Department of Radiation Oncology, Brigham and Women's Hospital, Dana-Farber Cancer Institute, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
Harvard Medical School, Boston, Massachusetts.
Transplant Cell Ther. 2022 Aug;28(8):502.e1-502.e12. doi: 10.1016/j.jtct.2022.05.028. Epub 2022 May 25.
Pulmonary toxicity after allogeneic hematopoietic stem cell transplantation (allo-HSCT) for childhood leukemia and myelodysplastic syndrome (MDS), along with the impact of different myeloablative conditioning regimens, remain incompletely described. Here we compared the acute and long-term incidence of pulmonary toxicity (PT) after total body irradiation (TBI)- and busulfan-based myeloablative conditioning. We conducted this retrospective cohort study of 311 consecutive pediatric patients with leukemia or MDS who underwent allo-HSCT at Dana-Farber Cancer Institute/Boston Children's Hospital between 2008 and 2018. PT was graded using Common Terminology Criteria for Adverse Events version 5.0. The primary objective was to compare the cumulative incidence of grade ≥3 and grade 5 PT after TBI-based and busulfan-based myeloablative conditioning using Gray's test. Secondary objectives were to determine factors associated with PT and overall survival (OS) using competing risk analysis and Cox regression analyses, respectively. There was no significant difference between the TBI-conditioned group (n = 227) and the busulfan-conditioned group (n = 84) in the incidence of grade ≥3 PT (29.2% versus 34.7% at 2 years; P = .26) or grade 5 pulmonary toxicity (6.2% versus 6.1% at 2 years; P = .47). Age (hazard ratio [HR], 1.70, 95% confidence interval [CI], 1.11 to 2.59; P = .01), grade ≥2 PT prior to allo-HSCT or preexisting pulmonary conditions (HR, 1.84, 95% CI, 1.24 to 2.72; P < .01), acute graft-versus-host disease (GVHD) (HR, 2.50; 95% CI, 1.51 to 4.14; P < .01), and chronic GVHD (HR, 2.61; 95% CI, 1.26 to 5.42; P = .01) were associated with grade ≥3 PT on multivariable analysis. Grade ≥3 PT was associated with worse OS (81.1% versus 61.5% at 2 years; P < .01). In pediatric allo-HSCT recipients, rates of PT were similar in recipients of TBI-based and recipients of busulfan-based myeloablative conditioning regimens. Age, the presence of PT or preexisting pulmonary conditions prior to transplantation, and the development of either acute or chronic GVHD were associated with grade ≥3 PT post-transplantation. Furthermore, the occurrence of grade 3-4 PT post-transplantation was associated with inferior OS.
异基因造血干细胞移植(allo-HSCT)后儿童白血病和骨髓增生异常综合征(MDS)的肺毒性(PT),以及不同的清髓性预处理方案的影响,仍不完全清楚。在这里,我们比较了全身照射(TBI)和白消安为基础的清髓性预处理后的急性和长期 PT 发生率。我们对 2008 年至 2018 年间在 Dana-Farber 癌症研究所/波士顿儿童医院接受 allo-HSCT 的 311 例连续白血病或 MDS 儿科患者进行了回顾性队列研究。PT 使用不良事件常用术语标准 5.0 进行分级。主要目的是使用 Gray 检验比较 TBI 为基础和白消安为基础的清髓性预处理后≥3 级和 5 级 PT 的累积发生率。次要目的分别是使用竞争风险分析和 Cox 回归分析确定与 PT 和总生存(OS)相关的因素。TBI 预处理组(n=227)和白消安预处理组(n=84)在≥3 级 PT 的发生率(2 年时分别为 29.2%和 34.7%;P=0.26)或 5 级肺毒性(2 年时分别为 6.2%和 6.1%;P=0.47)方面无显著差异。年龄(风险比[HR],1.70,95%置信区间[CI],1.11 至 2.59;P=0.01)、allo-HSCT 前≥2 级 PT 或预先存在的肺部疾病(HR,1.84,95%CI,1.24 至 2.72;P<.01)、急性移植物抗宿主病(GVHD)(HR,2.50;95%CI,1.51 至 4.14;P<.01)和慢性 GVHD(HR,2.61;95%CI,1.26 至 5.42;P=0.01)在多变量分析中与≥3 级 PT 相关。≥3 级 PT 与较差的 OS 相关(2 年时分别为 81.1%和 61.5%;P<.01)。在儿科 allo-HSCT 受者中,TBI 为基础和白消安为基础的清髓性预处理方案的 PT 发生率相似。年龄、移植前 PT 或预先存在的肺部疾病的存在以及急性或慢性 GVHD 的发生与移植后≥3 级 PT 相关。此外,移植后发生 3-4 级 PT 与较差的 OS 相关。