Yu Qiuxia, Wang Gaoxiang, Wang Jue, Zhang Wei, Meng Li, Cao Yang
Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, People's Republic of China.
Cancer Manag Res. 2022 Apr 21;14:1507-1514. doi: 10.2147/CMAR.S353022. eCollection 2022.
Philadelphia chromosome positive B cell lymphoblastic lymphoma (Ph+ B-LBL) is an extremely rare disease. We report a 27-year-old patient diagnosed with primary testicular and cutaneous Ph+ B-LBL without bone marrow involvement. The CCCG-LBL-2016 regimen (https://clinicaltrials.gov/ct2/show/NCT02845882) was initially administered due to the fast pathological diagnosis as B-LBL that was first obtained. To identify potential therapeutic targets, RNA sequencing (RNAseq) was also performed on lymph node specimens as a part of the routine diagnostic workup in our center. Unexpectedly, IKZF1 deletions and BCR-ABL1 fusion transcripts were detected. Based on these results, we retrospectively performed fluorescence in situ hybridization (FISH) for BCR/ABL1 rearrangements in the same lymph node specimen, and a 70% positive signal was detected. The patient subsequently received the CCCG-LBL-2016 protocol combined with the BCR-ABL tyrosine kinase inhibitor (TKI) dasatinib, along with prophylactic intrathecal infusion. Then, the patient underwent TBI-based haploidentical (haplo) allogeneic hematopoietic stem cell transplantation (haplo-allo-HSCT) as consolidation following the achievement of remission and continued taking dasatinib as maintenance therapy. The patient was still in complete remission 1 year after diagnosis. This case indicates that the detection of potential molecular targets, especially those targets that can be pharmacologically treated, such as BCR/ABL1 fusion transcripts, is of important value to both LBL diagnosis and therapeutic strategy choices. FISH, reverse transcriptase polymerase chain reaction (RT-PCR) and/or RNAseq should be routinely carried out in lymphoma specimens to depict its genetic landscape for the further execution of a precise therapy strategy.
费城染色体阳性B细胞淋巴母细胞淋巴瘤(Ph+ B-LBL)是一种极其罕见的疾病。我们报告了一名27岁的患者,被诊断为原发性睾丸和皮肤Ph+ B-LBL,无骨髓受累。由于最初快速病理诊断为B-LBL,首先给予CCCG-LBL-2016方案(https://clinicaltrials.gov/ct2/show/NCT02845882)。为了确定潜在的治疗靶点,作为我们中心常规诊断检查的一部分,还对淋巴结标本进行了RNA测序(RNAseq)。出乎意料的是,检测到IKZF1缺失和BCR-ABL1融合转录本。基于这些结果,我们对同一淋巴结标本进行了BCR/ABL1重排的回顾性荧光原位杂交(FISH),检测到70%的阳性信号。该患者随后接受了CCCG-LBL-2016方案联合BCR-ABL酪氨酸激酶抑制剂(TKI)达沙替尼治疗,并进行了预防性鞘内注射。然后,患者在达到缓解后接受了基于全身照射(TBI)的单倍体同基因(haplo)异基因造血干细胞移植(haplo-allo-HSCT)作为巩固治疗,并继续服用达沙替尼作为维持治疗。诊断后1年患者仍处于完全缓解状态。该病例表明,潜在分子靶点的检测,尤其是那些可以进行药物治疗的靶点,如BCR/ABL1融合转录本,对LBL诊断和治疗策略选择均具有重要价值。应在淋巴瘤标本中常规进行FISH、逆转录聚合酶链反应(RT-PCR)和/或RNAseq,以描绘其基因图谱,从而进一步实施精确的治疗策略。