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先前使用吉妥珠单抗奥佐米星和异基因造血干细胞移植后静脉闭塞性疾病的风险。

Prior treatment with gemtuzumab ozogamicin and the risk of veno-occlusive disease after allogeneic haematopoietic stem cell transplantation.

机构信息

Service d'Hématologie Clinique, CHU Hotel-Dieu, Nantes, Cedex 01, France.

出版信息

Bone Marrow Transplant. 2010 Jan;45(1):165-70. doi: 10.1038/bmt.2009.153. Epub 2009 Jul 6.

Abstract

This was a retrospective multicenter study including 44 acute leukaemia patients who have received allogeneic haematopoietic SCT (allo-HSCT) after prior exposure to Gemtuzumab Ozogamicin (GO) + chemotherapy. Median interval between last administration of GO and allo-HSCT was 4.2 (range, 0.8-26.3) months. At time of allo-HSCT, 33 patients were in CR. The majority of patients (n=36) received a reduced-intensity conditioning (RIC) regimen before allo-HSCT. All but one patient received low-dose heparin for veno-occlusive disease (VOD) prophylaxis. With a median follow-up of 15 (range, 1.1-63) months, overall survival and disease-free survival after allo-HSCT were 45% (95% confidence interval (CI), 30-61%) and 38% (95% CI, 24-54%) at 2 years, respectively. The cumulative incidence of grade 3-4 hyperbilirubinemia was 13.5% (n=6), with this being 21% in patients with a short (< or =3.5 months) GO-allo-HSCT interval (n=4/19) vs 8% in all others (P=NS). Overall, the cumulative incidence of VOD was 7% (n=3), with this being 10.5% (n=2/19) in patients with a short GO-allograft interval (< or =3.5 months) vs 4% (n=1/25) for all others (P=NS), and 5.5% (n=2/36) in patients receiving an RIC regimen vs 12.5% for the others (n=1/8) (P=NS). These results suggest that GO-based chemotherapy before allo-HSCT is feasible and does not result in an excessive rate of liver toxicity, especially VOD, after allo-HSCT.

摘要

这是一项回顾性多中心研究,共纳入 44 例先前接受过吉妥珠单抗奥佐米星(GO)+化疗的急性白血病患者,这些患者随后接受了异基因造血干细胞移植(allo-HSCT)。GO 末次给药与 allo-HSCT 之间的中位间隔为 4.2 个月(范围 0.8-26.3)。allo-HSCT 时,33 例患者处于完全缓解(CR)。大多数患者(n=36)在 allo-HSCT 前接受了强度降低的预处理方案。除 1 例患者外,所有患者均接受低剂量肝素预防静脉闭塞病(VOD)。中位随访 15 个月(范围 1.1-63),allo-HSCT 后 2 年的总生存率和无病生存率分别为 45%(95%置信区间[CI],30-61%)和 38%(95% CI,24-54%)。3-4 级高胆红素血症的累积发生率为 13.5%(n=6),GO-allo-HSCT 间隔时间较短(<或=3.5 个月,n=4/19)者发生率为 21%,而其他患者为 8%(P=NS)。总体而言,VOD 的累积发生率为 7%(n=3),GO 移植物间隔时间较短(<或=3.5 个月,n=19)的患者发生率为 10.5%,而其他患者为 4%(n=25)(P=NS),接受强度降低预处理方案的患者发生率为 5.5%,而其他患者为 12.5%(n=1/8)(P=NS)。这些结果表明,allo-HSCT 前基于 GO 的化疗是可行的,不会导致 allo-HSCT 后肝毒性(尤其是 VOD)发生率过高。

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