Recommendations on prevention of infections during chimeric antigen receptor T-cell and bispecific antibody therapy in multiple myeloma

被引:43
作者
Mohan, Meera [1 ]
Chakraborty, Rajshekhar [2 ]
Bal, Susan [3 ]
Nellore, Anoma [4 ]
Baljevic, Muhamed [5 ]
D'Souza, Anita [1 ]
Pappas, Peter G. [4 ]
Berdeja, Jesus G. [6 ]
Callander, Natalie [7 ]
Costa, Luciano J. [3 ]
机构
[1] Med Coll Wisconsin, Div Hematol Oncol, Milwaukee, WI USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, Multiple Myeloma & Amyloidosis Program, New York, NY USA
[3] Univ Alabama Birmingham, Div Hematol & Med Oncol, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Div Infect Dis, Birmingham, AL USA
[5] Vanderbilt Ingram Canc Ctr, Div Hematol Oncol, Nashville, TN USA
[6] Sarah Cannon Res Inst, Nashville, TN USA
[7] Univ Wisconsin, Dept Med, Div Hematol & Oncologye, Madison, WI USA
关键词
bispecific T-cell; chimeric antigen receptor T-cell; immunotherapy; infection; multiple myeloma; INTRAVENOUS IMMUNOGLOBULIN; CILTACABTAGENE AUTOLEUCEL; BCMA; COMPLICATIONS; 1ST-IN-HUMAN; PROPHYLAXIS; SURVIVAL; RISK;
D O I
10.1111/bjh.18909
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chimeric antigen receptor T (CAR T) cell and bispecific antibody therapies have shown unprecedented efficacy in heavily pretreated patients with multiple myeloma (MM). However, their use is associated with a significant risk of severe infections, which can be attributed to various factors such as hypogammaglobulinemia, neutropenia, lymphopenia, T-cell exhaustion, cytokine-release syndrome and immune-effector cell-associated neurotoxicity syndrome. As these therapies have been recently approved by regulatory agencies, it is crucial to establish practical guidelines for infection monitoring and prevention until robust data from prospective clinical trials become available. To address this issue, a panel of experienced investigators from the Academic Consortium to Overcome Multiple Myeloma through Innovative Trials (COMMIT) developed consensus recommendations for mitigating infections associated with CAR T-cell and bispecific antibody therapies in MM patients.
引用
收藏
页码:736 / 746
页数:11
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