第二代ALK抑制剂布加替尼、大剂量化疗和异体干细胞移植联合治疗难治性间变性大细胞淋巴瘤1例报告及文献复习

Giulia Caddeo, Cristina Tecchio, Matteo Chinello, Rita Balter, Ada Zaccaron, Virginia Vitale, Vincenza Pezzella, Elisa Bonetti, Marta Pillon, Elisa Carraro, Lara Mussolin, Simone Cesaro
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引用次数: 1

摘要

难治性或复发性间变性大细胞淋巴瘤(ALCL)患儿的治疗仍然是一个重大挑战。除了传统的化疗和干细胞移植,新的治疗选择,如抗cd30药物和间变性淋巴瘤激酶(ALK)抑制剂,最近已经在这种情况下被引入。在ALK抑制剂中,只有第一代分子克里唑替尼被批准用于儿科,而第二代分子,如布加替尼,仍在研究中。在这里,我们报告了一个13岁的男孩被诊断为IV期ALCL,对一线常规化疗和抗CD30抗体-药物偶联brentuximab-vedotin二线治疗难以耐受,在常规大剂量化疗和第二代ALK抑制剂布加替尼联合治疗后最终获得缓解。选择后者是因为它能够穿透血脑屏障,因为它持续累及患者的脑神经系统。随后,患者接受了来自非亲属供体的同种异体造血干细胞移植(HSCT),使用全身照射的清髓调节。移植后24个月,患者完全缓解,活得很好。提供了关于ALK抑制剂在ALCL患者中使用的最新综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Refractory Anaplastic Large Cell Lymphoma Rescued by the Combination of the Second-Generation ALK Inhibitor Brigatinib, High-dose Chemotherapy and Allogeneic Stem Cell Transplantation: A Case Report and Review of the Literature.

The treatment of pediatric patients with refractory or relapsed anaplastic large cell lymphoma (ALCL) is still a major challenge. In addition to conventional chemotherapy and stem cell transplantation, new therapeutic options such as anti-CD30 drugs and anaplastic lymphoma kinase (ALK) inhibitors have been recently introduced in this setting. Among ALK inhibitors, only the first-generation molecule crizotinib is approved for pediatric use, while second-generation molecules, such as brigatinib, are still under investigation. Here we report the case of a 13-year-old boy diagnosed with stage IV ALCL, refractory to first-line conventional chemotherapy and second-line therapy with the anti CD30 antibody-drug conjugate brentuximab-vedotin, who finally achieved remission after a combination of conventional high-dose chemotherapy and the second-generation ALK inhibitor brigatinib. The latter was chosen for its ability to penetrate through the blood-brain barrier, due to the persistent involvement of the patient's cerebral nervous system. The remission was then consolidated with an allogeneic hematopoietic stem cell transplantation (HSCT) from an unrelated donor using myeloablative conditioning with total body irradiation. At 24 months after HSCT, the patient is in complete remission, alive and well. An updated review regarding the use of ALK inhibitors in ALCL patients is provided.

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