CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Prolonged COVID-19 Pneumonitis and Severe Lung Injury in a Patient with a History of Diffuse Large B-cell Lymphoma after CAR-T Therapy: Highlighting the Role of Corticosteroids.
Prolonged COVID-19 Pneumonitis and Severe Lung Injury in a Patient with a History of Diffuse Large B-cell Lymphoma after CAR-T Therapy: Highlighting the Role of Corticosteroids.
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COVID-19 对既往有血液系统恶性肿瘤病史的患者构成更高的风险,并可导致严重的呼吸窘迫和死亡。研究表明,迁延性肺炎可能需要使用皮质类固醇才能改善。然而,关于管理迁延性 COVID-19 肺炎的合适方案的数据仍然缺乏。本病例凸显了在合并血液系统恶性肿瘤的免疫功能低下个体中治疗 COVID-19 感染的挑战。皮质类固醇治疗显示出获益,但剂量和疗程应基于患者个体的反应。延长监测、个体化治疗方案以及研究对于优化这一脆弱人群的结局至关重要。
COVID-19 可对免疫功能低下者造成严重后果,包括血液系统恶性肿瘤患者。在接受CAR-T 细胞治疗的弥漫性大 B 细胞淋巴瘤(DLBCL)患者中,导致肺炎和肺损伤的迁延性感染较为罕见。病例报告:一名 43 岁男性,有 DLBCL 病史,CAR-T 治疗后缓解 2 年,出现持续性 COVID 感染,经聚合酶链反应阳性证实。该感染缓慢进展为有症状的低氧性肺炎,活检证实为弥漫性肺泡损伤,经皮质类固醇治疗后有反应。
INTRODUCTION: COVID-19 can have severe consequences for immunocompromised individuals, including those with hematological malignancies. Prolonged infections causing pneumonia and lung injury are rare in patients with diffuse large B-cell lymphoma (DLBCL) treated with chimeric antigen receptor T-cell (CAR-T). CASE PRESENTATION: A 43-year-old male with a history of DLBCL, in remission for 2 years after CAR-T therapy, developed a persistent COVID infection, as confirmed via positive polymerase chain reaction. This slowly progressed to symptomatic hypoxemic pneumonitis and biopsy-proven diffuse alveolar damage, which responded to corticosteroid treatment. DISCUSSION: COVID-19 poses increased risks to patients with a history of hematologic malignancies and can lead to severe respiratory distress and mortality. Studies have shown prolonged pneumonitis may require corticosteroids for improvement. However, data on appropriate regimen for managing prolonged COVID-19 pneumonitis are lacking. CONCLUSIONS: This case highlights challenges of the treatment of COVID-19 infections in immunocompromised individuals with hematological malignancies. Corticosteroid treatment shows benefits, but dosing and duration should be based on individual patient response. Extended monitoring, individualized treatment plans, and research are crucial for optimizing outcomes in this vulnerable population.
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