单抗和苯达莫司汀治疗前的常规检查发现了SARS-CoV-2感染。由于她处于免疫抑制状态且被认为疾病加重风险高,立即给予了莫努匹拉韦,其SARS-CoV-2抗原水平下降。然而,抗原未完全清除,6周时病情复发,出现了冠状病毒病2019(COVID-19)症状。尽管对SARS-CoV-2感染进行了强化治疗,包括使用瑞德西韦、巴瑞替尼、托珠单抗和静脉注射免疫球蛋白,但她的SARS-CoV-2抗原滴度从未转阴,最终死于SARS-CoV-2感染时间延长导致的呼吸衰竭。本文讨论了临床病程中SARS-CoV-2抗原滴度的系列变化以及免疫抑制患者的治疗策略。