Zhu Yang-Min, Wu Zhao, Tan You-Ping, Du Yuan-Yuan, Liu Zhi, Ou Rui-Ming, Liu Shuang, Pu Cheng-Fei, Jiang Jing, Wang Jin-Ping, Xiao Lei, Zhang Qing
Department of Hematology, Guangdong No. 2 Provincial People's Hospital, Guangzhou Innovative Cellular Therapeutics Co., Ltd. (Formerly SiDanSai Biotechnology Co., Ltd), Shanghai, China.
Medicine (Baltimore). 2016 Dec;95(51):e5676. doi: 10.1097/MD.0000000000005676.
The presence of the Philadelphia chromosome (Ph) in acute lymphoblastic leukemia (ALL) has been associated with a high risk of disease relapse and a poor prognosis. Allogeneic hematopoietic stem cell transplantation (HSCT) is an established treatment for adults with Ph-positive ALL, but relapse remains the primary cause of treatment failure, and is associated with an extremely poor prognosis. The emergence of resistance to tyrosine kinase inhibitors (TKIs) poses a challenge for patients with disease relapses after initial treatment with TKI-containing regimens.
Two patients with TKI-resistant recurrent Ph-positive ALL.
Ph-positive ALL.
Anti-CD19 CAR T-cell infusion.
One patient's bone marrow blasts decreased significantly, and the other reached negative minimal residual disease (MRD). However, we first recorded the development of new-onset acute graft-versus-host disease (aGVHD) after anti-CD19 CAR T-cell infusion in a patient who received allogeneic HSCT. Our 2 case reports also demonstrate the efficacy of anti-CD19 CAR T-cell therapy in the treatment of TKI-resistant Ph-positive ALL.
Our report suggests that anti-CD19 CAR T-cell therapy may be a promising option for the treatment of relapsed Ph-positive ALL after conventional chemotherapy or allogeneic HSCT. However, caution is due given the possibility of the adverse effects of cytokine release syndrome (CRS)-induced aGVHD for patients receiving allogeneic HSCT.