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因诺妥珠单抗奥唑米星作为替沙格韦单抗治疗后复发的儿童BCP-ALL患者干细胞移植的桥梁:病例系列

Inotuzumab Ozogamicin as a Bridge to Stem Cell Transplantation in Relapsed Pediatric BCP-ALL After Tisagenlecleucel: A Case Series.

作者信息

Aertgeerts Margo, Renard Marleen, Uyttebroeck Anne, Boeckx Nancy, Segers Heidi

机构信息

Department of Oncology, KU Leuven, Leuven, Belgium.

Center for Cancer Biology, VIB, Leuven, Belgium.

出版信息

Cancer Rep (Hoboken). 2025 Mar;8(3):e70177. doi: 10.1002/cnr2.70177.

Abstract

BACKGROUND

CD19-directed chimeric antigen receptor T-cell therapy tisagenlecleucel has shown promising results in the treatment of pediatric patients with relapsed/refractory B-cell precursor acute lymphoblastic leukemia (BCP-ALL). However, around 50% of patients relapse after tisagenlecleucel. Following multiple relapses, limited treatment options are left, and the prognosis is dismal. We report on four pediatric patients who relapsed after tisagenlecleucel and were treated with inotuzumab ozogamicin (InO).

CASE

Four patients with BCP-ALL received tisagenlecleucel after second relapse (3/4) or refractory disease at first relapse (1/4). Three patients relapsed with CD19/CD22 BCP-ALL, one with CD19/CD22 BCP-ALL. Following relapse, they received treatment with InO. After the first InO cycle, all achieved complete remission (CR), three without measurable residual disease. After two or three InO cycles, they underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT). One patient developed an isolated extramedullary relapse (IEM) in both anterior eye chambers six and nine months after allo-HSCT and received palliative radiotherapy. This patient was in CR at the last follow-up 25 months later. The other patients were also in CR at the last follow-up (mean 31.3 months).

CONCLUSION

InO can be used successfully and safely for the treatment of CD22 BCP-ALL relapse after tisagenlecleucel as a bridge to allo-HSCT in heavily pretreated pediatric patients.

摘要

背景

靶向CD19的嵌合抗原受体T细胞疗法tisagenlecleucel在治疗复发/难治性B细胞前体急性淋巴细胞白血病(BCP-ALL)的儿科患者中已显示出有前景的结果。然而,约50%的患者在接受tisagenlecleucel治疗后复发。多次复发后,治疗选择有限,预后不佳。我们报告了4例在接受tisagenlecleucel治疗后复发并接受吉妥珠单抗奥唑米星(InO)治疗的儿科患者。

病例

4例BCP-ALL患者在第二次复发(3/4)或首次复发时为难治性疾病(1/4)后接受了tisagenlecleucel治疗。3例患者复发为CD19/CD22 BCP-ALL,1例复发为CD19/CD22 BCP-ALL。复发后,他们接受了InO治疗。在第一个InO周期后,所有患者均实现完全缓解(CR),3例无微小残留病。在两个或三个InO周期后,他们接受了异基因造血干细胞移植(allo-HSCT)。1例患者在allo-HSCT后6个月和9个月时在前房均出现孤立性髓外复发(IEM),并接受了姑息性放疗。该患者在25个月后的最后一次随访时处于CR状态。其他患者在最后一次随访时也处于CR状态(平均31.3个月)。

结论

InO可成功且安全地用于治疗tisagenlecleucel治疗后复发的CD22 BCP-ALL,作为重度预处理儿科患者allo-HSCT的桥梁。

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