Baig Muhammad U, Rytting Michael, Roth Michael, Morani Ajaykumar C, Nunez Cesar, Lin Pei, Cuglievan Branko
Departments of Pediatrics.
Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX.
J Pediatr Hematol Oncol. 2021 Oct 1;43(7):e991-e996. doi: 10.1097/MPH.0000000000002050.
Overall survival of adolescents with relapsed T-cell lymphoblastic lymphoma (T-LL) remains poor with limited options for salvage therapy. The BCL-2 inhibitor venetoclax combined with hypomethylating agents like decitabine, has shown favorable responses in elderly patients with acute myeloid leukemia.
We present the case of a 19-year-old adolescent with stage III relapsed and refractory T-LL who did not respond to 3 lines of salvage therapy. The patient was treated with venetoclax and decitabine and achieved a dramatic response.
This case highlights the potential clinical activity of venetoclax and decitabine in relapsed T-LL.
复发的T细胞淋巴母细胞淋巴瘤(T-LL)青少年患者的总生存期仍然很差,挽救治疗选择有限。BCL-2抑制剂维奈托克联合地西他滨等去甲基化药物,已在老年急性髓系白血病患者中显示出良好疗效。
我们报告了一例19岁的III期复发难治性T-LL青少年患者,该患者对3线挽救治疗均无反应。该患者接受维奈托克和地西他滨治疗后取得了显著疗效。
该病例突出了维奈托克和地西他滨在复发T-LL中的潜在临床活性。