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Clinical outcomes of myeloid/lymphoid neoplasms with fibroblast growth factor receptor-1 ( FGFR1 ) rearrangement

机译:具有成纤维细胞生长因子受体1(FGFR1)重排的髓样/淋巴样肿瘤的临床结果

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Objective: Myeloid/lymphoid neoplasms with fibroblast growth factor receptor-1 (FGFR1) rearrangement are hematopoietic stem cell disorders with a poor prognosis, but no established standard therapy. Methods: We experienced a patient with T-lymphoblastic lymphoma (LBL) associated with FGFR1 rearrangement who underwent cord blood transplantation, but died of pulmonary complication. We collected the clinical data of patients with FGFR1 rearrangement from the medical literature and analyzed 45 patients, including our patient. Results: The primary diagnoses were myeloproliferative neoplasm (MPN) or myelodysplastic syndromes (MDS) in 14 and acute leukemia or LBL in 31. In MPN and MDS patients, the cumulative incidence of transformation to blast phase (BP) at 12 months was 46.2%. The 1-year overall survival (OS) from diagnosis in all cases was 43.1%. With regard to the impact of treatment response on survival, the achievement of complete response with a landmark at 2 months after diagnosis of BP was associated with a superior OS (40.0% vs. 26.0% P?=?0.011 for 1-year OS from BP). Allogeneic hematopoietic stem cell transplantation (HSCT) was performed in 13 patients, and the 1-year OS from allogeneic HSCT was 61.5%. The hazard ratio for mortality was 0.34 (95% CI, 0.08–1.51, P?=?0.15) for allogeneic HSCT treated as a time-dependent covariate, which suggests that allogeneic HSCT may confer a clinical benefit. Conclusion : The further accumulation of clinical data is needed to determine the optimal therapeutic approach for these neoplasms.
机译:目的:具有成纤维细胞生长因子受体1(FGFR1)重排的骨髓/淋巴瘤是造血干细胞疾病,预后较差,但尚无标准治疗方法。方法:我们经历了一名患有FGFR1重排的T淋巴细胞淋巴瘤(LBL)患者,该患者接受了脐血移植,但死于肺部并发症。我们从医学文献中收集了FGFR1重排患者的临床数据,并分析了45例患者,包括我们的患者。结果:主要诊断为14例骨髓增生性肿瘤(MPN)或骨髓增生异常综合征(MDS)和31例急性白血病或LBL。在MPN和MDS患者中,在12个月时转化为成胚期(BP)的累积发生率为46.2% 。在所有情况下,从诊断得出的1年总生存率(OS)为43.1%。关于治疗反应对生存的影响,在诊断出BP后2个月达到完全反应并达到标志性目标与较高的OS相关(从1年OS的40.0%对比26.0%P = 0.011)。 BP)。异基因造血干细胞移植(HSCT)进行了13例患者,异基因HSCT的1年OS为61.5%。将异基因HSCT视为时间依赖性协变量,死亡率的危险比为0.34(95%CI,0.08-1.51,P <=?0.15),这表明异基因HSCT可能带来临床益处。结论:需要进一步积累临床数据,以确定这些肿瘤的最佳治疗方法。

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