Suppr超能文献

伴有细胞形态学急变的慢性髓性白血病患者的预后因素和临床结局。

Prognostic Factors and Clinical Outcomes in Patients with Blast Phase Chronic Myeloid Leukemia.

出版信息

Clin Lab. 2024 Jul 1;70(7). doi: 10.7754/Clin.Lab.2024.231206.

Abstract

BACKGROUND

Given the low incidence of patients with advanced chronic myeloid leukemia (CML), comprehensive clinical characteristics and outcomes of cohort studies of patients diagnosed with blast phase chronic myeloid leukemia (BP-CML) are limited. We examined the clinical features of blast phase CML, including the TKI selection, treatment response, and whether they have had hematopoietic stem cell transplantation (HSCT) or not.

METHODS

We performed a retrospective cohort study, including BP-CML patients diagnosed in our center from January 2013 to December 2022. Clinical features, treatment therapy, and overall survival (OS) were investigated.

RESULTS

Out of the 11 patients, 2 were myeloid type, eight patients were B-lymphoid, and one was T-lymphoid. Four patients suffered from chromosome abnormalities. Four patients were identified with BCR-ABL1 kinase domain mutation, including T315I, E255K, M244v, and E279K. The overall CR, CRi, PR, and MLFS rates were 9%, 54%, 27%, and 9%, respectively. The median follow-up was 21 months (9.5 - 33 months). At the end of the follow-up time, seven patients died. CML patients with lymphoids tended to get a better OS than patients with a type of myeloid, but the difference was not statistically significant (p > 0.05). Patients who received HSCT had an improved OS by two years compared to those who had not received HSCT.

CONCLUSIONS

The prognosis of BP-CML patients was poor. Given the rarity of BP-CML and the limitation of clinical trial data, large-scale multi-center prospective studies are urgently needed to confirm and improve the treatment of patients with BP-CML in the future.

摘要

背景

鉴于晚期慢性髓性白血病(CML)患者的发病率较低,因此对诊断为急变期 CML(BP-CML)的患者的队列研究的综合临床特征和结局的了解有限。我们检查了 BP-CML 的临床特征,包括 TKI 的选择、治疗反应,以及他们是否进行了造血干细胞移植(HSCT)。

方法

我们进行了一项回顾性队列研究,纳入了 2013 年 1 月至 2022 年 12 月在我们中心诊断为 BP-CML 的患者。研究了临床特征、治疗方法和总生存期(OS)。

结果

11 例患者中,2 例为髓样型,8 例为 B 淋巴细胞型,1 例为 T 淋巴细胞型。4 例患者伴有染色体异常。4 例患者存在 BCR-ABL1 激酶结构域突变,包括 T315I、E255K、M244v 和 E279K。总的完全缓解(CR)、CR 伴不完全血液学恢复(CRi)、部分缓解(PR)和白血病无进展生存(MLFS)率分别为 9%、54%、27%和 9%。中位随访时间为 21 个月(9.5-33 个月)。随访结束时,7 例患者死亡。淋巴细胞型 CML 患者的 OS 倾向于优于髓样型患者,但差异无统计学意义(p>0.05)。接受 HSCT 的患者的 OS 比未接受 HSCT 的患者延长了两年。

结论

BP-CML 患者的预后较差。鉴于 BP-CML 的罕见性和临床试验数据的局限性,迫切需要进行大规模多中心前瞻性研究,以在未来证实和改善 BP-CML 患者的治疗。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验