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:Complications of Autologous Stem Cell Transplantation in Multiple Myeloma: Results from the CALM Study.
Complications of Autologous Stem Cell Transplantation in Multiple Myeloma: Results from the CALM Study.
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淋巴瘤和骨髓瘤自体移植结局合作研究(CALM)的事后分析主要评估多发性骨髓瘤(MM)患者接受自体造血干细胞移植(ASCT)后短期和长期感染性及非感染性并发症发生率。
分析纳入所有参加CALM研究并接受至少一次ASCT的MM患者。主要终点为ASCT后感染性和非感染性并发症发生率,并比较三个时期:移植后0至100天、101天至1年及超过1年。
共纳入3,552名患者,中位随访56.7个月(范围0.4至108.1个月)。并发症发生率随ASCT后时间延长而降低:移植后第0至100天为每100患者年24.85例,自第101天起低于每100患者年2.31例。ASCT后100天时,45.7%的患者出现并发症,感染事件约为非感染性并发症的两倍。早期最常见事件为细菌感染(每100患者年6.5例,95%置信区间6.1–7.0)和胃肠道并发症(每100患者年4.7例,95%置信区间4.3–5.1)。并发症类型随ASCT后时间而变化。ASCT后是否出现并发症与总生存期无关。
本研究数据为比较ASCT相关并发症与多发性骨髓瘤新兴治疗(如CAR-T 细胞疗法和其他免疫疗法)导致的并发症提供了可靠依据。
Background: The main goal of this post hoc analysis of the Collaboration to Collect Autologous Transplant Outcomes in Lymphoma and Myeloma (CALM) study was to evaluate the rate of short- and long-term infectious and non-infectious complications occurring after ASCT in patients with multiple myeloma (MM). Methods: The analysis included all patients with MM from the CALM study who underwent 1 ASCT. The primary endpoint of the analysis was to determine the rate of infectious and non-infectious complications after ASCT and to compare them in three time periods: 0 100 days, 101 days 1 year, and >1 year after the first transplant. Results: The analysis included a total of 3552 patients followed up for a median of 56. 7 months (range 0. 4 108. 1). Complication rates decreased with the time from ASCT with 24.
85 cases per 100 patient-years from day 0 to 100 days after the transplant, and <2. 31 cases per 100 patient-years from the 101st day. At 100 days after ASC T, 45. 7% of patients had complications, with infectious events being twice as frequent as non-infectious complications. Bacterial infections (6. 5 cases per 100 patient-years, 95% CI: 6. 1 7. 0) and gastrointestinal complications (4.
7 cases per 100 patient-years, 95% CI: 4. 3 5. 1) were the most common early events. The pattern of complications changed with time from ASCT. The presence of complications after ASCT was not associated with overall survival. Conclusions: Our data provide a solid basis for comparing ASCT-related complications to those caused by emerging treatments in multiple myeloma, such as CAR T-cell therapy and other immunotherapies.
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