Kono Asuka, Tanaka Keisuke, Shimada Tomohito, Bando Kana, Takahata Atsushi, Koi Satoshi, Yamamoto Masahide, Mori Takehiko, Toyota Shigeo
Department of Hematology, Yokosuka Kyosai Hospital.
Department of Hematology, Tokyo Medical and Dental University (TMDU).
Rinsho Ketsueki. 2024;65(3):158-163. doi: 10.11406/rinketsu.65.158.
Although alectinib is effective for relapsed or refractory ALK-positive anaplastic large cell lymphoma (ALCL) and has a favorable safety profile, its role as a bridging therapy for allogeneic hematopoietic stem cell transplantation (allo-HSCT) and the role of allo-HSCT itself in this setting are unknown. A 35-year-old man with ALK-positive ALCL experienced relapse after first-line therapy with CHOP. Brentuximab vedotin led to partial response and high-dose chemotherapy combined with autologous HSCT was performed. However, disease progressed 15 months after transplantation, and alectinib was initiated. Complete response (CR) was achieved after three months of treatment, and alectinib was continued for 5 months. After cessation of alectinib, allogeneic bone marrow transplantation from an HLA 1-locus mismatched unrelated donor was performed after conditioning with fludarabine, busulfan, and total body irradiation. GVHD prophylaxis consisted of tacrolimus and short-term methotrexate. The post-transplant course was unremarkable except for grade I acute GVHD. The lymphoma has not recurred for 2 years after allo-HSCT without resuming alectinib. The clinical course of our case suggests that alectinib bridging therapy and allo-HSCT are effective in relapsed/refractory ALK-positive ALCL.
尽管阿来替尼对复发或难治性ALK阳性间变性大细胞淋巴瘤(ALCL)有效且安全性良好,但其作为异基因造血干细胞移植(allo-HSCT)的桥接治疗的作用以及allo-HSCT本身在这种情况下的作用尚不清楚。一名35岁的ALK阳性ALCL男性在接受CHOP一线治疗后复发。 Brentuximab vedotin导致部分缓解,并进行了高剂量化疗联合自体HSCT。然而,移植后15个月疾病进展,开始使用阿来替尼。治疗三个月后达到完全缓解(CR),并持续使用阿来替尼5个月。停用阿来替尼后,在使用氟达拉滨、白消安和全身照射进行预处理后,接受了来自HLA 1位点错配无关供体的异基因骨髓移植。移植物抗宿主病(GVHD)预防包括他克莫司和短期甲氨蝶呤。除I级急性GVHD外,移植后过程无异常。在allo-HSCT后2年,淋巴瘤未复发,未恢复使用阿来替尼。我们病例的临床过程表明,阿来替尼桥接治疗和allo-HSCT对复发/难治性ALK阳性ALCL有效。