Long-term remission of primary refractory ALK-positive anaplastic large cell lymphoma after allogeneic hematopoietic stem cell transplantation.

IF 0.9 Q4 HEMATOLOGY Journal of Clinical and Experimental Hematopathology Pub Date : 2022-09-28 Epub Date: 2022-06-22 DOI:10.3960/jslrt.22003
Masahiro Miyazaki, Satoshi Ichikawa, Yasushi Onishi, Noriko Fukuhara, Eijiro Furukawa, Koichi Onodera, Hisayuki Yokoyama, Ryo Ichinohasama, Hideo Harigae
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Abstract

ALK-positive anaplastic large cell lymphoma (ALK+ ALCL) has a favorable prognosis in general; however, some cases are resistant to chemotherapy, which leads to a poor clinical outcome. We herein report the case of a 32-year-old male with aggressive ALK+ ALCL who presented with hemorrhage from a large tumor in the duodenum and multiple tumors in the lungs, mediastinum, and peritoneal cavity. Although induction chemotherapy resulted in a marked reduction of the tumor lesions, premature progression with massive pulmonary infiltration and central nervous system invasion occurred immediately after the completion of chemotherapy. The patient was then promptly treated with brentuximab vedotin (BV) and high-dose methotrexate, which resulted in complete remission. Subsequently, he successfully underwent allogeneic hematopoietic stem cell transplantation (allo-HSCT) from an unrelated donor and has been healthy and did not relapse for more than 3 years after transplantation without any additional therapy. Allo-HSCT may be a promising treatment option for ALK+ ALCL due to its graft-versus-lymphoma effect. In addition, molecular targeting agents, such as BV, may be promising as a bridging therapy before allo-HSCT to achieve disease remission.

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同种异体造血干细胞移植后原发性难治性alk阳性间变性大细胞淋巴瘤的长期缓解。
ALK阳性间变性大细胞淋巴瘤(ALK+ ALCL)一般预后良好;然而,一些病例对化疗有耐药性,导致临床结果不佳。我们在此报告一例32岁男性侵袭性ALK+ ALCL患者,其表现为十二指肠大肿瘤出血,肺部、纵隔和腹膜腔多发肿瘤。虽然诱导化疗导致肿瘤病变明显减少,但化疗完成后立即出现大量肺部浸润和中枢神经系统侵犯的过早进展。随后,患者立即接受brentuximab vedotin (BV)和大剂量甲氨蝶呤治疗,完全缓解。随后,他成功地接受了来自非亲属供体的同种异体造血干细胞移植(alloo - hsct),并且在移植后没有任何额外治疗的情况下健康且没有复发超过3年。由于其移植物抗淋巴瘤作用,同种异体造血干细胞移植可能是ALK+ ALCL的一种有希望的治疗选择。此外,分子靶向药物,如BV,可能有希望作为同种异体造血干细胞移植前的桥接治疗,以实现疾病缓解。
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来源期刊
CiteScore
2.00
自引率
6.70%
发文量
25
审稿时长
11 weeks
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