Department of Hematology, Shinko Hospital, 1-4-47, Wakihamacho, Chuo-Ku, Kobe, Hyogo, 651-0072, Japan.
Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Int J Hematol. 2024 Jun;119(6):762-767. doi: 10.1007/s12185-024-03762-8. Epub 2024 Mar 25.
Allogenic hematopoietic stem cell transplantation (allo-HSCT) is not a standard therapy for solid cancer because of its high toxicity and insufficient evidence levels. However, the potential graft-versus-solid-tumor (GVT) effect of this therapy has been discussed. Many case reports have also described treatment effects of allo-HSCT in patients with hematologic malignancies and active solid tumors. A 38-year-old woman treated with fulvestrant and abemaciclib for recurrent breast cancer with multiple lung metastases was diagnosed with myelodysplastic syndrome (MDS) with increased blasts 2. She was classified as adverse risk by the 2017 European LeukemiaNet risk stratification and as very high risk by the Molecular International Prognostic Scoring System. Breast cancer treatment was interrupted and venetoclax and azacitidine therapy was started. Complete hematologic response was achieved after three cycles. However, multiple lung metastases from the breast cancer remained. The patient then underwent umbilical cord blood transplantation. She has maintained complete remission of MDS as of 1 year post-transplantation, without serious complications. Lung metastatic activity on FDG-PET/CT scan also completely disappeared by half a year post-transplantation, and this response has continued as of 1 year post-transplantation. This favorable treatment course suggests the existence of a GVT effect.
异基因造血干细胞移植(allo-HSCT)并非实体瘤的标准治疗方法,因其毒性较高且证据水平不足。然而,这种治疗方法的潜在移植物抗肿瘤(GVT)效应已被讨论。许多病例报告也描述了 allo-HSCT 在血液系统恶性肿瘤和活动性实体瘤患者中的治疗效果。
一名 38 岁女性因复发性乳腺癌伴多发肺转移接受氟维司群和阿贝西利治疗,后被诊断为骨髓增生异常综合征(MDS)伴原始细胞增多 2。根据 2017 年欧洲白血病网风险分层,她被归类为不良风险,根据分子国际预后评分系统,她被归类为极高危。乳腺癌治疗中断,开始使用维奈克拉和阿扎胞苷治疗。三个周期后达到完全血液学缓解。然而,乳腺癌的多个肺转移仍存在。随后,患者接受了脐带血移植。截至移植后 1 年,患者维持 MDS 完全缓解,无严重并发症。移植后半年,FDG-PET/CT 扫描显示肺转移活性完全消失,且该缓解持续至移植后 1 年。这一良好的治疗过程提示存在 GVT 效应。