4.7 Article

Unity brings strength: Combination of CAR-T cell therapy and HSCT

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CANCER LETTERS
卷 549, 期 -, 页码 -

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ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2022.215721

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  1. Science and Technology Innovation Special Project of Social Undertakings and People's Livelihood Security of Chongqing [CSTC2016shms-ztzx10003]
  2. Improvement of Scientific and Technological Innovation Youth Cultivation Special Project of Army Medical University [2021XQN16]
  3. Scientific Research Cultivation Project for Undergraduates of Army Medical University [202021]
  4. Special Funding for the Frontiers of Military Medical Basics [2018YQYLY002]

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With the rapid development of therapies, hemopoietic stem cell transplantation (HSCT) and chimeric antigen receptor T (CAR-T) cell therapy have emerged as promising treatments for hematological malignancies. However, disease relapse, complications, and side effects continue to pose challenges. This review aims to explore ways to maximize the benefits of each therapy and improve patient prognosis.
With the rapid revolution of therapies, hemopoietic stem cell transplantation (HSCT) has become a widely promoted treatment for hematological malignancies. High-dose chemotherapy (HDCT) followed by autologous blood cell (ABC) transplantation is a standard procedure for patients with primary relapse B-cell non-Hodgkin lymphoma (NHL) and multiple myeloma (MM), and allogeneic HSCT is one of the few treatments for patients with acute leukemia. However, refractory and recurrent disease has a negative impact on disease-free survival (DFS) for patients after HSCT. Furthermore, complications such as GVHD and infection significantly impair the quality of life and life expectancy of patients who receive allogeneic HSCT. The promising efficacy of chimeric antigen receptor T (CAR-T) cell therapy for relapsed or refractory B-cell acute lymphoblast leukemia (ALL) has offered hope for patients with R/R hematological malignancies. However, the long-term survival of patients after CAR-T cell therapy is also threatened by recurrent disease, and relapse occurs in half of patients who achieve remission. In addition, the rapid proliferation of CAR-T cells will cause damage to the balance of the immune system, leading to cytokine release syndrome (CRS) and CAR-T cell-related encephalopathy syndrome (CRES). Although therapeutic regimens such as IL-6 pathway blockers have obvious impacts on the side effects related to CAR-T cell therapy, there are still reports of patient deaths in past clinical trials. Based on the characteristics of HSCT and CAR-T cell therapy, it is unclear whether there is a better combination of cutting-edge immune cell therapy and traditional transplantation to improve the prognosis of patients. This review focuses on the possible ways to take full advantage of each therapy in the treatment of hematological malignancies.

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