Chidamide in combination with chemotherapy in refractory and relapsed T lymphoblastic lymphoma/leukemia.
Wei GuanYu JingLiping DouMaoquan WangYang XiaoLi YuPublished in: Leukemia & lymphoma (2019)
Chidamide, a novel histone deacetylase inhibitor, has exerted effects in T-cell tumors through various mechanisms. Seventeen patients with refractory or relapsed T-cell acute lymphoblastic lymphoma/leukemia (T-LBL/ALL) received Chidamide combined with chemotherapy as salvage treatment. Historical data was analyzed as comparison as chemotherapy group. Complete response (CR) rate and overall response rate (ORR) of Chidamide + chemotherapy group were higher than that of chemotherapy group after one course. Chidamide + chemotherapy group had a better progress-free survival (PFS) compared to chemotherapy group. No difference in overall survival (OS) was observed. Grade 3/4 nonhematological adverse events (>10%) of patients in Chidamide + chemotherapy group included febrile neutropenia (64.7%), drug-induced liver failure (17.6%), decreased fibrinogen (11.8%), sepsis (11.8%), pneumonitis (11.8%), and oral mucositis (11.8%). This study demonstrates that Chidamide included regimen may be a new treatment strategy with an acceptable safety profile for refractory or relapsed T-LBL/ALL patients but requires further investigation.
Keyphrases
- locally advanced
- liver failure
- chemotherapy induced
- acute myeloid leukemia
- drug induced
- diffuse large b cell lymphoma
- end stage renal disease
- newly diagnosed
- acute lymphoblastic leukemia
- ejection fraction
- liver injury
- multiple myeloma
- rectal cancer
- histone deacetylase
- hepatitis b virus
- squamous cell carcinoma
- hodgkin lymphoma
- acute kidney injury
- prognostic factors
- idiopathic pulmonary fibrosis
- extracorporeal membrane oxygenation
- respiratory failure
- mechanical ventilation
- urinary tract infection