The experience of relapsed Burkitt lymphoma treatment with targeted drugs and autologous/allogeneic stem cell transplantation

T. T. Valiev, A. A. Khachatryan, S. V. Goryacheva, N. Batmanova, K. Kirgizov, S. Varfolomeeva
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Abstract

The use of high-effective, multicomponent, risk-adopted chemoimmunotherapy schemes in children with Burkitt lymphoma reached advanced long-term progression-free survival over 90 % even for high risk patients. Unfortunately, conventional therapeutic strategy for relapsed/refractory disease is not accepted, and the effectiveness of carboplat‑in- and gemcitabine-containing regimens is unsatisfactory. Clinical experience of rituximab, ibrutinib and nivolumab in combination with polychemotherapy and own clinical case of successful relapsed Burkitt lymphoma treatment with targeted therapy and following autologous and allogeneic hematopoietic stem cell transplantation are presented. Proposed program could achieve a complete remission of Burkitt lymphoma, but short-term after allogeneic hematopoietic stem cell transplantation diagnosed T-cell precursor acute lymphoblastic leukemia became fatal for the patient.
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使用靶向药物和自体/异体干细胞移植治疗复发伯基特淋巴瘤的经验
在儿童伯基特淋巴瘤患者中采用高效、多组分、风险适应性化疗免疫疗法方案后,即使是高危患者的长期无进展生存率也超过了90%。遗憾的是,复发/难治性疾病的传统治疗策略并不被接受,含卡铂和吉西他滨方案的疗效并不令人满意。本文介绍了利妥昔单抗、伊布替尼和尼沃单抗联合多化疗的临床经验,以及用靶向疗法和自体及异体造血干细胞移植成功治疗复发伯基特淋巴瘤的临床病例。所提出的方案可使伯基特淋巴瘤完全缓解,但在异基因造血干细胞移植后短期内,诊断出的T细胞前体急性淋巴细胞白血病对患者来说却成为致命的疾病。
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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