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伊马替尼时代耐药慢性髓性白血病中 与 突变的共存:是否存在相关性?

Co-existence of and mutation in resistant chronic myeloid leukemia in the imatinib era: Is there a correlation?

作者信息

Frikha Rim, Turki Fatma, Kassar Olfa, Elloumi Moez, Kamoun Hassen

机构信息

Department of Medical Genetics, University Hospital of Sfax, Sfax, Tunisia.

Department of Haematology, University Hospital of Sfax, Sfax, Tunisia.

出版信息

J Oncol Pharm Pract. 2021 Oct;27(7):1784-1789. doi: 10.1177/1078155221991646. Epub 2021 Feb 10.

Abstract

INTRODUCTION

Diagnoses of myeloproliferative disorder is based on molecular marker. Chronic Myeloid Leukemia and Myeloproliferative neoplasms were considered mutually exclusive and co-existence of BCR/ABL1 and JAK2 mutation is a rare phenomenon.

CASE REPORT

Here, we present two cases of co-existence of BCR-ABL and JAK2V617F positivity. We characterize the course of the disease, mainly the minimal residual disease. The two cases was initially managed as Chronic Myeloid Leukemia and treated by TKI inhibitors. The first one was diagnosed in 2010. He started the first line of TKI, and then switched to second line without obtaining a major molecular response. Hence he was tested for JAK2V617F mutation and positivity was diagnosed. The second patient showed Chronic Myeloid Leukemia phenotype with coexistence of BCR/ABL1 and JAK2 mutation at diagnosis. Molecular monitoring reveals a high BCR-ABL1 transcript level (20%) at the last follow-up (12 months).

DISCUSSION

Ours results highlight that JAK2V617F/BCR-ABL double positivity may be a potential marker of resistance in Chronic Myeloid Leukemia and clonal molecular analysis is mandatory to elucidate the mechanism. Moreover, the combination of JAK and TKI inhibitors might be effective and potentially be guided by molecular monitoring of minimal residual disease.

摘要

引言

骨髓增殖性疾病的诊断基于分子标志物。慢性髓性白血病和骨髓增殖性肿瘤曾被认为是相互排斥的,而BCR/ABL1和JAK2突变同时存在是一种罕见现象。

病例报告

在此,我们呈现两例BCR-ABL和JAK2V617F均呈阳性的病例。我们描述了疾病的进程,主要是微小残留病。这两例最初均按照慢性髓性白血病进行处理,并接受酪氨酸激酶抑制剂(TKI)治疗。第一例于2010年确诊。他开始使用一线TKI,之后转换为二线治疗,但未获得主要分子学缓解。因此,对他进行了JAK2V617F突变检测,结果确诊为阳性。第二例患者在诊断时表现为慢性髓性白血病表型,同时存在BCR/ABL1和JAK2突变。分子监测显示,在最后一次随访(12个月)时,BCR-ABL1转录水平较高(20%)。

讨论

我们的结果表明,JAK2V617F/BCR-ABL双阳性可能是慢性髓性白血病耐药的一个潜在标志物,克隆分子分析对于阐明其机制必不可少。此外,JAK抑制剂和TKI抑制剂联合使用可能有效,并且可能需要通过微小残留病的分子监测来指导。

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