Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts, USA.
CIBMTR® (Center for International Blood and Marrow Transplant Research), Department of Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Pediatr Blood Cancer. 2021 Aug;68(8):e29067. doi: 10.1002/pbc.29067. Epub 2021 Apr 19.
Gemtuzumab ozogamicin (GO) administered before allogeneic hematopoietic cell transplantation (alloHCT) has been linked to an increased risk of hepatic veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS).
This retrospective analysis examined VOD/SOS risk and clinical outcomes in pediatric patients with acute myeloid leukemia who received myeloablative alloHCT in 2008-2011 with (n = 148) and without (n = 348; controls) prior GO exposure and were reported to the Center for International Blood and Marrow Transplant Research.
Cumulative incidences (95% confidence interval [CI]) of VOD/SOS and severe VOD/SOS, respectively, at 100 days were 16% (11-23%) and 8% (4-13%) for GO-exposed patients and 10% (7-13%) and 3% (2-5%) for controls. With a median follow-up of approximately 7 years, the 5-year adjusted overall survival probability (95% CI) after alloHCT was 51% (43-58%) and 55% (50-60%) for GO-exposed patients and controls, respectively; three (4%) and one (<1%) deaths were attributed to VOD/SOS. In multivariate analyses, GO exposure was observed to be associated with an increased risk of VOD/SOS at 100 days, but was not associated with overall survival, disease-free survival, relapse, or nonrelapse mortality.
Results suggest that GO treatment prior to alloHCT in pediatric patients may increase the risk of VOD/SOS but not death.
在异基因造血细胞移植(alloHCT)前使用吉妥珠单抗奥佐米星(GO)与肝静脉闭塞病/窦状隙阻塞综合征(VOD/SOS)的风险增加有关。
本回顾性分析检查了在 2008 年至 2011 年间接受清髓性 alloHCT 的患有急性髓细胞白血病的儿科患者的 VOD/SOS 风险和临床结果,这些患者(n=148)和未暴露于 GO(n=348;对照组),并向国际血液和骨髓移植研究中心报告。
GO 暴露组和对照组在 100 天的 VOD/SOS 和重度 VOD/SOS 的累积发生率(95%置信区间[CI])分别为 16%(11-23%)和 8%(4-13%)和 10%(7-13%)和 3%(2-5%)。在中位随访时间约为 7 年之后,alloHCT 后的 5 年调整总生存率概率(95%CI)分别为 GO 暴露组和对照组的 51%(43-58%)和 55%(50-60%);有三例(4%)和一例(<1%)死亡归因于 VOD/SOS。多变量分析显示,GO 暴露与 100 天的 VOD/SOS 风险增加相关,但与总生存率、无病生存率、复发率或非复发死亡率无关。
结果表明,GO 治疗在儿科患者 alloHCT 前可能会增加 VOD/SOS 的风险,但不会增加死亡风险。