不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Outcome of early treatment of SARS-CoV-2 infection in patients with haematological disorders.
Outcome of early treatment of SARS-CoV-2 infection in patients with haematological disorders.
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血液系统恶性肿瘤(HM)患者早期接受抗病毒药物或抗刺突蛋白单克隆抗体(MAb)治疗COVID-19的结局尚不明确。本研究回顾性分析了2021年3月至2022年7月接受轻至中度COVID-19治疗的HM患者。主要复合终点为治疗失败(重症COVID-19或COVID-19相关死亡)。研究纳入328例连续患者:120例(37%)接受MAb治疗(其中73例使用sotrovimab),208例(63%)接受抗病毒药物治疗(其中116例使用nirmatrelvir/ritonavir);从症状出现到治疗的中位时间为2天。111例(33.8%)患有非霍奇金淋巴瘤(NHL),89例(27%)为移植或CAR-T 细胞治疗受者。大多数感染(309例,94%)发生在Omicron流行期。
31例(9.5%)发生治疗失败。治疗失败的独立预测因素包括年龄较大、接种疫苗剂次较少及接受MAb治疗。Omicron流行期的失败率低于其前期(7.8%比36.8%,p<0.001)。在Omicron流行期,失败的预测因素为年龄较大、接种疫苗剂次较少,以及急性髓系白血病/骨髓增生异常综合征(AML/MDS)诊断。病毒排出时间较长的独立预测因素包括年龄、合并症、确诊时住院、NHL/慢性淋巴细胞白血病(CLL)以及MAb治疗。COVID-19相关死亡率为3.4%(11例);在Omicron流行期,早期治疗后进展为重症COVID-19患者的死亡率为26%。即使在Omicron流行期,HM患者早期治疗仍存在显著失败风险,且死亡率较高。
Outcome of early treatment of COVID-19 with antivirals or anti-spike monoclonal antibodies (MABs) in patients with haematological malignancies (HM) is unknown. A retrospective study of HM patients treated for mild/moderate COVID-19 between March 2021 and July 2022 was performed. The main composite end-point was treatment failure (severe COVID-19 or COVID-19-related death).
We included 328 consecutive patients who received MABs (n = 120, 37%; sotrovimab, n = 73) or antivirals (n = 208, 63%; nirmatrelvir/ritonavir, n = 116) over a median of two days after symptoms started; 111 (33. 8%) had non-Hodgkin lymphoma (NHL); 89 (27%) were transplant/CAR-T (chimaeric antigen receptor T-cell therapy) recipients. Most infections (n = 309, 94%) occurred during the Omicron period. Failure developed in 31 patients (9. 5%). Its independent predictors were older age, fewer vaccine doses, and treatment with MABs. Rate of failure was lower in the Omicron versus the pre-Omicron period (7.
8% versus 36. 8%, p < 0. 001). During the Omicron period, predictors of failure were age, fewer vaccine doses and diagnosis of acute myeloid leukaemia/myelodysplastic syndrome (AML/MDS). Independent predictors of longer viral shedding were age, comorbidities, hospital admission at diagnosis, NHL/CLL, treatment with MABs.
COVID-19-associated mortality was 3. 4% (n = 11). The mortality in those who developed severe COVID-19 after early treatment was 26% in the Omicron period. Patients with HM had a significant risk of failure of early treatment, even during the Omicron period, with high mortality rate.
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