Mayo Clinic Alix School of Medicine.
Division of Pediatric Hematology/Oncology, Department of Pediatric and Adolescent Medicine.
J Pediatr Hematol Oncol. 2023 Jul 1;45(5):e624-e627. doi: 10.1097/MPH.0000000000002629. Epub 2023 Jan 26.
Post-transplant lymphoproliferative disorder (PTLD) is a complication of immunosuppressive therapy following solid organ or hematopoietic cell transplantation. Initial treatment typically includes a reduction of immunosuppression with or without rituximab. However, the optimal therapy for PTLD with plasmacytic differentiation is unclear. We present 3 cases of pediatric patients with plasmacytic PTLD. Two patients received a standard rituximab-based approach and relapsed, prompting additional chemotherapy. The third patient was treated with a novel regimen of bortezomib, dexamethasone, and daratumumab. This regimen was safe, well-tolerated, and resulted in a 2-year remission. Larger studies are needed to further explore this regimen.
移植后淋巴组织增生性疾病 (PTLD) 是实体器官或造血细胞移植后免疫抑制治疗的并发症。初始治疗通常包括减少免疫抑制药物剂量,联合或不联合利妥昔单抗。然而,浆细胞分化型 PTLD 的最佳治疗方法尚不清楚。我们报告了 3 例儿科患者的浆细胞 PTLD 病例。2 例患者接受了标准的利妥昔单抗为基础的治疗方案,但复发,随后接受了额外的化疗。第 3 例患者接受了硼替佐米、地塞米松和达雷妥尤单抗的新型治疗方案。该方案安全、耐受良好,且 2 年无疾病复发。需要更大规模的研究来进一步探索该方案。