Characteristics and therapeutic approaches for patients diagnosed with T-ALL/LBL exhibiting t(8;14)(q24;q11)/TCRA/D:MYC translocation.
Xian ZhangTong WangYang ZhangFang WangJiaqi ChenJingbo NiRuijuan SunZhijie WeiGailing ZhangWenqian LiJingjing LiPeihua LuPublished in: Leukemia & lymphoma (2023)
T-acute lymphoblastic leukemia/lymphoma (T-ALL/LBL) patients with t(8;14)(q24;q11)/TCRA/D::MYC translocation represent a rare subgroup, with an aggressive course. In our retrospective analysis of 14 patients, all were identified during refractory or relapsed stages (5 primary tumor, 9 relapse). Notably, extramedullary invasion was detected in most patients. Four exhibited STIL::TAL1 translocation, and six demonstrated CDKN2A/B gene loss. The therapeutic outcomes were notably poor for all seven patients who received only chemotherapy or allogeneic hematopoietic stem cell transplantation (HSCT); all eventually succumbed to the disease with a median OS of 3 months. In the application of CD7 CAR-T therapy in six patients, five achieved CR. Of the four patients who underwent HSCT following CAR-T therapy, all have remained disease-free. The prognosis for T-ALL/LBL patients with t(8;14) translocation remains bleak, but interventions involving CD7 CAR-T may offer a potential pathway to CR. HSCT following CAR-T could be a viable strategy for long-term survival.
Keyphrases
- acute lymphoblastic leukemia
- end stage renal disease
- newly diagnosed
- allogeneic hematopoietic stem cell transplantation
- prognostic factors
- peritoneal dialysis
- type diabetes
- risk assessment
- randomized controlled trial
- gene expression
- squamous cell carcinoma
- stem cells
- transcription factor
- patient reported outcomes
- skeletal muscle
- adipose tissue
- metabolic syndrome
- genome wide
- diffuse large b cell lymphoma
- insulin resistance
- dna methylation
- radiation therapy
- cross sectional
- locally advanced
- hematopoietic stem cell
- genome wide identification