Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Lund, Sweden.
Division of Clinical Genetics, Lund University, Lund, Sweden.
Genes Chromosomes Cancer. 2024 Aug;63(8):e23261. doi: 10.1002/gcc.23261.
Chromosomal rearrangements involving Janus kinase 2 (JAK2) are rare but recurrent findings in lymphoid or myeloid neoplasia. Detection of JAK2 fusion genes is important as patients with aberrantly activated JAK2 may benefit from treatment with tyrosine kinase inhibitors such as ruxolitinib. Here, we report a novel fusion gene between the transcriptional co-repressor-encoding gene transducin-like enhancer of split 3 (TLE3) and JAK2 in a patient initially diagnosed with chronic eosinophilic leukemia with additional mutations in PTPN11 and NRAS. The patient was successfully treated with the JAK2 inhibitor ruxolitinib for 8 months before additional somatic mutations were acquired and the disease progressed into an acute lymphoblastic T-cell leukemia/lymphoma. The present case shows similarities to previously reported cases with PCM1::JAK2 and BCR::JAK2 with regard to disease phenotype and response to ruxolitinib, and importantly, provides an example that also patients harboring other JAK2 fusion genes may benefit from treatment with JAK2 inhibitors.
涉及 Janus 激酶 2 (JAK2) 的染色体重排是淋巴样或髓样肿瘤中罕见但反复出现的发现。检测 JAK2 融合基因很重要,因为异常激活的 JAK2 患者可能受益于酪氨酸激酶抑制剂(如鲁索利替尼)的治疗。在这里,我们报告了一名最初诊断为伴有额外 PTPN11 和 NRAS 突变的慢性嗜酸性粒细胞白血病患者中 TLE3 和 JAK2 之间的新型融合基因。该患者成功接受 JAK2 抑制剂鲁索利替尼治疗 8 个月,随后获得额外的体细胞突变,疾病进展为急性淋巴细胞 T 细胞白血病/淋巴瘤。本病例在疾病表型和对鲁索利替尼的反应方面与先前报道的 PCM1::JAK2 和 BCR::JAK2 病例相似,重要的是,提供了一个示例,即其他 JAK2 融合基因的患者也可能受益于 JAK2 抑制剂的治疗。