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多发性骨髓瘤患者输注递增低剂量供体淋巴细胞后血清学完全缓解与同时出现新的骨溶解性病变之间的差异:一例报告

Discrepancy between serological complete remission and concomitant new bone lytic lesions after infusion of escalating low doses of donor lymphocytes in multiple myeloma: a case report.

作者信息

Rondelli D, Bandini G, Cavo M, Re F, Motta M, Senese B, Leopardi G, Stanzani M, Tura S

机构信息

Institute of Hematology and Medical Oncology 'Seràgnoli', University of Bologna, Italy.

出版信息

Bone Marrow Transplant. 1999 Sep;24(6):685-7. doi: 10.1038/sj.bmt.1701960.

DOI:10.1038/sj.bmt.1701960
PMID:10490737
Abstract

A graft-versus-myeloma effect has been previously induced by infusing high numbers of donor lymphocytes after allogeneic stem cell transplantation in relapsed/refractory multiple myeloma (MM) patients. A 43-year-old patient with MM refractory to standard chemotherapy and autologous transplantation received an allogeneic HLA-matched T cell-depleted marrow transplant from his sister after conditioning with single dose total-body irradiation, melphalan and cyclophosphamide. Twenty-four months after transplant neither a significant reduction of serum M protein nor evidence of acute or chronic graft-versus-host disease (GVHD) were observed. The patient was then treated with four escalating low doses of donor lymphocyte infusions (DLI) (0.1, 1.0, 5.0 and 5.0 x 106 CD3+ T cells/kg, respectively) over a 13 month period. Following the second infusion a mild liver acute GVHD and a partial, but transient, response occurred. After the last DLI the patient achieved a complete remission and developed extensive chronic GVHD. However, concomitant with the disappearance of clonal plasma cells from the marrow and of serum M protein, two new bone lytic lesions appeared requiring treatment with radiotherapy. In conclusion, escalating low doses of DLI may be effective in MM and may prevent severe acute but not chronic GVHD. However, the efficacy of DLI in extramedullary MM lesions is still unclear.

摘要

先前在复发/难治性多发性骨髓瘤(MM)患者接受异基因干细胞移植后输注大量供体淋巴细胞,已诱导出移植物抗骨髓瘤效应。一名43岁对标准化疗和自体移植难治的MM患者,在接受单剂量全身照射、美法仑和环磷酰胺预处理后,接受了来自其妹妹的 HLA 匹配的去 T 细胞骨髓移植。移植后24个月,未观察到血清M蛋白显著降低,也未发现急性或慢性移植物抗宿主病(GVHD)的证据。然后在13个月期间,该患者接受了四次递增的低剂量供体淋巴细胞输注(DLI)(分别为0.1、1.0、5.0和5.0×10⁶ CD3⁺ T细胞/kg)。第二次输注后,出现了轻度肝脏急性GVHD以及部分但短暂的反应。最后一次DLI后,患者达到完全缓解并出现广泛的慢性GVHD。然而,随着骨髓中克隆性浆细胞和血清M蛋白消失,出现了两处新的骨溶解性病变,需要进行放射治疗。总之,递增的低剂量DLI可能对MM有效,且可预防严重急性GVHD,但不能预防慢性GVHD。然而,DLI对髓外MM病变的疗效仍不清楚。

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